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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