Autopsy report · NCT00414024
Safety and Efficacy of Tegaserod in Opioid-induced Constipation in Patients With Non-cancer Pain.
Cause of deathRegulatory or ethics
“This study was terminated early as a result of regulatory action suspending tegaserod use in 2007”
Life of this trial
- Registered 2 months before it started.
- Ran for about 3 months before it stopped.
- 11 participants enrolled.
- No results are posted on the registry.
Vital statistics
- Status
- Terminated
- Phase
- Phase 3
- Sponsor
- Novartis
- Sponsor type
- Industry
- Conditions
- Opioid-induced Constipation
- Interventions
- Tegaserod
- Participants
- 11
- Sites
- 6
- Countries
- China, Egypt, Singapore, Taiwan, United States, Venezuela
Trials that died the same way
- Safety and Efficacy of AT-1501 in Patients With IgA Nephropathy (IgAN)
“An administrative decision was made to terminate the AT-1501-N205 study. This voluntary business-related decision was not related to the safety of tegoprubart (AT-1501). Available safety data demonstrated tegoprubart to be safe and well tolerated.” - Common Safety Follow-up Trial of Tecemotide (L-BLP25)
“The study is terminated prematurely as the sponsor decided to discontinue program with Tecemotide in NSCLC.” - Relative Bioavailability Study of Ropinirole Implants in Parkinson's Patients on L-Dopa Switched From Oral Ropinirole
“This study was terminated for reasons not related to efficacy or safety” - A Study of TCD601 (Siplizumab) in New Onset Type 1 Diabetes Patients
“The study has been early terminated due to business reasons. This decision is not related to any safety, efficacy, or regulatory concerns.” - A Dose Exploration Study With Birabresib (MK-8628) in Participants With Selected Hematologic Malignancies (MK-8628-005)
“This study was terminated due to limited efficacy and not due to safety reasons”
Look deeper
- The official registry record (the source of truth)
- Record history: every change the sponsor made
- Open it in the database
Everything here comes from the current ClinicalTrials.gov record. The timeline uses the record’s dates; dates marked planned are the sponsor’s plans. The cause of death is an automatic, unverified label. This is research information, not medical advice.