Sickle Cell Disease Clinical Trials in Chicago, Illinois
14 studies are recruiting for sickle cell disease in Chicago, Illinois right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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A Research Study Looking at Long-term Treatment With Etavopivat in People With Sickle Cell Disease or Thalassaemia
Etavopivat is a new medicine under development for treating blood disorders like sickle cell disease and thalassaemia. Sickle cell disease and thalassaemia are inherited blood disorders that affect haemoglobin. Haemoglobin is the protein that carries oxygen through the body. This study is looking i…
- Stage
- Phase 3
- Ages
- 2 and older
- Site
- Univer Of Illinois at Chicago, Chicago, Illinois
- Locations
- 107 in total
- Run by
- Novo Nordisk A/S
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A Study to Evaluate How Well Etavopivat Works in People With Sickle Cell Disease
This study is conducted to confirm whether etavopivat works well at reducing the number of Vaso-occlusive crisis VOCs (sickle cell pain crises) caused by obstructions in blood vessels in adults and adolescents living with sickle cell disease. The study will also evaluate how well etavopivat can red…
- Stage
- Phase 3
- Ages
- 12 and older
- Site
- Childrens Hospital of Chicago, Chicago, Illinois
- Locations
- 175 in total
- Run by
- Novo Nordisk A/S
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A Phase 1b, Open-Label Study of DISC-3405 in Participants With Sickle Cell Disease (SCD)
This is an open-label, multicenter, within-participant dose-escalation study examining up to 3 dose levels of DISC-3405 and will assess the safety, tolerability, PK, and PD of DISC 3405 in participants with sickle cell disease.
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Illinois Hospital and Health Sciences System, Chicago, Illinois
- Locations
- 9 in total
- Run by
- Disc Medicine, Inc
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Tocilizumab for Acute Chest Syndrome
The investigators are evaluating the role of a low dose of tocilizumab in treating acute chest syndrome in patients with sickle cell disease. Tocilizumab inhibits interleukin-6 (IL-6) receptors and is used to treat rheumatoid arthritis and severe cytokine release syndrome, which can be seen with ch…
- Stage
- Phase 2
- Ages
- 12 and older
- Site
- University of Chicago, Chicago, Illinois
- Run by
- University of Chicago
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A Study to Investigate the Efficacy and Safety of Crizanlizumab (5 mg/kg) Compared With Placebo in Adolescent and Adult Sickle Cell Disease Patients Who Experience Frequent Vaso-Occlusive Crises (SPARKLE)
A phase III, multi-center, randomized, placebo-controlled, double-blind study to assess efficacy and safety of crizanlizumab (5 mg/kg) versus placebo, with or without hydroxyurea/hydroxycarbamide therapy, in adolescent and adult Sickle Cell Disease patients with frequent vaso-occlusive crises.
- Stage
- Phase 3
- Ages
- 12 to 100
- Site
- Uni of Illinois Hospital and HSC, Chicago, Illinois
- Locations
- 35 in total
- Run by
- Novartis Pharmaceuticals
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A Phase 2/3 Study of Osivelotor in Adult and Adolescent Participants With SCD
The purpose of this study is to evaluate the safety, tolerability, efficacy, pharmacokinetics and pharmacodynamics of osivelotor.
- Stage
- Phase 2
- Ages
- 12 and older
- Site
- University of Illinois at Chicago Clinical Research Center, Chicago, Illinois
- Locations
- 80 in total
- Run by
- Pfizer
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ATHN Transcends: A Natural History Study of Non-Neoplastic Hematologic Disorders
In parallel with the growth of ATHN's clinical studies, the number of new therapies for all blood disorders is increasing significantly. Some of the recently FDA-approved therapies for congenital and acquired hematologic conditions have not yet demonstrated long-term safety and effectiveness beyond…
- Stage
- Not phased
- Ages
- Any age
- Site
- Rush University Medical Center, Chicago, Illinois
- Locations
- 76 in total
- Run by
- American Thrombosis and Hemostasis Network
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The Efficacy and Safety of Rilzabrutinib in Participants Aged 10 to 65 Years With Sickle-cell Disease
This is a multicenter, randomized, double-blind, placebo-controlled, parallel-group, flexible-adaptive, group-sequential study (Part A), followed by an open-label LTE period (Part B) to investigate the efficacy, and safety of rilzabrutinib in participants with sickle-cell disease (SCD). Study detai…
- Stage
- Phase 3
- Ages
- 10 to 65
- Site
- University of Illinois-Chicago - College of Medicine- Site Number : 8400054, Chicago, Illinois
- Locations
- 53 in total
- Run by
- Sanofi
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Study of HLA-Haploidentical Stem Cell Transplantation to Treat Clinically Aggressive Sickle Cell Disease
The study is a Phase II clinical trial. Patients will receive intensity modulated total body irradiation (TBI) at a dose of 3 Gy with standard fludarabine/ i.v. cyclophosphamide conditioning prior to human leukocyte antigen (HLA)-haploidentical hematopoietic stem cell transplant (HSCT). The primary…
- Stage
- Phase 2
- Ages
- 16 to 60
- Site
- University of Illinois at Chicago, Chicago, Illinois
- Run by
- University of Illinois at Chicago
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Delivering Patient-Facing Evidence-Based Guidelines Through mHealth to Adults With Sickle Cell Disease
In a hybrid type I effectiveness-implementation trial, our three-center research teams aim to examine whether empowering adults with sickle cell disease (SCD) with patient-facing SCD-specific guidelines through an mHealth application with booklets will decrease acute healthcare utilization and be c…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Illinois at Chicago, Chicago, Illinois
- Locations
- 4 in total
- Run by
- Ohio State University
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Minimizing Toxicity in HLA-identical Sibling Donor Transplantation for Children With Sickle Cell Disease
This multisite prospective study seeks to determine if HLA-identical sibling donor transplantation using alemtuzumab, low dose total-body irradiation, and sirolimus (Sickle transplant Using a Nonmyeloablative approach, "SUN") can decrease the toxicity of transplant while achieving a high cure rate …
- Stage
- Phase 2
- Ages
- 2 to 25
- Site
- Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois
- Locations
- 7 in total
- Run by
- Robert Nickel
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Peer Support for Adolescents and Emerging Adults With Sickle Cell Pain
The study, known as the Peer suppoRt for adolescents and Emerging adults with Sickle cell pain: promoting ENgagement in Cognitive behavioral thErapy (PRESENCE), aims to determine the effectiveness of digital CBT in reducing pain, opioid use, and healthcare utilization among AYAs with SCD. It also s…
- Stage
- Not phased
- Ages
- 16 to 30
- Site
- Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois
- Locations
- 14 in total
- Run by
- University of Pittsburgh
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Recruitment and Engagement in Care to Impact Practice Enhancement (RECIPE) for Sickle Cell Disease
The goal of this observational study is to help us understand more about the best ways to help individuals living with Sickle Cell Disease (SCD) get the best care. The main question it aims to answer is: How to find individuals unaffiliated from SCD specialist care use three distinct pathways? Once…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- University of Illinois, Chicago, Illinois
- Locations
- 9 in total
- Run by
- RTI International
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A Study of Nicotinamide With Oral Tetrahydrouridine and Decitabine to Treat High Risk Sickle Cell Disease
A randomized control trial in 20 subjects with sickle cell disease comparing oral THU-decitabine to nicotinamide and in combination (THU, decitabine and nicotinamide).
- Stage
- Phase 1
- Ages
- 18 and older
- Site
- University of Illinois at Chicago College of Medicine, Chicago, Illinois
- Run by
- EpiDestiny, Inc.
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
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