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NCT03236649
Phase 3Interventional
Includes trials conducted after preliminary evidence suggesting effectiveness of the drug has been obtained, and are intended to gather additional information to evaluate the overall benefit-risk relationship of the drug.
View on ClinicalTrials.gov ↗Timeline
- Start date
- Aug 30, 2017
- Primary completion
- Aug 31, 2019
- Completion date
- Aug 31, 2019
- First posted
- —
- Last posted
- —
- Enrollment
- 200
- Arms / groups
- 2 / —
- Source
- AACT · ingestion pipeline
Sponsors
- Beijing Shenogen Biomedical Co., LtdLead sponsor
- Soochow UniversityCollaborator
- Nanjing Medical UniversityCollaborator
- Chinese Academy of Medical SciencesOverall official - principal investigator
- China Academy of Chinese Medical SciencesCollaborator
- Harbin Medical UniversityCollaborator
- Hebei UniversityCollaborator
- Jilin UniversityCollaborator
- Nantong UniversityCollaborator
- Tianjin Medical UniversityCollaborator
- People's Liberation Army of ChinaOverall official - principal investigator
- Southern Medical UniversityCollaborator
- Fudan UniversityCollaborator
- People's Liberation Army of ChinaCollaborator
- Anhui Medical UniversityCollaborator
- Peking UniversityCollaborator
- Henan Medical UniversityCollaborator
- Capital Medical UniversityCollaborator
- Central South UniversityCollaborator
- Jinan UniversityCollaborator
- Jilin Provincial Tumor HospitalCollaborator
- Guangzhou Medical UniversityCollaborator
- Chinese Academy of Medical SciencesCollaborator
- Bengbu Medical CollegeCollaborator
- Foshan First People's HospitalCollaborator
- General Hospital of Chinese Armed Police ForcesCollaborator
- Linyi Tumour HospitalCollaborator
- Huazhong University of Science and TechnologyCollaborator
Drugs studied
Indications studied
CDEK-curated fields only — the ClinicalTrials.gov results mirror (baseline measures, adverse events, participant flow) is a separate, currently-dormant pipeline; see MIGRATION_PLAN.md.