Condition
Sickle Cell Disease clinical trials and research
As of November 12, 2026, Find a Trial lists 124 Sickle Cell Disease clinical trials that are recruiting, at sites in 41 countries (most in United States (91), France (14), Nigeria (9)). By phase: Phase 2 (24), Phase 1/2 (10), Phase 3 (10), Phase 1 (9). The most active sponsors are St. Jude Children's Research Hospital (14), National Institutes of Health Clinical Center (CC) (7), Children's National Research Institute (5). There are also 215 NIH-funded research projects on Sickle Cell Disease, with $118.2 million in listed awards. Every study is explained in plain English. Data from ClinicalTrials.gov and NIH RePORTER, updated November 12, 2026.
- 124Clinical trials
- 215NIH research projects
- 41Countries
Newest Sickle Cell Disease clinical trials
All recruiting trials (124)
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Cerebrovascular Reactivity Testing with HD-DOT in Sickle Cell Patients
This study tests whether high-density diffuse optical tomography can measure brain blood flow and oxygen use in people with sickle cell disease, to see how these signals relate to stroke risk.
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Adapting and testing PEN-Plus in Zambian primary care
Aiming to see if the PEN-Plus package can be adapted and used in two Zambian hospitals to better manage chronic diseases like heart disease, diabetes, hypertension, and sickle cell in primary care.
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Newborn Sickle Cell Screening in Mozambique
We’re testing a three-part plan to help babies in Mozambique get diagnosed early for sickle cell disease and start care quickly.
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Optimizing Hydroxyurea in Children with Sickle Cell in Africa
This study tests whether raising hydroxyurea to a maximum tolerated dose is safe and beneficial for Ugandan children with sickle cell anemia already taking a fixed daily dose.
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Hematopoietic stem cell editing to treat sickle cell disease
This study tests whether a patient’s own blood stem cells can be edited to remove the sickle cell triggering gene and then returned to the patient.
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Virtual reality options to help with VOC pain in adults with SCD
This study tests whether headset-based virtual reality can help reduce pain for adults with sickle cell disease during vaso-occlusive crises treated in an infusion center.
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Mitapivat for reducing transfusion needs in sickle cell disease
This study tests whether mitapivat, compared with placebo, can lower the number of blood transfusions needed by people with sickle cell disease.
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Haploidentical donor transplant for sickle cell disease in young patients
This trial tests a gentler conditioning regimen and a post-transplant medication plan to see if children and young adults with sickle cell disease can have a successful haploidentical hematopoietic cell transplant with limited GVHD.
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SCD SIMCS: a mobile system to help screen newborns for sickle cell disease in Ugandan clinics
A cluster randomized trial will test a mobile information system (SIMCS) that helps health workers screen newborns for sickle cell disease and coordinate care, compared with usual screening in Uganda.
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Partial stem cell transplant for sickle cell disease and beta-thalassemia using matched donors
This study tests a partial stem cell transplant from matched donors to help people with severe sickle cell disease or beta-thalassemia see if more donor cells can persist long-term.
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Music therapy for pain and quality of life in youth with sickle cell disease
This study tests whether a 4-week music therapy program can reduce pain and improve well-being in young people with sickle cell disease.
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Hydroxyurea Use in Sickle Cell Disease: Personalizing Dose in Nigerian Patients
This observational study tests how genetic, pharmacokinetic, and pharmacodynamic differences affect hydroxyurea response in Nigerian people with sickle cell disease to help tailor dosing.
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SickleFit: exercise and nutrition program for adults with sickle cell disease
This program will test whether a personalized exercise plan plus dietitian-guided nutrition helps adults aged 35 and older with sickle cell disease feel and function better.
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Gene therapy using corrected β-globin and a silencing RNA in your own CD34+ stem cells for severe sickle cell disease
This trial will try a one-time gene therapy using a patient’s own modified CD34+ stem cells to reduce painful vaso-occlusive crises and long-term organ damage in people aged 12–35 with severe sickle cell disease.
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Ovarian reserve during puberty in girls with sickle cell disease
This project will test whether AMH blood levels, a marker of ovarian reserve, differ during puberty in girls aged 10 to <19 with sickle cell disease compared with healthy girls.
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Long-term follow-up after BEAM-101 treatment
This follow-up will see how people with sickle cell disease who received BEAM-101 are doing over 15 years.
