Haematological Disorders
Conditions
Interventions
Sponsors
Forma Therapeutics Inc
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patient has confirmed diagnosis of SCD • Documentation of SCD genotype (HbSS, HbSß0-thalassemia or other sickle cell syndrome variants) based on prior history of laboratory testing. Molecular genotyping is not required. SCD genotype may be determined from the results of Hb electrophoresis, high-performance liquid chromatography (HPLC), or similar testing. Note that Hb electrophoresis is performed by the local laboratory at Screening. 2. Hemoglobin = 5.5 and 100 mg/g on 2 measures (separated by = 1 month) as an indicator of early renal disease • History of a conditional TCD in the last 12 months, but not currently being treated with chronic transfusion therapy. Conditional TCD is defined as a TAMMV of 170-199 cm/s by TCD or 155-184 cm/s by imaging TCD (TCDi). 4. For participants taking HU, the dose of HU (mg/kg) must be stable (no more than a 20% change in dosing) for at least 90 days prior to start of study treatment with no anticipated need for dose adjustments during the study, in the opinion of the Investigator 5. Patients on crizanlizumab or L-glutamine treatment at the time of consent may be eligible if they: • Have been on a stable dose for = 12 months at the time of consent (ie, no changes to the dose except for changes to weight or for safety reasons) • For patients on crizanlizumab, have been = 80% compliant with the planned regimen during the 12 months prior to the time of consent
Exclusion criteria
Exclusion criteria: Medical Conditions 1. More than 10 VOCs within the past 12 months that required a hospital, emergency room(ER), or clinic visit 2. Hospitalized for sickle cell crisis or other vaso-occlusive event within 14 days of Screening 3. Abnormal TCD in the prior 12 months Prior/Concomitant Therapy 4. Patients receiving regularly scheduled blood (RBC) transfusion therapy (also termed chronic, prophylactic, or preventive transfusion) 5. Received any blood products within 30 days of starting study treatment 6. Receiving or use of concomitant medications that are strong inducers of cytochrome P450 (CYP) 3A4/5 within 2 weeks of starting study treatment 7. Use of voxelotor within 28 days prior to starting study treatment or anticipated need for this agent during the study 8. Receipt of erythropoietin or other hematopoietic growth factor treatment within 28 days of starting study treatment or anticipated need for such agents during the study 9. Receipt of prior cellular based therapy (eg, hematopoietic cell transplant, gene modification therapy)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To assess the PK of etavopivat in patients with SCD;To assess the safety and tolerability of etavopivat during the 24-week primary treatment period | — |
Secondary
| Measure | Time frame |
|---|---|
| To assess the safety and tolerability of etavopivat during the 72-week treatment extension period;To assess the effects of etavopivat on hemoglobin (Hb) response;To describe the occurrence of VOCs in enrolled patients;To assess changes in fatigue of patients with SCD taking etavopivat;To assess changes in cerebral blood flow in patients with SCD taking etavopivat | — |
Countries
Kenya, Nigeria
Contacts
Public ContactMichelle Botha
Regulatory
Outcome results
None listed