Gilteritinib Astellas is indicated as monotherapy for the treatment of adult patients who have relapsed or refractory acute myeloid leukaemia (AML) with a FLT3 mutation (see sections 4.2 and 5.1).

Treatment with Gilteritinib Astellas should be initiated and supervised by a physician experienced in the use of anti-cancer therapies. Before taking gilteritinib, relapsed or refractory AML patients must have confirmation of FMS-like tyrosine kinase 3 (FLT3) mutation (internal tandem duplication [ITD] or tyrosine kinase domain [TKD]) using a validated test. Gilteritinib Astellas may be re-initiated in patients following haematopoietic stem cell transplantation (HSCT) (see Table 1). Posology The recommended starting dose is 120 mg gilteritinib (three 40 mg tablets) once daily. Blood chemistries, including creatine phosphokinase, should be assessed prior to initiation of treatment, on day 15 and monthly for the duration of treatment (see section 4.4). An electrocardiogram (ECG) should be performed before initiation of gilteritinib treatment, on day 8 and 15 of cycle 1 and prior to the start of the next three subsequent months of treatment (see sections 4.4 and 4.8). Females of reproductive potential should be advised to have a pregnancy test within seven days prior to starting treatment with Gilteritinib Astellas (see sections 4.4 and 4.6). 2 Treatment should continue until the patient is no longer clinically benefiting from Gilteritinib Astellas or until unacceptable toxicity occurs. Response may be delayed; therefore, continuation of treatment at the prescribed dose for up to 6 months should be considered to allow time for a clinical response. In the absence of a response [patient did not achieve a composite complete remission (CRc)] after 4 weeks of treatment, the dose can be increased to 200 mg (five 40 mg tablets) once daily, if tolerated or clinically warranted. Dose modifications Table 1: Gilteritinib Astellas dose interruption, reduction and discontinuation recommendations in patients with relapsed or refractory AML Criteria Gilteritinib Astellas dosing Differentiation syndrome • If differentiation syndrome is suspected, administer corticosteroids and initiate hemodynamic monitoring (see section 4.4). • Interrupt gilteritinib if severe signs and/or symptoms persist for more than 48 hours after initiation of corticosteroids. • Resume gilteritinib at the same dose when signs and symptoms improve to Grade 2a or lower. Posterior reversible encephalopathy syndrome • Discontinue gilteritinib. QTcF interval >500 msec • Interrupt gilteritinib. • Resume gilteritinib at a reduced dose (80 mg or 120 mgb) when QTcF interval returns to within 30 msec of baseline or =480 msec. QTcF interval increased by >30 msec on ECG on day 8 of cycle 1 • Confirm with ECG on day 9. • If confirmed, consider dose reduction to 80 mg. Pancreatitis • Interrupt gilteritinib until pancreatitis is resolved. • Resume treatment with gilteritinib at a reduced dose (80 mg or 120 mgb). Other Grade 3a or higher toxicity considered related to treatment. • Interrupt gilteritinib until toxicity resolves or improves to Grade 1a. • Resume treatment with gilteritinib at a reduced dose (80 mg or 120 mgb). Planned HSCT • Interrupt treatment with gilteritinib one week prior to administration of the conditioning regimen for HSCT. • Treatment can be resumed 30 days after HSCT if engraftment was successful, the patient did not have grade =2 acute graft versus host disease and was in CRcc. a. Grade 1 is mild, Grade 2 is moderate, Grade 3 is severe, Grade 4 is life-threatening. b. The daily dose can be reduced from 120 mg to 80 mg or from 200 mg to 120 mg. c. CRc is defined as the remission rate of all CR (see section 5.1 for definition of CR), CRp [achieved CR except for incomplete platelet recovery (<100 x 109/L)] and CRi (achieved all criteria for CR except for incomplete haematological recovery with residual neutropenia <1 x 109/L with or without complete platelet recovery). 3 Elderly No dose adjustment is required in patients =65 years of age (see section 5.2). Hepatic impairment No dose adjustment is required for patients with mild (Child-Pugh Class A) or moderate (Child-Pugh Class B) hepatic impairment. Gilteritinib Astellas is not recommended for use in patients with severe (Child-Pugh Class C) hepatic impairment, as safety and efficacy have not been evaluated in this population (see section 5.2). Renal impairment No dose adjustment is necessary in patients with mild, moderate or severe renal impairment (see sections 4.4 and 5.2). Paediatric population The safety and efficacy of Gilteritinib Astellas in children aged below 18 years has not yet been established. No data are available. Due to in vitro binding to 5HT2B (see section 4.5), there is a potential impact on cardiac development in patients less than 6 months of age. Method of administration Gilteritinib Astellas is for oral use. The tablets can be taken with or without food. They should be swallowed whole with water and should not be broken or crushed. Gilteritinib Astellas should be administered at about the same time each day. If a dose is missed or not taken at the usual time, the dose should be administered as soon as possible on the same day, and patients should return to the normal schedule the following day. If vomiting occurs after dosing, patients should not take another dose but should return to the normal schedule the following day.

