Clinical trial
A Single-Arm, Multi-Center, Open-Label, Phase 2 Study to Evaluate Efficacy and Safety of Tislelizumab (BGB-A317), an Anti-PD-1 Monoclonal Antibody, as Monotherapy in Patients With Previously-Treated Locally Advanced Unresectable or Metastatic Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Solid Tumors
NCT03736889 is registered in ClinicalTrials.gov with BeiGene as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Single-Arm, Multi-Center, Open-Label, Phase 2 Study to Evaluate Efficacy and Safety of Tislelizumab (BGB-A317), an Anti-PD-1 Monoclonal Antibody, as Monotherapy in Patients With Previously-Treated Locally Advanced Unresectable or Metastatic Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient (dMMR) Solid Tumors
- Lead sponsor
- BeiGene
- Phase
- Phase 2
- Overall status
- Recruiting
- Start date
- September 19, 2018
- Completion date
- September 30, 2027
- Enrollment
- 200 (estimated)
- Sites
- 30
Conditions
As the registry lists them; a condition with its own page is linked.
msi-h/dmmr solid tumors