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RECRUITING
NCT07444580
PHASE1

PrP-targeting siRNA Safety & Mechanism Study

Sponsor: Broad Institute of MIT and Harvard

View on ClinicalTrials.gov

Summary

The purpose of this trial is to evaluate safety, tolerability, pharmacokinetics and pharmacodynamic impact of PrP-siRNA in symptomatic prion disease patients and in pre-symptomatic adults at genetic risk for prion disease.

Official title: An Open-label, Single Ascending Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Intrathecally Administered PrP-siRNA in Adults Diagnosed With Symptomatic Prion Disease and in Pre-symptomatic Adults at Genetic Risk for Prion Disease.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

45

Start Date

2026-05-15

Completion Date

2029-08-14

Last Updated

2026-10-16

Healthy Volunteers

No

Conditions

Interventions

DRUG

PrP-siRNA

Intrathecally administered divalent siRNA designed to target the PRNP mRNA. The structure has been published in PMID: 42033217

Locations (5)

Massachusetts General Hospital

Boston, Massachusetts, United States

Mayo Clinic

Rochester, Minnesota, United States

Columbia University Medical Center

New York, New York, United States

University Hospitals Cleveland Medical Center

Cleveland, Ohio, United States

Vanderbilt University Medical Center

Nashville, Tennessee, United States