Phase 1Completed

Bioequivalence Study of Baricitinib From Barcimiant 4 mg Film Coated Tablets (Horus Pharma, Egypt) and Olumiant 4 mg Film Coated Tablets (Eli Lilly Nederland B.V., The Netherlands)

Comparative Randomized, Single Dose, Three Way Three Sequence Two Treatment Partial Replicate Crossover Study to Determine the Bioequivalence of Baricitinib From Barcimiant 4 mg Film Coated Tablets (Horus Pharma, Egypt) and Olumiant 4 mg Film Coated Tablets (Eli Lilly Nederland B.V., The Netherlands)

Sponsor
Genuine Research Center, Egypt (Industry)
Enrollment
30 enrolled
Conditions
Healthy
Interventions
Barcimiant; Olumiant (first dose); Olumiant (second dose)
Ages
adults
Registry
NCT05006768

Full record on ClinicalTrials.gov

From the registry

Comparative randomized, single dose, three-way, three-sequence, two treatment, partial replicate, crossover, open-label study to determine the bioequivalence of Baricitinib from Barcimiant 4 mg Film Coated Tablets (Horus Pharma, Egypt) and Olumiant 4 mg Film Coated Tablets (Eli Lilly Nederland B.V., The Netherlands)

Primary outcomes

  • Cmax

History

  1. Registered

  2. Study completion

  3. Primary completion

  4. Started