Clinical trial
A Phase 1/2 Multicenter, Open-label, Dose-escalation, Safety, Pharmacodynamic, and Pharmacokinetic Study of Q901Administered Via Intravenous Infusion as Monotherapy and in Combination With Pembrolizumab in Adult Patients With Selected Advanced Solid Tumors With Cohort Expansions at the Recommended Phase 2 Dose
NCT05394103 is registered in ClinicalTrials.gov with Qurient Co., Ltd. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase 1/2 Multicenter, Open-label, Dose-escalation, Safety, Pharmacodynamic, and Pharmacokinetic Study of Q901Administered Via Intravenous Infusion as Monotherapy and in Combination With Pembrolizumab in Adult Patients With Selected Advanced Solid Tumors With Cohort Expansions at the Recommended Phase 2 Dose
- Lead sponsor
- Qurient Co., Ltd.
- Phase
- Phase 1/2
- Overall status
- Recruiting
- Start date
- August 30, 2022
- Completion date
- August 30, 2026
- Enrollment
- 130 (estimated)
- Sites
- 11
Conditions
As the registry lists them; a condition with its own page is linked.
advanced cancer, metastatic cancer