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Clinical trial

A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Profiles and Preliminary Efficacy of Subcutaneous Injection of Recombinant Humanized Anti-CD20 Monoclonal Antibody in the Treatment of Primary Membranous Nephropathy

NCT05668403 is registered in ClinicalTrials.gov with Shanghai Jiaolian Drug Research and Development Co., Ltd as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Profiles and Preliminary Efficacy of Subcutaneous Injection of Recombinant Humanized Anti-CD20 Monoclonal Antibody in the Treatment of Primary Membranous Nephropathy
Lead sponsor
Shanghai Jiaolian Drug Research and Development Co., Ltd
Phase
Phase 1
Overall status
Recruiting
Start date
March 2, 2023
Completion date
December 30, 2027
Enrollment
52 (estimated)
Sites
6

Conditions

As the registry lists them; a condition with its own page is linked.

primary membranous nephropathy