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Low-dose ketamine for sickle cell vaso-occlusive pain in children and young adults
This trial will test whether adding a low (sub-dissociative) dose ketamine infusion to usual IV opioid pain medicine helps children and young adults (ages 5–20) with sickle cell disease have better pain relief and remain safe during a vaso-occlusive episode.
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Checking measles vaccine response in children with sickle cell disease
This study tests whether infants and young children with sickle cell disease develop enough protection in the weeks after their measles vaccine.
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Mindfulness and stress-management program for adults with sickle cell disease
This program will try a six-week mindfulness and stress-management course to see if it improves quality of life for adults with sickle cell disease who live near Philadelphia.
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Senicapoc for Sickle Cell Disease with Hemolytic Phenotype
A mid-stage study tests whether daily senicapoc helps people with sickle cell disease who have ongoing red blood cell breakdown and low hemoglobin, despite hydroxyurea, by comparing it to a placebo over 24 weeks.
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Ruxolitinib-enhanced haploidentical transplant for children and young adults with sickle cell disease
This trial will test whether adding ruxolitinib to a reduced-intensity haploidentical transplant lowers the risk of graft failure in children and young adults with sickle cell disease.
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Single-dose 21-valent pneumococcal conjugate vaccine for children and teens with sickle cell disease
This trial tests whether a single dose of the new PCV21 vaccine is safe and helps children and teens (ages 2–17) with sickle cell disease make protective antibodies compared with the licensed 20-valent pneumococcal vaccine.
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Morphine removal and kidney filtering in adults with sickle cell crises in intensive care
This project will test how quickly morphine is cleared from the body in adults with sickle cell disease admitted to intensive care for vaso-occlusive crisis or acute chest syndrome, and whether faster kidney filtering leads to lower morphine levels.
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Methylphenidate for attention and executive problems in children with sickle cell disease
This study will test whether once-daily extended-release methylphenidate for 4 weeks helps attention and thinking skills in children 8–17 with sickle cell disease while monitoring side effects and adherence.
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Testing Anumigilimab (CSL324) safety in adults with sickle cell disease
This study will test whether subcutaneous Anumigilimab is safe for adults with sickle cell disease who had 1–12 painful vaso-occlusive crises in the past year.
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Songwriting to Reduce Anxiety in Teens with Sickle Cell Disease
This program will try songwriting and performing original songs to see if it helps reduce anxiety in adolescents (ages 11–18) with sickle cell disease.
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Integrated diagnosis for sickle cell disease and other rare anemias
This project tests whether combining genetic testing, LoRRca ektacytometry, and microfluidic analysis can improve diagnosis and predict disease course for people with sickle cell disease and other inherited anemias.
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DISC-3405 for adults with sickle cell disease
This will test DISC-3405 in adults with sickle cell disease who have had recent pain crises or other complications to see if it is safe and how the body handles it.
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Trans-auricular nerve stimulation for pain in children with sickle cell disease
This trial will test whether gentle electrical stimulation of nerves at the outer ear can reduce pain in children with sickle cell disease who are hospitalized for pain crises.
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Bone health, muscle strength, and frailty in postmenopausal women of African descent with sickle cell trait
We will see if postmenopausal women of African descent who have sickle cell trait are more likely to have thinner bones, weaker muscles, or greater frailty than women without the trait.
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Early heart screening and treatment for people with sickle cell disease
This study tests whether regular heart checks and early iron-removing treatment can prevent heart problems and cut hospital stays in adults with sickle cell disease who have high iron or heart symptoms.
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EMDR to reduce pain interference in children with sickle cell disease
This will test EMDR therapy to see if it reduces how much pain gets in the way of daily life for children and adolescents (6–18) with sickle cell disease.
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Regional anesthesia to reduce inflammation during vaso‑occlusive crises in sickle cell disease
This project will test whether giving regional (loco‑regional) anesthesia to adults hospitalized for sickle cell vaso‑occlusive crises reduces inflammatory markers and speeds recovery compared with usual care.
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Why dengue is more severe in people with sickle cell disease
This project will test whether immune cells and tiny blood particles from young people with SC or SS sickle cell disease respond differently to dengue virus compared with healthy controls, which could explain more severe infections.
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Evaluating Rilzabrutinib for Sickle Cell Disease in Patients Aged 10 to 65
This study is testing a new medication called rilzabrutinib to see if it can help people aged 10 to 65 with sickle cell disease have fewer pain crises and improve their overall health.
