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Trial · NCT00856492

Results by group252

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

OutcomeGroupCategoryValueSpreadUnits
Number of Patients With Pathological Complete Response RateArm 1 (Nab-Paclitaxel + Bevacizumab - AC+PEG-G))35Participants
Number of Patients With Pathological Complete Response RateArm 2/3 (Nab-Paclitaxel/AC+PEG-G))24Participants
Overall SurvivalArm 1 (Nab-Paclitaxel + Bevacizumab - AC+PEG-G))14deaths
Overall SurvivalArm 2/3 (Nab-Paclitaxel/AC+PEG-G))17deaths
Event-free SurvivalArm 1 (Nab-Paclitaxel + Bevacizumab - AC+PEG-G))20participants
Event-free SurvivalArm 2/3 (Nab-Paclitaxel/AC+PEG-G))24participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm I (Nab-Paclitaxel + Bevacizumab - AC+PEG-G))Abdominal pain2Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm II (Nab-Paclitaxel - AC+PEG-G)Abdominal pain0Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm III (AC+PEG-G - Nab-Paclitaxel)Abdominal pain0Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm I (Nab-Paclitaxel + Bevacizumab - AC+PEG-G))Adult respiratory distress syndrome1Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm II (Nab-Paclitaxel - AC+PEG-G)Adult respiratory distress syndrome0Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm III (AC+PEG-G - Nab-Paclitaxel)Adult respiratory distress syndrome0Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm I (Nab-Paclitaxel + Bevacizumab - AC+PEG-G))Alanine aminotransferase increased2Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm II (Nab-Paclitaxel - AC+PEG-G)Alanine aminotransferase increased2Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm III (AC+PEG-G - Nab-Paclitaxel)Alanine aminotransferase increased1Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm I (Nab-Paclitaxel + Bevacizumab - AC+PEG-G))Anemia13Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm II (Nab-Paclitaxel - AC+PEG-G)Anemia6Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm III (AC+PEG-G - Nab-Paclitaxel)Anemia13Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm I (Nab-Paclitaxel + Bevacizumab - AC+PEG-G))Anorectal infection2Participants
Number of Adverse Events That Are Possibly, Probably or Definitely Related to Study DrugArm II (Nab-Paclitaxel - AC+PEG-G)Anorectal infection0Participants

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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