Lytgobi drug information

2 DOSAGE AND ADMINISTRATION Confirm the presence of an FGFR2 gene fusion or other rearrangement prior to initiation of treatment with LYTGOBI. ( 2.1 ) Recommended dose is 20 mg orally (five 4 mg tablets or one 16 mg tablet and one 4 mg tablet) once daily until disease progression or unacceptable toxicity occurs. ( 2.2 ) Swallow tablet whole, with or without food. ( 2.2 ) 2.1 Patient Selection Select patients for the treatment of unresectable, locally advanced or metastatic intrahepatic cholangiocarcinoma with LYTGOBI based on the presence of an FGFR2 gene fusion or rearrangement [see Clinical Studies (14.1) ]. An FDA-approved test for detection of FGFR2 gene fusions or other rearrangements in patients with unresectable, locally advanced, or metastatic intrahepatic cholangiocarcinoma for selecting patients for treatment with LYTGOBI is not available. 2.2 Recommended Dosage The recommended dosage of LYTGOBI is 20 mg (five 4 mg tablets or one 16 mg and one 4 mg tablet) taken orally once daily until disease progression or unacceptable toxicity occurs. Take LYTGOBI with or without food at approximately the same time each day [see Clinical Pharmacology (12.3) ] . Swallow tablets whole. Do not crush, chew, split, or dissolve tablets. If the patient misses a dose of LYTGOBI for more than 12 hours or if vomiting occurs, resume dosing with the next scheduled dose. 2.3 Dosage Modification for Adverse Reactions The recommended dose reductions for adverse reactions are provided in Table 1 . Table 1: Recommended Dose Reductions for LYTGOBI for Adverse Reactions Dose Reduction Recommended Dosage First dose reduction 16 mg (four 4 mg tablets or one 16 mg tablet) orally once daily Second dose reduction Permanently discontinue LYTGOBI if unable to tolerate 12 mg orally once daily. 12 mg (three 4 mg tablets) orally once daily Recommended dosage modifications for adverse reactions are provided in Table 2 . Table 2: Recommended Dosage Modifications for LYTGOBI Adverse Reactions Adverse Reaction Severity LYTGOBI Dosage Modifications a Severity as defined by National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE version 4.03). Retinal Pigment Epithelial Detachment (RPED) [see Warnings and Precautions (5.1) ] Not applicable Continue LYTGOBI at the current dose and continue periodic ophthalmic evaluation: If resolving within 14 days, continue LYTGOBI at the current dose. If not resolving within 14 days, withhold LYTGOBI until resolving; then resume LYTGOBI at previous or a lower dose. Hyperphosphatemia [see Warnings and Precautions (5.2) ] Serum phosphate ≥5.5 - ≤7 mg/dL Continue LYTGOBI at the current dose and initiate phosphate lowering therapy. Monitor serum phosphate weekly. Serum phosphate >7 - ≤10 mg/dL Initiate or adjust phosphate lowering therapy. Monitor serum phosphate weekly and Dose reduce LYTGOBI to next lower dose - If the serum phosphate resolves to ≤7 mg/dL within 2 weeks after dose reduction, continue at this reduced dose. - If serum phosphate is not ≤7 mg/dL within 2 weeks, further reduce LYTGOBI to the next lower dose. - If serum phosphate is not ≤7 mg/dL within 2 weeks after the second dose reduction, withhold LYTGOBI until serum phosphate is ≤7 mg/dL and resume at the dose prior to suspending. Serum phosphate >10 mg/dL Initiate or adjust phosphate lowering therapy and monitor serum phosphate weekly and Withhold LYTGOBI until phosphate is ≤7 mg/dL and resume LYTGOBI at the next lower dose. - Permanently discontinue LYTGOBI if serum phosphate is not ≤7 mg/dL within 2 weeks following 2 dose interruptions and reductions. Other Adverse Reactions Grade 3 a Withhold LYTGOBI until toxicity resolves to Grade 1 or baseline, then resume LYTGOBI - for hematological toxicities resolving within 1 week, at the dose prior to suspending. - for other adverse reactions, at next lower dose. Grade 4 a Permanently discontinue LYTGOBI Table text from source: Table 1: Recommended Dose Reductions for LYTGOBI for Adverse Reactions | Dose Reduction | Recommended Dosage | First dose reduction | 16 mg (four 4 mg tablets or one 16 mg tablet) orally once daily | Second dose reductionPermanently discontinue LYTGOBI if unable to tolerate 12 mg orally once daily. | 12 mg (three 4 mg tablets) orally once daily Table 2: Recommended Dosage Modifications for LYTGOBI Adverse Reactions | Adverse Reaction | Severity | LYTGOBI Dosage Modifications | a Severity as defined by National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE version 4.03). | Retinal Pigment Epithelial Detachment (RPED) [see Warnings and Precautions (5.1)] | Not applicable | Continue LYTGOBI at the current dose and continue periodic ophthalmic evaluation: If resolving within 14 days, continue LYTGOBI at the current dose.If not resolving within 14 days, withhold LYTGOBI until resolving; then resume LYTGOBI at previous or a lower dose. | Hyperphosphatemia [see Warnings and Precautions (5.2)] | Serum phosphate ≥5.5 - ≤7 mg/dL | Continue LYTGOBI at the current dose and initiate phosphate lowering therapy. Monitor serum phosphate weekly. | Serum phosphate >7 - ≤10 mg/dL | Initiate or adjust phosphate lowering therapy. Monitor serum phosphate weekly andDose reduce LYTGOBI to next lower dose -If the serum phosphate resolves to ≤7 mg/dL within 2 weeks after dose reduction, continue at this reduced dose.-If serum phosphate is not ≤7 mg/dL within 2 weeks, further reduce LYTGOBI to the next lower dose. -If serum phosphate is not ≤7 mg/dL within 2 weeks after the second dose reduction, withhold LYTGOBI until serum phosphate is ≤7 mg/dL and resume at the dose prior to suspending. | Serum phosphate >10 mg/dL | Initiate or adjust phosphate lowering therapy and monitor serum phosphate weekly andWithhold LYTGOBI until phosphate is ≤7 mg/dL and resume LYTGOBI at the next lower dose. -Permanently discontinue LYTGOBI if serum phosphate is not ≤7 mg/dL within 2 weeks following 2 dose interruptions and reductions. | Other Adverse Reactions | Grade 3a | Withhold LYTGOBI until toxicity resolves to Grade 1 or baseline, then resume LYTGOBI -for hematological toxicities resolving within 1 week, at the dose prior to suspending.-for other adverse reactions, at next lower dose. | Grade 4a | Permanently discontinue LYTGOBI

3 DOSAGE FORMS AND STRENGTHS Tablets: 4 mg, round, white, film-coated tablets debossed with “4MG” on one side, and “FBN” on the other side. 16 mg, round, white, film-coated tablets debossed with “16MG” on one side and “FBN” on the other side. Tablets: 4 mg and 16 mg ( 3 )

