Table I.
Trial | NCT identifier | Status | Reported results |
---|---|---|---|
Study of decitabine and THU in patients with SCD | NCT01685515 | Active, not recruiting | N/A |
Gum arabic as a HbF agent in SCA | NCT02467257 | Completed | None |
Hydroxyurea and erythropoietin to treat SCA | NCT00270478 | Completed | None |
Study to determine the maximum tolerated dose, safety and effectiveness of pomalidomide for patients with SCD | NCT01522547 | Completed | None |
Effects of HQK-1001 in patients with SCD | NCT01601340 | Completed | None |
Decitabine for high-risk SCD | NCT01375608 | Completed | 4·8% average HbF increase |
Effectiveness of arginine as a treatment for SCA | NCT00513617 | Completed | None for HbF induction |
Fetal haemoglobin induction treatment with metformin | NCT02981329 | Recruiting | N/A |
Gene transfer for patients with SCD | NCT02186418 | Recruiting | N/A |
Study of panobinostat in patients with SCD | NCT01245179 | Recruiting | N/A |
A study to evaluate safety, pharmacokinetic, and biological activity of INCB059872 | NCT03132324 | Recruiting | N/A |
Efficacy of vorinostat to induce HbF in SCD | NCT01000155 | Terminated | None; closed for slow accrual |
HbF, fetal haemoglobin; N/A, not applicable; NCT, National Clinical Trial registry (https://clinicaltrials.gov/); None, closed or completed without reported results; SCA, sickle cell anaemia; SCD, sickle cell disease; THU, tetrahydrouridine.