WHO ICTRP trial

A Bioequivalence Study of Two Formulations of Fixed Dose Combination Tablets of…

TCTR20200605001 · Thai Clinical Trials Registry (TCTR) · Not Recruiting

Key facts

Trial ID TCTR20200605001
Public title A Bioequivalence Study of Two Formulations of Fixed Dose Combination Tablets of Sitagliptin Phosphate Equivalent to Sitagliptin 50 mg and Metformin Hydrochloride 1000 mg in Healthy Thai Volunteers under Fed Conditions
Scientific title A Bioequivalence Study of Two Formulations of Fixed Dose Combination Tablets of Sitagliptin Phosphate Equivalent to Sitagliptin 50 mg and Metformin Hydrochloride 1000 mg in Healthy Thai Volunteers under Fed Conditions
Primary sponsor Novartis (Thailand) Ltd.
Registry Thai Clinical Trials Registry (TCTR)
Recruitment status Not Recruiting
Study type Interventional
Phase Phase 1
Countries Thailand
Conditions Healthy volunteers Healthy volunteers Bioequivalence Sitagliptin Metiformin Fixed dose combunation tablets Pharmacokinetic study;Healthy volunteers Bioequivalence Sitagliptin Metiformin Fixed dose combunation tablets Pharmacokinetic study
Interventions A single dose of Sitagliptin/Metformin 50/1000-mg Tablets, Test Product,A single dose of Sitagliptin/Metformin 50/1000-mg Tablets, Reference Product;Experimental Drug,Active Comparator Drug;SITAGLIPTIN METFORMIN SANDOZ (50/1000),JanumetTM
Registration date May 6, 2020
Target size 32
Registry page thaiclinicaltrials.org

At a glance

  • No Results available

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About WHO ICTRP trial registrations

The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.

Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

Browse all WHO ICTRP trial registrations