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Trial · NCT00557856

Results by group1,210

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

OutcomeGroupCategoryValueSpreadUnits
Maximum Tolerated Dose (MTD): Part 1PF-0344696210.0milligram/kilogram (mg/kg)
Recommended Phase 2 Dose (RP2D): Part 1PF-034469627.0mg/kg
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 0.5 mg/kg: Part 1All causalities5participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 1 mg/kgAll causalities5participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 2 mg/kg : Part 1All causalities6participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 3 mg/kg: Part 1All causalities3participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 4.5 mg/kg: Part 1All causalities4participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 6.75 mg/kg: Part 1All causalities8participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 10 mg/kg: Part 1All causalities7participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 15 mg/kg: Part 1All causalities6participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 7 mg/kg: Part 2All causalities24participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 0.5 mg/kg: Part 1Treatment-related4participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 1 mg/kgTreatment-related2participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 2 mg/kg : Part 1Treatment-related4participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 3 mg/kg: Part 1Treatment-related1participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 4.5 mg/kg: Part 1Treatment-related3participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 6.75 mg/kg: Part 1Treatment-related7participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 10 mg/kg: Part 1Treatment-related6participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 15 mg/kg: Part 1Treatment-related2participants
Number of Participants With Treatment-Emergent Adverse Events (AEs): Part 1 and Part 2PF-03446962 7 mg/kg: Part 2Treatment-related20participants

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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