Pridopidine Phase 3 Study to Evaluate Efficacy and Safety in ALS
Part of paid clinical trials in San Francisco, California.
- Sponsor
- Prilenia
- Study ID
- NCT07322003
- Phase
- PHASE3
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Pridopidine — DRUGPridopidine hard gelatin capsule.
- Placebo — DRUGPlacebo hard gelatin capsule.
Study Details
The goal of this clinical trial is to learn if the drug pridopidine works to treat amyotrophic lateral sclerosis in adults. It will also help to learn about the safety of pridopidine. The main question it aims to answer is: Does pridopidine slow disease progression of ALS? Researchers will compare pridopidine to a placebo (a look-alike substance that contains no drug) to see if pridopidine works to treat ALS. Participants will: Take pridopidine or a placebo by mouth every day for 48 weeks. Afterwards, all participants will take pridopidine for another 48 weeks. Visit the clinic once every 1-3 months for checkups and tests
Key Dates
- First listed
- Jan 7, 2026
- Start date
- Feb 1, 2026
- Status verified
- Jun 2026
- Primary completion
- Mar 31, 2028
- Completion
- Mar 31, 2029
Study Design
- Enrollment
- 500 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: PridopidinePridopidine hard gelatin capsules of 45 mg strength. During titration period 1 capsule taken orally in the morning for 2 weeks. During the main treatment period, 1 capsule in the morning and 1 capsule in the afternoon taken orally. Total daily dose of 90 mg.
- Placebo Comparator: PlaceboPlacebo hard gelatin capsules. During titration period 1 capsule taken orally in the morning for 2 weeks. During the main treatment period, 1 capsule in the morning and 1 capsule in the afternoon taken orally.
Primary Outcome Measure
Change from baseline through Week 26 and Week 48 in the Revised ALS Functional Rating Scale (ALSFRS-R) total score adjusted for mortality [ Time Frame: Baseline to Week 48 ]
Central Contacts
- Prilenia Medical Information857-574-5755
Locations (15)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| California Pacific Medical Center | San Francisco | California | 94109 | Christie Linh |
| Mayo Clinic | Jacksonville | Florida | 32224 | - |
| University of South Florida | Tampa | Florida | 33612 | |
| Emory University | Atlanta | Georgia | 30322 | |
| Northwestern University | Chicago | Illinois | 60611 | Candace James |
| University of Kansas | Fairway | Kansas | 66205 | |
| Sean M. Healey & AMG Center for ALS | Boston | Massachusetts | 02114 | |
| Washington University | St Louis | Missouri | 63110 | 844-257-2273 |
| Somnos Clinical Research | Lincoln | Nebraska | 68506 | 402-770-7403 |
| Eleanor and Lou Gehrig ALS Center at Columbia University | New York | New York | 10032 | Arish Jamil |
| Neuroscience Department at LKSM at Temple University | Philadelphia | Pennsylvania | 19140 | |
| Texas Neurology | Dallas | Texas | 75206 | 214-827-3610 |
| Baylor College of Medicine; McNair Medical Campus | Houston | Texas | 77030 | |
| Swedish Medical Center | Seattle | Washington | 98122 | |
| University of Washington | Seattle | Washington | 98195 | - |
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