Novum Pharmaceutical Research Services
Pittsburgh, Pennsylvania, 15206, United States
NCT Number: NCT00840203
The objective of this study is to evaluate the relative bioavailability of the test formulation of mesalamine suspension rectal enema with the already marketed reference formulation Rowasa® in healthy, adult subjects.
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Notify Me18 year and older
All sexes
Interventional
Phase 1
Pittsburgh, Pennsylvania, 15206, United States
Criteria for Evaluation: FDA Bioequivalence Criteria
Statistical Methods: FDA bioequivalence statistical methods
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
1 x 4 gm/60 mL, single-dose
1 x 4 gm/60 mL, single-dose
Time frame: Blood samples collected over 48 hour period
Bioequivalence based on Cmax
Time frame: Blood samples collected over 48 hour period
Bioequivalence based on AUC0-inf
Time frame: Blood samples collected over 48 hour period
Bioequivalence based on AUC0-t
Time frame: Blood samples collected over 48 hour period
Cmax results for N-Acetylmesalamine metabolite
Time frame: Blood samples collected over 48 hour period
AUC0-inf results for N-Acetylmesalamine metabolite
Time frame: Blood samples collected over 48 hour period
AUC0-t results for N-Acetylmesalamine metabolite
Teva Pharmaceuticals USA
Industry
A Study to Evaluate the Relative Bioavailability of Two Mesalamine 4 gm/60 mL Rectal Enema Formulations
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