Hypersensitivity to the active substance or to any of the excipients listed in section 6.1.

Differentiation syndrome Gilteritinib has been associated with differentiation syndrome (see section 4.8). Differentiation syndrome is associated with rapid proliferation and differentiation of myeloid cells and may be life-threatening or fatal if not treated. Symptoms and clinical findings of differentiation syndrome include fever, dyspnoea, pleural effusion, pericardial effusion, pulmonary oedema, hypotension, rapid weight gain, peripheral oedema, rash, and renal dysfunction. If differentiation syndrome is suspected, corticosteroid therapy should be initiated along with hemodynamic monitoring until symptom resolution. If severe signs and/or symptoms persist for more than 48 hours after initiation of corticosteroids, gilteritinib should be interrupted until signs and symptoms are no longer severe (see sections 4.2 and 4.8). Corticosteroids can be tapered after resolution of symptoms and should be administered for a minimum of 3 days. Symptoms of differentiation syndrome may recur with premature discontinuation of corticosteroid treatment. 4 Posterior reversible encephalopathy syndrome There have been reports of posterior reversible encephalopathy syndrome (PRES) in patients receiving gilteritinib (see section 4.8). PRES is a rare, reversible, neurological disorder which can present with rapidly evolving symptoms including seizure, headache, confusion, visual and neurological disturbances, with or without associated hypertension and altered mental status. If PRES is suspected, it should be confirmed by brain imaging, preferably magnetic resonance imaging (MRI). Discontinuation of gilteritinib in patients who develop PRES is recommended (see sections 4.2 and 4.8). Prolonged QT interval Gilteritinib has been associated with prolonged cardiac ventricular repolarisation (QT Interval) (see sections 4.8 and 5.1). QT prolongation can be observed in the first three months of treatment with gilteritinib. Therefore, electrocardiogram (ECG) should be performed prior to initiation of treatment, on day 8 and 15 of cycle 1, and prior to the start of the next three subsequent months of treatment. Caution is warranted in patients with relevant cardiac history. Hypokalaemia or hypomagnesaemia may increase the QT prolongation risk. Hypokalaemia or hypomagnesaemia should therefore be corrected prior to and during gilteritinib treatment. Gilteritinib should be interrupted in patients who have a QTcF >500 msec (see section 4.2). The decision to re-introduce gilteritinib treatment after an event of QT prolongation should be based on a careful consideration of benefits and risks. If gilteritinib is re-introduced at a reduced dose, ECG should be performed after 15 days of dosing, and prior to the start of the next three subsequent months of treatment. In clinical studies, 12 patients had QTcF >500 msec. Three patients interrupted and re-initiated treatment without recurrence of QT prolongation. Pancreatitis There have been reports of pancreatitis. Patients who develop signs and symptoms suggestive of pancreatitis should be evaluated and monitored. Gilteritinib should be interrupted and can be resumed at a reduced dose when the signs and symptoms of pancreatitis have resolved (see section 4.2). Severe renal impairment Gilteritinib exposure may be increased in patients with severe renal impairment or end stage renal disease. Patients should be closely monitored for toxicities and QT prolongation during administration of gilteritinib (see section 5.2).

