Clinical Trials in the UK / NCT06989359
Recruiting
Phase 2
Phase 2 Study of ADX-038 in Complement-Mediated Kidney Disease
NCT06989359 · tracked via the Priya Life Science UK tracker
Condition(s) studied
IgANC3GComplement-mediated Kidney DiseaseIgA Nephropathy (IgAN)IC-MPGN
Investigational drug(s) / intervention(s)
ADX-038 Dose Level 2ADX-038 Dose Level 1
ADX-038 Dose Level 2: siRNA duplex oligonucleotide
ADX-038 Dose Level 1: siRNA duplex oligonucleotide
Study summary
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
Inclusion Criteria:
* 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
Exclusion Criteria:
* Hereditary or acquired complement deficiency
* Kidney transplant or renal replacement therapy
* History of solid organ transplant
* Other kidney disease
* History of recurrent invasive infections
* Received complement inhibitor treatments
* Active systemic viral, bacterial, or fungal infection
* Abnormal liver function
Primary outcome measure(s)
- Evaluate the safety and tolerability of ADX-038 — Length of study - 36 months
Incidence and severity of TEAEs
Trial sites (38)
| Facility | City | Region | Status |
|---|---|---|---|
| ADARx Clinical Site | Doral | Florida | Withdrawn |
| ADARx Clinical Site | Miami | Florida | Recruiting |
| ADARx Clinical Site | Pembroke Pines | Florida | Withdrawn |
| ADARx Clinical Site | Iowa City | Iowa | Recruiting |
| ADARx Clinical Site | Shreveport | Louisiana | Withdrawn |
| ADARx Clinical Site | Shelby | Michigan | Recruiting |
| ADARx Clinical Site | Great Neck | New York | Recruiting |
| ADARx Clinical Site | Columbus | Ohio | Recruiting |
| ADARx Clinical Site | Dakota Dunes | South Dakota | Recruiting |
| ADARx Clinical Site | Dallas | Texas | Withdrawn |
| ADARx Clinical Site | Houston | Texas | Recruiting |
| ADARx Clinical Site | Liverpool | New South Wales | Recruiting |
| ADARx Clinical Site | Wollongong | New South Wales | Recruiting |
| ADARx Clinical Site | Sydney | Australia | Recruiting |
| ADARx Clinical Site | Woolloongabba | Australia | Recruiting |
| ADARx Clinical Site | Hong Kong | Hong Kong | Recruiting |
| ADARx Clinical Site | Shatin | Hong Kong | Recruiting |
| ADARx Clinical Site | Bergamo | Italy | Recruiting |
| ADARx Clinical Site | Bologna | Italy | Recruiting |
| ADARx Clinical Site | Pavia | Italy | Recruiting |
| ADARx Clinical Site | Wŏnju | Gangwon-do | Recruiting |
| ADARx Clinical Site | Gyeonggi-do | Gurogu | Recruiting |
| ADARx Clinical Site | Seoul | Gurogu | Recruiting |
| ADARx Clinical Site | Cheonan | South Korea | Recruiting |
| ADARx Clinical Site | Daegu | South Korea | Recruiting |
| ADARx Clinical Site | Gyeonggi-do | South Korea | Recruiting |
| ADARx Clinical Site | Seoul | South Korea | Recruiting |
| ADARx Clinical Site | Seoul | South Korea | Recruiting |
| ADARx Clinical Site | Seoul | South Korea | Recruiting |
| ADARx Clinical Site | Seoul | South Korea | Recruiting |
| ADARx Clinical Site | Barcelona | Spain | Recruiting |
| ADARx Clinical Site | Madrid | Spain | Recruiting |
| ADARx Clinical Site | Madrid | Spain | Recruiting |
| ADARx Clinical Site | Seville | Spain | Recruiting |
| ADARx Clinical Site | Kaohsiung City | Taiwan | Not Yet Recruiting |
| ADARx Clinical Site | New Taipei City | Taiwan | Recruiting |
| ADARx Clinical Site | Leicester | BC | Recruiting |
| ADARx Clinical Site | Newcastle upon Tyne | United Kingdom | Recruiting |
More ADARx Pharmaceuticals, Inc. trials in the UK
STOP-HAE: A Phase 3 Study of ADX-324 in HAE
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Other trials for the same condition
Study of Ravulizumab in Immunoglobulin A Nephropathy (IgAN)
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06989359 on ClinicalTrials.gov ↗ ← All trials in the UK