ALXN2350 in Adult Participants With BAG3-Associated Dilated Cardiomyopathy
Condition(s) studied
Investigational drug(s) / intervention(s)
ALXN2350: ALXN2350 is a gene therapy product consisting of an AAV9 capsid containing BAG3 transgene. It is administered as a single intravenous (IV) infusion.
Study summary
This Phase 1/2 study is an open-label, dose finding and dose expansion study investigating the safety, tolerability, and efficacy of a single IV infusion of ALXN2350 in adult participants with BAG3 associated DCM.
Eligibility
Primary outcome measure(s)
- Part A: Number of Participants With Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs) — Baseline up to Week 78
Trial sites (11)
| Facility | City | Region | Status |
|---|---|---|---|
| Research Site | Birmingham | Alabama | Recruiting |
| Research Site | Palo Alto | California | Recruiting |
| Research Site | Boston | Massachusetts | Recruiting |
| Research Site | Cincinnati | Ohio | Recruiting |
| Research Site | Portland | Oregon | Recruiting |
| Research Site | Philadelphia | Pennsylvania | Recruiting |
| Research Site | Houston | Texas | Recruiting |
| Research Site | Massa | Italy | Recruiting |
| Research Site | Barcelona | Spain | Recruiting |
| Research Site | Majadahonda | Spain | Recruiting |
| Research Site | London | United Kingdom | Recruiting |
More Alexion Pharmaceuticals, Inc. trials in Italy
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 NCT07218887 on ClinicalTrials.gov ↗ ← All trials in Italy