Gilteritinib is primarily metabolised by CYP3A enzymes, which can be induced or inhibited by a number of concomitant medicinal products. Effects of other medicinal products on Gilteritinib Astellas CYP3A/P-gp inducers Concomitant use of Gilteritinib Astellas with strong CYP3A/P-gp inducers (e.g., phenytoin, rifampin and St. John’s wort) should be avoided because they can decrease gilteritinib plasma concentrations. In healthy subjects, co-administration of rifampicin (600 mg), a strong CYP3A/P-gp inducer, to steady state with a single 20 mg dose of gilteritinib decreased gilteritinib mean Cmax by 27% and mean AUCinf by 70%, respectively, compared to subjects administered a single dose of gilteritinib alone (see section 4.4). CYP3A, P-gp and/or BCRP inhibitors Strong inhibitors of CYP3A, P-gp and/or BCRP (e.g., voriconazole, itraconazole, posaconazole, clarithromycin, erythromycin, captopril, carvedilol, ritonavir, azithromycin) can increase gilteritinib plasma concentrations. A single, 10 mg dose of gilteritinib co-administered with itraconazole (200 mg once daily for 28 days), a strong CYP3A, P-gp and BCRP inhibitor, to healthy subjects resulted in an approximate 20% increase in mean Cmax and 2.2-fold increase in mean AUCinf relative to subjects administered a single dose of gilteritinib alone. Gilteritinib exposure increased approximately 1.5-fold in patients with relapsed or refractory AML when co-administered with a strong CYP3A, P-gp and/or BCRP inhibitor (see section 4.4). Effects of Gilteritinib Astellas on other medicinal products Gilteritinib as an inhibitor or inducer Gilteritinib is not an inhibitor or inducer of CYP3A4 or an inhibitor of MATE1 in vivo. The pharmacokinetics of midazolam (a sensitive CYP3A4 substrate) were not significantly (Cmax and AUC increased approximately 10%) affected after once-daily administration of gilteritinib (300 mg) for 15 days in patients with FLT3-mutated relapsed or refractory AML. Additionally, the pharmacokinetics of cephalexin (a sensitive MATE1 substrate) were not significantly (Cmax and AUC decreased by less than 10%) affected after once daily administration of gilteritinib (200 mg) for 15 days in patients with FLT3-mutated relapsed or refractory AML. Gilteritinib is an inhibitor of P-gp, BCRP and OCT1 in vitro. As no clinical data is available, it cannot be excluded that gilteritinib could inhibit these transporters at a therapeutic dose. 6 Caution is advised during co-administration of gilteritinib with substrates of P-gp (e.g., digoxin, dabigatran etexilate), BCRP (e.g., mitoxantrone, methotrexate, rosuvastatin) and OCT1 (e.g., metformin). 5HT2B receptor or sigma nonspecific receptor Based on in vitro data, gilteritinib may reduce the effects of medicinal products that target 5HT2B receptor or sigma nonspecific receptor (selective serotonin reuptake inhibitors e.g., escitalopram, fluoxetine, sertraline). Avoid concomitant use of these medicinal products with gilteritinib unless use is considered essential for the care of the patient.

