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A comparative bioavailability of reformulated ibuprofen 2% and 4% oral suspensions (Berlin Chemie AG) and reference ibuprofen (Nurofen®) 200 mg/5 ml oral suspension in healthy male and female adult subjects under fasting conditions: an open-label, randomized, single-dose, three-period, three-treatment, three-sequence crossover study

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2023-503703-28-00
Acronym
BCLT/22/IBU-BE/001
Enrollment
75
Registered
2023-08-24
Start date
2023-10-25
Completion date
2024-04-02
Last updated
2024-04-16

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

Conditions

In this study will be no subjects involved with any specific medical condition or disease

Interventions

None listed

Sponsors

Berlin-Chemie AG
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to 64 Years

Countries

Lithuania

Outcome results

None listed

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