RecruitingPhase 3NCT06008106

Comparing Tunlametinib Capsules and Combination Chemotherapy in Advanced NRAS-mutant Melanoma

Studying Hinman syndrome

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Key facts

Sponsor
Shanghai Kechow Pharma, Inc.
Principal Investigator
Hongqi Tian, phD
Shanghai Kechow Pharma, Inc.
Intervention
tunlametinib(drug)
Enrollment
165 target
Eligibility
18 years · All sexes
Timeline
20232027

Study locations (1)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06008106 on ClinicalTrials.gov

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