4 CONTRAINDICATIONS None. None ( 4 )

5 WARNINGS AND PRECAUTIONS Ocular Toxicity: LYTGOBI can cause retinal pigment epithelial detachment (RPED). Perform a comprehensive ophthalmological examination including optical coherence tomography (OCT) prior to initiation of therapy, every 2 months for the first 6 months, and every 3 months thereafter and urgently at any time for visual symptoms. ( 2.3 , 5.1 ) Hyperphosphatemia and Soft Tissue Mineralization: Increases in phosphate levels can cause hyperphosphatemia leading to soft tissue mineralization, calcinosis, nonuremic calciphylaxis and vascular calcification. Monitor for hyperphosphatemia and withhold, reduce the dose, or permanently discontinue based on duration and severity of hyperphosphatemia. ( 2.3 , 5.2 ) Embryo-Fetal Toxicity: Can cause fetal harm. Advise patients of reproductive potential of the potential risk to the fetus and to use effective contraception. ( 5.3 , 8.1 , 8.3 ) 5.1 Ocular Toxicity Retinal Pigment Epithelial Detachment (RPED) LYTGOBI can cause RPED, which may cause symptoms such as blurred vision. Among 318 patients who received LYTGOBI across clinical trials [see Adverse Reactions (6.1) ] where ophthalmologic monitoring did not routinely include optical coherence tomography (OCT), RPED occurred in 9% of patients. The median time to first onset of RPED was 40 days. RPED led to dose interruption of LYTGOBI in 1.3% of patients, dose reduction in 1.6% of patients, and permanent discontinuation in 0.3% of patients. Perform a comprehensive ophthalmological examination, including OCT of the macula, prior to initiation of therapy, every 2 months for the first 6 months, and every 3 months thereafter. For onset of visual symptoms, refer patients for ophthalmologic evaluation urgently, with follow-up every 3 weeks until resolution or discontinuation of LYTGOBI. Withhold or reduce the dose of LYTGOBI as recommended [see Dosage and Administration (2.3) ]. Dry Eye/Corneal Keratitis Among 318 patients who received LYTGOBI across clinical trials [see Adverse Reactions (6.1) ] , dry eye occurred in 15% of patients. Treat patients with ocular demulcents as needed. 5.2 Hyperphosphatemia and Soft Tissue Mineralization LYTGOBI can cause hyperphosphatemia leading to soft tissue mineralization, calcinosis, nonuremic calciphylaxis, and vascular calcification. Increases in phosphate levels are a pharmacodynamic effect of LYTGOBI [see Clinical Pharmacology (12.2) ] . Among 318 patients who received LYTGOBI across clinical trials [see Adverse Reactions (6.1) ] , hyperphosphatemia was reported in 88% of patients based on laboratory values above the upper limit of normal. The median time to onset of hyperphosphatemia was 5 days (range 3-117). Phosphate binders were received by 77% of patients who received LYTGOBI. Monitor for hyperphosphatemia throughout treatment. Initiate a low phosphate diet and phosphate lowering therapy when serum phosphate level is ≥5.5 mg/dL. For serum phosphate levels >7 mg/dL, initiate or intensify phosphate lowering therapy and dose reduce, withhold, or permanently discontinue LYTGOBI based on duration and severity of hyperphosphatemia [see Dosage and Administration (2.3) ] . 5.3 Embryo-Fetal Toxicity Based on findings in an animal study and its mechanism of action, LYTGOBI can cause fetal harm when administered to a pregnant woman. Oral administration of futibatinib to pregnant rats during the period of organogenesis caused fetal malformations, fetal growth retardation, and embryo-fetal death at maternal exposures lower than the human exposure at the clinical dose of 20 mg based on area under the curve (AUC). Advise pregnant women of the potential risk to the fetus. Advise female patients of reproductive potential to use effective contraception during treatment with LYTGOBI and for 1 week after the last dose of LYTGOBI. Advise males with female partners of reproductive potential to use effective contraception during treatment with LYTGOBI and for 1 week after the last dose [see Use in Specific Populations (8.1 , 8.3) ] .

