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A phase 1, double-blind, placebo-controlled, randomized, single ascending dose and multiple ascending dose study to assess the safety, tolerability, and pharmacokinetics of GHF-201 in healthy adult volunteers

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-519813-74-00
Acronym
CGH24001
Enrollment
32
Registered
2025-04-17
Start date
2025-06-27
Completion date
Unknown
Last updated
2025-04-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adult polyglucosan body disease (APBD).

Interventions

None listed

Sponsors

CCDRD Cooperative Clinical Drug Research and Development AG, GHF-Golden Heart Flower Ltd.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Countries

Bulgaria

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026