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NCT07522099RecruitingPhase 2

Chinese Adults With Kidney Disease

A Phase 2 Study to Assess ADX-038 in Chinese Adults With Complement-Mediated Kidney Disease

Source: ClinicalTrials.gov · Last updated 3 Sept 2026

Brief summary (registry, in English)

This is a Phase 2 study to assess the safety, efficacy, pharmacokinetics (PK) and pharmacodynamics of ADX-038 in adults with complement-mediated kidney diseases. The study will enroll Chinese adults with IgA nephropathy, complement 3 glomerulopathy (C3G) and immune complex membranoproliferative glomerulonephritis (IC-MPGN). The study will evaluate ADX-038 administered alone (Part A) and in combination with telitacicept (Part B).

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
30 (estimated)
First submitted
27 Feb 2026
Start date
21 May 2026
Primary completion date
10 Jul 2028
Lead sponsor
ADARx Pharmaceuticals, Inc.
NCT number
NCT07522099

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 30
  • From 21 May 2026 to the primary completion date, 10 Jul 2028
  • 9 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous kidney transplant or major solid organ transplant
  • Required renal replacement therapy for more than 72 hours
  • Current or previous use of C5 or CFB inhibitors (such as eculizumab, ravulizumab or iptacopan)

Other illness

  • History of recurrent invasive infection
  • Active TB, HIV or other systemic infection

Other

  • Rapidly progressive glomerular nephritis or acute kidney injury
  • Abnormal liver function

Who the study is looking for

  • 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
  • Primary diagnosis of IgAN, C3G or IC-MPGN confirmed by a kidney biopsy

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (9)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
ADARx Clinical Site
Coordinator of this site? Confirm its status
BaotouChinaRecruiting
ADARx Clinical Site
Coordinator of this site? Confirm its status
BeijingChinaRecruiting
ADARx Clinical Site
Coordinator of this site? Confirm its status
GuiyangChinaRecruiting
ADARx Clinical Site
Coordinator of this site? Confirm its status
ShandongChinaRecruiting
ADARx Clinical Site
Coordinator of this site? Confirm its status
ShanghaiChinaRecruiting
ADARx Clinical Site
Coordinator of this site? Confirm its status
ShenzhenChinaRecruiting
ADARx Clinical Site
Coordinator of this site? Confirm its status
WuxiChinaRecruiting
ADARx Clinical Site
Coordinator of this site? Confirm its status
YantaiChinaRecruiting
ADARx Clinical Site
Coordinator of this site? Confirm its status
ZhengzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.