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Usnoflast Neuromuscular Investigation for Treatment Efficacy in Amyotrophic Lateral Sclerosis
NCT07023835 · View on ClinicalTrials.gov ↗
Study Summary
Usnoflast Neuromuscular Investigation for Treatment Efficacy in Amyotrophic Lateral Sclerosis
Conditions Studied
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
| Field | Value |
|---|---|
| Enrollment Target | 240 participants |
| Start Date | 2025-09-17 |
| Est. Completion | 2028-10 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07023835
The ClinicalTrials.gov registry entry for NCT07023835 describes a study currently listed as active not recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 240 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Zydus Therapeutics, which has 36 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT07023835 reports 17 study locations spanning 14 distinct geographic areas — top geographies include California, Texas, Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
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). These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT07023835?
The interventions under investigation include: Placebo (DRUG), 50 mg Usnoflast (DRUG), 75 mg Usnoflast (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT07023835?
This trial is sponsored by Zydus Therapeutics, which has 36 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
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.
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