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Trial · NCT02850406

Adverse events1,568

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherSickle cell anaemia with crisisBlood and lymphatic system disordersPart A: Participants Aged 12 to 17 Years: Voxelotor 600 mg17
otherSickle cell anaemia with crisisBlood and lymphatic system disordersPart A: Participants Aged 6 to 11 Years: Voxelotor 600 mg16
otherSickle cell anaemia with crisisBlood and lymphatic system disordersPart B: Voxelotor 900 mg QD525
otherSickle cell anaemia with crisisBlood and lymphatic system disordersPart B: Voxelotor 1500 mg QD315
otherSickle cell anaemia with crisisBlood and lymphatic system disordersPart C: Participants Aged 4 to 11 Years: Voxelotor 1500 mg QD1051
otherSickle cell anaemia with crisisBlood and lymphatic system disordersPart C: Participants Aged 12 to 17 Years: Voxelotor 1500 mg QD211
otherSickle cell anaemia with crisisBlood and lymphatic system disordersPart D: Participants Aged 6 Months to <2 Years: Voxelotor 1500 mg QD59
otherSickle cell anaemia with crisisBlood and lymphatic system disordersPart D: Participants Aged 2 to <4 Years: Voxelotor 1500 mg QD1023
otherAcute chest syndromeRespiratory, thoracic and mediastinal disordersPart A: Participants Aged 12 to 17 Years: Voxelotor 600 mg07
otherAcute chest syndromeRespiratory, thoracic and mediastinal disordersPart A: Participants Aged 6 to 11 Years: Voxelotor 600 mg06
otherAcute chest syndromeRespiratory, thoracic and mediastinal disordersPart B: Voxelotor 900 mg QD225
otherAcute chest syndromeRespiratory, thoracic and mediastinal disordersPart B: Voxelotor 1500 mg QD015
otherAcute chest syndromeRespiratory, thoracic and mediastinal disordersPart C: Participants Aged 4 to 11 Years: Voxelotor 1500 mg QD051
otherAcute chest syndromeRespiratory, thoracic and mediastinal disordersPart C: Participants Aged 12 to 17 Years: Voxelotor 1500 mg QD011
otherAcute chest syndromeRespiratory, thoracic and mediastinal disordersPart D: Participants Aged 6 Months to <2 Years: Voxelotor 1500 mg QD09
otherAcute chest syndromeRespiratory, thoracic and mediastinal disordersPart D: Participants Aged 2 to <4 Years: Voxelotor 1500 mg QD023
otherOsteonecrosisMusculoskeletal and connective tissue disordersPart A: Participants Aged 12 to 17 Years: Voxelotor 600 mg07
otherOsteonecrosisMusculoskeletal and connective tissue disordersPart A: Participants Aged 6 to 11 Years: Voxelotor 600 mg06
otherOsteonecrosisMusculoskeletal and connective tissue disordersPart B: Voxelotor 900 mg QD125
otherOsteonecrosisMusculoskeletal and connective tissue disordersPart B: Voxelotor 1500 mg QD015

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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