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NCT07023835 · ClinicalTrials.gov registry record · Phase 2

Usnoflast Neuromuscular Investigation for Treatment Efficacy in Amyotrophic Lateral Sclerosis

A Phase 2 study of Amyotrophic Lateral Sclerosis (ALS), sponsored by Zydus Therapeutics.

Active
Registry status
Phase 2
Development phase
240
Enrollment target
17
Study locations

NCT07023835 is a Phase 2 study of Amyotrophic Lateral Sclerosis (ALS) that is active but no longer recruiting, run by Zydus Therapeutics. The registered enrollment target is 240 participants, roughly in line with the 247-participant average among 17 other Amyotrophic Lateral Sclerosis (ALS) trials with a reported enrollment target. The trial reports 17 study locations across 14 states.

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The verdict

NCT07023835, a Phase 2 study of Amyotrophic Lateral Sclerosis (ALS), is active but no longer recruiting, sponsored by Zydus Therapeutics.

ACTIVE NOT RECRUITING
Registry status
Phase 2
Development phase
240 participants
Enrollment target
17
Study locations

Study Summary

Usnoflast Neuromuscular Investigation for Treatment Efficacy in Amyotrophic Lateral Sclerosis

Interventions

  • DRUG Placebo
  • DRUG 50 mg Usnoflast
  • DRUG 75 mg Usnoflast

Study Locations (17)

California

  • Zydus US015 - La Jolla
  • Zydus US008 - Orange
  • Zydus US013 - San Francisco

Texas

  • Zydus US001 - Dallas
  • Zydus US002 - Houston

Connecticut

  • Zydus US005 - New Britain

Florida

  • Zydus US012 - Tampa

Georgia

  • Zydus US007 - Atlanta

Massachusetts

  • Zydus US010 - Boston

Michigan

  • Zydus US006 - Detroit

Nebraska

  • Zydus US014 - Lincoln

Trial Details

FieldValue
Enrollment Target 240 participants
Start Date 2025-09-17
Est. Completion 2028-10
Phase Phase 2

Sponsor

Zydus Therapeutics

15 total trials

What the Registry Record Tells You About NCT07023835

The ClinicalTrials.gov registry entry for NCT07023835 describes a study currently listed as active not recruiting, categorized as Phase 2. The registered enrollment target is 240 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 247-participant average among 17 other Amyotrophic Lateral Sclerosis (ALS) trials with a reported enrollment target. The listed sponsor is Zydus Therapeutics, which has 15 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Amyotrophic Lateral Sclerosis (ALS) appearing as the primary indexed condition, and to 3 interventions - of which Placebo is the first listed.

NCT07023835 reports 17 study locations spanning 14 distinct geographic areas - top geographies include California, Texas, Connecticut.

Frequently Asked Questions

What is clinical trial NCT07023835 about?

NCT07023835 is a clinical study titled "Usnoflast Neuromuscular Investigation for Treatment Efficacy in Amyotrophic Lateral Sclerosis". Usnoflast Neuromuscular Investigation for Treatment Efficacy in Amyotrophic Lateral Sclerosis

What is the current status of trial NCT07023835?

This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 240 participants. The study started on 2025-09-17. Estimated completion is 2028-10.

What conditions does trial NCT07023835 study?

This clinical trial studies the following conditions: Amyotrophic Lateral Sclerosis (ALS).

What interventions are being tested in trial NCT07023835?

The interventions under investigation include: Placebo (DRUG), 50 mg Usnoflast (DRUG), 75 mg Usnoflast (DRUG).

Who is sponsoring clinical trial NCT07023835?

This trial is sponsored by Zydus Therapeutics, which has 15 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07023835 being conducted?

This trial has 17 study locations across California, Connecticut, Florida, Georgia, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Amyotrophic Lateral Sclerosis (ALS)

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.