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Bioequivalence of Nilotinib 200 mg Capsules in Healthy Participants Under Fasting Conditions.

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-514448-10-00
Acronym
BLCL-NIL-FDA-02
Enrollment
88
Registered
2024-07-12
Start date
2024-08-09
Completion date
2024-09-27
Last updated
2024-07-12

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

Conditions

No medical condition.

Interventions

None listed

Sponsors

Bluepharma Industria Farmaceutica S.A.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Countries

Portugal

Outcome results

None listed

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