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Trial · NCT01210482

Results by group20

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Number of Participants With Adverse Drug ReactionsTORISEL Injection (Temsirolimus)ADR778Participants
Number of Participants With Adverse Drug ReactionsTORISEL Injection (Temsirolimus)Serious ADR352Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Mucositis related adverse events279Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Skin disorder209Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Interstitial lung disease174Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Interstitial lung disease suspected events3Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Infections141Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Hypercholesterolaemia/hyperlipidaemia140Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Diabetes/hyperglycaemia131Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Diarrhoea43Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Hypophosphataemia39Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Dyspnea35Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Acute renal failure17Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Hypokalaemia14Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Hypersensitivity reaction11Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Gastrointestinal perforation1Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Intracerebral hemorrhage1Participants
Number of Participants With Adverse Drug Reactions of Major Investigation ItemsTORISEL Injection (Temsirolimus)Wound healing abnormal1Participants
Overall Response RateTORISEL Injection (Temsirolimus)6.795% Confidence Interval 4.9 to 8.9Percentage of Participants
Response Rate Excluding Participants Evaluated as UnassessableTORISEL Injection (Temsirolimus)7.4Percentage of Participants

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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