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Understanding genetic risks of immune responses after blood transfusions in sickle cell disease
This study is trying to find out how genetics affect the immune response to blood transfusions in people with sickle cell disease to help improve their treatment.
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Cannabidiol (CBD) treatment for adults with sickle cell disease
This trial will try three doses of oral cannabidiol taken twice daily for 4 weeks in adults with sickle cell disease, compared with placebo, to see if it lowers inflammation and pain-related measures.
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Evaluating the safety and effectiveness of Xromi in young children with sickle cell disease
This study is testing if the medication Xromi is safe and effective for young children with sickle cell disease.
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Mobile app plus printed booklets to help adults manage sickle cell disease
This project will test whether a mobile app combined with printed patient-facing sickle cell guidelines helps adults with sickle cell disease use less emergency and hospital care than printed booklets alone.
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Donor transplant for high risk blood disorders
This study is testing if a stem cell transplant from a matched sibling can help people with high-risk blood disorders like sickle cell disease and thalassemia feel better.
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Using music therapy to improve quality of life in sickle cell disease
This study is testing if music therapy can help improve the quality of life for teenagers and adults with sickle cell disease.
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Endurance training for patients with sickle cell disease
This study is testing whether a long-term endurance training program can help improve health, fitness, and quality of life for both adults and children with sickle cell disease.
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ATHNdataset registry for people with bleeding and clotting disorders
This registry collects health, treatment, and patient-reported information from people with bleeding and clotting disorders seen at ATHN-affiliated centers to help improve care and outcomes.
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Tocilizumab for Acute Chest Syndrome in Sickle Cell Disease
This study tests whether a single infusion of tocilizumab can help people with sickle cell disease and acute chest syndrome come off oxygen and respiratory support faster.
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Using virtual reality to help manage pain in children with sickle cell disease
This study tests if using virtual reality can help children with sickle cell disease feel less pain during their hospital stays compared to just standard pain management.
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Digital cognitive rehabilitation for youth with sickle cell disease
This study is testing a digital program that helps kids and teens with sickle cell disease improve their thinking skills and memory while also providing social support.
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Improving lung function in sickle cell disease with acupuncture-like stimulation
This study is testing whether combining breathing exercises with a special type of electrical stimulation can help improve lung function in people with sickle cell disease.
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Acupuncture for pain in sickle cell disease
This trial will test whether traditional needle acupuncture or non‑needle laser acupuncture can reduce pain and change brain and sensory responses in adolescents and adults with sickle cell disease.
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Training program to help teens with sickle cell pain
This study is testing a new training program to see if it can help teens with sickle cell disease manage their pain and improve their daily activities.
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A tool to improve family communication in pediatric stem cell transplant decisions
This study is testing a new tool to help families talk better and make decisions together about stem cell transplants for kids aged 8 to 17.
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Adapting a fatigue-management program for adults with sickle cell disease
This trial will test a combined cognitive-behavioral and energy-conservation program (Drépa-FACETS) to reduce fatigue in French-speaking adults with sickle cell disease.
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Gene editing of your own blood stem cells to boost fetal hemoglobin for severe sickle cell disease and beta-thalassemia
This trial will test whether editing a specific gene in patients' own blood stem cells can raise fetal hemoglobin and reduce symptoms in people aged 13–40 with severe sickle cell disease or transfusion-dependent beta-thalassemia.
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Using intravenous L-citrulline to treat pain in sickle cell disease
This study is testing if giving L-citrulline through an IV can help kids and young adults with sickle cell disease feel better faster during painful episodes.
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Evaluating Etavopivat for Sickle Cell Disease
This study is testing if a new drug called etavopivat can help reduce painful crises and improve overall health in adults and teens with sickle cell disease.
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Long-term treatment with Etavopivat for sickle cell disease and thalassemia
This study is testing how safe and effective a new medication called Etavopivat is for people with sickle cell disease and thalassemia who have already seen benefits from it.
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Evaluating Hydroxycarbamide for Children with Sickle Cell Disease
This study is testing if a new form of Hydroxycarbamide can safely help children with Sickle Cell Disease feel better over a year of treatment.
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CS-206 treatment for sickle cell disease
This study is testing a new injection called CS-101 to see if it can safely help people with sickle cell disease by boosting their production of fetal hemoglobin.
