A Phase 1 Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ARO-SOD1 in Adult Patients With Amyotrophic Lateral Sclerosis Harboring a Superoxide Dismutase-1 Mutation Considered to be Causative of Amyotrophic Lateral Sclerosis

Status: Withdrawn prior to enrolment

Phase of Trial: Phase I

Latest Information Update: 22 Apr 2024

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At a glance

Drugs ARO SOD1 (Primary)
Indications Amyotrophic lateral sclerosis
Focus Adverse reactions
Sponsors Arrowhead Pharmaceuticals

Most Recent Events

16 Apr 2024 Status changed from not yet recruiting to withdrawn prior to enrolment.
14 Dec 2023 Planned End Date changed from 1 Jan 2025 to 1 Mar 2025.
14 Dec 2023 Planned primary completion date changed from 1 Jan 2025 to 1 Mar 2025.

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