Women of childbearing potential / Contraception in males and females Pregnancy testing is recommended for females of reproductive potential seven days prior to initiating gilteritinib treatment. Women of childbearing potential are recommended to use effective contraception (methods that result in less than 1% pregnancy rates) during and up to 6 months after treatment. It is unknown whether gilteritinib may reduce the effectiveness of hormonal contraceptives, and therefore women using hormonal contraceptives should add a barrier method of contraception. Males of reproductive potential should be advised to use effective contraception during treatment and for at least 4 months after the last dose of gilteritinib (see section 4.4). Pregnancy Gilteritinib can cause foetal harm when administered to pregnant women. There are no or limited amount of data from the use of gilteritinib in pregnant women. Reproductive studies in rats have shown that gilteritinib caused suppressed foetal growth, embryo-foetal deaths and teratogenicity (see section 5.3). Gilteritinib is not recommended during pregnancy and in women of childbearing potential not using effective contraception. Breast-feeding It is unknown whether gilteritinib or its metabolites are excreted in human milk. Available animal data have shown excretion of gilteritinib and its metabolites in the animal milk of lactating rats and distribution to the tissues in infant rats via the milk (see section 5.3). A risk to breast-fed children cannot be excluded. Breast-feeding should be discontinued during treatment with gilteritinib and for at least two months after the last dose. Fertility There are no data on the effect of gilteritinib on human fertility.

Gilteritinib has minor influence on the ability to drive and use machines. Dizziness has been reported in patients taking gilteritinib and should be considered when assessing a patient’s ability to drive or use machines (see section 4.8).

Summary of the safety profile The safety of Gilteritinib Astellas was evaluated in 319 patients with relapsed or refractory AML who have received at least one dose of 120 mg gilteritinib. 7 The most frequent adverse reactions with gilteritinib were alanine aminotransferase (ALT) increased (82.1%), aspartate aminotransferase (AST) increased (80.6%), blood alkaline phosphatase increased (68.7%), blood creatine phosphokinase increased (53.9%), diarrhoea (35.1%), fatigue (30.4%), nausea (29.8%), constipation (28.2%), cough (28.2%), peripheral oedema (24.1%), dyspnea (24.1%), dizziness (20.4%), hypotension (17.2%), pain in extremity (14.7%), asthenia (13.8%), arthralgia (12.5%) and myalgia (12.5%). The most frequent serious adverse reactions were acute kidney injury (6.6%), diarrhoea (4.7%), ALT increased (4.1%), dyspnea (3.4%), AST increased (3.1%) and hypotension (2.8%). Other clinically significant serious adverse reactions included differentiation syndrome (2.2%), electrocardiogram QT prolonged (0.9%) and posterior reversible encephalopathy syndrome (0.6%). Tabulated list of adverse reactions Adverse reactions observed during clinical studies are listed below by MedDRA system organ class and by frequency category. Frequency categories are defined as follows: very common (=1/10); common (=1/100 to <1/10); uncommon (=1/1 000 to <1/100); rare (=1/10 000 to <1/1 000); very rare (<1/10 000); not known (cannot be estimated from the available data). Within each frequency grouping, adverse reactions are presented in order of decreasing seriousness. Table 2: Adverse reactions MedDRA system organ class Preferred Term All Grades % Grades =3 % Frequency category Immune system disorders Anaphylactic reaction 1.3 1.3 Common Nervous system disorders Dizziness 20.4 0.3 Very common Posterior reversible