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Clinical trial

A Single-arm, Multi-center Phase II Trial to Evaluate the Efficacy and Safety of the Combination of HL-085 and Vemurafenib in Advanced Melanoma Patients With BRAF V600E/K Mutation

NCT05263453 is registered in ClinicalTrials.gov with Shanghai Kechow Pharma, Inc. as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Single-arm, Multi-center Phase II Trial to Evaluate the Efficacy and Safety of the Combination of HL-085 and Vemurafenib in Advanced Melanoma Patients With BRAF V600E/K Mutation
Lead sponsor
Shanghai Kechow Pharma, Inc.
Phase
Phase 2
Overall status
Unknown status
Start date
September 6, 2021
Completion date
December 31, 2024
Enrollment
104 (estimated)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.