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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 is a Phase 2 study that is actively recruiting participants, run by AstraZeneca. The registered enrollment target is 326 participants.

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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).

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

Sponsor

AstraZeneca

1,285 total trials

What the Registry Record Tells You About NCT07608354

The ClinicalTrials.gov registry entry for NCT07608354 describes a study currently listed as recruiting, categorized as Phase 2. The registered enrollment target is 326 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AstraZeneca, which has 1,285 total studies on file at ClinicalTrials.gov.

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

NCT07608354 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.