About this trial

This Phase 2 study is designed to assess the safety, efficacy, pharmacokinetics (PK) and pharmacodynamics (PD) of ADX-038 in adults with complement-mediated kidney diseases.

Eligibility criteria

Qualifiers

Mean eGFR greater than or equal to 30 mL/min/1.73m2

Clinical evidence of active kidney disease

Treated with supportive care including an ACE inhibitor or ARB if applicable

Willing to receive required vaccinations

Disqualifiers

Hereditary or acquired complement deficiency

Kidney transplant or renal replacement therapy

History of solid organ transplant

Other kidney disease

Trial design

Treatments tested in this trial

  • ADX-038 Dose Level 2
  • ADX-038 Dose Level 1

Treatment groups

45 Participants
are divided into 3 treatment groups

Locations

29
Australia
ADARx Clinical Site2170, LiverpoolNew South Wales, Australia
ADARx Clinical Site2500, WollongongNew South Wales, Australia
ADARx Clinical SiteNSW 2139, Sydney Australia
ADARx Clinical SiteQLD 4102, Woolloongabba Australia

Sponsors and collaborators

ADARx Pharmaceuticals, Inc.

Lead sponsor