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 — DRUG
    Pridopidine hard gelatin capsule.
  • Placebo — DRUG
    Placebo 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: Pridopidine
    Pridopidine 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: Placebo
    Placebo 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

Locations (15)

FacilityCityStateZIPSite coordinators
California Pacific Medical CenterSan FranciscoCalifornia94109
Christie Linh
Mayo ClinicJacksonvilleFlorida32224-
University of South FloridaTampaFlorida33612
Jessica Shaw
(813) 974-9413
Emory UniversityAtlantaGeorgia30322
Wanda Sanchez
404-727-1273
Northwestern UniversityChicagoIllinois60611
Candace James
University of KansasFairwayKansas66205
Sean M. Healey & AMG Center for ALSBostonMassachusetts02114
Julia Stein
617-726-1398
Washington UniversitySt LouisMissouri63110
844-257-2273
Somnos Clinical ResearchLincolnNebraska68506
402-770-7403
Eleanor and Lou Gehrig ALS Center at Columbia UniversityNew YorkNew York10032
Neuroscience Department at LKSM at Temple UniversityPhiladelphiaPennsylvania19140
Kathleen Hatala
215-707-4171
Christine Barr
215-707-5440
Texas NeurologyDallasTexas75206
214-827-3610
Baylor College of Medicine; McNair Medical CampusHoustonTexas77030
Jorge E. Zaragoza Zapiain
713-798-0106
Swedish Medical CenterSeattleWashington98122
Laura Johnson
206-320-7115
University of WashingtonSeattleWashington98195-

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