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Trial · NCT01236547

Results by group16

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

OutcomeGroupCategoryValueSpreadUnits
(Phase II) Overall Survival(Phase II) Pazopanib, Paclitaxel, IMRT37.195% Confidence Interval 21.1 to 53.2percentage of participants
(Phase II) Overall Survival(Phase II) Placebo, Paclitaxel, IMRT29.095% Confidence Interval 13.2 to 44.8percentage of participants
(Phase I) Number of Participants With Treatment-related Grade 4 Hemorrhage, Grade 4 Febrile Neutropenia, or Grade 5 Adverse Event (AE), or Discontinuation of Treatment Due to Toxicity [Adverse Events of Concern (AEC)]
(Run-in 1) Pazopanib, Paclitaxel, IMRT0Participants
(Phase I) Number of Participants With Treatment-related Grade 4 Hemorrhage, Grade 4 Febrile Neutropenia, or Grade 5 Adverse Event (AE), or Discontinuation of Treatment Due to Toxicity [Adverse Events of Concern (AEC)]
(Run-in 2) Pazopanib, Paclitaxil, IMRT0Participants
(Phase I) Number of Participants With Treatment-related Grade 4 Hemorrhage, Grade 4 Febrile Neutropenia, or Grade 5 Adverse Event (AE), or Discontinuation of Treatment Due to Toxicity [Adverse Events of Concern (AEC)]
(Run-in 3) Pazopanib, Paclitaxel, IMRT2Participants
(Phase I) Number of Participants With Treatment-related Grade 4 Hemorrhage, Grade 4 Febrile Neutropenia, or Grade 5 Adverse Event (AE), or Discontinuation of Treatment Due to Toxicity [Adverse Events of Concern (AEC)]
(Phase II) Pazopanib, Paclitaxel, IMRT0Participants
(Phase II) Local-regional Control(Phase II) Pazopanib, Paclitaxel, IMRT6 months20.095% Confidence Interval 8.6 to 34.8percentage of participants
(Phase II) Local-regional Control(Phase II) Placebo, Paclitaxel, IMRT6 months27.395% Confidence Interval 13.3 to 43.3percentage of participants
(Phase II) Local-regional Control(Phase II) Pazopanib, Paclitaxel, IMRT1 year28.695% Confidence Interval 14.6 to 44.3percentage of participants
(Phase II) Local-regional Control(Phase II) Placebo, Paclitaxel, IMRT1 year33.695% Confidence Interval 17.9 to 50.0percentage of participants
(Phase II) Percentage of Participants With Treatment-related Grade 4 Hemorrhage, Grade 4 Febrile Neutropenia, or Grade 5 Adverse Event, or Discontinuation of Treatment Due to Toxicity [Adverse Events of Concern]
(Phase II) Pazopanib, Paclitaxel, IMRT2.895% Confidence Interval 0.1 to 14.5percentage of participants
(Phase II) Percentage of Participants With Treatment-related Grade 4 Hemorrhage, Grade 4 Febrile Neutropenia, or Grade 5 Adverse Event, or Discontinuation of Treatment Due to Toxicity [Adverse Events of Concern]
(Phase II) Placebo, Paclitaxel, IMRT11.895% Confidence Interval 3.3 to 27.5percentage of participants
(Phase II) Percentage of Participants With Treatment-related Grade 3 or 4 Adverse Events Other Than Grade 4 Hemorrhage or Grade 4 Febrile Neutropenia [Not Adverse Events of Concern](Phase II) Pazopanib, Paclitaxel, IMRT86.195% Confidence Interval 70.5 to 95.3percentage of participants
(Phase II) Percentage of Participants With Treatment-related Grade 3 or 4 Adverse Events Other Than Grade 4 Hemorrhage or Grade 4 Febrile Neutropenia [Not Adverse Events of Concern](Phase II) Placebo, Paclitaxel, IMRT85.395% Confidence Interval 68.9 to 95.0percentage of participants
(Phase II) Percentage of Participants With Complete or Partial Response of the Primary Site After Chemoradiation Per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1(Phase II) Pazopanib, Paclitaxel, IMRT30.495% Confidence Interval 13.2 to 52.9percentage of participants
(Phase II) Percentage of Participants With Complete or Partial Response of the Primary Site After Chemoradiation Per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1(Phase II) Placebo, Paclitaxel, IMRT33.395% Confidence Interval 16.5 to 54.0percentage 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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