encephalopathy syndrome 0.6 0.6 Uncommon Cardiac disorders Electrocardiogram QT prolonged 8.8 2.5 Common Pericardial effusion 4.1 0.9 Common Pericarditis 1.6 0 Common Cardiac failure 1.3 1.3 Common Vascular disorders Hypotension 17.2 7.2 Very common Respiratory, thoracic and mediastinal disorders Cough 28.2 0.3 Very common Dyspnoea 24.1 4.4 Very common Differentiation syndrome 3.4 2.2 Common Gastrointestinal disorders Diarrhoea 35.1 4.1 Very common Nausea 29.8 1.9 Very common Constipation 28.2 0.6 Very common Hepatobiliary disorders Alanine aminotransferase increased* 82.1 12.9 Very common Aspartate aminotransferase increased* 80.6 10.3 Very common Musculoskeletal and connective tissue disorders Blood creatine phosphokinase increased* 53.9 6.3 Very common Blood alkaline phosphatase increased* 68.7 1.6 Very common 8 MedDRA system organ class Preferred Term All Grades % Grades =3 % Frequency category Pain in extremity 14.7 0.6 Very common Arthralgia 12.5 1.3 Very common Myalgia 12.5 0.3 Very common Musculoskeletal pain 4.1 0.3 Common Renal and urinary disorders Acute kidney injury 6.6 2.2 Common General disorders and administration site conditions Fatigue 30.4 3.1 Very common Peripheral oedema 24.1 0.3 Very common Asthenia 13.8 2.5 Very common Malaise 4.4 0 Common * Frequency is based on central laboratory values. Description of selected adverse reactions Differentiation syndrome Of 319 patients treated with Gilteritinib Astellas in the clinical studies, 11 (3%) experienced differentiation syndrome. Differentiation syndrome is associated with rapid proliferation and differentiation of myeloid cells and may be life-threatening or fatal if not treated. Symptoms and clinical findings of differentiation syndrome in patients treated with Gilteritinib Astellas included fever, dyspnoea, pleural effusion, pericardial effusion, pulmonary oedema, hypotension, rapid weight gain, peripheral oedema, rash, and renal dysfunction. Some cases had concomitant acute febrile neutrophilic dermatosis. Differentiation syndrome occurred as early as one day and up to 82 days after Gilteritinib Astellas initiation and has been observed with or without concomitant leukocytosis. Of the 11 patients who experienced differentiation syndrome, 9 (82%) recovered after treatment or after dose interruption of Gilteritinib Astellas. For recommendations in case of suspected differentiation syndrome (see sections 4.2 and 4.4). PRES Of the 319 patients treated with Gilteritinib Astellas in the clinical studies, 0.6% experienced posterior reversible encephalopathy syndrome (PRES). PRES is a rare, reversible, neurological disorder, which can present with rapidly evolving symptoms including seizure, headache, confusion, visual and neurological disturbances, with or without associated hypertension. Symptoms have resolved after discontinuation of treatment (see sections 4.2 and 4.4). QT prolongation Of the 317 patients treated with Gilteritinib Astellas at 120 mg with a post-baseline QTC value in clinical studies, 4 patients (1%) experienced a QTcF >500 msec. Additionally, across all doses, 12 patients (2.3%) with relapsed/refractory AML had a maximum post-baseline QTcF interval >500 msec (see sections 4.2, 4.4 and 5.1). Reporting of suspected adverse reactions Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via the Yellow Card Scheme at: www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store. 9

There is no known specific antidote for Gilteritinib Astellas. In the event of an , treatment with Gilteritinib Astellas should be stopped. Patients must be closely monitored for signs or symptoms of adverse reactions, and appropriate symptomatic and supportive treatment initiated, taking into consideration the long half-life estimated at 113 hours.

