Trials / Conditions / To Determine Bioequivalence Under Fed Conditions

To Determine Bioequivalence Under Fed Conditions

10 registered clinical trials studyying To Determine Bioequivalence Under Fed Conditions.

Status	Trial	Sponsor	Phase
Completed	The Study Intends to Show Bioequivalence of the Test Product and the Reference Reference Product in a Crossove NCT05329857	AET Laboratories Private Limited	N/A
Completed	The Study Aims to Show Bioequivalence of the Test Product and the Reference Reference Product in a Crossover D NCT05337969	AET Laboratories Private Limited	N/A
Completed	Bioavailability Study of Propranolol Under Fed Conditions NCT00652600	Par Pharmaceutical, Inc.	Phase 1
Completed	Bioavailability Study of Leflunomide Tablets Under Fed Conditions NCT00653003	Par Pharmaceutical, Inc.	Phase 1
Completed	Bioavailability Study of Tramadol/APAP Tablets Under Fed Conditions NCT00652821	Par Pharmaceutical, Inc.	Phase 1
Completed	Bioequivalence Study of Cabergoline Tablets and Dostinex Under Fed Conditions NCT00652873	Par Pharmaceutical, Inc.	Phase 1
Completed	Bioequivalence Study of Doxycycline Monohydrate Tablets Under Fed Conditions NCT01380496	Par Pharmaceutical, Inc.	Phase 1
Completed	A Comparative Bioavailability Study of Lisinopril Tablets, 40 mg - Effect of Food Study NCT01380431	Par Pharmaceutical, Inc.	Phase 1
Completed	Bioavailability Study of Doxycycline Monohydrate Capsules and Monodox Under Fasting and Fed Conditions NCT00652704	Par Pharmaceutical, Inc.	Phase 1
Completed	Bioavailability Study of (Buspar) Buspirone HCl Tablets Under Fasting and Fed Conditions NCT00652730	Par Pharmaceutical, Inc.	Phase 1