Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07223203 · ClinicalTrials.gov registry record · Phase 3

TRITON-PN: A Study to Evaluate the Efficacy and Safety of Nucresiran in Patients With Hereditary Transthyretin Amyloidosis With Polyneuropathy

A Phase 3 study of Hereditary Transthyretin-Mediated Amyloidosis With Polyneuropathy and hATTR-PN, sponsored by Alnylam Pharmaceuticals.

Recruiting
Registry status
Phase 3
Development phase
125
Enrollment target
1
Study location

NCT07223203 is a Phase 3 study of Hereditary Transthyretin-Mediated Amyloidosis With Polyneuropathy and hATTR-PN that is actively recruiting participants, run by Alnylam Pharmaceuticals. The registered enrollment target is 125 participants. The trial reports 1 study location across 1 state.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07223203, a Phase 3 study of Hereditary Transthyretin-Mediated Amyloidosis With Polyneuropathy and hATTR-PN, is actively recruiting participants, sponsored by Alnylam Pharmaceuticals.

RECRUITING
Registry status
Phase 3
Development phase
125 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to: * Determine the efficacy of nucresiran in patients with hATTR-PN by evaluating the effect on neurologic impairment, quality of life, nutritional status, disability, and gait speed * Demonstrate superiority of nucresiran compared to in-study vutrisiran with respect to serum transthyretin (TTR) levels

Interventions

  • DRUG Nucresiran
  • DRUG Vutrisiran

Study Locations (1)

Massachusetts

  • Clinical Trial Site - Boston

Trial Details

FieldValue
Enrollment Target 125 participants
Start Date 2026-01-16
Est. Completion 2031-06-12
Phase Phase 3

Sponsor

Alnylam Pharmaceuticals

49 total trials

What the Registry Record Tells You About NCT07223203

The ClinicalTrials.gov registry entry for NCT07223203 describes a study currently listed as recruiting, categorized as Phase 3. The registered enrollment target is 125 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Alnylam Pharmaceuticals, which has 49 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Hereditary Transthyretin-Mediated Amyloidosis With Polyneuropathy appearing as the primary indexed condition, and to 2 interventions - of which Nucresiran is the first listed.

NCT07223203 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT07223203 about?

NCT07223203 is a clinical study titled "TRITON-PN: A Study to Evaluate the Efficacy and Safety of Nucresiran in Patients With Hereditary Transthyretin Amyloidosis With Polyneuropathy". The purpose of this study is to: * Determine the efficacy of nucresiran in patients with hATTR-PN by evaluating the effect on neurologic impairment, quality of life, nutritional status, disability, and gait speed * Demonstrate superiority of nucresiran compared to in-study vutrisiran with respect t...

What is the current status of trial NCT07223203?

This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 125 participants. The study started on 2026-01-16. Estimated completion is 2031-06-12.

What conditions does trial NCT07223203 study?

This clinical trial studies the following conditions: Hereditary Transthyretin-Mediated Amyloidosis With Polyneuropathy, hATTR-PN.

What interventions are being tested in trial NCT07223203?

The interventions under investigation include: Nucresiran (DRUG), Vutrisiran (DRUG).

Who is sponsoring clinical trial NCT07223203?

This trial is sponsored by Alnylam Pharmaceuticals, which has 49 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07223203 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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.