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Resilience support for adolescents and young adults with sickle cell disease
This project will test a resilience-building program (PRISM) delivered through a collaborative care model for adolescents and young adults with sickle cell disease to see if it is feasible and acceptable.
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Evaluating ITU512 for Sickle Cell Disease and Healthy Participants
This study is testing a new drug called ITU512 to see if it is safe and effective for people with sickle cell disease and healthy adults.
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Preventing strokes in children with sickle cell disease in Nigeria using hydroxyurea
This study is testing if hydroxyurea can help prevent strokes in children with sickle cell disease in Nigeria who are at high risk.
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Gene editing treatment for sickle cell disease
This study is testing a new gene editing treatment for people with severe sickle cell disease to see if it can improve their health.
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Examining sleep and brain function in children with sickle cell disease
This study is trying to see how sleep quality affects brain function in children with sickle cell disease by using special devices at home and tests at the clinic.
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Using motixafortide to collect stem cells in sickle cell disease patients
This study is testing if a new drug called motixafortide can safely help people with sickle cell disease collect stem cells for future treatments.
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Investigating Crizanlizumab for Sickle Cell Disease in Adolescents and Adults
This study is testing if a new medication called crizanlizumab can help reduce painful episodes in adolescents and adults with sickle cell disease.
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Gene therapy using BAH243 for treating sickle cell disease
This study is testing a new gene therapy called BAH243 to see if it can safely help people with sickle cell disease feel better after receiving a stem cell transplant.
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Finding and Engaging Patients with Sickle Cell Disease
This study is trying to find people with Sickle Cell Disease who aren't getting the care they need and connect them with support to improve their treatment and quality of life.
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Digital cognitive behavioral therapy with peer support for young adults with sickle cell pain
This study is testing if a new online therapy with peer support can help young adults with sickle cell disease manage their pain better than standard care.
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School readiness program for preschool children with sickle cell disease
This study is testing a special online school readiness program for preschool kids with sickle cell disease to see if it helps them get ready for school better than regular resources.
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Transplant for Sickle Cell Disease Using a Nonmyeloablative Approach
This study is testing a new way to help people with sickle cell disease who have certain antibodies receive a safer type of stem cell transplant from a sibling to see if it can improve their chances of recovery.
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Improving hydroxyurea use for sickle cell disease in Nigeria
This study is testing a special training program for healthcare workers in Nigeria to see if it can help more people with sickle cell disease start using hydroxyurea treatment.
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Understanding red blood cell lifespan in sickle cell disease and hemoglobin disorders
This study is trying to see how long red blood cells last in people with sickle cell disease and other blood disorders to help improve their treatment.
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Mapping the prevalence of sickle cell disease in Uganda
This study is trying to find out how common sickle cell trait and sickle cell disease are in Uganda by testing blood samples from infants to help improve health strategies for these conditions.
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Zinc supplements for bone health in sickle cell disease
This 12-week test gives two different daily zinc doses (25 mg or 40 mg) to people aged 15 to 40 with homozygous sickle cell disease to see which dose most changes blood markers of bone turnover.
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European platform for collecting data on rare anemia disorders
This study is trying to gather important information from people with rare anemia disorders across Europe to help improve their treatment and care.
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Evaluating Etavopivat for Pediatric Sickle Cell Disease
This study is testing a new oral medication called etavopivat in teenagers with sickle cell disease to see how it works in their bodies and if it helps them feel better over 96 weeks.
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Using virtual reality to help manage pain in sickle cell disease patients
This study is testing if using virtual reality can help adults with sickle cell disease feel less pain during painful episodes.
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Non-invasive prenatal diagnosis for single gene disorders
This study is testing a new way to safely diagnose single-gene disorders in unborn babies using a simple blood test from the mother, starting as early as 9 weeks into the pregnancy.
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Identifying Pain Predictors in Sickle Cell Disease
This study is trying to find out what factors can predict severe pain in people with sickle cell disease to help improve pain management.
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Web-based intervention for teens and young adults with sickle cell disease
This study is testing a mobile app designed to help teens and young adults with sickle cell disease manage their symptoms and improve their overall health.
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Using alendronate to treat osteonecrosis in adults with sickle cell disease
This study is testing if a weekly medication called alendronate can help adults with sickle cell disease who have bone pain from osteonecrosis feel better and improve their bone health.
