Clinical Trials in the USA / NCT07807995
Enrolling by invitation
Phase 3
A Phase 3 Open-Label Study of Long-term Treatment With Povetacicept in Adults With Immunoglobulin A Nephropathy
NCT07807995 · tracked via the Priya Life Science USA tracker
Condition(s) studied
Immunoglobulin A Nephropathy
Investigational drug(s) / intervention(s)
Povetacicept: Subcutaneous injection administration.
Study summary
The purpose of this study is to evaluate the long-term safety, tolerability and efficacy of povetacicept in participants with immunoglobulin A nephropathy (IgAN).
Eligibility
Key Inclusion Criteria:
* Completed the Week 104 visit in the parent study VX24-AIS-D08 (NCT06564142) and has not permanently discontinued study drug
* Estimated glomerular filtration rate (eGFR) greater than or equal to (≥) 15 milliliters per minute (mL/min)/1.73 square meter (m\^2) within 45 days of Day 1 of this study
Key Exclusion Criteria:
\- Planned participation in another interventional, therapeutic clinical trial (other than the parent study).
Other protocol defined Inclusion/Exclusion criteria may apply.
Primary outcome measure(s)
- Safety and Tolerability as Assessed by Number of Participants with Adverse Events (AEs) and Serious Adverse Events (SAEs) — From Day 1 up to Week 112
Trial sites (4)
| Facility | City | Region | Status |
|---|---|---|---|
| Western Nephrology - Arvada | Arvada | Colorado | |
| CTR Oakwater, LLC | Orlando | Florida | |
| Idaho Kidney Institute- Idaho Falls | Idaho Falls | Idaho | |
| Prolato Clinical Research Center - Kirby Dr | Houston | Texas |
More Vertex Pharmaceuticals Incorporated trials in the USA
A Phase 2 Study to Evaluate Povetacicept in Adults With Generalized Myasthenia Gravis
Active, not recruiting
Other trials for the same condition
Study of Ravulizumab in Immunoglobulin A Nephropathy (IgAN)
Active, not recruiting
Atrasentan in Patients With IgA Nephropathy
Active, not recruiting
A Study of Zigakibart in Adults With IgA Nephropathy
Active, not recruiting
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 NCT07807995 on ClinicalTrials.gov ↗ ← All trials in the USA