drugset / Trial / NCT07223203
TRITON-PN: A Study to Evaluate the Efficacy and Safety of Nucresiran in Patients With Hereditary Transthyretin Amyloidosis With Polyneuropathy
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Nucresiran | Unknown | 300 mg | Subcutaneous |
| Comparator | Vutrisiran | Small interfering RNA (siRNA) | 25 mg | Subcutaneous |