6 ADVERSE REACTIONS The following adverse reactions are discussed elsewhere in the labeling: Ocular Toxicity [see Warnings and Precautions (5.1) ] Hyperphosphatemia and Soft Tissue Mineralization [see Warnings and Precautions (5.2) ] Most common (≥20%) adverse reactions were nail toxicity, musculoskeletal pain, constipation, diarrhea, fatigue, dry mouth, alopecia, stomatitis, abdominal pain, dry skin, arthralgia, dysgeusia, dry eye, nausea, decreased appetite, urinary tract infection, palmar-plantar erythrodysesthesia syndrome, and vomiting. ( 6.1 ) Most common laboratory abnormalities (≥20%) were increased phosphate, increased creatinine, decreased hemoglobin, increased glucose, increased calcium, decreased sodium, decreased phosphate, increased alanine aminotransferase, increased alkaline phosphatase, decreased lymphocytes, increased aspartate aminotransferase, decreased platelets, increased activated partial thromboplastin time, decreased leukocytes, decreased albumin, decreased neutrophils, increased creatine kinase, increased bilirubin, decreased glucose, increased prothrombin international normalized ratio, and decreased potassium. ( 6.1 ) To report SUSPECTED ADVERSE REACTIONS, contact Taiho Oncology Inc. at 1-844-878-2446 or FDA at 1-800-FDA-1088 or http://www.fda.gov/medwatch . 6.1 Clinical Trials Experience Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in practice. The pooled safety population described in the WARNINGS AND PRECAUTIONS reflect exposure to LYTGOBI as a single agent at 20 mg orally once daily in 318 patients including 145 patients with cholangiocarcinoma and 173 patients with other advanced solid tumors. Among 318 patients who received LYTGOBI, 37% were exposed for 6 months or longer and 13% were exposed for greater than 12 months. Previously Treated, Unresectable Locally Advanced or Metastatic Intrahepatic Cholangiocarcinoma The safety of LYTGOBI was evaluated in Study TAS-120-101, which included 103 patients with previously treated, unresectable locally advanced or metastatic intrahepatic cholangiocarcinoma harboring FGFR2 fusions or other gene rearrangements [see Clinical Studies (14.1) ] . Patients were treated with LYTGOBI 20 mg orally once daily until disease progression or unacceptable toxicity. The median duration of treatment was 9 months (range: 0.5 - 25 months). Serious adverse reactions occurred in 39% of patients receiving LYTGOBI. Serious adverse reactions in ≥2% of patients who received LYTGOBI included pyrexia (3.9%), gastrointestinal hemorrhage (3.9%), ascites (2.9%), musculoskeletal pain (2.9%), and bile duct obstruction (2.9%). Permanent discontinuation due to an adverse reaction occurred in 4.9% of patients who received LYTGOBI. Adverse reactions requiring permanent discontinuation of LYTGOBI in one patient each were esophagitis, oral dysesthesia, bile duct obstruction, dizziness, and anemia. Dosage interruptions due to an adverse reaction occurred in 66% of patients who received LYTGOBI. Adverse reactions requiring dosage interruption in ≥5% of patients included hyperphosphatemia, palmar-plantar erythrodysesthesia syndrome, increased alanine aminotransferase, increased aspartate aminotransferase, and fatigue. Dose reductions due to an adverse reaction occurred in 58% of patients who received LYTGOBI. Adverse reactions requiring dosage reductions in ≥2% of patients who received LYTGOBI included hyperphosphatemia, palmar-plantar erythrodysesthesia syndrome, fatigue, increased alanine aminotransferase, increased aspartate aminotransferase, nail toxicity, and stomatitis. The most common (≥20%) adverse reactions were nail toxicity, musculoskeletal pain, constipation, diarrhea, fatigue, dry mouth, alopecia, stomatitis, abdominal pain, dry skin, arthralgia, dysgeusia, dry eye, nausea, decreased appetite, urinary tract infection, palmar-plantar erythrodysesthesia syndrome, and vomiting. The most common laboratory abnormalities (≥20%) were increased phosphate, increased creatinine, decreased hemoglobin, increased glucose, increased calcium, decreased sodium, decreased phosphate, increased alanine aminotransferase, increased alkaline phosphatase, decreased lymphocyte, increased aspartate aminotransferase, decreased platelets, increased activated partial thromboplastin time, decreased leukocytes, decreased albumin, decreased neutrophils, increased creatine kinase, increased bilirubin, decreased glucose, increased prothrombin international normalized ratio, and decreased potassium. Table 3 summarizes the adverse reactions in TAS-120-101. Table 4 summarizes laboratory abnormalities in TAS-120-101. Table 3: Adverse Reactions (≥15%) in Patients Receiving LYTGOBI in Study TAS-120-101 LYTGOBI N = 103 Adverse Reaction All Grades a (%) Grade 3 (%) a Graded per NCI CTCAE 4.03. b Includes nail toxicity, nail disorder, nail discoloration, nail dystrophy, nail hypertrophy, nail infection, nail pigmentation, onychalgia, onychoclasis, onycholysis, onychomadesis, onychomycosis, and paronychia. c Includes diarrhea, colitis, and gastroenteritis. d Includes stomatitis, glossitis, mouth ulceration, mucosal inflammation, pharyngeal inflammation, and tongue ulceration. e Includes abdominal pain, abdominal discomfort, abdominal pain upper, gastrointestinal pain, and hepatic pain. f Includes vomiting and hematemesis. g Includes fatigue and asthenia. h Includes back pain, bone pain, musculoskeletal chest pain, musculoskeletal discomfort, musculoskeletal pain, musculoskeletal stiffness, myalgia, neck pain, non-cardiac chest pain, pain in extremity, and spinal pain. i Includes arthralgia and arthritis. j Includes dry eye, keratitis, lacrimation increased, photokeratitis, punctate keratitis, and ulcerative keratitis. k Includes dysgeusia, ageusia, and taste disorder. l Includes urinary tract infection, cystitis, and dysuria. Skin and subcutaneous tissue disorders Nail toxicity b 47 1.9 Alopecia 34 0 Dry skin 29 0 Palmar-plantar erythrodysesthesia syndrome 21 4.9 Gastrointestinal disorders Constipation 39 0 Diarrhea c 39 1 Dry mouth 35 0 Stomatitis d 30 6 Abdominal pain e 30 2.9 Nausea 24 1.9 Vomiting f 20 1 General disorders Fatigue g 37 8 Metabolism and nutrition disorders Decreased appetite 23 2.9 Musculoskeletal and connective tissue disorder Musculoskeletal pain h 43 3.9 Arthralgia i 25 0 Eye disorders Dry eye j 25 1 Nervous system disorders Dysgeusia k 25 0 Infections Urinary tract infection l 23 2.9 Investigations Weight decreased 18 3.9 Clinically relevant adverse reactions occurring in ≤15% of patients included retinal pigment epithelial detachment (RPED, 7.8%). Table 4: Select Laboratory Abnormalities (≥10%) Worsening from Baseline in Patients Receiving LYTGOBI in TAS-120-101 LYTGOBI N = 103 Laboratory Abnormality a All Grades b (%) Grades 3 or 4 (%) a Graded per NCI CTCAE 4.03. b Percentages are based on patients with data at both baseline and at least one post-baseline data value. c NCI CTCAE 4.03 does not define grades for increased phosphate. Laboratory value shift table categories were used to assess increased phosphorus levels (Grades ≥3 defined as >7 mg/dL). d Graded based on comparison to upper limit of normal. Hematology Decreased hemoglobin 52 6 Decreased lymphocytes 46 10 Decreased platelets 42 1 Decreased leukocytes 33 1.1 Decreased neutrophils 31 1.6 Chemistry Increased phosphate c 97 39 Increased creatinine d 58 0 Increased glucose 52 4.9 Increased calcium 51 1.2 Decreased sodium 51 15 Decreased phosphate 50 20 Increased alanine aminotransferase 50 7 Increased alkaline phosphatase 47 4.9 Increased aspartate aminotransferase 46 13 Decreased albumin 31 2.4 Increased creatine kinase 31 5 Increased bilirubin 28 0 Decreased glucose 25 0 Decreased potassium 22 2.1 Increased potassium 16 2 Coagulation Increased activated partial thromboplastin time 36 8 Increased prothrombin international normalized ratio 25 0 Table text from source: Table 3: Adverse Reactions (≥15%) in Patients Receiving LYTGOBI in Study TAS-120-101 | | LYTGOBI N = 103 | Adverse Reaction | All Grades a (%) | Grade 3 (%) | a Graded per NCI CTCAE 4.03. b Includes nail toxicity, nail disorder, nail discoloration, nail dystrophy, nail hypertrophy, nail infection, nail pigmentation, onychalgia, onychoclasis, onycholysis, onychomadesis, onychomycosis, and paronychia. c Includes diarrhea, colitis, and gastroenteritis. d Includes stomatitis, glossitis, mouth ulceration, mucosal inflammation, pharyngeal inflammation, and tongue ulceration. e Includes abdominal pain, abdominal discomfort, abdominal pain upper, gastrointestinal pain, and hepatic pain. f Includes vomiting and hematemesis. g Includes fatigue and asthenia. h Includes back pain, bone pain, musculoskeletal chest pain, musculoskeletal discomfort, musculoskeletal pain, musculoskeletal stiffness, myalgia, neck pain, non-cardiac chest pain, pain in extremity, and spinal pain. i Includes arthralgia and arthritis. j Includes dry eye, keratitis, lacrimation increased, photokeratitis, punctate keratitis, and ulcerative keratitis. k Includes dysgeusia, ageusia, and taste disorder. l Includes urinary tract infection, cystitis, and dysuria. | Skin and subcutaneous tissue disorders | Nail toxicity b | 47 | 1.9 | Alopecia | 34 | 0 | Dry skin | 29 | 0 | Palmar-plantar erythrodysesthesia syndrome | 21 | 4.9 | Gastrointestinal disorders | Constipation | 39 | 0 | Diarrhea c | 39 | 1 | Dry mouth | 35 | 0 | Stomatitis d | 30 | 6 | Abdominal pain e | 30 | 2.9 | Nausea | 24 | 1.9 | Vomiting f | 20 | 1 | General disorders | Fatigue g | 37 | 8 | Metabolism and nutrition disorders | Decreased appetite | 23 | 2.9 | Musculoskeletal and connective tissue disorder | Musculoskeletal pain h | 43 | 3.9 | Arthralgia i | 25 | 0 | Eye disorders | Dry eye j | 25 | 1 | Nervous system disorders | Dysgeusia k | 25 | 0 | Infections | Urinary tract infection l | 23 | 2.9 | Investigations | Weight decreased | 18 | 3.9 Table 4: Select Laboratory Abnormalities (≥10%) Worsening from Baseline in Patients Receiving LYTGOBI in TAS-120-101 | | LYTGOBI N = 103 | Laboratory Abnormality a | All Grades b (%) | Grades 3 or 4 (%) | a Graded per NCI CTCAE 4.03. b Percentages are based on patients with data at both baseline and at least one post-baseline data value. c NCI CTCAE 4.03 does not define grades for increased phosphate. Laboratory value shift table categories were used to assess increased phosphorus levels (Grades ≥3 defined as >7 mg/dL). d Graded based on comparison to upper limit of normal. | Hematology | Decreased hemoglobin | 52 | 6 | Decreased lymphocytes | 46 | 10 | Decreased platelets | 42 | 1 | Decreased leukocytes | 33 | 1.1 | Decreased neutrophils | 31 | 1.6 | Chemistry | Increased phosphate c | 97 | 39 | Increased creatinine d | 58 | 0 | Increased glucose | 52 | 4.9 | Increased calcium | 51 | 1.2 | Decreased sodium | 51 | 15 | Decreased phosphate | 50 | 20 | Increased alanine aminotransferase | 50 | 7 | Increased alkaline phosphatase | 47 | 4.9 | Increased aspartate aminotransferase | 46 | 13 | Decreased albumin | 31 | 2.4 | Increased creatine kinase | 31 | 5 | Increased bilirubin | 28 | 0 | Decreased glucose | 25 | 0 | Decreased potassium | 22 | 2.1 | Increased potassium | 16 | 2 | Coagulation | Increased activated partial thromboplastin time | 36 | 8 | Increased prothrombin international normalized ratio | 25 | 0

