IMM01
DrugIV infusion
Other names: Timdarpacept
NCT Number: NCT06647862
This study is a randomized, controlled, double-blind, multicenter, phase Ⅲ clinical study to evaluate the efficacy of IMM01(timdarpacept) in combination with azacitidine versus placebo in combination with azacitidine in patients with newly diagnosed chronic leukemia monocytic (CMML1-2).Primary endpoint are Complete remission rate and Overall survival.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 3
Anhui Provincial Hospital, Hefei, Anhui, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
IV infusion
Other names: Timdarpacept
subcutaneous injection
IV infusion
Time frame: approximately 24 months
CR rate: CR rate determined by Independent Review Committee (IRC) based on IWG2006 MDS efficacy evaluation criteria;
Time frame: approximately 24 months
Overall survival (OS): Time from randomization to death from any cause;
Time frame: approximately 24 months
Time from randomization to transformation to AML or death from any cause, whichever occurs first
Time frame: approximately 24 months
Time from randomization to transformation to AML or death from any cause, whichever occurs first
Time frame: approximately 24 months
time from first dose to first occurrence of CR, partial remission (PR), marrow complete remission (mCR) ± hematologic improvement (HI), HI, assessed by IRC and investigators, respectively
Time frame: approximately 24 months
is defined as the proportion of the analysis population achieving CR, PR, mCR±HI, or HI
Time frame: approximately 24 months
is defined as the time from the first occurrence of CR, PR, mCR±HI, or HI to disease progression or death from any cause, whichever occurs first
Time frame: approximately 24 months
the proportion of patients who did not receive red blood cell (or whole blood) transfusion for 8 consecutive weeks during the study treatment period among patients who required transfusion at baseline.
Time frame: approximately 24 months
CR rate determined by IRC based on IWG2006 MDS efficacy evaluation criteria assessed by the investigator;
Time frame: approximately 24 months
Time from initiation of study treatment to transformation to AML; defined as ≥ 20% blasts in the bone marrow or peripheral blood by manual differential count, according to the 2016 WHO classification criteria.
Contact information is provided by the study sponsor or research team.
ImmuneOnco Biopharmaceuticals (Shanghai) Inc.
Other
A Randomized, Controlled, Double-Blind, Multicenter, Phase Ⅲ Study to Evaluate the Efficacy and Safety of IMM01 (Timdarpacept) in Combination With Azacitidine in Patients With Newly Diagnosed Chronic Myelomonocytic Leukemia (CMML1-2)
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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