You will receive a link to create a new password via email.
NCT04336982
Recruiting
April 7, 2020
March 14, 2022
Brief summary:
CC-90009-AML-002 is an exploratory Phase 1b open-label multi-arm trial to evaluate the safety and efficacy of CC-90009 in combination with anti-leukemia agents in subjects with acute myeloid leukemia (AML).
Study CC-90009-AML-002 is an open-label, multi-arm, parallel multi-cohort, multicenter, Phase 1b study to determine the safety, tolerability, PK, and efficacy of CC 90009 in combination with anti-leukemia agents used for the treatment of AML. CC 90009 will be given as a combination therapy to subjects with newly diagnosed (ND) or relapsed or refractory (R/R) AML. The dose and schedule finding part (Part A) of the study will evaluate the safety, PK and PD data, and preliminary efficacy information and determine the Part B dose and schedule for each arm. The expansion part (Part B) of the study will further evaluate the safety and efficacy of the CC-90009 containing combination at or below the maximum tolerated dose (MTD) in the selected cohorts in order to determine the recommended Phase 2 dose (RP2D) for subjects with AML.
| Arm | Intervention/treatment |
|---|---|
| Experimental: CC-90009 in combination with venetoclax and azacitidine CC-90009 will be administered intravenously per dosing schedule in a 28-day cycle. Venetoclax will be administered orally QD. Azacitidine will be administered intravenously or subcutaneously on planned dosing days for each cycle. |
Drug: CC-90009 Injection Drug: Venetoclax Tablet Drug: Azacitidine Injection |
| Experimental: CC-90009 in combination with gilteritinib CC-90009 will be administered intravenously per dosing schedule in a 28-day cycle. Gilteritinib will be administered orally QD. |
Drug: Gilteritinib Tablet |
Inclusion Criteria: Adult subject must understand and voluntarily sign an ICF prior to any study-related assessments/procedures being conducted. Arm A (CC-90009 + venetoclax/azacitidine): Newly diagnosed AML and is ≥ 75 years of age or intensive chemotherapy ineligible OR Refractory AML and is ≥ 18 years of age Arm B (CC-90009 + gilteritinib): Subject is ≥ 18 years of age. FLT3-ITD positive relapsed or refractory AML. Gilteritinib treatment naïve Subject has Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2. Subject must have the following screening laboratory values: Total White Blood Cell count (WBC) < 25 x 10^9 prior to study treatments. Treatment with hydroxyurea to achieve this level is allowed. Selected electrolytes within normal limits or correctable with supplements. Participant must have adequate liver function as demonstrated by: Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 x upper limit of normal (ULN) and bilirubin ≤ 1.5 x ULN Participant has adequate renal function as demonstrated by an estimated serum creatinine clearance of ≥ 60 mL/min using the Cockcroft-Gault equation. Agree to follow the CC-90009 Pregnancy Prevention Plan (PPP) and combination agents' requirements. Exclusion Criteria: Subject with acute promyelocytic leukemia (APL) Subject has received systemic anticancer therapy (including investigational therapy) or radiotherapy < 28 days or 5 half-lives, whichever is shorter, prior to the start of study treatment Patients with prior autologous hematopoietic stem cell transplant (HSCT) who, in the investigator's judgment, have not fully recovered from the effects of the last transplant (eg, transplant related side effects) Prior allogeneic HSCT with either standard or reduced intensity conditioning ≤ 6 months prior to dosing Subject on systemic immunosuppressive therapy post HSCT at the time of screening, or with clinically significant graft-versus-host disease (GVHD). The use of topical steroids for ongoing skin or ocular GVHD is permitted Subject has persistent, clinically significant non-hematologic toxicities from prior therapies which have not recovered to < Grade 2 Subject has or is suspected of having central nervous system (CNS) leukemia. Evaluation of cerebrospinal fluid is only required if CNS involvement by leukemia is suspected during screening. Disorders or conditions disrupting normal calcium homeostasis or preventing calcium supplementation. Impaired cardiac function or clinically significant cardiac diseases, including any of the following: Left ventricular ejection fraction (LVEF) < 45% as determined by multiple gated acquisition (MUGA) scan or echocardiogram (ECHO). Complete left bundle branch or bifascicular block. Congenital long QT syndrome. Persistent or clinically meaningful ventricular arrhythmias. QTcF ≥ 470 ms (Arm A) or > 450 ms (Arm B) on Screening electrocardiogram (ECG) Unstable angina pectoris or myocardial infarction ≤ 6 months prior to starting study treatments or unstable arrhythmia. Cardiovascular disability status of New York Heart Association Class ≥2. Class 2 is defined as cardiac disease in which patients are comfortable at rest but ordinary physical activity results in fatigue, palpitations, dyspnea, or anginal pain. Subject is a pregnant or lactating female Additional exclusion criteria based on combination agent: a. For Combination Arm A (venetoclax/azacitidine): Received strong or moderate CYP3A inhibitors or inducers or P-gp inhibitors within 7 days prior to initiation of first venetoclax dose. Subject has consumed grapefruit, grapefruit products, Seville oranges (including marmalade containing Seville oranges), or Star fruit within 3 days prior to first venetoclax dose through last dose of venetoclax. Previous SARS-CoV-2 infection within 10 days for mild or asymptomatic infections or 20 days for severe/critical illness prior to C1D1. a. Acute symptoms must have resolved and based on investigator assessment in consultation with the medical monitor, there are no sequelae that would place the participant at a higher risk of receiving study treatment. Previous SARS-CoV-2 vaccine within 14 days of C1D1.
Contact: BMS Study Connect Contact Center www.BMSStudyConnect.com 855-907-3286 Clinical.Trials@bms.com
Contact: First line of the email MUST contain the NCT# and Site #
United States, California
University of California, San Francisco
San Francisco
United States, Connecticut
Yale New Haven Hospital
New Haven
United States, Massachusetts
Dana-Farber/Mass General Brigham Cancer Care, Inc
Boston
United States, Missouri
Washington University School of Medicine
Saint Louis
United States, New Jersey
Hackensack University Medical Center
Hackensack
United States, Texas
The University of Texas - MD Anderson Cancer Center
Houston
United States, Washington
Fred Hutchinson Cancer Research Center
Seattle
Canada, Alberta
University of Alberta
Edmonton
Canada, Ontario
Princess Margaret Cancer Centre
Toronto
Canada, Quebec
Hopital Maisonneuve-Rosemont
Montreal
France
Institut Paoli-Calmettes
Marseille
France
Hopital Haut Leveque
Pessac Cedex
France
Institut Universitaire du Cancer de Toulouse (IUCT) - Oncopole
Toulouse Cedex 9
United Kingdom
John Radcliffe Hospital
Oxford
Celgene
AbbVie
Study Director: Bristol-Myers Squibb Bristol-Myers Squibb