7 DRUG INTERACTIONS Strong CYP3A inhibitors : Avoid concomitant use. ( 7.1 ) Strong CYP3A inducers : Avoid concomitant use. ( 7.1 ) 7.1 Effect of Other Drugs on LYTGOBI Strong CYP3A Inhibitors Avoid concomitant use of strong CYP3A inhibitors with LYTGOBI. Futibatinib is a CYP3A substrate [see Clinical Pharmacology (12.3) ] . Concomitant use of a strong CYP3A inhibitor increases futibatinib exposure [see Clinical Pharmacology (12.3) ] , which may increase the risk of adverse reactions. Strong CYP3A Inducers Avoid concomitant use of strong CYP3A inducers with LYTGOBI. Futibatinib is a CYP3A substrate [see Clinical Pharmacology (12.3) ] . Concomitant use of a strong CYP3A inducer decreases futibatinib exposure [see Clinical Pharmacology (12.3) ] , which may reduce the effectiveness of LYTGOBI.

8 USE IN SPECIFIC POPULATIONS Lactation: Advise not to breastfeed. ( 8.2 ) 8.1 Pregnancy Risk Summary Based on findings in an animal study and its mechanism of action, LYTGOBI can cause fetal harm or loss of pregnancy when administered to a pregnant woman [see Clinical Pharmacology (12.1) ] . There are no available data on the use of LYTGOBI in pregnant women. Oral administration of futibatinib to pregnant rats during the period of organogenesis at maternal plasma exposures below the human exposure at the clinical dose of 20 mg resulted in fetal malformations, fetal growth retardation, and embryo-fetal death ( see Data ). Advise pregnant women of the potential risk to a fetus. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. Data Animal Data Once daily oral administration of futibatinib to pregnant rats during the period of organogenesis resulted in 100% embryofetal mortality due to post-implantation loss at doses ≥10 mg/kg (approximately 5 times the recommended clinical dose of 20 mg based on body surface area, BSA). Fetal survival was unaffected at 0.5 mg/kg per day; however, once daily oral administration of futibatinib at the 0.5 mg/kg dose level (approximately 0.2 times the recommended clinical dose of 20 mg based on BSA) resulted in reduced mean fetal body weight and an increase in fetal skeletal and visceral malformations, major blood vessel variations, and reduced ossification. 8.2 Lactation Risk Summary There are no data on the presence of futibatinib or its metabolites in human milk or their effects on either the breastfed child or on milk production. Because of the potential for serious adverse reactions from LYTGOBI in breastfed children, advise women not to breastfeed during treatment and for 1 week after the last dose. 8.3 Females and Males of Reproductive Potential LYTGOBI can cause fetal harm when administered to a pregnant woman [see Use in Specific Populations (8.1) ] . Pregnancy Testing Verify pregnancy status of females of reproductive potential prior to initiating LYTGOBI [see Use in Specific Populations (8.1) ] . Contraception Females Advise females of reproductive potential to use effective contraception during treatment with LYTGOBI and for 1 week after the last dose. Males Advise males with female partners of reproductive potential or who are pregnant to use effective contraception during treatment with LYTGOBI and for 1 week after the last dose. 8.4 Pediatric Use The safety and effectiveness of LYTGOBI have not been established in pediatric patients. Animal Toxicity Data In 4- or 13-week repeat-dose toxicology studies in adult rats and dogs, findings included increased inorganic phosphorus and calcium in plasma, ectopic mineralization in various organs and tissues, and lesions in bone/cartilage at futibatinib exposures lower than the human exposure at the clinical dose of 20 mg. Findings in rats also included corneal lesions. Evidence of recovery in rats and dogs was observed four weeks after cessation of dosing except for the ectopic mineralization. 8.5 Geriatric Use Of the 103 patients treated with LYTGOBI in Study TAS-120-101, 22% were 65 years or older. Based on available data, no overall differences in safety or effectiveness of LYTGOBI have been observed between patients 65 years of age and older and younger adult patients. 8.7 Hepatic Impairment There are limited data in patients treated with LYTGOBI with total bilirubin >1.5🞨 ULN, and patients with cholangiocarcinoma with total bilirubin >3🞨 ULN were excluded from enrollment in clinical trials. Patients with cirrhosis and total bilirubin >1.5🞨 ULN to 3🞨 ULN may have the potential for increased adverse reactions compared to patients with normal hepatic function due to higher unbound futibatinib exposure [see Clinical Pharmacology (12.3) ] .

8.1 Pregnancy Risk Summary Based on findings in an animal study and its mechanism of action, LYTGOBI can cause fetal harm or loss of pregnancy when administered to a pregnant woman [see Clinical Pharmacology (12.1) ] . There are no available data on the use of LYTGOBI in pregnant women. Oral administration of futibatinib to pregnant rats during the period of organogenesis at maternal plasma exposures below the human exposure at the clinical dose of 20 mg resulted in fetal malformations, fetal growth retardation, and embryo-fetal death ( see Data ). Advise pregnant women of the potential risk to a fetus. In the U.S. general population, the estimated background risk of major birth defects and miscarriage in clinically recognized pregnancies is 2% to 4% and 15% to 20%, respectively. Data Animal Data Once daily oral administration of futibatinib to pregnant rats during the period of organogenesis resulted in 100% embryofetal mortality due to post-implantation loss at doses ≥10 mg/kg (approximately 5 times the recommended clinical dose of 20 mg based on body surface area, BSA). Fetal survival was unaffected at 0.5 mg/kg per day; however, once daily oral administration of futibatinib at the 0.5 mg/kg dose level (approximately 0.2 times the recommended clinical dose of 20 mg based on BSA) resulted in reduced mean fetal body weight and an increase in fetal skeletal and visceral malformations, major blood vessel variations, and reduced ossification.

8.4 Pediatric Use The safety and effectiveness of LYTGOBI have not been established in pediatric patients. Animal Toxicity Data In 4- or 13-week repeat-dose toxicology studies in adult rats and dogs, findings included increased inorganic phosphorus and calcium in plasma, ectopic mineralization in various organs and tissues, and lesions in bone/cartilage at futibatinib exposures lower than the human exposure at the clinical dose of 20 mg. Findings in rats also included corneal lesions. Evidence of recovery in rats and dogs was observed four weeks after cessation of dosing except for the ectopic mineralization.

8.5 Geriatric Use Of the 103 patients treated with LYTGOBI in Study TAS-120-101, 22% were 65 years or older. Based on available data, no overall differences in safety or effectiveness of LYTGOBI have been observed between patients 65 years of age and older and younger adult patients.