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Evaluating Etavopivat for Pediatric Sickle Cell Disease Patients at Risk for Stroke
This study is testing if a new medication called etavopivat can help prevent strokes in kids aged 12 to 16 with sickle cell disease who are at higher risk.
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Evaluating the safety of fostamatinib for sickle cell disease
This study is testing whether a new medication called fostamatinib is safe for adults with stable sickle cell disease and if it can help improve their blood cell function and reduce inflammation.
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Understanding patient needs for gene therapy in sickle cell disease
This study talks to patients and their families about what they think and need to know about gene therapy for sickle cell disease to help create better educational resources for them.
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Investigating genetic factors in blood disorders
This study is trying to find out how genes affect blood disorders like sickle cell disease and thalassemia by looking at the DNA of many people with these conditions.
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Immune suppression treatment for sickle cell disease and beta-thalassemia patients receiving stem cell transplants
This study is testing if a new immune suppression treatment can help people with sickle cell disease or beta-thalassemia have better outcomes when they receive stem cell transplants.
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Using tocilizumab to treat acute chest syndrome in sickle cell disease
This study is testing if a low dose of tocilizumab can help people with sickle cell disease who have acute chest syndrome feel better during their hospital stay.
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Investigating heart blood flow and function in sickle cell disease
This study is testing how blood flow and heart function are affected in people with sickle cell disease to see if it leads to heart problems.
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Using cannabinoids to reduce inflammation and pain in sickle cell disease
This study is testing if a cannabinoid called dronabinol can help adults with sickle cell disease feel less pain and improve their quality of life.
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Evaluating a single dose of CTX001 for treating transfusion-dependent beta-thalassemia and severe sickle cell disease
This study is testing a single dose of a new treatment called CTX001 to see if it can help people with transfusion-dependent beta-thalassemia or severe sickle cell disease feel better.
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Phase 2/3 testing of osivelotor in adults and adolescents with sickle cell disease.
This trial tests whether an oral medicine called osivelotor can safely reduce pain crises and improve blood measures in people aged 12–65 with sickle cell disease.
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Haploidentical stem cell transplantation for adults with severe sickle cell disease
This study is testing if a special type of stem cell transplant can help adults with severe sickle cell disease who haven't found relief with other treatments.
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Helping young people with sickle cell disease make treatment decisions
This study is testing a new way to help young people with sickle cell disease and their caregivers make better treatment decisions by using virtual reality alongside regular education materials.
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Early-life exposures and breastfeeding in children with sickle cell disease
This project will try a community breastfeeding support group for mothers of infants with sickle cell disease to see if breastfeeding and related supports improve early-life exposures and child health.
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Exploring the effects of exercise on children's health with chronic diseases
This study is testing how exercise can improve the health of children with chronic diseases like cystic fibrosis and sickle cell disease to find safe ways for them to be active.
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Telehealth intervention to help adolescents with sickle cell disease transition to adult care
This study is testing a telehealth program to help teenagers with sickle cell disease improve their thinking skills and self-care as they transition to adult healthcare.
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Using Hydroxyurea to Treat Sickle Cell Anemia in Children in Africa
This study is testing if hydroxyurea can safely help children with sickle cell anemia in Africa feel better and improve their treatment options.
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Assessing skin hydration in patients with sickle cell disease
This study is testing a new skin sensor to see if it can help people with sickle cell disease manage their hydration better, especially during painful episodes.
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Understanding diet and nutrition in adults with Sickle Cell Disease
This study looks at how diet and nutrition affect the health of adults with Sickle Cell Disease to see what changes might help them feel better.
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Training program to improve attention in children with sickle cell disease
This study is testing a fun, game-like training program to see if it can help children with sickle cell disease improve their attention and thinking skills.
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Gene correction therapy for severe sickle cell disease
This study is testing a new gene therapy called nula-cel to see if it can safely improve the health of young people with severe sickle cell disease.
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Infusion of modified stem cells for severe Sickle Cell Disease
This study is testing if a new treatment using modified stem cells can safely help young people with severe Sickle Cell Disease.
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Continuation of crizanlizumab treatment for sickle cell disease patients
This study is for people with sickle cell disease who have already tried crizanlizumab and want to keep using it to see how well it works and if it's safe over a longer time.
