Phase 2 Sickle cell disease trials recruiting now
All Sickle cell disease trials, every phase
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Phase 2 recruiting
Other phases for Sickle cell disease
Phase 2 Sickle cell disease trials
- A Phase 2 Open-label Study to Evaluate the Activity of Etavopivat on Transcranial Doppler Velocities in Pediatric Patients With Sickle Cell Disease Who Are at Increased Risk for Primary Stroke
- A Phase 2/3 Study of Osivelotor in Adult and Adolescent Participants With SCD
- A Phase I/II Study of ITU512 in Healthy Participants and Patients With Sickle Cell Disease
- A Study of Immune Suppression Treatment for People With Sickle Cell Disease or β-Thalassemia Who Are Going to Receive an Allogeneic Hematopoietic Cell Transplantation (HCT)
- A Study to Evaluate BMS-986470 in Healthy Volunteers and Participants With Sickle Cell Disease
- A Study to Evaluate the Pharmacokinetics and Safety of Etavopivat in Pediatric Patients With Sickle Cell Disease
- A Trial to Assess Haploidentical T-depleted Stem Cell Transplantation in Patients With SCD
- Acceptance and Commitment Therapy for Adolescents and Young Adults With Sickle Cell Disease
- Alendronate for Osteonecrosis in Adults With Sickle Cell Disease
- Allo HSCT for High Risk Hemoglobinopathies
- AlloSCT for Malignant and Non-malignant Hematologic Diseases Utilizing Alpha/Beta T Cell and CD19+ B Cell Depletion
- Arginine Therapy for the Treatment of Pain in Children With Sickle Cell Disease
- Cannabidiol in Sickle Cell Disease
- Cannabinoids for the Reduction of Inflammation and Sickle Cell Related Pain
- Cognitive Remediation Intervention to Prepare for Transition of Care
- Early Screening and Treatment of Heart Complication in Sickle Cell Disease
- Efficacy Safety Study of Gene Therapy for Sickle Cell DiseaseSCD Using Autologous CD34+ Cells Transduced ex Vivo, Carrying a Corrected Globin Gene and a Silencing RNA.
- Efficacy and Safety of SIL-8301 for Control of Hemolysis in a Uniform Sickle Cell Disease Endotype
- Gene Correction in Autologous CD34+ Hematopoietic Stem Cells (HbS to HbA) to Treat Severe Sickle Cell Disease
- Haploidentical Donor Hematopoietic Cell Transplant for Sickle Cell Disease
- Intravenous L-Citrulline for Vaso-occlusive Pain Episode in Sickle Cell Disease
- Investigation Into the Use of BAH243 Lentiviral Vector for Gene Therapy in Treating Sickle Cell Disease
- Minimizing Toxicity in HLA-identical Sibling Donor Transplantation for Children With Sickle Cell Disease
- Myeloablative Conditioning, Prophylactic Defibrotide and Haplo AlloSCT for Patients With Sickle Cell Disease
- Nonmyeloablative Stem Cell Transplant in Children With Sickle Cell Disease and a Major ABO-Incompatible Matched Sibling Donor
- Optimizing Hydroxyurea Dosage With Pharmakokinetic in Patients Suffering of Moderate to Severe Sickle Cell Anemia
- Optimizing Hydroxyurea Therapy in Children With Sickle Cell Anemia In Malaria Endemic Areas: The NOHARM Maximum Tolerated Dose (MTD) Study
- Partial Stem Cell Transplant for Sickle Cell Disease From Matched Donors
- Pharmacokinetics, Efficacy and Safety of Twice Daily Dosing Regimen of Hydroxycarbamide Dispersible Tablets in Children With Sickle Cell Disease
- RH Genotype Matched RBC Transfusions
- Reduced Intensity Conditioning and Familial HLA-Mismatched BMT for Non-Malignant Disorders
- Reduced Intensity Conditioning for Non-Malignant Disorders Undergoing UCBT, BMT or PBSCT
- Relationship Between Abnormal Myocardial Perfusion and Diastolic Dysfunction in Sickle Cell Disease Using PET
- Repeat Peripheral Blood Stem Cell Transplantation for Patients With Sickle Cell Disease and Falling Donor Myeloid Chimerism Levels
- Ruxolitinib-Enhanced Haplo HCT for Children and Young Adults With Sickle Cell Disease
- Safety of Anumigilimab (CSL324) in Adults With Sickle Cell Disease (SCD)
- Safety, Efficacy, and Pharmacokinetics of CSL889 in Adults and Adolescents With Sickle Cell Disease During Vaso-Occlusive Crisis
- Sickle Cell Disease Transplant Using a Nonmyeloablative Approach for Patients With Anti-donor Red Cell Antibody
- Study of HLA-Haploidentical Stem Cell Transplantation to Treat Clinically Aggressive Sickle Cell Disease
- Sub-dissociative Dose Ketamine in Treatment of Vaso-occlusive Pain Event in Children and Young Adults
- T-Cell Depleted Alternative Donor Bone Marrow Transplant for Sickle Cell Disease (SCD) and Other Anemias
- Targeting the Pathophysiology of Sickle Cell-Related Kidney Disease Using the SGLT2 Inhibitors, Empagliflozin
- Tocilizumab for Acute Chest Syndrome
- Transplantation of Clustered Regularly Interspaced Short Palindromic Repeats Modified Hematopoietic Progenitor Stem Cells (CRISPR_SCD001) in Patients With Severe Sickle Cell Disease
- Zinc Supplementation in Sickle Cell Disease: A Precursor to the Think Zinc for Bones Trial
Common questions
What does Phase 2 mean?
Is this list complete?
No. For the full record, search ClinicalTrials.gov.