Phase 1Completed

Bioequivalence Study of Vildagliptin From Gliptus 50 mg Tablet (EVA Pharma, Egypt) and Galvus 50 mg Tablet (NOVARTIS PHARMA, GERMANY)

Open Label, Randomized, Single Dose, Two-way Crossover Bioequivalence Study of Vildagliptin From Gliptus 50 mg Tablet (EVA Pharma, Egypt) and Galvus 50 mg Tablet (NOVARTIS PHARMA, GERMANY)

Sponsor
Genuine Research Center, Egypt (Industry)
Enrollment
24 enrolled
Conditions
Healthy
Interventions
Vildagliptin; Vildagliptin
Ages
adults
Registry
NCT02816970

Full record on ClinicalTrials.gov

From the registry

An open label randomized, single dose, two-way crossover bioequivalence study to determine the bioequivalence of Vildagliptin from Gliptus 50 mg tablet (EVA pharma, Egypt) and Galvus 50 mg tablet (NOVARTIS PHARMA, GERMANY) in Healthy Human Volunteers Under Fasting Condition

Primary outcomes

  • Maximal measured plasma concentration (Cmax)

History

  1. Registered

  2. Study completion

  3. Started

  4. Primary completion