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Genomic and gene therapy needs for families and patients with sickle cell disease
This project uses interviews and surveys to see if better information and a web-based tool can help parents and teens with sickle cell disease understand genomic sequencing and treatment options.
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Long-term observation of non-cancer blood disorders
This study is tracking people with blood disorders like hemophilia and thrombosis for at least 15 years to see how their conditions change over time and gather useful information for doctors and researchers.
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Haploidentical stem cell transplantation for sickle cell disease
This study is testing a new type of stem cell transplant for people with sickle cell disease to see if it can cure the disease while causing fewer complications.
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Monitoring brain health in children with Sickle Cell Disease
This study is trying to see how Sickle Cell Disease affects brain health in children aged 8-18 by using special imaging techniques to check blood flow and oxygen levels in the brain.
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Understanding brain blood flow and metabolism in children
This study is trying to see how blood flow and metabolism in the brain affect development in children, especially those with sickle cell disease and stroke, by using advanced MRI techniques.
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Stem cell transplantation for blood disorders using specific cell depletion techniques
This study is testing a new way of using stem cell transplants for children and young adults with blood disorders to see if removing certain cells helps them recover better and improve their quality of life.
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Understanding hydroxyurea effects during pregnancy and breastfeeding in women with sickle cell disease
This study looks at how taking hydroxyurea during pregnancy and breastfeeding affects women with sickle cell disease and their babies to better understand the risks and outcomes.
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Treatment for high-risk sickle cell disease using nicotinamide and other medications
This study is testing if a combination of three medications can help people with high-risk sickle cell disease feel better and manage their symptoms more effectively.
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Collecting biological samples to study blood disorders
This study is collecting samples from people with blood disorders and healthy volunteers to see how certain genetic factors affect these conditions and overall health.
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Program to help teenagers with sickle cell disease transition to adult care
This study tests a program designed to help teenagers with sickle cell disease smoothly move from children's healthcare to adult care by providing both medical and emotional support.
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Reducing toxicity in sibling donor transplants for children with sickle cell disease
This study is testing a gentler transplant method for children with sickle cell disease using cells from their siblings to see if it reduces side effects while still helping them stay healthy.
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Using virtual reality to manage pain in sickle cell disease crises
This study is testing if using virtual reality can help people with sickle cell disease feel less pain during painful crises when combined with their usual treatment.
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Registry for Sickle Cell Disease in German-speaking Europe
This study is collecting information about people with sickle cell disease in Germany, Austria, and Switzerland to see how the disease affects them and improve future care and treatment.
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Nonmyeloablative stem cell transplant for children with sickle cell disease and incompatible donors
This study is testing a new way to do a stem cell transplant for children with sickle cell disease who have a donor that doesn't perfectly match to see if it can help them get better.
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HLA-haploidentical stem cell transplantation for aggressive sickle cell disease
This study is testing a new type of stem cell transplant to see if it can help people with severe sickle cell disease feel better.
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Biofluidic chip technology for studying sickle cell disease
This study is testing a new technology that looks closely at the cells of people with sickle cell disease to better understand how their cells behave and interact.
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Investigation of genetics related to blood diseases
This study is trying to understand the genetics behind blood diseases by collecting samples and health information from people with these conditions and their family members.
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Using Defibrotide to Improve Stem Cell Transplant Outcomes for Sickle Cell Disease
This study is testing if giving Defibrotide before a stem cell transplant can help people with sickle cell disease avoid serious complications and have better outcomes.
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Arginine treatment for pain relief in children with sickle cell disease
This study is testing if giving arginine to children with sickle cell disease can help reduce their pain during painful episodes and lessen their need for pain medications.
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Observational program for sickle cell disease management and outcomes
This study is tracking people with sickle cell disease from childhood to adulthood to see how their condition changes over time and how treatments like hydroxyurea affect their health.
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Testing panobinostat for treating sickle cell disease
This study is testing if a new drug called panobinostat can help adults with sickle cell disease who haven't found relief with standard treatment.
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Collecting blood samples to study sickle cell disease
This study is collecting blood samples from healthy people and those with sickle cell disease to see if new drugs can help stop red blood cells from sickling.
NIH-funded research (newest 40 of 215)
Early-stage science funded by the US National Institutes of Health. Most of these projects don't enroll patients, but they show what is being worked on.
