Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT04835805 · ClinicalTrials.gov registry record · Phase 1
A Study to Evaluate the Safety and Activity of Belvarafenib as a Single Agent and in Combination With Either Cobimetinib or Cobimetinib Plus Nivolumab in Patients With NRAS-mutant Advanced Melanoma.
A Phase 1 study of Melanoma, sponsored by Genentech.
- Active
- Registry status
- Phase 1
- Development phase
- 65
- Enrollment target
- 17
- Study locations
NCT04835805 is a Phase 1 study of Melanoma that is active but no longer recruiting, run by Genentech. The registered enrollment target is 65 participants, below the 706-participant average among 266 other Melanoma trials with a reported enrollment target (91% lower). The trial reports 17 study locations across 10 states.
The verdict
NCT04835805, a Phase 1 study of Melanoma, is active but no longer recruiting, sponsored by Genentech.
- ACTIVE NOT RECRUITING
- Registry status
- Phase 1
- Development phase
- 65 participants
- Enrollment target
- 17
- Study locations
Study Summary
This study will evaluate the safety, pharmacokinetics, and activity of belvarafenib as a single agent and in combination with either cobimetinib or cobimetinib plus nivolumab in patients with NRAS-mutant advanced melanoma who have received anti-PD-1/PD-L1 therapy.
Conditions Studied
Interventions
- DRUG Nivolumab
- DRUG Cobimetinib
- DRUG Belvarafenib
Study Locations (17)
Other
- Charité - Universitätsmedizin Berlin - Berlin
- Universitätsklinikum Hamburg-Eppendorf - Hamburg
- Klinikum Mannheim GmbH Universitätsklinikum - Mannheim
- Universitatsklinikum Tubingen - Tübingen
- Universitätsklinikum Würzburg - Würzburg
- Asan Medical Center - PPDS - Seoul
California
- California Pacific Medical Center Research Institute - San Francisco
- UCSF Helen Diller Family CCC - San Francisco
Ontario
- Ottawa Hospital Regional Cancer Centre - Ottawa
- Princess Margaret Hospital - Toronto
Colorado
- University of Colorado Cancer Center - Aurora
Maryland
- Johns Hopkins Sidney Kimmel Comprehensive Cancer Center - Baltimore
Missouri
- Washington University School of Medicine - St Louis
New York
- Memorial Sloan Kettering - New York
New South Wales
- Calvary Mater Newcastle - Waratah
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 65 participants |
| Start Date | 2021-05-13 |
| Est. Completion | 2027-06-30 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04835805
The ClinicalTrials.gov registry entry for NCT04835805 describes a study currently listed as active not recruiting, categorized as Phase 1. The registered enrollment target is 65 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 706-participant average among 266 other Melanoma trials with a reported enrollment target (91% lower). The listed sponsor is Genentech, which has 332 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Melanoma appearing as the primary indexed condition, and to 3 interventions - of which Nivolumab is the first listed.
NCT04835805 reports 17 study locations spanning 10 distinct geographic areas - top geographies include Other, California, Ontario.
Frequently Asked Questions
What is clinical trial NCT04835805 about?
NCT04835805 is a clinical study titled "A Study to Evaluate the Safety and Activity of Belvarafenib as a Single Agent and in Combination With Either Cobimetinib or Cobimetinib Plus Nivolumab in Patients With NRAS-mutant Advanced Melanoma.". This study will evaluate the safety, pharmacokinetics, and activity of belvarafenib as a single agent and in combination with either cobimetinib or cobimetinib plus nivolumab in patients with NRAS-mutant advanced melanoma who have received anti-PD-1/PD-L1 therapy.
What is the current status of trial NCT04835805?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 65 participants. The study started on 2021-05-13. Estimated completion is 2027-06-30.
What conditions does trial NCT04835805 study?
This clinical trial studies the following conditions: Melanoma.
What interventions are being tested in trial NCT04835805?
The interventions under investigation include: Nivolumab (DRUG), Cobimetinib (DRUG), Belvarafenib (DRUG).
Who is sponsoring clinical trial NCT04835805?
This trial is sponsored by Genentech, which has 332 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT04835805 being conducted?
This trial has 17 study locations across California, Colorado, Maryland, Missouri, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Melanoma
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
Ulixertinib/Palbociclib in Patients With Advanced Pancreatic and Other Solid Tumors
RECRUITING · Phase 1
-
A Study of MQ710 With and Without Pembrolizumab in People With Solid Tumor Cancer
RECRUITING · Phase 1
-
Study of Autologous Tumor-Infiltrating Lymphocytes in Pediatric, Adolescent, and Young Adult Participants
RECRUITING · Phase 1
-
A Study to Investigate the Safety and Efficacy of NST-628 Oral Tablets in Subjects With Solid Tumors
RECRUITING · Phase 1
-
A Study to Learn About the Study Medicine Called PF-07799544 as Monotherapy or in Combination in People With Advanced Solid Tumors
RECRUITING · Phase 1
-
BI-1808 as a Single Agent and With Pembrolizumab (KEYTRUDA® ) in Treatment of Advanced Malignancies(Keynote-D20)
RECRUITING · Phase 1
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.