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Last Updated: May 18, 2024

CLINICAL TRIALS PROFILE FOR IDASANUTLIN


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Clinical Trials for Idasanutlin

Trial ID Title Status Sponsor Phase Summary
NCT02545283 ↗ A Study of Idasanutlin With Cytarabine Versus Cytarabine Plus Placebo in Participants With Relapsed or Refractory Acute Myeloid Leukemia (AML) Terminated Hoffmann-La Roche Phase 3 This is a multicenter, double-blind, randomized, placebo-controlled study designed to compare overall survival in participants with relapsed or refractory AML treated with idasanutlin in combination with cytarabine versus participants treated with placebo and cytarabine. Participants will receive induction treatment with idasanutlin/placebo and cytarabine (Cycle 1). Responding participants may continue to receive a maximum of further two cycles of consolidation (Cycle 2 and Cycle 3). Complete remission (CR), CR with incomplete platelet count recovery (CRp), overall remission rate (ORR), event-free survival (EFS) and percentage of participants with an allogeneic hematopoietic stem cell transplant (HSCT) will also be compared between treatment arms. This study will include participants with and without TP53 wild type (TP53 WT) mutations.
NCT02624986 ↗ A Study of Idasanutlin in Combination With Obinutuzumab in Relapsed/Refractory (R/R) Follicular Lymphoma (FL) and in Combination With Rituximab in R/R Diffuse Large B-Cell Lymphoma (DLBCL) Participants Terminated Hoffmann-La Roche Phase 1/Phase 2 This is a open-label, multicenter, non-randomized, study to evaluate the safety, efficacy, and pharmacokinetics of idasanutlin in combination with obinutuzumab in participants with R/R FL and rituximab in combination with idasanutlin in R/R DLBCL. The study will include an initial dose-escalation phase followed by an expansion phase. The dose-escalation phase is designed to determine the recommended phase 2 dose (RP2D) for idasanutlin in combination with obinutuzumab for FL and in combination with rituximab for DLBCL. The expansion phase is designed to further assess the safety and efficacy of obinutuzumab in combination with idasanutlin at the RP2D with the selected regimen in participants with R/R FL and of rituximab in combination with idasanutlin at the RP2D in participants with R/R DLBCL.
NCT02633059 ↗ Idasanutlin, Ixazomib Citrate, and Dexamethasone in Treating Patients With Relapsed Multiple Myeloma Active, not recruiting National Cancer Institute (NCI) Phase 1/Phase 2 This phase I/II trial studies the side effects and best dose of idasanutlin and ixazomib citrate when given together with dexamethasone in treating patients with multiple myeloma that has returned after a period of improvement. Drugs used in chemotherapy, such as idasanutlin and dexamethasone, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Ixazomib citrate may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving idasanutlin, ixazomib citrate, and dexamethasone together may work better in treating patients with multiple myeloma.
NCT02633059 ↗ Idasanutlin, Ixazomib Citrate, and Dexamethasone in Treating Patients With Relapsed Multiple Myeloma Active, not recruiting Mayo Clinic Phase 1/Phase 2 This phase I/II trial studies the side effects and best dose of idasanutlin and ixazomib citrate when given together with dexamethasone in treating patients with multiple myeloma that has returned after a period of improvement. Drugs used in chemotherapy, such as idasanutlin and dexamethasone, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Ixazomib citrate may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving idasanutlin, ixazomib citrate, and dexamethasone together may work better in treating patients with multiple myeloma.
NCT02670044 ↗ A Study of Venetoclax in Combination With Cobimetinib and Venetoclax in Combination With Idasanutlin in Patients With Relapsed or Refractory Acute Myeloid Leukemia Who Are Not Eligible for Cytotoxic Therapy Completed Hoffmann-La Roche Phase 1 The primary objective for this study is to assess the safety and tolerability as well as preliminary efficacy of venetoclax in combination with cobimetinib, and venetoclax in combination with idasanutlin in patients with relapsed or refractory acute myeloid leukemia (R/R) AML who are not eligible for cytotoxic therapy.
>Trial ID >Title >Status >Phase >Summary

Clinical Trial Conditions for Idasanutlin

Condition Name

Condition Name for
Intervention Trials
Solid Tumors 4
Leukemia, Myeloid, Acute 2
HER2/Neu Negative 1
Stage IIIA Breast Cancer 1
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Condition MeSH

Condition MeSH for
Intervention Trials
Leukemia 4
Leukemia, Myeloid, Acute 4
Leukemia, Myeloid 3
Lymphoma, Large B-Cell, Diffuse 2
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Clinical Trial Locations for Idasanutlin

Trials by Country

Trials by Country for
Location Trials
United States 101
Italy 19
Australia 17
Canada 12
Spain 8
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Trials by US State

Trials by US State for
Location Trials
New York 9
Texas 7
Colorado 6
Pennsylvania 6
California 6
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Clinical Trial Progress for Idasanutlin

Clinical Trial Phase

Clinical Trial Phase for
Clinical Trial Phase Trials
Phase 3 1
Phase 2 2
Phase 1/Phase 2 8
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Clinical Trial Status

Clinical Trial Status for
Clinical Trial Phase Trials
Terminated 6
Recruiting 4
Completed 3
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Clinical Trial Sponsors for Idasanutlin

Sponsor Name

Sponsor Name for
Sponsor Trials
Hoffmann-La Roche 11
National Cancer Institute (NCI) 1
Mayo Clinic 1
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Sponsor Type

Sponsor Type for
Sponsor Trials
Industry 12
Other 7
NIH 1
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