The Food and Drug Administration (FDA) has granted a priority review to a new drug application (NDA) for gilteritinib for the treatment of adult patients with FLT3 mutation–positive relapsed or refractory acute myeloid leukemia (AML), according to Astellas Pharma, the manufacturer of the FLT3 inhibitor.
The Food and Drug Administration (FDA) has granted a priority review to a new drug application (NDA) for gilteritinib for the treatment of adult patients with FLT3 mutation—positive relapsed or refractory acute myeloid leukemia (AML), according to Astellas Pharma, the manufacturer of the FLT3 inhibitor.
The NDA is based on data from the ongoing phase 3 ADMIRAL study, which is comparing gilteritinib with salvage chemotherapy in adult patients with FLT3-positive relapse/refractory AML. Data from the ADMIRAL trial have not yet been made available. Under the Prescription Drug User Fee Act, the FDA is scheduled to make its decision on the NDA by Nov. 29, 2018.
"FLT3 mutations impact approximately 30 percent of AML patients and are often associated with poor survival outcomes. Many with this condition relapse after treatment or don't respond to currently available treatments. Simply put, they need more options," Steven Benner, M.D., senior vice president and global therapeutic area head, Oncology Development, Astellas, said in a statement.
“The FDA's acceptance of this NDA, with priority review, represents a significant milestone for gilteritinib and Astellas in our mission to help AML patients and the physicians who treat them,” added Benner.
In October 2017, the FDA granted Fast Track designation to gilteritinib for adult patients with FLT3 mutation-positive relapsed/refractory acute myeloid leukemia AML. The Fast Track program is designed to accelerate the development, review, and approval of drugs that treat serious and life-threatening conditions.
In results from a phase 1/2 dose-escalation (23 patients) and dose-expansion (229 patients) study published in The Lancet Oncology, investigators concluded that the maximum-tolerated dose of gilteritinib was 300 mg daily and determined that the treatment was generally well tolerated. Among patients included in the safety analysis (252 patients), the most common grade 3/4 adverse events (AEs) were febrile neutropenia (39 percent), anemia (24 percent), thrombocytopenia (13 percent), sepsis (11 percent) and pneumonia (11 percent).
The most common treatment-related adverse events AEs were similar to those associated with other AML drugs: diarrhea, fatigue, elevated aspartate aminotransferase and increased alanine aminotransferase. Ten percent of patients required dose reductions, most commonly for diarrhea (1 percent) or fatigue (1 percent).
Serious AEs were relatively rare. The most common (5 percent or more) included febrile neutropenia (39 percent), sepsis (14 percent), pneumonia (11 percent), acute renal failure (10 percent), pyrexia (8 percent), bacteremia (6 percent) and respiratory failure (6 percent). Only febrile neutropenia, acute renal failure, pyrexia, sepsis, and bacteremia were determined to be treatment-related.
From October 2013 to August 2015, a total of 265 patients enrolled in the study. By November 2015, 88 percent had discontinued treatment and 12 percent remained on-study. Median treatment duration was 25.9 weeks.
Investigators locally confirmed internal tandem duplication mutations in FLT3 in 162 patients at screening. Thirteen patients had a point mutation in the D835 codon and 16 had both types of FLT3 mutation. All 31 patients who remained on treatment after November 2015 had an internal tandem duplication mutation in FLT3.
Patients in the dose-escalation phase were assigned to 1 of 7 gilteritinib daily dosing regimens, from 20 mg to 450 mg. Investigators established the 300 mg per day schedule as the maximum-tolerated dose after 2 of 3 patients in the 450-mg cohort experienced dose-limiting grade 3 diarrhea and grade 3 elevated aspartate aminotransferase.
Of 75 patients who achieved a composite complete remission, 2 (1 percent) received the 20 mg/day dose, 7 (3 percent) received the 80 mg/day dose, 27 (11 percent) received the 120 mg/day dose, 36 (14 percent) received the 200 mg/day dose, and 3 (1 percent) received the 300 mg/day dose. The median duration of response was 17 weeks (95 percent CI, 14-29).
The research team observed antidisease activity at all dose levels. Of the 249 patients included in the full analysis, 40 percent had a response to treatment including 19 (8 percent) who had a complete response, 10 (4 percent) had complete remission with incomplete platelet recovery, 46 (18 percent) had complete remission with incomplete hematological recovery, and 25 (10 percent) had partial remission.
Concentrations in plasma of gilteritinib after oral daily dosing were generally dose-proportional and showed substantial accumulation until steady-state levels at treatment day 15. Investigators noted potent target inhibition at all dose levels, prompting expansion of all dose cohorts ranging from 20 mg/day to 300 mg/day.
Exposure-related inhibition of FLT3 phosphorylation increased along with increasing gilteritinib concentrations in plasma. Most patients receiving a daily dose of 80 mg or higher had at least 90 percent of FLT3 phosphorylation inhibition by day 8. In-vivo inhibition of FLT3 occurred at all dose levels.