11 DESCRIPTION Futibatinib is a kinase inhibitor with the chemical name 1-[(3 S )-3-{4-amino-3-[(3,5-dimethoxyphenyl)ethynyl]- 1 H -pyrazolo[3,4- d ]pyrimidin-1-yl}pyrrolidin-1-yl]prop-2-en-1-one. Futibatinib has a molecular formula of C 22 H 22 N 6 O 3 and molecular mass of 418.45 g/mole. Futibatinib has the following chemical structure: Futibatinib is a white crystalline powder. The solubility of futibatinib is pH dependent with decreasing solubility with increasing pH, being practically insoluble at pH 3 or higher. Futibatinib is insoluble in water and poorly soluble in common solvents. LYTGOBI is supplied as 4 mg and 16 mg film-coated tablets for oral administration. Each tablet contains inactive ingredients of corn starch, crospovidone, hydroxypropyl cellulose, lactose monohydrate, magnesium stearate, mannitol, microcrystalline cellulose, and sodium lauryl sulfate. The film coating material contains hypromellose, magnesium stearate, polyethylene glycol, and titanium dioxide. Futibatinib Str

12 CLINICAL PHARMACOLOGY 12.1 Mechanism of Action Futibatinib is a small molecule kinase inhibitor of FGFR 1, 2, 3, and 4 with IC 50 values of less than 4 nM. Futibatinib covalently binds FGFR. Constitutive FGFR signaling can support the proliferation and survival of malignant cells. Futibatinib inhibited FGFR phosphorylation and downstream signaling and decreased cell viability in cancer cell lines with FGFR alterations including FGFR fusions/rearrangements, amplifications, and mutations. Futibatinib demonstrated anti-tumor activity in mouse and rat xenograft models of human tumors with activating FGFR genetic alterations. 12.2 Pharmacodynamics Serum Phosphate Futibatinib increased serum phosphate levels due to FGFR inhibition. Serum phosphate increased with increasing futibatinib exposure across the dose range of 4 to 24 mg orally once daily (0.2 to 1.2 times the recommended dose), with increased risk of hyperphosphatemia at higher futibatinib exposure. Cardiac Electrophysiology At four times the approved recommended dose, LYTGOBI does not cause clinically significant QTc interval prolongation. 12.3 Pharmacokinetics The pharmacokinetics of futibatinib were observed at steady state in patients with advanced solid tumors unless otherwise specified at the approved recommended dosage and are presented as mean (%CV) unless otherwise specified. Futibatinib maximum concentration (C max ) is 144 mg/mL (50%) and systemic exposure (AUC) is 790 ng∙hr/mL (45%). Futibatinib exposure (AUC) increased in dose proportional manner over the dose range from 4 to 24 mg orally once daily (0.2 to 1.2 times the approved recommended dosage). No accumulation is observed at steady state. Absorption Futibatinib median (min, max) time to maximum plasma concentration (T max ) is 2 hours (1.2, 23 hours). Effect of Food Futibatinib C max decreased by 42% with no clinically significant differences in AUC in healthy subjects following administration of LYTGOBI with a high-fat and high-calorie meal (900 to 1000 calories with approximately 50% from fat). Distribution The apparent (oral) volume of distribution is 66 L (18%). Futibatinib plasma protein binding is 95%, primarily to albumin and α1-acid glycoprotein. Elimination Futibatinib elimination half-life is 2.9 hours (27%) with an apparent (oral) clearance of 20 L/hr (23%). Metabolism Futibatinib is primarily metabolized by CYP3A and to a lesser extent by CYP2C9 and CYP2D6. Unchanged futibatinib accounts for 59% of radioactivity in plasma in healthy subjects. Excretion Following a single oral dose of radiolabeled futibatinib 20 mg, approximately 91% of the dose was recovered in feces and 9% in urine. Specific Populations No clinically significant differences in the pharmacokinetics of futibatinib were observed based on age (18 to 82 years), sex, race (White, Asian, and African American), body weight (36 to 152 kg), or creatinine clearance (CLcr) 30 to 89 mL/min (estimated by Cockcroft-Gault). The effect of CLcr of 15 to 29 mL/min or renal dialysis in end-stage renal disease (CLcr <15 mL/min) on futibatinib pharmacokinetics is unknown. Patients with Hepatic Impairment No clinically significant differences in the pharmacokinetics of futibatinib were observed in subjects with mild hepatic impairment (total bilirubin ≤ ULN and AST > ULN or total bilirubin >1 to 1.5🞨 ULN and any AST or Child-Pugh A) or moderate to severe hepatic impairment (Child-Pugh B to C) with total bilirubin < 1.5 🞨 ULN. The effect of moderate to severe hepatic impairment without cirrhosis on futibatinib pharmacokinetics is unknown. In subjects with cirrhosis and total bilirubin >1 to 1.5🞨 ULN, mean unbound futibatinib AUC and C max increased by 1.7-fold relative to subjects with normal hepatic function. In subjects with cirrhosis and total bilirubin >1.5🞨 ULN, mean unbound futibatinib AUC and C max increased by 3.2-fold and 2.4-fold, respectively, compared to values in healthy subjects. Drug Interaction Studies Clinical Studies Strong CYP3A inhibitors : Futibatinib C max increased by 1.5-fold and AUC by 1.4-fold following concomitant use of multiple doses of itraconazole (strong CYP3A inhibitor). Strong CYP3A inducers : Futibatinib C max decreased by 53% and AUC by 64% following concomitant use of multiple doses of rifampin (strong CYP3A inducer). Other Drugs : No clinically significant differences in futibatinib pharmacokinetics were observed with concomitant use of multiple doses of quinidine (P-gp inhibitor) or lansoprazole (proton pump inhibitor). No clinically significant differences in the pharmacokinetics of the following drugs were observed following concomitant use of multiple doses of LYTGOBI: midazolam (CYP3A substrate), digoxin (P-pg substrate), and rosuvastatin (BCRP substrate). In Vitro Studies CYP Enzymes : Futibatinib does not inhibit CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, or CYP2D6 and does not induce CYP1A2 or CYP2B6. Transporter Systems : Futibatinib is not a substrate of OATP1B1 or OATP1B3. Futibatinib does not inhibit OAT1, OAT3, OCT2, OATP1B1, OATP1B3, MATE1, or MATE2K.

12.1 Mechanism of Action Futibatinib is a small molecule kinase inhibitor of FGFR 1, 2, 3, and 4 with IC 50 values of less than 4 nM. Futibatinib covalently binds FGFR. Constitutive FGFR signaling can support the proliferation and survival of malignant cells. Futibatinib inhibited FGFR phosphorylation and downstream signaling and decreased cell viability in cancer cell lines with FGFR alterations including FGFR fusions/rearrangements, amplifications, and mutations. Futibatinib demonstrated anti-tumor activity in mouse and rat xenograft models of human tumors with activating FGFR genetic alterations.

12.2 Pharmacodynamics Serum Phosphate Futibatinib increased serum phosphate levels due to FGFR inhibition. Serum phosphate increased with increasing futibatinib exposure across the dose range of 4 to 24 mg orally once daily (0.2 to 1.2 times the recommended dose), with increased risk of hyperphosphatemia at higher futibatinib exposure. Cardiac Electrophysiology At four times the approved recommended dose, LYTGOBI does not cause clinically significant QTc interval prolongation.

