Changeflow GovPing Pharma & Drug Safety HBS-301 Tablet Phase 3 for Idiopathic Hypersomnia
Routine Notice Added Final

HBS-301 Tablet Phase 3 for Idiopathic Hypersomnia

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Detected March 31st, 2026
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Summary

The National Institutes of Health posted a new clinical trial registration on ClinicalTrials.gov for HBS-301 tablets in Phase 3 evaluation for idiopathic hypersomnia. The trial is listed as currently recruiting participants. This registry posting does not impose new regulatory requirements but reflects compliance with clinical trial registration obligations.

What changed

ClinicalTrials.gov has published a new trial registration for HBS-301 tablets, a Phase 3 investigational treatment for idiopathic hypersomnia (NCT07500090). The registry entry documents trial identification, phase classification, therapeutic indication, and recruitment status. No new regulatory requirements, reporting obligations, or compliance deadlines are established by this posting.

Pharmaceutical companies and clinical investigators should update internal clinical trial management systems to reflect this new Phase 3 study. Healthcare providers treating idiopathic hypersomnia patients may use this registry to identify trial access opportunities for eligible patients. This is a routine registry posting; no immediate regulatory action or deadline is triggered.

Source document (simplified)

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Source

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Classification

Agency
NLM
Instrument
Notice
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
NCT07500090

Who this affects

Applies to
Pharmaceutical companies Clinical investigators Healthcare providers
Industry sector
3254 Pharmaceutical Manufacturing
Activity scope
Drug Development Clinical Research
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Pharmaceuticals Consumer Protection

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