Phase 1Completed

Bioequivalence Study of Empagliflozin & Metformin HCL From Empagliform 12.5/1000 mg F.C.T (Hikma Pharma, Egypt) and Synjardy 12.5/1000 mg F.C.T (Boehringer Ingelheim International GmbH, Germany)

Comparative, Randomized, Single Dose, Two-way Crossover Bioequivalence Study to Determine the Bioequivalence of Empagliflozin & Metformin From Empagliform 12.5/1000 mg F.C.T (Hikma Pharma, Egypt) and Synjardy 12.5/1000 mg F.C.T (Boehringer Ingelheim International GmbH, Germany)

Sponsor
Genuine Research Center, Egypt (Industry)
Enrollment
26 enrolled
Conditions
Healthy
Interventions
Empagliflozin & Metformin (Test); Empagliflozin & Metformin (Reference)
Ages
adults
Registry
NCT05132023

Full record on ClinicalTrials.gov

From the registry

Comparative randomized, single dose, two-way crossover open-label study to determine the bioequivalence of Empagliflozin \& Metformin HCL from Empagliform 12.5/1000 mg F.C.T (Hikma Pharma, Egypt) and Synjardy 12.5/1000 mg F.C.T (Boehringer Ingelheim International GmbH, Germany)

Primary outcomes

  • Cmax

History

  1. Registered

  2. Study completion

  3. Primary completion

  4. Started