12.3 Pharmacokinetics The pharmacokinetics of futibatinib were observed at steady state in patients with advanced solid tumors unless otherwise specified at the approved recommended dosage and are presented as mean (%CV) unless otherwise specified. Futibatinib maximum concentration (C max ) is 144 mg/mL (50%) and systemic exposure (AUC) is 790 ng∙hr/mL (45%). Futibatinib exposure (AUC) increased in dose proportional manner over the dose range from 4 to 24 mg orally once daily (0.2 to 1.2 times the approved recommended dosage). No accumulation is observed at steady state. Absorption Futibatinib median (min, max) time to maximum plasma concentration (T max ) is 2 hours (1.2, 23 hours). Effect of Food Futibatinib C max decreased by 42% with no clinically significant differences in AUC in healthy subjects following administration of LYTGOBI with a high-fat and high-calorie meal (900 to 1000 calories with approximately 50% from fat). Distribution The apparent (oral) volume of distribution is 66 L (18%). Futibatinib plasma protein binding is 95%, primarily to albumin and α1-acid glycoprotein. Elimination Futibatinib elimination half-life is 2.9 hours (27%) with an apparent (oral) clearance of 20 L/hr (23%). Metabolism Futibatinib is primarily metabolized by CYP3A and to a lesser extent by CYP2C9 and CYP2D6. Unchanged futibatinib accounts for 59% of radioactivity in plasma in healthy subjects. Excretion Following a single oral dose of radiolabeled futibatinib 20 mg, approximately 91% of the dose was recovered in feces and 9% in urine. Specific Populations No clinically significant differences in the pharmacokinetics of futibatinib were observed based on age (18 to 82 years), sex, race (White, Asian, and African American), body weight (36 to 152 kg), or creatinine clearance (CLcr) 30 to 89 mL/min (estimated by Cockcroft-Gault). The effect of CLcr of 15 to 29 mL/min or renal dialysis in end-stage renal disease (CLcr <15 mL/min) on futibatinib pharmacokinetics is unknown. Patients with Hepatic Impairment No clinically significant differences in the pharmacokinetics of futibatinib were observed in subjects with mild hepatic impairment (total bilirubin ≤ ULN and AST > ULN or total bilirubin >1 to 1.5🞨 ULN and any AST or Child-Pugh A) or moderate to severe hepatic impairment (Child-Pugh B to C) with total bilirubin < 1.5 🞨 ULN. The effect of moderate to severe hepatic impairment without cirrhosis on futibatinib pharmacokinetics is unknown. In subjects with cirrhosis and total bilirubin >1 to 1.5🞨 ULN, mean unbound futibatinib AUC and C max increased by 1.7-fold relative to subjects with normal hepatic function. In subjects with cirrhosis and total bilirubin >1.5🞨 ULN, mean unbound futibatinib AUC and C max increased by 3.2-fold and 2.4-fold, respectively, compared to values in healthy subjects. Drug Interaction Studies Clinical Studies Strong CYP3A inhibitors : Futibatinib C max increased by 1.5-fold and AUC by 1.4-fold following concomitant use of multiple doses of itraconazole (strong CYP3A inhibitor). Strong CYP3A inducers : Futibatinib C max decreased by 53% and AUC by 64% following concomitant use of multiple doses of rifampin (strong CYP3A inducer). Other Drugs : No clinically significant differences in futibatinib pharmacokinetics were observed with concomitant use of multiple doses of quinidine (P-gp inhibitor) or lansoprazole (proton pump inhibitor). No clinically significant differences in the pharmacokinetics of the following drugs were observed following concomitant use of multiple doses of LYTGOBI: midazolam (CYP3A substrate), digoxin (P-pg substrate), and rosuvastatin (BCRP substrate). In Vitro Studies CYP Enzymes : Futibatinib does not inhibit CYP1A2, CYP2B6, CYP2C8, CYP2C9, CYP2C19, or CYP2D6 and does not induce CYP1A2 or CYP2B6. Transporter Systems : Futibatinib is not a substrate of OATP1B1 or OATP1B3. Futibatinib does not inhibit OAT1, OAT3, OCT2, OATP1B1, OATP1B3, MATE1, or MATE2K.

13 NONCLINICAL TOXICOLOGY 13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility Carcinogenicity studies have not been conducted with futibatinib. Futibatinib was not mutagenic in an in vitro bacterial reverse mutation (Ames) assay. Futibatinib was clastogenic in an in vitro chromosomal aberration assay. Futibatinib was not clastogenic in a rat bone marrow micronucleus assay or a rat DNA damaging (Comet) assay. Dedicated fertility studies with futibatinib have not been conducted.

13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility Carcinogenicity studies have not been conducted with futibatinib. Futibatinib was not mutagenic in an in vitro bacterial reverse mutation (Ames) assay. Futibatinib was clastogenic in an in vitro chromosomal aberration assay. Futibatinib was not clastogenic in a rat bone marrow micronucleus assay or a rat DNA damaging (Comet) assay. Dedicated fertility studies with futibatinib have not been conducted.

14 CLINICAL STUDIES 14.1 Cholangiocarcinoma TAS-120-101 (NCT02052778), a multicenter, open-label, single-arm trial, evaluated the efficacy of LYTGOBI in 103 patients with previously treated, unresectable, locally advanced or metastatic intrahepatic cholangiocarcinoma. The presence of FGFR2 fusions or other rearrangements was determined in 102 enrolled patients (99%) using next generation sequencing (NGS) testing. Qualifying in-frame fusions and other rearrangements were predicted to have a breakpoint within intron 17/exon 18 of the FGFR2 gene leaving the FGFR2 kinase domain intact. Patients received LYTGOBI at a dosage of 20 mg orally once daily until disease progression or unacceptable toxicity. The major efficacy outcome measures were overall response rate (ORR) and duration of response (DoR) as determined by an independent review committee (IRC) according to Response Evaluation Criteria in Solid Tumors (RECIST) v1.1. The trial population characteristics were: Median age was 58 years (range: 22 to 79 years) with 22% of patients ≥65 years, 56% were female, race was: 50% White, 29% Asian, 8% Black or African American, 1% Native Hawaiian or Other Pacific Islander, 13% unknown, baseline Eastern Cooperative Oncology Group (ECOG) performance status of 0 (47%) or 1 (53%). Seventy-eight percent (78%) of patients had in-frame FGFR2 gene fusions and the most commonly identified FGFR2 fusion partner was BICC1 (n=24, 23%). Twenty-two percent (22%) of patients had other FGFR2 rearrangements that may not be in-frame with the partner gene or the partner gene was not identifiable. All patients had received at least 1 prior systemic therapy, 30% had 2 prior lines of therapy, and 23% had 3 or more prior lines of therapy. All patients received a prior platinum-based therapy including 91% with prior gemcitabine/cisplatin. Efficacy results are summarized in Table 5 . The median time to response was 2.5 months (range 0.7 – 7.4 months). Table 5: Efficacy Results in TAS-120-101 Efficacy Parameter LYTGOBI N = 103 a The 95% confidence interval (CI) was calculated using Clopper–Pearson method. b The 95% confidence interval (CI) was constructed based on a log-log transformed CI for the survival function. ORR (95% CI) a 42% (32, 52) Partial response, n (%) 43 (42%) Median DoR (months) (95% CI) b 9.7 (7.6, 17.1) DoR ≥6 months, n (%) 31 (72%) DoR ≥12 months, n (%) 6 (14%) Table text from source: Table 5: Efficacy Results in TAS-120-101 | Efficacy Parameter | LYTGOBI N = 103 | a The 95% confidence interval (CI) was calculated using Clopper–Pearson method. b The 95% confidence interval (CI) was constructed based on a log-log transformed CI for the survival function. | ORR (95% CI)a | 42% (32, 52) | Partial response, n (%) | 43 (42%) | Median DoR (months) (95% CI)b | 9.7 (7.6, 17.1) | DoR ≥6 months, n (%) | 31 (72%) | DoR ≥12 months, n (%) | 6 (14%)

16 HOW SUPPLIED/STORAGE AND HANDLING LYTGOBI tablets are round, white, and film-coated. The 4 mg tablets are debossed with “4MG” on one side, and “FBN” on the other side. The 16 mg tablets are debossed with “16MG” on one side, and “FBN” on the other. Tablets are packaged in blister cards and supplied in child-resistant DosePak ® as follows: 20 mg daily dose: Each carton contains 1 blister card containing a 7-day supply (35 tablets; 4 mg futibatinib per tablet). [NDC-64842-0120-6] 20 mg daily dose: Each carton contains 1 blister card containing a 7-day supply (14 tablets; 7 tablets each of 4 mg and 16 mg futibatinib per tablet). [NDC-64842-0128-8] 16 mg daily dose: Each carton contains 1 blister card containing a 7-day supply (28 tablets; 4 mg futibatinib per tablet). [NDC-64842-0120-5] 16 mg daily dose: Each carton contains 1 blister card containing a 7-day supply (7 tablets; 16 mg futibatinib per tablet). [NDC-64842-0127-7] 12 mg daily dose: Each carton contains 1 blister card containing a 7-day supply (21 tablets; 4 mg futibatinib per tablet). [NDC-64842-0120-4] Store LYTGOBI tablets at room temperature 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C and 30°C (59°F to 86°F). ([see USP Controlled Room Temperature]).