Pharmacotherapeutic group: antineoplastic agents, protein kinase inhibitors, ATC code: L01EX13 Mechanism of action Gilteritinib fumarate is a FLT3 and AXL inhibitor. Gilteritinib inhibits FLT3 receptor signalling and proliferation in cells exogenously expressing FLT3 including FLT3-ITD, FLT3-D835Y, and FLT3-ITD-D835Y, and it induces apoptosis in leukemic cells expressing FLT3-ITD. Pharmacodynamic effects In patients with relapsed or refractory AML receiving gilteritinib 120 mg, substantial (>90%) inhibition of FLT3 phosphorylation was rapid (within 24 hours after first dose) and sustained, as characterised by an ex vivo plasma inhibitory activity (PIA) assay. Prolonged QT interval A concentration-related increase in change from baseline of QTcF was observed across gilteritinib doses ranging from 20 to 450 mg. The predicted mean change from baseline of QTcF at the mean steady-state Cmax (282.0 ng/mL) at the 120 mg daily dose was 4.96 msec with an upper 1-sided 95% CI = 6.20 msec. Clinical efficacy and safety Relapsed or refractory AML Efficacy and safety were evaluated in the active-controlled, phase 3 study (2215-CL-0301). ADMIRAL study (2215-CL-0301) The ADMIRAL study is a Phase 3, open-label, multicentre, randomised clinical study of adult patients with relapsed or refractory AML with a FLT3 mutation as determined by the LeukoStrat® CDx FLT3 Mutation Assay. In this study, 371 patients were randomised in a 2:1 ratio to receive gilteritinib or one of the following salvage chemotherapies (247 in the gilteritinib arm and 124 in the salvage chemotherapy arm): • cytarabine 20 mg twice daily by subcutaneous injection (SC) or intravenous infusion (IV) for 10 days (days 1 through 10) (LoDAC) • azacitidine 75 mg/m2 once daily by SC or IV for 7 days (days 1 through 7) • mitoxantrone 8 mg/m2, etoposide 100 mg/m2 and cytarabine 1000 mg/m2 once daily by IV for 5 days (days 1 through 5) (MEC) • granulocyte colony-stimulating factor 300 mcg/m2 once daily by SC for 5 days (days 1 to 5), fludarabine 30 mg/m2 once daily by IV for 5 days (days 2 through 6), cytarabine 2000 mg/m2 once daily by IV for 5 days (days 2 through 6), idarubicin 10 mg/m2 once daily by IV for 3 days (days 2 through 4) (FLAG-Ida). 10 Patients included were relapsed or refractory after first line AML therapy and were stratified by response to prior AML treatment and preselected chemotherapy i.e. high or low intensity. While the study included patients with various AML-related cytogenetic abnormalities, patients with acute promyelocytic leukaemia (APL) or therapy-related AML were excluded. Sixteen patients were randomised but not treated in the study (1 patient in the gilteritinib arm and 15 patients in the chemotherapy arm). Gilteritinib was given orally at a starting dose of 120 mg daily until unacceptable toxicity or lack of clinical benefit. Dose reductions were allowed, to manage adverse reactions, and dose increases were allowed, for those patients who did not respond at the starting dose of 120 mg. Of the patients who were pre-selected to receive salvage chemotherapy, 60.5% were randomised to high intensity and 39.5% to low intensity. MEC and FLAG-Ida were given for up to two cycles depending on response to first cycle. LoDAC and azacitidine were given in continuous 4-week cycles until unacceptable toxicity or lack of clinical benefit. The demographic and baseline characteristics were well-balanced between the two treatment arms. The median age at randomisation was 62 years (range 20 to 84 years) in the gilteritinib arm and 62 years (range 19 to 85 years) in the salvage chemotherapy arm. In the study 42% of patients were 65 years or older and 12% were 75 years or older. Fifty-four percent of the patients were female. Most patients in the study were Caucasian (59.3%); 27.5% Asian, 5.7% Black, 4% other races and 3.5% unknown. The majority of patients (83.8%) had an ECOG performance status score