Active, not recruitingNCT04666272
Effectiveness and Safety of Dabrafenib in Combination With Trametinib as Adjuvant Treatment for Chinese Patients With Stage III BRAF V600 Mutation-positive Melanoma After Complete Resection
Studying Germ cell tumor
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Novartis Pharmaceuticals
- Principal Investigator
- Novartis PharmaceuticalsNovartis Pharmaceuticals
- Intervention
- dabrafenib(drug)
- Enrollment
- 78 target
- Eligibility
- 18-100 years · All sexes
- Timeline
- 2020 – 2028
Study locations (8)
- Novartis Investigative Site, Fuzhou, Fujian, China
- Novartis Investigative Site, Zhengzhou, Henan, China
- Novartis Investigative Site, Wuhan, Hubei, China
- Novartis Investigative Site, Changsha, Hunan, China
- Novartis Investigative Site, Nanjing, Jiangsu, China
- Novartis Investigative Site, Kunming, Yunnan, China
- Novartis Investigative Site, Hangzhou, Zhejiang, China
- Novartis Investigative Site, Beijing, China
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.
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