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Digital twins of the spleen to help design better therapies for sickle cell disease
A computer-driven replica of the spleen is being developed to speed up creating safer and more effective treatments for people with sickle cell disease.
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Accelerating hydroxyurea use for sickle cell disease in Nigeria
A pragmatic study in Nigeria aims to help doctors use hydroxyurea more consistently for people with sickle cell disease.
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Immune and nerve signals behind acupuncture relief for sickle cell pain
This NIH grant explores how acupuncture helps reduce pain and opioid use for people with sickle cell disease.
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Mindfulness-based Support for Pain and Sleep in Young People with Sickle Cell Disease
A digital mindfulness program is being tailored for adolescents and young adults with sickle cell disease to help with pain and sleep and is being tested for practicality and early effectiveness.
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How diet affects white blood cells and sickle cell disease
A study looks at how nutrition, from early life to adulthood, influences sickle cell disease by examining neutrophils and disease severity in people with SCD and in a mouse model.
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Nutrition-based plan to ease pain in sickle cell disease
A nutrition-based approach is being tested to reduce pain for people living with sickle cell disease.
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Understanding how environment and microbiome affect health in children with sickle cell disease
A research project will explore how environmental exposures shape immune responses and airway microbiomes in children with sickle cell disease and how these factors relate to health outcomes.
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Gene-editing delivery for sickle cell disease using safer, non-viral nanoparticles
A researcher is developing a safer, non-viral nanoparticle method to deliver gene edits to a patient’s own blood-forming cells to treat sickle cell disease.
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Using Real-World Data to Improve Infection Prevention in Children with Sickle Cell Disease
This project uses real-world data to understand how current antibiotic and disease-modifying therapies work together to prevent serious infections in children with sickle cell disease.
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MAP SCD: How place-based factors affect sickle cell disease
A study to understand how where people live and their daily environment influence the illness and pain in sickle cell disease.
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Gut microbiome targets to ease sickle cell pain in patients
Researchers are studying how gut microbes affect chronic pain in people with sickle cell disease and how penicillin prophylaxis in babies might change pain pathways.
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Predicting which febrile kids with sickle cell disease are at low risk for bacteremia
A small, patient-facing prediction rule is being developed to help doctors decide which febrile children with sickle cell disease really need aggressive testing and antibiotics.
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Admixture mapping to find genetic modifiers of sickle cell disease in adults
A study in adults with sickle cell disease will look for inherited genes that change how the disease shows up, beyond the main HbS mutation.
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Retinal clues to brain injury in children with sickle cell disease
This study looks at whether eye blood vessels measured with OCT scans can reflect brain injury in kids with sickle cell disease.
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Partnering with adolescents and young adults with sickle cell disease in treatment decisions
This grant explores how to better involve teens and young adults with sickle cell disease in choosing their therapies to improve how well they stick with treatment.
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Access to preventive dental care may improve health in children with sickle cell disease
Aiming to see if regular preventive dental visits help improve health outcomes for kids with sickle cell disease who rely on Medicaid.
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Understanding how individual differences shape pain in sickle cell disease (MIDAS)
Aims to build a patient-focused model using real-world health data from Black adolescents and young adults with sickle cell disease to better predict and manage severe pain crises.
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KYC: a new drug aiming to stop painful VOC in adults with sickle cell disease
A new drug called KYC could help adults with sickle cell disease who come to the ER with painful vaso-occlusive crises by reducing blood vessel blockage and pain.
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Molecular mechanisms of HIV resistance in people with Sickle Cell Disease and Trait
A scientist at Howard University is studying why people with sickle cell disease or trait might be more resistant to HIV, in order to uncover clues for better protection and treatment.
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Donor red blood cells and how long they last in people with sickle cell disease
This project looks at how donated red blood cells behave after transfusions in people with sickle cell disease to understand why some lasts longer than others.
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RECIPE: Connecting Sickle Cell Patients to Care for Better Outcomes
A program to help adults with sickle cell disease get the care they need by identifying those not currently seeing a specialist and linking them to guideline-based services.
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Understanding how platelets behave in sickle cell disease
A physician-scientist-in-training will study how platelets function differently in people with sickle cell disease to find better ways to prevent painful crises.
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Accelerating hydroxyurea adoption for sickle cell disease in Nigeria
A pragmatic study in Nigeria aims to help more people with sickle cell disease get hydroxyurea, a treatment that reduces painful crises and hospitalizations.
