Study of ALXN2220 Versus Placebo in Adults With ATTR-CM
Condition(s) studied
Investigational drug(s) / intervention(s)
ALXN2220: Participants will receive ALXN2220 via IV infusion.
Placebo: Participants will receive placebo via IV infusion.
Study summary
The primary objective of this study is to access the efficacy of ALXN2220 in the treatment of adult participants with ATTR-CM by evaluating the difference between the ALXN2220 and placebo groups as assessed by the total occurrences of all-cause mortality (ACM) and cardiovascular (CV) clinical events.
Eligibility
Primary outcome measure(s)
- Total Occurrence of ACM and CV clinical events during the Blinded Treatment Period — Baseline up to the end of study (up to Month 48)
Trial sites (213)
| Facility | City | Region | Status |
|---|---|---|---|
| Research Site | Irvine | California | |
| Research Site | La Jolla | California | |
| Research Site | Palo Alto | California | |
| Research Site | San Francisco | California | |
| Research Site | Aurora | Colorado | |
| Research Site | Washington D.C. | District of Columbia | |
| Research Site | Jacksonville | Florida | |
| Research Site | Weston | Florida | |
| Research Site | Atlanta | Georgia | |
| Research Site | Atlanta | Georgia | |
| Research Site | Chicago | Illinois | |
| Research Site | Indianapolis | Indiana | |
| Research Site | Boston | Massachusetts | |
| Research Site | Boston | Massachusetts | |
| Research Site | Kansas City | Missouri | |
| Research Site | St Louis | Missouri | |
| Research Site | New York | New York | |
| Research Site | New York | New York | |
| Research Site | Stony Brook | New York | |
| Research Site | Chapel Hill | North Carolina | |
| Research Site | Durham | North Carolina | |
| Research Site | Cleveland | Ohio | |
| Research Site | Columbus | Ohio | |
| Research Site | Portland | Oregon | |
| Research Site | Danville | Pennsylvania | |
| Research Site | Philadelphia | Pennsylvania | |
| Research Site | Charleston | South Carolina | |
| Research Site | Greenville | South Carolina | |
| Research Site | Memphis | Tennessee | |
| Research Site | Fort Worth | Texas | |
| Research Site | Houston | Texas | |
| Research Site | Salt Lake City | Utah | |
| Research Site | Falls Church | Virginia | |
| Research Site | Richmond | Virginia | |
| Research Site | Seattle | Washington | |
| Research Site | Madison | Wisconsin | |
| Research Site | Buenos Aires | Argentina | |
| Research Site | CABA | Argentina | |
| Research Site | Ciudad de Buenos Aires | Argentina | |
| Research Site | Ciudad de Buenos Aires | Argentina |
+ 173 more sites — see the full list on the official registry below.
More Alexion Pharmaceuticals, Inc. trials in Italy
Other trials for the same condition
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 NCT06183931 on ClinicalTrials.gov ↗ ← All trials in Italy