Clinical trial
A Phase 1 Open-label, Multicenter, Dose Escalation Study of the Safety, Tolerability, and Pharmacokinetics of HPN217 in Patients With Relapsed/Refractory Multiple Myeloma
NCT04184050 is registered in ClinicalTrials.gov with Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA) as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase 1 Open-label, Multicenter, Dose Escalation Study of the Safety, Tolerability, and Pharmacokinetics of HPN217 in Patients With Relapsed/Refractory Multiple Myeloma
- Lead sponsor
- Harpoon Therapeutics, Inc., a subsidiary of Merck & Co., Inc. (Rahway, New Jersey USA)
- Phase
- Phase 1
- Overall status
- Active, not recruiting
- Start date
- April 13, 2020
- Completion date
- December 31, 2026
- Enrollment
- 100 (actual)
- Sites
- 12
Conditions
As the registry lists them; a condition with its own page is linked.
multiple myeloma, multiple myeloma in relapse, multiple myeloma of bone, multiple myeloma with failed remission