Mesalamine 4 gm/60 mL Rectal Enema
This study has been completed.
Sponsor:
Teva Pharmaceuticals USA
Information provided by:
Teva Pharmaceuticals USA
ClinicalTrials.gov Identifier:
NCT00840203
First received: February 6, 2009
Last updated: September 1, 2009
Last verified: September 2009
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Purpose
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.
| Condition | Intervention | Phase |
|---|---|---|
|
Healthy |
Drug: Rowasa® 4 gm/60 mL Rectal Enema Drug: Mesalamine 4 gm/60 mL Rectal Enema |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Bio-equivalence Study Intervention Model: Crossover Assignment Masking: Open Label |
| Official Title: | A Study to Evaluate the Relative Bioavailability of Two Mesalamine 4 gm/60 mL Rectal Enema Formulations |
Resource links provided by NLM:
Further study details as provided by Teva Pharmaceuticals USA:
Primary Outcome Measures:
- Cmax - Maximum Observed Concentration [ Time Frame: Blood samples collected over 48 hour period ] [ Designated as safety issue: No ]
- AUC0-inf - Area Under the Concentration-time Curve From Time Zero to Infinity (Extrapolated) [ Time Frame: Blood samples collected over 48 hour period ] [ Designated as safety issue: No ]
- AUC0-t - Area Under the Concentration-time Curve From Time Zero to Time of Last Non-zero Concentration (Per Participant) [ Time Frame: Blood samples collected over 48 hour period ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Cmax - Maximum Observed Concentration [ Time Frame: Blood samples collected over 48 hour period ] [ Designated as safety issue: No ]
- AUC0-inf - Area Under the Concentration-time Curve From Time Zero to Infinity (Extrapolated) [ Time Frame: Blood samples collected over 48 hour period ] [ Designated as safety issue: No ]
- AUC0-t - Area Under the Concentration-time Curve From Time Zero to Time of Last Non-zero Concentration (Per Participant) [ Time Frame: Blood samples collected over 48 hour period ] [ Designated as safety issue: No ]
| Enrollment: | 72 |
| Study Start Date: | May 2003 |
| Study Completion Date: | June 2003 |
| Primary Completion Date: | June 2003 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Mesalamine
Mesalamine 4gm/60mL Rectal Enema (test) dosed in first period followed by Rowasa® 4gm/60mL Rectal Enema (reference) dosed in second period
|
Drug: Mesalamine 4 gm/60 mL Rectal Enema
1 x 4 gm/60 mL, single-dose
|
|
Active Comparator: Rowasa®
Rowasa® 4gm/60mL Rectal Enema (reference) dosed in first period followed by Mesalamine 4gm/60mL Rectal Enema (test) dosed in second period
|
Drug: Rowasa® 4 gm/60 mL Rectal Enema
1 x 4 gm/60 mL, single-dose
|
Detailed Description:
Criteria for Evaluation: FDA Bioequivalence Criteria
Statistical Methods: FDA bioequivalence statistical methods
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Males and females, 18 years or older, with a body mass index (BMI) of 30 or less.
- Good health as determined by lack of clinically significant abnormalities in health assessments performed at screening.
- Signed informed consent form, which meets all criteria of current FDA regulations.
- If female and of child bearing potential prepared to abstain from sexual intercourse or use a reliable method of contraception during the study (e.g. condom, IUD, hormonal contraceptives).
Exclusion Criteria:
- If female pregnant, lactating, or likely to become pregnant during the study.
- History of allergy or sensitivity to mesalamine or other salicylic drugs (e.g. aspirin, sulfasalazine) or history of any drug hypersensitivity or intolerance which, in the opinion of the Investigator, would compromise the safety of the subject or the study.
- Colitis, hemorrhoids, anal fissures, or other disease of the anus, rectum or colon.
- Significant history or current evidence of chronic infections disease, system disorder or organ disorder.
- History of psychiatric disorders occuring within the last two years that required hospitalization or medication.
- Presence of a medical condition requiring regular treatment with prescription drugs (other than contraceptives).
- Use of pharmacologic agents known to significantly induce or inhibit drug-metabolizing enzymes within 30 days prior to dosing.
- Receipt of any drug as part of a research study within 30 days prior to dosing.
- Drug or alcohol addiction requiring treatment in the past 12 months.
- Donation or significant loss of whole blood (480 mL or more) within 30 days or plasma within 14 days prior to dosing.
- Positive test for HIV, Hepatitis B surface antigen, or Hepatitis C antibody.
- Positive test results for drugs of abuse at screening.
- Positive serum pregnancy test at screening.
- Unable or unwilling to tolerate multiple venipunctures.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00840203
Locations
| United States, Pennsylvania | |
| Novum Pharmaceutical Research Services | |
| Pittsburgh, Pennsylvania, United States, 15206 | |
Sponsors and Collaborators
Teva Pharmaceuticals USA
Investigators
| Principal Investigator: | Shirley Ann Kennedy, M.D. | Novum Pharmaceutical Research Services |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00840203 History of Changes |
| Other Study ID Numbers: | 10336014 |
| Study First Received: | February 6, 2009 |
| Results First Received: | June 30, 2009 |
| Last Updated: | September 1, 2009 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Teva Pharmaceuticals USA:
|
Bioequivalence Healthy Subjects |
Additional relevant MeSH terms:
|
Mesalamine Anti-Inflammatory Agents, Non-Steroidal Analgesics, Non-Narcotic Analgesics Sensory System Agents Peripheral Nervous System Agents |
Physiological Effects of Drugs Pharmacologic Actions Anti-Inflammatory Agents Therapeutic Uses Antirheumatic Agents Central Nervous System Agents |
ClinicalTrials.gov processed this record on May 16, 2013