Cobimetinib in Newly Diagnosed or HMA-treated CMML Patients With RAS Pathway Mutations (CONCERTO)
Phase 2 Trial of Cobimetinib in Newly Diagnosed or HMA-treated CMML Patients With RAS Pathway Mutations
Sponsor: Genentech, Inc.
Listed as NCT04409639, this observational or N/A phase trial focuses on Chronic Myelomonocytic Leukemia (CMML) and remains ongoing. Sponsored by Genentech, Inc., it has been updated 18 times since 2021, reflecting substantial change activity. This study contributes to the evolving evidence base for cancer treatment protocols.
Study Description(click to expand)This is an open-label, nonrandomized phase 2 trial to assess the efficacy of cobimetinib in RAS pathway activated CMML. Two cohorts of patients will be accrued using Simon's two-stage design (Simon, 1989) for both cohorts. Cohort 1 will enroll nine newly diagnosed patients in the first stage and if four or more responses are observed five additional patients will be enrolled in the second stage. Cohort 2 will enroll six HMA refractory patients in the first stage and if one or more responses are observed then nine additional patients will be enrolled in the second stage.
All eligible patients will be treated daily with cobimetinib in 28-day cycles. Cobimetinib will be administered consecutively for three weeks followed by a one week break prior to the start of the following cycle. Patients will remain on study therapy until treatment discontinuation criteria is met.
This is an open-label, nonrandomized phase 2 trial to assess the efficacy of cobimetinib in RAS pathway activated CMML. Two cohorts of patients will be accrued using Simon's two-stage design (Simon, 1989) for both cohorts. Cohort 1 will enroll nine newly diagnosed patients in the first stage and if four or more responses are observed five additional patients will be enrolled in the second stage. Cohort 2 will enroll six HMA refractory patients in the first stage and if one or more responses are observed then nine additional patients will be enrolled in the second stage.
All eligible patients will be treated daily with cobimetinib in 28-day cycles. Cobimetinib will be administered consecutively for three weeks followed by a one week break prior to the start of the following cycle. Patients will remain on study therapy until treatment discontinuation criteria is met.
Status Flow
Change History
18 versions recorded-
Apr 28, 2026 — Present [daily]
Active Not Recruiting
Phase: PHASE2 → None
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Feb 2026 — Apr 2026 [monthly]
Active Not Recruiting PHASE2
Status: Recruiting → Active Not Recruiting
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Dec 2025 — Feb 2026 [monthly]
Recruiting PHASE2
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Apr 2025 — Dec 2025 [monthly]
Recruiting PHASE2
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Sep 2024 — Apr 2025 [monthly]
Recruiting PHASE2
▶ Show 13 earlier versions
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Jul 2024 — Sep 2024 [monthly]
Recruiting PHASE2
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Mar 2024 — Jul 2024 [monthly]
Recruiting PHASE2
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Sep 2023 — Mar 2024 [monthly]
Recruiting PHASE2
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Jul 2023 — Sep 2023 [monthly]
Recruiting PHASE2
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Apr 2023 — Jul 2023 [monthly]
Recruiting PHASE2
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Jul 2022 — Apr 2023 [monthly]
Recruiting PHASE2
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Nov 2021 — Jul 2022 [monthly]
Recruiting PHASE2
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Apr 2021 — Nov 2021 [monthly]
Recruiting PHASE2
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Feb 2021 — Apr 2021 [monthly]
Recruiting PHASE2
Status: Not Yet Recruiting → Recruiting
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Jan 2021 — Feb 2021 [monthly]
Not Yet Recruiting PHASE2
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Dec 2020 — Jan 2021 [monthly]
Not Yet Recruiting PHASE2
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Oct 2020 — Dec 2020 [monthly]
Not Yet Recruiting PHASE2
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Jul 2020 — Oct 2020 [monthly]
Not Yet Recruiting PHASE2
First recorded
Eligibility Summary
This is an open-label, nonrandomized phase 2 trial to assess the efficacy of cobimetinib in RAS pathway activated CMML. All eligible patients will be treated daily with cobimetinib in 28-day cycles. Cobimetinib will be administered for three weeks followed by a one week break prior to the start of the following cycle. Patients will remain on study therapy until treatment discontinuation criteria is met.
Contact Information
- Genentech, Inc.
- University of Utah
For direct contact, visit the study record on ClinicalTrials.gov .