Changeflow GovPing Pharma & Drug Safety ALT001 drug trial for MSA-C cerebellar subtype
Routine Notice Added Final

ALT001 drug trial for MSA-C cerebellar subtype

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Detected April 7th, 2026
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Summary

The National Library of Medicine registered a new clinical trial on ClinicalTrials.gov for ALT001, an investigational drug for the cerebellar subtype of Multiple System Atrophy (MSA-C). The trial is categorized as an interventional study. ClinicalTrials.gov is a publicly accessible database operated by the NIH as required under FDA regulations for clinical trial registration and results reporting.

What changed

A new clinical trial registration (NCT07514923) for ALT001 targeting the cerebellar subtype of Multiple System Atrophy (MSA-C) was added to the ClinicalTrials.gov registry. The entry includes standard required fields: study title, intervention type, trial phase classification, enrollment information, locations, and contact details for investigators. Clinical trials are required to be registered on ClinicalTrials.gov under FDAAA 801 and FDA regulations.

For sponsors and investigators conducting MSA-C research, this registration signals active enrollment activity for an investigational therapy. Healthcare providers treating MSA-C patients may want to be aware of this trial for patient referral considerations. The registration is mandatory under US law for applicable clinical trials and contributes to transparency in drug development.

What to do next

  1. Monitor ClinicalTrials.gov for trial updates and results
  2. Review eligibility criteria when enrolling patients in MSA-C research studies

Source document (simplified)

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Source

Analysis generated by AI. Source diff and links are from the original.

Classification

Agency
NLM
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
NCT07514923

Who this affects

Applies to
Healthcare providers Pharmaceutical companies Clinical investigators
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Clinical trial registration Drug development research Patient enrollment
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Compliance frameworks
GxP
Topics
Pharmaceuticals Public Health

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