Usnoflast Neuromuscular Investigation for Treatment Efficacy in Amyotrophic Lateral Sclerosis

Recruiting now · Phase 2 · Has a placebo group

Conditions studied: Amyotrophic Lateral Sclerosis (ALS)

In brief

Key facts

Study ID: NCT07023835
Run by: Zydus Therapeutics Inc.
People needed: 240
Starts: 2025-09-17
Expected to finish: 2028-10-01
Last updated by the study team: 2026-07-28

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Diagnosis of probable or definite Amyotrophic lateral sclerosis, according to the revised version of the El Escorial World Federation of Neurology criteria
Time since onset of first symptom of Amyotrophic lateral sclerosis ≤24 months. Date of Amyotrophic lateral sclerosis symptom onset. For the purposes of this study, the date of symptom onset will be defined as the date the subject first had symptoms of their disease, i.e., limb weakness, dysarthria, dysphagia, shortness of breath, or fasciculations, from the screening visit.
Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised score of ≥35 at screening.
Slow vital capacity: ≥60% of predicted capacity at the screening visit.
Be able to swallow capsules.
Either not currently receiving riluzole/sodium phenylbutyrate and taurursodiol/tofersen or on a stable dose of riluzole/sodium phenylbutyrate and taurursodiol/tofersen for at least 4 weeks before the screening visit. Subjects receiving riluzole/sodium phenylbutyrate and taurursodiol/tofersen are expected to remain on the same dose throughout the duration of the study.
Either not currently receiving edaravone or on edaravone treatment. Subjects receiving edaravone must have completed at least 1 cycle of treatment before the screening visit and are expected to continue with a stable dose of edaravone treatment throughout the duration of the study.
Capable of providing informed consent and complying with study procedures in the opinion of the investigator

You may not qualify if…

Presence of unstable psychiatric disease, cognitive impairment, dementia, or substance abuse that would impair the ability of the subject to provide informed consent, in the opinion of the investigator.
Serious illness (e.g., pneumonia, septicemia) within 4 weeks of the screening visit; infection requiring hospitalization or treatment with intravenous antibiotics, antivirals, or antifungals within 4 weeks of screening; chronic bacterial infection (such as tuberculosis) deemed unacceptable as per the judgment of the investigator.
Active herpes zoster infection within 2 months prior to the screening visit.
Any medical condition that promotes suicidal attempt or behavior within 6 months prior to the screening visit and in the opinion of the investigator might interfere with subject's participation in the study or is a risk for a suicide attempt.
History of unstable or severe cardiac, pulmonary, oncological, hepatic, or renal disease or active cancer or another medically significant illness other than Amyotrophic lateral sclerosis, precluding safe participation of subject in this study in the opinion of the investigator.
Known allergy, sensitivity, or intolerance to Investigational product or excipients.
Subjects who have taken concomitant medications that are substrates of drug metaboliz-ing enzymes (Cytochrome P450 1A2 and/or Cytochrome P450 2B6) within 7 days or 5 half-lives of the medication (whichever is longer) before the first dose of Investigational product and throughout the study.
Use of any steroids, colchicine, or anti-IL-1 inhibitors within 7 days or 5 half-lives of the medication (whichever is longer) prior to the first dose of Investigational product administration.
Use of any investigational drug concurrently or within 4 weeks or 5 half-lives (whichever is longer) prior to the first dose of Investigational product administration.
Any clinically significant condition and/or laboratory significant value that would prevent the subject from participating in the study in the opinion of the investigator.
Received a live vaccine within 14 days before the screening visit or planning to receive during the study duration.
Subjects who have received stem cell or gene therapy for Amyotrophic lateral sclerosis at any time in the past.
Following laboratory test values at screening:
Alanine aminotransferase or Aspartate aminotransferase values >3.0 × Upper Limit of Normal
Bilirubin >1.5 × Upper Limit of Normal unless the subject has documented Gilbert's syndrome (isolated bilirubin >1.5 × Upper Limit of Normal is acceptable if bilirubin is fractionated, and direct bilirubin is <35%)
Estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m2
For those participating in the optional Cerebrospinal fluid collection, contraindications to lumbar puncture including but not limited to lumbar scoliosis, coagulopathy, infection at site of puncture, or use of anticoagulants.
Subjects with history of epilepsy within 6 months of screening visit.
Surgery within last 3 months or planned major surgery within next 3 months from the date of screening (other than minor cosmetic surgery and minor dental surgery).
Use or intended use of any medications/products known to alter drug absorption, metabolism, or elimination processes, including St. John's Wort, within 4 weeks of screening and up to end of study. Use of such medication will be considered on a case-by-case basis as per the opinion of the investigator and/or independent medical monitor.
Receiving an elemental diet or parenteral nutrition.
Received blood transfusion within 3 months prior to screening.
Subjects with Human immunodeficiency virus, hepatitis B, hepatitis C, coronary artery disease, or active gastrointestinal condition that might interfere with drug absorption.
Inability to be venipunctured or those not able to tolerate venous puncture.
Employee of the investigator or study site, with direct involvement in the proposed study or other studies under the direction of that investigator or study site, as well as family members of employees of investigator or the investigator.

Where it is running

Zydus US015 — La Jolla, California, United States (enrolling)
Zydus US014 — Lincoln, Nebraska, United States (enrolling)
Zydus US003 — Winston-Salem, North Carolina, United States (enrolling)
Zydus US001 — Dallas, Texas, United States (enrolling)
Zydus US002 — Houston, Texas, United States (enrolling)
Zydus US004 — Richmond, Virginia, United States (enrolling)
Zydus US011 — Seattle, Washington, United States (enrolling)
Zydus US005 — New Britain, Connecticut, United States (enrolling)
Zydus US012 — Tampa, Florida, United States (enrolling)
Zydus US010 — Boston, Massachusetts, United States (enrolling)
Zydus US006 — Detroit, Michigan, United States (enrolling)
Zydus US008 — Orange, California, United States
Zydus US013 — San Francisco, California, United States
Zydus US009 — Pittsburgh, Pennsylvania, United States
Zydus 101 — Toronto, Ontario, Canada
Zydus US007 — Atlanta, Georgia, United States
Zydus 100 — Québec, Quebec, Canada

Full record on ClinicalTrials.gov

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