An Open-label Phase 3b Study of Ivosidenib in Combination With Azacitidine in Adult Patients Newly Diagnosed With IDH1m Acute Myeloid Leukemia (AML) Ineligible for Intensive Induction Chemotherapy.

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorServier Affaires Médicales

About this trial

The purpose of this study is to learn more about the safety and efficacy of ivosidenib taken with azacitidine to treat adult patients with acute myeloid leukemia (AML) who are presenting a gene mutation called IDH1 (isocitrate dehydrogenase1 mutation-positive \[IDH1m\]) and cannot receive treatment with intensive chemotherapy (IC).

Eligibility criteria

Qualifiers

Has untreated Acute Myeloid Leukemia (AML)

Have a documented IDH1 R132 gene-mutated disease

Have at least one of the following making yourself ineligible for intensive chemotherapy (IC): 75 years or older, Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 2, or any comorbidity that the investigator judges to be incompatible with IC including but not limited to severe cardiac or pulmonary disorder, creatinine clearance less than 45 mL/minute, or bilirubin greater than 1.5 times the upper limit of normal

Has adequate hepatic (liver) and renal (kidney) function

Disqualifiers

Has received any prior treatment for AML, with the exception of hydroxyurea or leukapheresis for white blood cell count control

Has received prior treatment with an IDH1 inhibitor

Is a woman who is pregnant or breastfeeding

Has an active, uncontrolled, systemic fungal, bacterial, or viral infection (including human immunodeficiency virus [HIV], active hepatitis B (HBV), or hepatitis C virus [HCV]) without improvement despite appropriate antibiotics, antiviral therapy, and/or other treatment

Trial design

Treatments tested in this trial

  • Ivosidenib 500mg Oral Tablet
  • Azacitidine

Treatment groups

245 Participants
are divided into 1 treatment group

Sponsors and collaborators