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Clinical Trials in the EU / 2025-522582-30-00
Completed Phase I

A Phase 1, Randomized, Placebo-controlled Study with a Double-blind Period with Open-label Extension Period to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intrathecally Administered ALN-5288 in Adult Patients with Alzheimer’s Disease

2025-522582-30-00 · tracked via the Priya Life Science EU tracker
Sponsor
Alnylam Pharmaceuticals Inc.
Sponsor type
Pharmaceutical company
Therapeutic area
Nervous System Diseases
Decision date
10/02/2026
Enrollment target
15
Sites
Spain, Netherlands

Condition studied

Alzheimer’s Disease

Eligibility

Age group
18-64 years, 65+ years
Sex
Female, Male
Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2025-522582-30-00 on CTIS ↗ ← All trials in the EU