17 PATIENT COUNSELING INFORMATION Advise the patient to read the FDA-approved patient labeling ( Patient Information ). Ocular Toxicity Advise patients that LYTGOBI may cause ocular toxicity including RPED and to immediately inform their healthcare provider if they experience any visual changes [see Warnings and Precautions (5.1) ] . Advise patients to use artificial tears, or hydrating or lubricating eye gels to prevent or treat dry eyes [see Warnings and Precautions (5.1) ] . Hyperphosphatemia and Soft Tissue Mineralization Inform patients that LYTGOBI may cause hyperphosphatemia and soft tissue mineralization and to immediately inform their healthcare provider of any symptoms related to acute change in phosphate levels such as muscle cramps, numbness, or tingling around the mouth [see Warnings and Precautions 5.2) ] . Nail Disorders Advise patients that LYTGOBI may cause nail disorders [see Adverse Reactions (6.1) ]. Embryo-Fetal Toxicity Advise females to inform their healthcare provider if they are pregnant or become pregnant. Inform female patients of the risk to a fetus and potential loss of pregnancy [see Warnings and Precautions (5.3) and Use in Specific Populations (8.1) ]. Advise females of reproductive potential to use effective contraception while on LYTGOBI and for 1 week after the last dose [see Use in Specific Populations (8.3) ]. Advise males with female partners of reproductive potential or who are pregnant to use effective contraception during treatment and for 1 week after receiving the last dose of LYTGOBI [see Use in Specific Populations (8.3) ]. Lactation Advise patients not to breastfeed during treatment with LYTGOBI and for 1 week after the last dose [see Use in Specific Populations (8.2) ] . Administration Instruct patients to not crush, chew, split or dissolve tablets. Instruct patients if they miss a dose by 12 or more hours or if they vomit after taking a dose, resume dosing with the next scheduled dose. Extra tablets should not be taken to make up for the missed dose [see Dosage and Administration (2.2) ]. Drug Interactions Advise patients to inform their healthcare providers of all concomitant medications, including prescription medicines, over-the-counter drugs, and herbal products. Advise patients to avoid grapefruit products during treatment with LYTGOBI [see Drug Interactions (7.1) ] .

Manufactured for: Taiho Pharmaceutical Co., Ltd. Japan Distributed by: Taiho Oncology, Inc. Princeton, NJ 08540 USA LYTGOBI is a trademark of Taiho Pharmaceutical Co., Ltd. U.S. Patent Nos. 9,108,973, 10,434,103, and 11,833,151 © 2025 Taiho Oncology, Inc. All rights reserved

