CLINICAL_TRIALS
ClinicalTrials.gov record with results posted
A Phase 1/2/3 Study to Evaluate the Safety and Efficacy of a Single Dose of Autologous CRISPR-Cas9 Modified CD34+ Human Hematopoietic Stem and Progenitor Cells (CTX001) in Subjects With Severe Sickle Cell Disease
This page presents selected fields from the linked source record. It does not add a medical interpretation.
Record identity and dates
- Source
- ClinicalTrials.gov
- Source record ID
- NCT03745287
- Title field or adapter rule
- protocolSection.identificationModule.officialTitle
- Ingested At
- 2026-09-17T00:07:57.752294+00:00
- Published At
- 2026-09-16T00:00:00+00:00
- Record Updated At
- 2026-09-16
- Results Posted At
- 2026-09-16
- Timestamp Basis
- source retrieval time was not retained by the feed adapter
- Date limitation
- source retrieval time was not retained by the feed adapter
Fields recorded by this source
- protocolSection.conditionsModule.conditions
["Sickle Cell Disease", "Hematological Diseases", "Hemoglobinopathies"]- protocolSection.statusModule.lastUpdatePostDateStruct.date
"2026-09-16"- protocolSection.identificationModule.nctId
"NCT03745287"- protocolSection.identificationModule.officialTitle
"A Phase 1/2/3 Study to Evaluate the Safety and Efficacy of a Single Dose of Autologous CRISPR-Cas9 Modified CD34+ Human Hematopoietic Stem and Progenitor Cells (CTX001) in Subjects With Severe Sickle Cell Disease"- protocolSection.statusModule.overallStatus
"COMPLETED"- protocolSection.designModule.phases
["PHASE2", "PHASE3"]- protocolSection.statusModule.resultsFirstPostDateStruct.date
"2026-09-16"
Study condition terms
Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.
This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.