Clinical trial
AN INVESTIGATOR-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO ESTABLISH THERAPEUTIC EQUIVALENCE OF 1000 mg MESALAMINE RECTAL SUPPOSITORIES AND CANASA® RECTAL SUPPOSITORIES (1000 mg MESALAMINE, USP) IN THE TREATMENT OF MILD TO MODERATE ULCERATIVE PROCTITIS
NCT01172444 is registered in ClinicalTrials.gov with Sandoz as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- AN INVESTIGATOR-BLIND, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL-GROUP STUDY TO ESTABLISH THERAPEUTIC EQUIVALENCE OF 1000 mg MESALAMINE RECTAL SUPPOSITORIES AND CANASA® RECTAL SUPPOSITORIES (1000 mg MESALAMINE, USP) IN THE TREATMENT OF MILD TO MODERATE ULCERATIVE PROCTITIS
- Lead sponsor
- Sandoz
- Phase
- Phase 3
- Overall status
- Terminated
- Start date
- June 30, 2010
- Completion date
- December 31, 2012
- Enrollment
- 158 (actual)
- Sites
- 38
Conditions
As the registry lists them; a condition with its own page is linked.