drugset / Trial / NCT05160558

A Pharmacokinetics and Safety Study of BIIB132 in Adults With Spinocerebellar Ataxia 3

NCT05160558 ↗

Phase 1 Terminated 8 enrolled Biogen
RandomizedSequentialQuadruple-blindTreatment

Summary

The primary objective of this study is to evaluate the safety and tolerability of multiple ascending doses of BIIB132 administered via intrathecal (IT) injection to participants with spinocerebellar ataxia type 3 (SCA3). The secondary objective of this study is to characterize the multiple-dose pharmacokinetics (PK) of BIIB132 administered via IT injection to participants with SCA3.

Timeline

Start
2022-02-02
Primary completion
2023-07-25
Completion
2023-07-25

Outcome

Outcome not reported

Stopped: “Sponsor's Decision”

Drugs

EvaluationDrugModalityDoseRoute
Subject BIIB132 Antisense oligonucleotide — Intrathecal