drugset / Trial / NCT07223203

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

NCT07223203 ↗

Phase 3 Recruiting 125 enrolled Alnylam Pharmaceuticals
RandomizedParallel-groupOpen-labelTreatment

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

Timeline

Start
2025-12-12
Primary completion
2027-12-27
Completion
2031-06-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Nucresiran Unknown 300 mg Subcutaneous
Comparator Vutrisiran Small interfering RNA (siRNA) 25 mg Subcutaneous