Atlas Trials

To Determine Bioequivalence Under Fed Conditions

10 clinical trials · Condition

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RecordFirmDate
The Study Intends to Show Bioequivalence of the Test Product and the Reference Reference Product in a Crossover Design Study Healthy Volunteers. Additionally, the Safety Profile of Test Product Compared to Reference Product Will be Evaluated. (NCT05329857)AET Laboratories Private Limited2015-12-01
The Study Aims to Show Bioequivalence of the Test Product and the Reference Reference Product in a Crossover Design Study Healthy Volunteers. Additionally, the Safety Profile of Test Product Compared to Reference Product Will be Assessed. (NCT05337969)AET Laboratories Private Limited2015-12-01
Bioavailability Study of Propranolol Under Fed Conditions (NCT00652600)Par Pharmaceutical, Inc.2005-09-01
Bioavailability Study of Leflunomide Tablets Under Fed Conditions (NCT00653003)Par Pharmaceutical, Inc.2003-12-01
Bioavailability Study of Tramadol/APAP Tablets Under Fed Conditions (NCT00652821)Par Pharmaceutical, Inc.2002-05-01
Bioequivalence Study of Cabergoline Tablets and Dostinex Under Fed Conditions (NCT00652873)Par Pharmaceutical, Inc.2001-07-01
A Comparative Bioavailability Study of Lisinopril Tablets, 40 mg - Effect of Food Study (NCT01380431)Par Pharmaceutical, Inc.1999-08-01
Bioavailability Study of Doxycycline Monohydrate Capsules and Monodox Under Fasting and Fed Conditions (NCT00652704)Par Pharmaceutical, Inc.1999-07-01
Bioavailability Study of (Buspar) Buspirone HCl Tablets Under Fasting and Fed Conditions (NCT00652730)Par Pharmaceutical, Inc.1998-07-01

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