of 0 or 1. Patients had the following confirmed mutations: FLT3-ITD alone (88.4%), FLT3-TKD alone (8.4%) or both FLT3-ITD and FLT3-TKD (1.9%). Twelve percent of patients received previous treatment with another FLT3 inhibitor. A majority of patients had AML with intermediate risk cytogenetics (73%), 10% had unfavourable, 1.3% had favourable and 15.6% had unclassified cytogenetics. Prior to treatment with gilteritinib, 39.4% of patients had primary refractory AML and the majority of these patients were classified as refractory after 1 cycle of chemotherapy induction treatment, 19.7% had relapsed AML after an allogeneic haematopoietic stem cell transplant (HSCT) and 41% had relapsed AML with no allogeneic HSCT. The primary efficacy endpoint for the final analysis was OS in the intent-to-treat (ITT) population, measured from the date of randomisation until death by any cause (number of events analysed was 261). Patients randomised to the gilteritinib arm had significantly longer survival compared to the chemotherapy arm (HR 0.637; 95% CI 0.490 – 0.830; 1 sided p-value: 0.0004). The median OS was 9.3 months for patients receiving gilteritinib and 5.6 months for those receiving chemotherapy. Efficacy was further supported by the rate of complete remission (CR)/complete remission with partial haematologic recovery (CRh) (Table 3, Figure 1). Table 3: ADMIRAL study overall survival and complete remission in patients with relapsed or refractory AML Gilteritinib (N=247) Chemotherapy (N=124) Overall survival Deaths, n (%) 171 (69.2) 90 (72.6) Median in months (95% CI) 9.3 (7.7, 10.7) 5.6 (4.7, 7.3) Hazard Ratio (95% CI) 0.637 (0.490, 0.830) p-value (1-sided) 0.0004 1 year survival rate, % (95% CI) 37.1 (30.7, 43.6) 16.7 (9.9, 25) Complete remission CRa (95% CIb) 21.1% (16.1, 26.7) 10.5% (5.7, 17.3) 11 Gilteritinib (N=247) Chemotherapy (N=124) CRhc (95% CIb) 13% (9, 17.8) 4.8% (1.8, 10.2) CR/CRh (95% CIb) 34% (28.1, 40.3) 15.3% (9.5, 22.9) CI: confidence interval a. CR was defined as an absolute neutrophil count =1.0 x 109/L, platelets =100 x 109/L, normal marrow differential with <5% blasts, must have been red blood cells, platelet transfusion independent and no evidence of extramedullary leukemia. b. The 95% CI rate was calculated using the exact method based on binomial distribution. c. CRh was defined as marrow blasts <5%, partial haematologic recovery absolute neutrophil count =0.5 x 109/L and platelets =50 x 109/L, no evidence of extramedullary leukemia and could not have been classified as CR. Figure 1: Kaplan-Meier plot of overall survival in ADMIRAL study For patients who achieved a CR/CRh, the median time to first response was 3.7 months (range: 0.9 to 10.6 months) in the gilteritinib arm and 1.2 months (range: 1 to 2.6 months) in the salvage chemotherapy arm. The median time to best response of CR/CRh was 3.8 months (range: 0.9 to 16 months) in the gilteritinib arm and 1.2 months (range: 1 to 2.6 months) in the salvage chemotherapy arm. CHRYSALIS study (2215-CL-0101) The supportive Phase 1/2 dose-escalation study 2215-CL-0101 included 157 patients with FLT3 mutated AML treated with either 1 or >1 prior lines of treatment in the combined dose group (i.e. 80 mg, 120 mg or 200 mg); 31.2% received 1 prior line of treatment and 68.8% received >1 prior lines of treatment. The response rate (CR/CRh) observed in Study 2215-CL-0101 in the patients who received more than 1 line of prior therapy was 21.4% and 15.7% for the 120 mg dose and the combined dose levels, respectively. The median OS was 7.2 months and 7.1 months for the 120 mg dose and the combined dose levels, respectively. 12 Paediatric population The licensing authority has deferred the obligation to submit the results of studies with Gilteritinib Astellas in one or more subsets of the paediatric population in the treatment of acute myeloid leukaemia. See section 4.2 for information on paediatric use.