This Patient Information has been approved by the U.S. Food and Drug Administration. Revised: 10/2025 PATIENT INFORMATION LYTGOBI (light-GOH-bee) (futibatinib) tablets What is LYTGOBI? LYTGOBI is a prescription medicine that is used to treat adults with bile duct cancer (intrahepatic cholangiocarcinoma) that has spread or cannot be removed by surgery: who have already received a previous treatment, and whose tumor has a certain type of abnormal "FGFR2” gene. Your healthcare provider will test your cancer for a certain type of abnormal FGFR2 gene and make sure that LYTGOBI is right for you. It is not known if LYTGOBI is safe and effective in children. Before you take LYTGOBI, tell your healthcare provider about all of your medical conditions, including if you: have vision or eye problems. are pregnant or plan to become pregnant. LYTGOBI can harm your unborn baby or cause loss of your pregnancy (miscarriage). You should not become pregnant during treatment with LYTGOBI. Females who can become pregnant: Your healthcare provider should do a pregnancy test before you start treatment with LYTGOBI. You should use an effective method of birth control during treatment and for 1 week after your final dose of LYTGOBI. Talk to your healthcare provider about birth control methods that may be right for you. Tell your healthcare provider right away if you become pregnant or think that you may be pregnant. Males with female partners who can become pregnant: You should use effective birth control when sexually active during treatment with LYTGOBI and for 1 week after your last dose of LYTGOBI. are breastfeeding or plan to breastfeed. It is not known if LYTGOBI passes into your breast milk. Do not breastfeed during treatment and for 1 week after your last dose of LYTGOBI. Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. LYTGOBI and other medicines may affect each other causing side effects. LYTGOBI may affect the way other medicines work, and other medicines may affect how LYTGOBI works. How should I take LYTGOBI? Take LYTGOBI exactly as your healthcare provider tells you. Take LYTGOBI 1 time each day with or without food at about the same time each day. You will continue for as long as your healthcare provider tells you to. Swallow LYTGOBI tablets whole. Do not crush, chew, split, or dissolve LYTGOBI tablets. Tell your healthcare provider if you have problems swallowing LYTGOBI tablets whole. You should not eat or drink grapefruit products during treatment with LYTGOBI. Your healthcare provider may change your dose of LYTGOBI, or may temporarily or completely stop treatment if you get certain side effects. If you miss a dose of LYTGOBI, you can take the missed dose within 12 hours on the same day. If more than 12 hours have passed, do not make up the dose. Take your regular dose of LYTGOBI the next day at the usual time. Do not take more LYTGOBI than prescribed to make up for the missed dose. If you vomit after taking LYTGOBI, do not take another LYTGOBI tablet. Take your regular dose of LYTGOBI the next day at the usual time. What are the possible side effects of LYTGOBI? LYTGOBI may cause serious side effects, including: Eye problems. Certain eye problems are common with LYTGOBI but can also be serious. Eye problems include dry eye or inflamed eyes, inflamed cornea (front part of the eye), increased tears, and a disorder of the retina (an internal part of the eye). You will need to see an eye specialist for a complete eye exam before you begin treatment with LYTGOBI, every 2 months for the first 6 months, and every 3 months thereafter during treatment with LYTGOBI. Tell your healthcare provider right away if you develop any changes in your vision during treatment with LYTGOBI, including blurred vision, flashes of light, or seeing black spots. You may need to see an eye specialist right away. You should use artificial tears or substitutes, or hydrating or lubricating eye gels during treatment with LYTGOBI to prevent or treat dry eyes. High phosphate levels in your blood (hyperphosphatemia) and build up of minerals in different tissues in your body. Hyperphosphatemia is common with LYTGOBI but can also be serious. High levels of phosphate in your blood may lead to buildup of minerals such as calcium, in different tissues in your body. Your healthcare provider will check your blood phosphate levels during treatment with LYTGOBI. Your healthcare provider may prescribe changes in your diet or phosphate lowering therapy, or change, interrupt or stop LYTGOBI if needed. Tell your healthcare provider right away if you develop any muscle cramps, or numbness or tingling around your mouth. The most common side effects of LYTGOBI include: changes in kidney function blood tests increased blood glucose level decreased red blood cell, white blood cell, and platelet counts increased calcium level in the blood decreased sodium and phosphate levels in the blood changes in liver function blood tests nails separate from the bed or poor formation of the nail; change in the color of nails muscle pain constipation diarrhea feeling tired or weak changes in tests used to measure your blood clotting time dry mouth hair loss decreased protein level (albumin) in the blood mouth sores stomach area (abdominal) pain dry skin decreased glucose and potassium level in the blood joint pain changes in sense of taste dry eye nausea decrease in appetite urinary tract infection redness, swelling, peeling or tenderness, mainly on the hands or feet (hand-foot syndrome) vomiting These are not all the possible side effects of LYTGOBI. For more information, ask your healthcare provider or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. How should I store LYTGOBI? Store LYTGOBI at room temperature between 68°F to 77°F (20°C to 25°C). Keep LYTGOBI and all medicines out of the reach of children. General information about the safe and effective use of LYTGOBI. Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use LYTGOBI for a condition for which it is not prescribed. Do not give LYTGOBI to other people, even if they have the same symptoms you have. It may harm them. If you would like more information, talk with your healthcare provider. You can ask your pharmacist or healthcare provider for information that is written for healthcare professionals. What are the ingredients in LYTGOBI? Active ingredient: futibatinib Inactive ingredients: corn starch, crospovidone, hydroxypropyl cellulose, lactose monohydrate, magnesium stearate, mannitol, microcrystalline cellulose, and sodium lauryl sulfate. The film coating material contains: hypromellose, magnesium stearate, polyethylene glycol, and titanium dioxide. Manufactured for: Taiho Pharmaceutical Co., Ltd. Japan LYTGOBI is a trademark of Taiho Pharmaceutical Co., Ltd.; U.S. Patent Nos. 9,108,973, 10,434,103, and 11,833,151; © 2025 Taiho Oncology, Inc. All rights reserved For more information, go to www.LYTGOBI.com or call 1-844-878-2446. Table text from source: | This Patient Information has been approved by the U.S. Food and Drug Administration. | Revised: 10/2025 | PATIENT INFORMATION LYTGOBI (light-GOH-bee) (futibatinib) tablets | What is LYTGOBI? | LYTGOBI is a prescription medicine that is used to treat adults with bile duct cancer (intrahepatic cholangiocarcinoma) that has spread or cannot be removed by surgery: who have already received a previous treatment, andwhose tumor has a certain type of abnormal "FGFR2” gene.Your healthcare provider will test your cancer for a certain type of abnormal FGFR2 gene and make sure that LYTGOBI is right for you. It is not known if LYTGOBI is safe and effective in children. | | Before you take LYTGOBI, tell your healthcare provider about all of your medical conditions, including if you: have vision or eye problems.are pregnant or plan to become pregnant. LYTGOBI can harm your unborn baby or cause loss of your pregnancy (miscarriage). You should not become pregnant during treatment with LYTGOBI. Females who can become pregnant: Your healthcare provider should do a pregnancy test before you start treatment with LYTGOBI.You should use an effective method of birth control during treatment and for 1 week after your final dose of LYTGOBI. Talk to your healthcare provider about birth control methods that may be right for you.Tell your healthcare provider right away if you become pregnant or think that you may be pregnant. Males with female partners who can become pregnant:You should use effective birth control when sexually active during treatment with LYTGOBI and for 1 week after your last dose of LYTGOBI. are breastfeeding or plan to breastfeed. It is not known if LYTGOBI passes into your breast milk. Do not breastfeed during treatment and for 1 week after your last dose of LYTGOBI.Tell your healthcare provider about all the medicines you take, including prescription and over-the-counter medicines, vitamins, and herbal supplements. LYTGOBI and other medicines may affect each other causing side effects. LYTGOBI may affect the way other medicines work, and other medicines may affect how LYTGOBI works. | How should I take LYTGOBI? Take LYTGOBI exactly as your healthcare provider tells you.Take LYTGOBI 1 time each day with or without food at about the same time each day. You will continue for as long as your healthcare provider tells you to.Swallow LYTGOBI tablets whole. Do not crush, chew, split, or dissolve LYTGOBI tablets. Tell your healthcare provider if you have problems swallowing LYTGOBI tablets whole.You should not eat or drink grapefruit products during treatment with LYTGOBI.Your healthcare provider may change your dose of LYTGOBI, or may temporarily or completely stop treatment if you get certain side effects.If you miss a dose of LYTGOBI, you can take the missed dose within 12 hours on the same day. If more than 12 hours have passed, do not make up the dose. Take your regular dose of LYTGOBI the next day at the usual time. Do not take more LYTGOBI than prescribed to make up for the missed dose.If you vomit after taking LYTGOBI, do not take another LYTGOBI tablet. Take your regular dose of LYTGOBI the next day at the usual time. | What are the possible side effects of LYTGOBI?LYTGOBI may cause serious side effects, including:Eye problems. Certain eye problems are common with LYTGOBI but can also be serious. Eye problems include dry eye or inflamed eyes, inflamed cornea (front part of the eye), increased tears, and a disorder of the retina (an internal part of the eye). You will need to see an eye specialist for a complete eye exam before you begin treatment with LYTGOBI, every 2 months for the first 6 months, and every 3 months thereafter during treatment with LYTGOBI. Tell your healthcare provider right away if you develop any changes in your vision during treatment with LYTGOBI, including blurred vision, flashes of light, or seeing black spots. You may need to see an eye specialist right away. You should use artificial tears or substitutes, or hydrating or lubricating eye gels during treatment with LYTGOBI to prevent or treat dry eyes.High phosphate levels in your blood (hyperphosphatemia) and build up of minerals in different tissues in your body. Hyperphosphatemia is common with LYTGOBI but can also be serious. High levels of phosphate in your blood may lead to buildup of minerals such as calcium, in different tissues in your body. Your healthcare provider will check your blood phosphate levels during treatment with LYTGOBI. Your healthcare provider may prescribe changes in your diet or phosphate lowering therapy, or change, interrupt or stop LYTGOBI if needed.Tell your healthcare provider right away if you develop any muscle cramps, or numbness or tingling around your mouth. | The most common side effects of LYTGOBI include: | changes in kidney function blood testsincreased blood glucose leveldecreased red blood cell, white blood cell, and platelet countsincreased calcium level in the blooddecreased sodium and phosphate levels in the bloodchanges in liver function blood testsnails separate from the bed or poor formation of the nail; change in the color of nailsmuscle painconstipationdiarrheafeeling tired or weakchanges in tests used to measure your blood clotting timedry mouth | hair lossdecreased protein level (albumin) in the bloodmouth soresstomach area (abdominal) paindry skindecreased glucose and potassium level in the bloodjoint painchanges in sense of tastedry eyenauseadecrease in appetiteurinary tract infectionredness, swelling, peeling or tenderness, mainly on the hands or feet (hand-foot syndrome)vomiting | These are not all the possible side effects of LYTGOBI. For more information, ask your healthcare provider or pharmacist. Call your doctor for medical advice about side effects. You may report side effects to FDA at 1-800-FDA-1088. | How should I store LYTGOBI?Store LYTGOBI at room temperature between 68°F to 77°F (20°C to 25°C). | Keep LYTGOBI and all medicines out of the reach of children. | General information about the safe and effective use of LYTGOBI. | Medicines are sometimes prescribed for purposes other than those listed in a Patient Information leaflet. Do not use LYTGOBI for a condition for which it is not prescribed. Do not give LYTGOBI to other people, even if they have the same symptoms you have. It may harm them. If you would like more information, talk with your healthcare provider. You can ask your pharmacist or healthcare provider for information that is written for healthcare professionals. | What are the ingredients in LYTGOBI? | Active ingredient: futibatinib | Inactive ingredients: corn starch, crospovidone, hydroxypropyl cellulose, lactose monohydrate, magnesium stearate, mannitol, microcrystalline cellulose, and sodium lauryl sulfate. The film coating material contains: hypromellose, magnesium stearate, polyethylene glycol, and titanium dioxide. | Manufactured for: Taiho Pharmaceutical Co., Ltd. Japan | LYTGOBI is a trademark of Taiho Pharmaceutical Co., Ltd.; U.S. Patent Nos. 9,108,973, 10,434,103, and 11,833,151; © 2025 Taiho Oncology, Inc. All rights reserved For more information, go to www.LYTGOBI.com or call 1-844-878-2446.