ClinicalTrials.gov record
Active, not recruiting Phase 2 Interventional

Usnoflast Neuromuscular Investigation for Treatment Efficacy in Amyotrophic Lateral Sclerosis

ClinicalTrials.gov ID: NCT07023835

Public ClinicalTrials.gov record NCT07023835. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 4, 2026, 11:41 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2b, Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Usnoflast Administered to Adult Subjects With ALS

Study identification

NCT ID
NCT07023835
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Zydus Therapeutics Inc.
Industry
Enrollment
240 participants

Conditions and interventions

Interventions

  • 50 mg Usnoflast Drug
  • 75 mg Usnoflast Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 16, 2025
Primary completion
Feb 29, 2028
Completion
Sep 30, 2028
Last update posted
Feb 4, 2026

2025 – 2028

United States locations

U.S. sites
15
U.S. states
12
U.S. cities
15
Facility City State ZIP Site status
Zydus US015 La Jolla California 92037
Zydus US008 Orange California 92868
Zydus US013 San Francisco California 94109
Zydus US005 New Britain Connecticut 06053
Zydus US012 Tampa Florida 80045
Zydus US007 Atlanta Georgia 30322
Zydus US010 Boston Massachusetts 02114
Zydus US006 Detroit Michigan 48202
Zydus US014 Lincoln Nebraska 68510
Zydus US003 Winston-Salem North Carolina 27157
Zydus 009 Pittsburgh Pennsylvania 15212
Zydus US001 Dallas Texas 75206
Zydus US002 Houston Texas 77030
Zydus US004 Richmond Virginia 23298
Zydus US011 Seattle Washington 98122

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07023835, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 4, 2026 · Synced May 4, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07023835 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →