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Last Updated: October 19, 2019

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CLINICAL TRIALS PROFILE FOR CEFPROZIL

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Clinical Trials for Cefprozil

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00778245 Bioequivalence Study of Cefprozil Tablets, USP 500 mg Undef Fed Conditions Completed Ranbaxy Laboratories Limited N/A 2005-05-01 The objective of this study is to assess the single - dose relative bioavailability of Ranbaxy and Bristol-Myers Squibb Company (CEFZIL ®) 500 mg cefprozil tablets, under fed conditions.
NCT00778557 Bioequivalence Study of Cefprozil 250 mg/ 5mL Powder For Oral Suspension Under Fasting Conditions Completed Ranbaxy Laboratories Limited N/A 2005-06-01 The study was conducted as a blinded, randomized, 3-way crossover study to compare the single-dose relative bioavailability of Cefprozil 250 mg/5 mL Oral suspension versus Cefzil TM Powder for Oral Suspension (250 mg/5 mL) following one 5 mL dose under fasting conditions
NCT00778739 Bioequivalence Study of Cefprozil 250 mg/ 5mL Powder For Oral Suspension Under Fed Conditions Completed Ranbaxy Laboratories Limited N/A 2005-06-01 The study was conducted as an open-label, randomized, 2-way crossover study to compare the single-dose relative bioavailability of Cefprozil 250 mg/5 mL Oral suspension versus Cefzil TM Powder for Oral Suspension (250 mg/5 mL) following one 5 mL dose under fed conditions
NCT00778778 Bioequivalence Study of Cefprozil Tablets, USP 500 mg Under Fasting Conditions Completed Ranbaxy Laboratories Limited N/A 2005-05-01 The objective of this study was to assess the single-dose relative bioavailability of Ranbaxy and Bristol-Myers Squibb Company (CEFZIL ®) 500 mg cefprozil tablets, under fasting conditions.
NCT00835354 Cefprozil for Oral Suspension 250 mg/5 mL, Non-fasting Completed Teva Pharmaceuticals USA Phase 1 2004-05-01 The objective of this study is to compare the relative bioavailability of cefprozil for oral suspension 250 mg/5 mL (TEVA Pharmaceuticals USA) with that of CEFZIL® for Oral Suspension 250 mg/5 mL (Bristol-Myers Squibb) in healthy, non-smoking adults under non-fasting conditions.
NCT00835614 Cefprozil for Oral Suspension 250 mg/5 mL, Fasting Completed Teva Pharmaceuticals USA Phase 1 2004-04-01 The objective of this study is to compare the relative bioavailability of cefprozil for oral suspension 250 mg/5 mL (TEVA Pharmaceuticals USA) with that of CEFZIL® for Oral Suspension 250 mg/5 mL (Bristol-Myers Squibb) in healthy, non-smoking adults under fasting conditions.
NCT00840281 Cefprozil 500 mg Tablets Under Fasting Conditions Completed Teva Pharmaceuticals USA Phase 1 2003-09-01 The objective of this study is to compare the relative bioavailability of cefprozil 500 mg tablets (Teva Pharmaceuticals USA) with that of Cefzil® 500 mg tablets (Bristol-Myers Squibb) in healthy, non-smoking adults under fasting conditions.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Cefprozil

Condition Name

Condition Name for Cefprozil
Intervention Trials
Healthy 12
Osteomyelitis 1
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Condition MeSH

Condition MeSH for Cefprozil
Intervention Trials
Osteomyelitis 1
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Clinical Trial Locations for Cefprozil

Trials by Country

Trials by Country for Cefprozil
Location Trials
United States 7
Canada 4
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Trials by US State

Trials by US State for Cefprozil
Location Trials
Missouri 4
Texas 2
Kentucky 1
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Clinical Trial Progress for Cefprozil

Clinical Trial Phase

Clinical Trial Phase for Cefprozil
Clinical Trial Phase Trials
Phase 1 8
Phase 0 1
N/A 4
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Clinical Trial Status

Clinical Trial Status for Cefprozil
Clinical Trial Phase Trials
Completed 12
Not yet recruiting 1
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Clinical Trial Sponsors for Cefprozil

Sponsor Name

Sponsor Name for Cefprozil
Sponsor Trials
Teva Pharmaceuticals USA 4
Ranbaxy Laboratories Limited 4
Sandoz 4
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Sponsor Type

Sponsor Type for Cefprozil
Sponsor Trials
Industry 12
Other 3
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Serving leading biopharmaceutical companies globally:

Medtronic
Moodys
Dow
AstraZeneca
Johnson and Johnson
Express Scripts

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