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Trial · NCT04447287

Adverse events115

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherConstipationGastrointestinal disordersBuprenorphine/Naloxone4234
otherConstipationGastrointestinal disordersASP8062 in Combination With Buprenorphine/Naloxone (Investigational Period)0120
otherConstipationGastrointestinal disordersASP8062 in Combination With Buprenorphine/Naloxone (Down-titration Period)0120
otherConstipationGastrointestinal disordersPlacebo ASP8062 in Combination With Buprenorphine/Naloxone (Investigational Period)262
otherConstipationGastrointestinal disordersPlacebo ASP8062 in Combination With Buprenorphine/Naloxone (Down-titration Period)060
otherDyspepsiaGastrointestinal disordersBuprenorphine/Naloxone0230
otherDyspepsiaGastrointestinal disordersASP8062 in Combination With Buprenorphine/Naloxone (Investigational Period)0120
otherDyspepsiaGastrointestinal disordersASP8062 in Combination With Buprenorphine/Naloxone (Down-titration Period)1121
otherDyspepsiaGastrointestinal disordersPlacebo ASP8062 in Combination With Buprenorphine/Naloxone (Investigational Period)161
otherDyspepsiaGastrointestinal disordersPlacebo ASP8062 in Combination With Buprenorphine/Naloxone (Down-titration Period)060
otherNauseaGastrointestinal disordersBuprenorphine/Naloxone1231
otherNauseaGastrointestinal disordersASP8062 in Combination With Buprenorphine/Naloxone (Investigational Period)0120
otherNauseaGastrointestinal disordersASP8062 in Combination With Buprenorphine/Naloxone (Down-titration Period)0120
otherNauseaGastrointestinal disordersPlacebo ASP8062 in Combination With Buprenorphine/Naloxone (Investigational Period)161
otherNauseaGastrointestinal disordersPlacebo ASP8062 in Combination With Buprenorphine/Naloxone (Down-titration Period)060
otherSalivary hypersecretionGastrointestinal disordersBuprenorphine/Naloxone0230
otherSalivary hypersecretionGastrointestinal disordersASP8062 in Combination With Buprenorphine/Naloxone (Investigational Period)1121
otherSalivary hypersecretionGastrointestinal disordersASP8062 in Combination With Buprenorphine/Naloxone (Down-titration Period)0120
otherSalivary hypersecretionGastrointestinal disordersPlacebo ASP8062 in Combination With Buprenorphine/Naloxone (Investigational Period)060
otherSalivary hypersecretionGastrointestinal disordersPlacebo ASP8062 in Combination With Buprenorphine/Naloxone (Down-titration Period)060

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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