drugset / Trial / NCT03225833

Safety and Tolerability of WVE-120101 in Patients With Huntington's Disease

NCT03225833 ↗

Phase 1/2 Terminated 61 enrolled Wave Life Sciences USA, Inc.
RandomizedSequentialDouble-blindTreatment

Summary

PRECISION-HD1 is a Phase 1b/2a multicenter, randomized, double-blind, placebo-controlled study to evaluate the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of single and multiple doses of WVE-120101 in adult patients with early manifest Huntington's disease (HD) who carry a targeted single nucleotide polymorphism (SNP) rs362307 (SNP1).

Timeline

Start
2017-07-17
Primary completion
2021-05-11
Completion
2021-05-11

Outcome

Outcome not reported

Stopped: “Lack of Efficacy”

Drugs

EvaluationDrugModalityDoseRoute
Subject ROVANERSEN Antisense oligonucleotide — Intrathecal

Indications