Trial · NCT02850406
Adverse events1,568
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
1 to 20 of 1,568
Download this page as JSON| Type | Event | Organ system | Group | Affected | At risk | Events |
|---|---|---|---|---|---|---|
| other | Sickle cell anaemia with crisis | Blood and lymphatic system disorders | Part A: Participants Aged 12 to 17 Years: Voxelotor 600 mg | 1 | 7 | |
| other | Sickle cell anaemia with crisis | Blood and lymphatic system disorders | Part A: Participants Aged 6 to 11 Years: Voxelotor 600 mg | 1 | 6 | |
| other | Sickle cell anaemia with crisis | Blood and lymphatic system disorders | Part B: Voxelotor 900 mg QD | 5 | 25 | |
| other | Sickle cell anaemia with crisis | Blood and lymphatic system disorders | Part B: Voxelotor 1500 mg QD | 3 | 15 | |
| other | Sickle cell anaemia with crisis | Blood and lymphatic system disorders | Part C: Participants Aged 4 to 11 Years: Voxelotor 1500 mg QD | 10 | 51 | |
| other | Sickle cell anaemia with crisis | Blood and lymphatic system disorders | Part C: Participants Aged 12 to 17 Years: Voxelotor 1500 mg QD | 2 | 11 | |
| other | Sickle cell anaemia with crisis | Blood and lymphatic system disorders | Part D: Participants Aged 6 Months to <2 Years: Voxelotor 1500 mg QD | 5 | 9 | |
| other | Sickle cell anaemia with crisis | Blood and lymphatic system disorders | Part D: Participants Aged 2 to <4 Years: Voxelotor 1500 mg QD | 10 | 23 | |
| other | Acute chest syndrome | Respiratory, thoracic and mediastinal disorders | Part A: Participants Aged 12 to 17 Years: Voxelotor 600 mg | 0 | 7 | |
| other | Acute chest syndrome | Respiratory, thoracic and mediastinal disorders | Part A: Participants Aged 6 to 11 Years: Voxelotor 600 mg | 0 | 6 | |
| other | Acute chest syndrome | Respiratory, thoracic and mediastinal disorders | Part B: Voxelotor 900 mg QD | 2 | 25 | |
| other | Acute chest syndrome | Respiratory, thoracic and mediastinal disorders | Part B: Voxelotor 1500 mg QD | 0 | 15 | |
| other | Acute chest syndrome | Respiratory, thoracic and mediastinal disorders | Part C: Participants Aged 4 to 11 Years: Voxelotor 1500 mg QD | 0 | 51 | |
| other | Acute chest syndrome | Respiratory, thoracic and mediastinal disorders | Part C: Participants Aged 12 to 17 Years: Voxelotor 1500 mg QD | 0 | 11 | |
| other | Acute chest syndrome | Respiratory, thoracic and mediastinal disorders | Part D: Participants Aged 6 Months to <2 Years: Voxelotor 1500 mg QD | 0 | 9 | |
| other | Acute chest syndrome | Respiratory, thoracic and mediastinal disorders | Part D: Participants Aged 2 to <4 Years: Voxelotor 1500 mg QD | 0 | 23 | |
| other | Osteonecrosis | Musculoskeletal and connective tissue disorders | Part A: Participants Aged 12 to 17 Years: Voxelotor 600 mg | 0 | 7 | |
| other | Osteonecrosis | Musculoskeletal and connective tissue disorders | Part A: Participants Aged 6 to 11 Years: Voxelotor 600 mg | 0 | 6 | |
| other | Osteonecrosis | Musculoskeletal and connective tissue disorders | Part B: Voxelotor 900 mg QD | 1 | 25 | |
| other | Osteonecrosis | Musculoskeletal and connective tissue disorders | Part B: Voxelotor 1500 mg QD | 0 | 15 |
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.
For software
Read this list from software.
Twenty rows a page, as JSON. No key.
GET https://conductscience.org/api/trials/v1/NCT02850406/events