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NCT07608354 · ClinicalTrials.gov registry record · Phase 2

A Study to Evaluate the Efficacy and Safety of Concomitant Use of Eplontersen and ALXN2220 Compared With Eplontersen and Placebo for Adults Participants With ATTR-CM

A Phase 2 study, sponsored by AstraZeneca.

Recruiting
Registry status
Phase 2
Development phase
326
Enrollment target

NCT07608354: Recruiting Phase 2 study, sponsored by AstraZeneca.

NCT07608354 is a Phase 2 study that is actively recruiting participants, run by AstraZeneca. The registered enrollment target is 326 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (145% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07608354, a Phase 2 study, is actively recruiting participants, sponsored by AstraZeneca.

RECRUITING
Registry status
Phase 2
Development phase
326 participants
Enrollment target

Study Summary

The purpose of this randomised, double-blind, placebo-controlled, multicenter study is to evaluate the efficacy and safety of concomitant use of eplontersen and ALXN2220 compared with eplontersen and placebo in adult participants with Transthyretin-mediated amyloid cardiomyopathy (ATTR-CM).

Primary Outcome

Change from baseline in Cardiopulmonary exercise test peak VO2 at week 52

Interventions

  • OTHER Placebo
  • DRUG Eplontersen
  • BIOLOGICAL ALXN2220

Trial Details

FieldValue
Enrollment Target 326 participants
Start Date 2026-06-11
Est. Completion 2029-02-06
Phase Phase 2
AstraZeneca

1,285 total trials

What NCT07608354 shows while recruiting

NCT07608354 is an interventional study that assigns participants to a tested intervention. The registered 326 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (145% higher).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT07608354 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07608354 about?

NCT07608354 is a clinical study titled "A Study to Evaluate the Efficacy and Safety of Concomitant Use of Eplontersen and ALXN2220 Compared With Eplontersen and Placebo for Adults Participants With ATTR-CM". The purpose of this randomised, double-blind, placebo-controlled, multicenter study is to evaluate the efficacy and safety of concomitant use of eplontersen and ALXN2220 compared with eplontersen and placebo in adult participants with Transthyretin-mediated amyloid cardiomyopathy (ATTR-CM).

What is the current status of trial NCT07608354?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 326 participants. The study started on 2026-06-11. Estimated completion is 2029-02-06.

What interventions are being tested in trial NCT07608354?

The interventions under investigation include: Placebo (OTHER), Eplontersen (DRUG), ALXN2220 (BIOLOGICAL).

Who is sponsoring clinical trial NCT07608354?

This trial is sponsored by AstraZeneca, which has 1,285 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07608354's enrollment target sits among peer trials

326 147th of 2000 higher than 1,853 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07608354, the US trial registry maintained by the National Library of Medicine. NCT07608354 (mid enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.