Clinical trial
A First-in-human, Open-label, Multiple Center Phase 1 Dose-Escalation Study to Evaluate Safety, Tolerability, Pharmacokinetic, Immunogenicity, and Preliminary Efficacy of F182112 in Patients With Relapsed or Refractory Multiple Myeloma.
NCT04984434 is registered in ClinicalTrials.gov with Shandong New Time Pharmaceutical Co., LTD as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A First-in-human, Open-label, Multiple Center Phase 1 Dose-Escalation Study to Evaluate Safety, Tolerability, Pharmacokinetic, Immunogenicity, and Preliminary Efficacy of F182112 in Patients With Relapsed or Refractory Multiple Myeloma.
- Lead sponsor
- Shandong New Time Pharmaceutical Co., LTD
- Phase
- Phase 1
- Overall status
- Unknown status
- Start date
- July 30, 2021
- Completion date
- December 30, 2023
- Enrollment
- 68 (estimated)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
dose-escalation study, relapsed or refractory multiple myeloma