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Trial · NCT01707472

Results by group30

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

OutcomeGroupCategoryValueSpreadUnits
Percentage of Participants Experiencing Treatment-Emergent Adverse EventsSimtuzumab in HIV Participants100percentage of participants
Percentage of Participants Experiencing Treatment-Emergent Adverse EventsSimtuzumab in HCV Participants100percentage of participants
Percentage of Participants Experiencing Treatment-Emergent Adverse EventsSimtuzumab in HIV/HCV Co-Infected Participants100percentage of participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HIV ParticipantsFibrosis improved: -20Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HCV ParticipantsFibrosis improved: -21Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HIV/HCV Co-Infected ParticipantsFibrosis improved: -20Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HIV ParticipantsFibrosis improved: -11Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HCV ParticipantsFibrosis improved: -11Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HIV/HCV Co-Infected ParticipantsFibrosis improved: -10Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HIV ParticipantsFibrosis did not change: 02Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HCV ParticipantsFibrosis did not change: 04Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HIV/HCV Co-Infected ParticipantsFibrosis did not change: 05Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HIV ParticipantsFibrosis worsened: 10Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HCV ParticipantsFibrosis worsened: 10Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HIV/HCV Co-Infected ParticipantsFibrosis worsened: 12Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HIV ParticipantsFibrosis worsened: 20Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HCV ParticipantsFibrosis worsened: 20Participants
Number of Participants With a Change From Baseline in Ishak Fibrosis Stage Score at Week 24Simtuzumab in HIV/HCV Co-Infected ParticipantsFibrosis worsened: 21Participants
Change From Baseline in HVPG at Week 24Simtuzumab in HIV Participants2Standard Deviation 2.4mm Hg
Change From Baseline in HVPG at Week 24Simtuzumab in HCV Participants0Standard Deviation 3.4mm Hg

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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