Skip to content

Bioequivalence of Cladribine 10 mg from two different products

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-508656-19-00
Acronym
CPO23001
Enrollment
76
Registered
2024-02-06
Start date
2024-03-01
Completion date
2024-05-02
Last updated
2024-02-06

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

Conditions

No therapeutic indication in the current trial with healthy volunteers. The intended indication is for treatment of adult patients with highly active relapsing multiple sclerosis (MS).

Interventions

None listed

Sponsors

CCDRD Cooperative Clinical Drug Research and Development AG, Pharos Pharmaceutical Oriented Services Ltd.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
Male
Age
18 Years to 64 Years

Countries

Bulgaria

Outcome results

None listed

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