Condition: Melanoma · Sponsor: Shanghai Kechow Pharma, Inc.
This is a multicenter, two-arm, open-label, randomized controlled phase III clinical trial to evaluate the efficacy and safety of tunlametinib capsule in comparison with the combination chemotherapy of investigator's choice in advanced melanoma patients with NRAS mutation who have received immunotherapy before. Subjects were stratified according to the baseline lactate dehydrogenase level and chemotherapy.
This description comes directly from the study's public registry record.
Lixia Gong, Master · 15800569407 · gonglx@kechowpharma.com
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| Beijing Cancer Hospital | Beijing, Beijing Municipality, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06008106