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Base editing and prime editing for sickle cell disease
Aims to improve treatment for adults with sickle cell disease by using precise genome editing to boost fetal hemoglobin or correct the sickle mutation.
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Sex hormones, inflammation, and pain in sickle cell disease
This project explores how female hormones may boost inflammation and influence painful episodes in women with sickle cell disease.
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Dual nitric oxide donor therapy for sickle cell–related acute chest syndrome
A new medicine (DMX-201) being developed to help people with sickle cell disease who develop acute chest syndrome by delivering nitric oxide more safely.
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Delivering patient-facing guidelines for adults with sickle cell disease using a mobile app and booklets
A multi-center study will provide adults with sickle cell disease with easy-to-use, evidence-based guidelines through a mobile app and printed booklets.
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Glycan-based at-home treatment to shorten painful VOEs in sickle cell disease
A new at-home therapy called IHP-102 aims to modify the disease’s pain crises in adults with sickle cell disease.
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CD39-bearing tiny vesicles may guard lungs in SCD patients
A study in people with sickle cell disease explores whether extracellular vesicles carrying CD39 protect the lungs from blood clots during acute illness.
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Sickle Cell Disease Pain Analgesia and Integrative Network for Better Pain Care
A national network is being built to better understand and manage pain in adults with sickle cell disease using integrative, whole-health approaches.
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Gene editing to raise fetal hemoglobin for sickle cell disease
A new gene-editing therapy using patient’s own stem cells to boost fetal hemoglobin could potentially correct sickle cell disease.
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Transfusion-driven hyperhemolysis in sickle cell disease
Aimed at understanding why some sickle cell patients have severe, dangerous reactions to blood transfusions and finding ways to prevent it.
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Bringing hydroxyurea to people with sickle cell disease in Nigeria
This project helps clinics in Nigeria screen for sickle cell disease and use hydroxyurea more often so people with SCD can get a proven medicine that lowers pain and complications.
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Modeling HbS polymerization in sickle cell disease at the single-cell level
A research project uses computer and lab models to understand how sickle hemoglobin polymerizes inside individual red blood cells, with goal of guiding future treatments for people with sickle cell disease.
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RBCs that activate neutrophils in sickle cell disease
This grant tests how red blood cells from people with sickle cell disease make neutrophils more sticky and inflammatory, which could worsen painful events and organ damage.
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Factor XII and blood clots in sickle cell disease
A research project tests how Factor XII affects blood clotting and inflammation in people with sickle cell disease to understand how it contributes to painful crises, clots, and organ damage.
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Senescence-targeting therapies to boost blood stem cell health in sickle cell disease
A study tests aging-related treatments to protect and improve blood stem cells in people with sickle cell disease.
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Understanding and reducing unintended large gene changes in sickle cell gene editing
A study in people with sickle cell disease looks at unexpected large DNA changes that can happen when repairing genes with CRISPR and aims to figure out how to prevent them.
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Chronic dehydration as a warning sign to prevent sickle cell pain crises
This project looks at whether ongoing mild dehydration can help spot people with sickle cell disease who are more likely to have painful vaso-occlusive crises.
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Gene editing to raise fetal hemoglobin levels in adults with sickle cell disease
This project edits a patient’s own blood stem cells with CRISPR to turn on fetal hemoglobin and help adults with sickle cell disease have fewer sickled red cells and painful episodes.
Related topics
Quick answers
How many Sickle Cell Disease clinical trials are recruiting right now?
124, as of November 12, 2026. We update this list each time we refresh our data from ClinicalTrials.gov.
Where are these trials running?
In 41 countries. The most sites are in United States (91 trials), France (14 trials), Nigeria (9 trials), United Kingdom (8 trials), Turkey (Türkiye) (7 trials). Each study page lists its sites and which ones are recruiting.
What phases are they in?
Phase 2: 24, Phase 1/2: 10, Phase 3: 10, Phase 1: 9. Trials with no phase listed are usually device, behavioural or observational studies.
How do I join one?
Open a study, check the "Is this trial a fit for you?" section, then contact the study team listed on the page. They will ask a few screening questions. Asking is free and does not commit you to anything. Talk it over with your doctor first.
Find the studies that fit you
A list is a starting point. Tell us your situation in your own words and we'll rank the studies that match and explain why. It's free and needs no account.