Clinical Study of CM338 in the Treatment of Immunoglobulin A Nephropathy

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorKeymed Biosciences Co.Ltd

About this trial

This study is a multicenter, randomized phase II clinical study to evaluate Efficacy and safety, while observing pharmacokinetic profiles, pharmacodynamic effects, and immunogenicity of CM338 in subjects with Immunoglobulin A(IgA) nephropathy.

Eligibility criteria

Qualifiers

Male or female aged 18-75.

Understand the nature of the study and sign the Informed Consent Form voluntarily.

Take effective contraception measures throughout the study period.

Disqualifiers

Used other investigational drugs within 30 days before the first study administration.

With previous history of Human immunodeficiency virus(HIV) infection.

Treponema pallidum antibody positive in screening period.

May have active Mycobacterium tuberculosis infection.

Trial design

Treatments tested in this trial

  • CM338

Treatment groups

70 Participants
are divided into 3 treatment groups

Sponsors and collaborators