Absorption Following oral administration of gilteritinib, peak plasma concentrations are observed at a median tmax approximately between 4 and 6 hours in healthy volunteers and patients with relapsed or refractory AML. Gilteritinib undergoes first-order absorption with an estimated absorption rate (ka) of 0.43 h-1 with a lag time of 0.34 hours based on population PK modelling. Median steady-state maximum concentration (Cmax) is 282.0 ng/mL (CV% = 50.8), and area under the plasma concentration curve during 24-hour dosing interval (AUC0-24) is 6180 ng·h/mL (CV% = 46.4) after once-daily dosing of 120 mg gilteritinib. Steady-state plasma levels are reached within 15 days of once-daily dosing with an approximate 10-fold accumulation. Effect of food In healthy adults, gilteritinib Cmax and AUC decreased by approximately 26% and less than 10%, respectively, when a single 40 mg dose of gilteritinib was co-administered with a high fat meal compared to gilteritinib exposure in fasted state. Median tmax was delayed 2 hours when gilteritinib was administered with a high-fat meal. Distribution The population estimate of central and peripheral volume of distribution were 1092 L and 1100 L, respectively. These data indicate gilteritinib distributes extensively outside of plasma, which may indicate extensive tissue distribution. In vivo plasma protein binding in humans is approximately 90% and gilteritinib is primarily bound to albumin. Biotransformation Based on in vitro data, gilteritinib is primarily metabolised via CYP3A4. The primary metabolites in humans include M17 (formed via N-dealkylation and oxidation), M16 and M10 (both formed via N-dealkylation) and were observed in animals. None of these three metabolites exceeded 10% of overall parent exposure. The pharmacological activity of the metabolites against FLT3 and AXL receptors is unknown. Transporter drug-drug

Adverse reactions not observed in clinical studies, but seen in animals (safety pharmacology/repeat dose toxicity) at exposure levels similar to clinical exposure levels and with possible relevance to clinical use were as follows: Safety pharmacology In rats, decreased urination at 30 mg/kg and higher and decreased defecation at 100 mg/kg were observed. In dogs, positive faecal occult blood at 10 mg/kg and higher, a decrease in the blood calcium concentration at 30 mg/kg, and salivation and an increase followed by a decrease in the blood calcium concentration at 100 mg/kg were observed. These changes were observed at plasma exposure levels similar to or less than clinical exposure levels. A possible clinical relevance of these findings is unknown. Repeat dose toxicity In the repeated dose toxicity studies in rats and dogs, target organs of toxicity were the gastrointestinal tract (heamorrhage in dogs), lymphohaematopoietic system (lymphocyte necrosis and bone marrow hypocellularity with changes in haematological parameters), eye (inflammation and lens opacity in rats, fundus colour change in dogs, retinal vacuolation), lung (interstitial pneumonia in rats and inflammation in dogs), kidney (renal tubule changes 14 with a positive urine occult blood reaction) and liver (hepatocyte vacuolation), urinary bladder (epithelial vacuolation), epithelial tissue (ulcer and inflammation), and phospholipidosis (lung and kidney in rats). These changes were observed at plasma exposure levels similar to or less than clinical exposure levels. Reversibility of most of the changes was indicated by the end of the 4-week recovery period. A possible clinical relevance of these findings is unknown. Genotoxicity Gilteritinib did not induce gene mutation or chromosomal aberrations in vitro. The in vivo micronucleus test showed that gilteritinib has a potential to induce micronuclei in mice. Reproductive toxicity Gilteritinib showed suppressed foetal growth, and induced embryo-foetal deaths and teratogenicity in the embryo-foetal development studies in rats at exposure levels similar to clinical exposure levels. Placental transfer of gilteritinib was shown in the rat resulting in transfer of radioactivity to the foetus similar to that observed in maternal plasma. Gilteritinib was excreted into the milk of lactating rats with milk concentrations being higher than in maternal plasma. Gilteritinib was distributed through the breast milk to different tissues, except for the brain, of suckling rats. Juvenile animal toxicity study In the juvenile toxicity study in rats, the minimum lethal dose level (2.5 mg/kg/day) was much lower than that of adult rats (20 mg/kg/day). The gastrointestinal tract was identified as one of the target organs similar as in adult rats.

Tablet core Mannitol (E421) Hydroxypropylcellulose Hydroxypropylcellulose, low-substituted Magnesium stearate Film-coating Hypromellose Talc Macrogol Titanium dioxide Iron oxide yellow (E172)

Not applicable

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