Ann and Robert H. Lurie Childrens Hospital of Chicago

Chicago, Illinois 60614-3363

22 studies enrolling now · 102 studies all time

What they study most

Achondroplasia, Acute Kidney Injury (AKI), Acute Lymphoblastic Leukemia, Acute Lymphoblastic Leukemia/Lymphoma, Acute Myelogenous Leukemia, Acute Renal Failure (ARF), Adenovirus Infection, Adrenal Insufficiency, Adult Nasal Type Extranodal NK/T-cell Lymphoma, Advanced Non CNS Tumors, Allergy, Peanut, Anaplastic Astrocytoma

Studies at this site

• Anesthetics and Analgesics in Children — Recruiting now
• A Study to Learn About Salanersen's (BIIB115) Effects on Movement and Its Safety When Given Before Symptoms Appear in Babies With Genetically Diagnosed Spinal Muscular Atrophy (SMA) — Recruiting now
• Pharmacokinetics and Safety of Commonly Used Drugs in Lactating Women and Breastfed Infants — Recruiting now
• Pharmacokinetics, Pharmacodynamics, and Safety Profile of Understudied Drugs Administered to Children Per Standard of Care (POPS) — Recruiting now
• A Clinical Trial of PR001 (LY3884961) in Patients With Peripheral Manifestations of Gaucher Disease (PROCEED) — Recruiting now
• A Study Evaluating the Real-World Experience of Givinostat in Patients With Duchenne Muscular Dystrophy — Recruiting now
• Early Signals of the Transition From Immune Quiescence to Activation in the Liver Allograft Microenvironment and in the Circulation — Recruiting now
• A Hybrid Effectiveness-implementation Trial to Reduce Diabetes Distress in Teenagers — Recruiting now
• A Study to Evaluate the Safety and Tolerability of Eravacycline in Pediatric Patients Aged 8 to 17 With Complicated Intra-abdominal Infections (cIAI) — Recruiting now
• rHSC-DIPGVax Plus Checkpoint Blockade for the Treatment of Newly Diagnosed DIPG and DMG — Recruiting now
• A Study of Pitolisant in Patients With Prader-Willi Syndrome — Recruiting now
• NS-089/NCNP-02-201 in Boys With Duchenne Muscular Dystrophy (DMD) — Recruiting now
• Open-Label Study of mRNA-3927 in Participants With Propionic Acidemia — Recruiting now
• Peer Support for Adolescents and Emerging Adults With Sickle Cell Pain — Recruiting now
• Soy Isoflavones For Inner City Infants At Risk For Asthma (SIRA) Study — Recruiting now
• OMEGA: Outcome Measures in Eosinophilic Gastrointestinal Disorders Across the Ages — Recruiting now
• A Study to Determine the Efficacy and Safety of Tividenofusp Alfa (DNL310) vs Idursulfase in Pediatric and Young Adult Participants With Neuronopathic (nMPS II) or Non-Neuronopathic Mucopolysaccharidosis Type II (nnMPS II) — Recruiting now
• The ExTINGUISH Trial of Inebilizumab in NMDAR Encephalitis — Recruiting now
• National Collaborative to Improve Care of Children With Complex Congenital Heart Disease — Recruiting now
• A Phase II Dose-escalation Study Characterizing the PK of Eltrombopag in Pediatric Patients With Previously Untreated or Relapsed Severe Aplastic Anemia or Recurrent Aplastic Anemia — Completed
• A Phase 1b Study to Investigate Safety and Tolerability of ARGX-119 in Adult Participants With DOK7-Congenital Myasthenic Syndromes (CMS) — Running, not enrolling
• Study to Evaluate the Safety and Efficacy of Pegvaliase in Adolescents (Ages 12-17) With Phenylketonuria — Running, not enrolling
• Autus Valve Pivotal Study — Running, not enrolling
• ARD-101 for Treatment of PWS: The Hunger Elimination or Reduction Objective Trial — Stopped early
• The Hunger Elimination or Reduction Objective (HERO ) Open -Label Extension (OLE) Trial — Stopped early
• An Extension Study of the Long-Term Safety, Tolerability, and Efficacy of Tividenofusp Alfa (DNL310) in Participants With Mucopolysaccharidosis Type II (MPS II) From Study DNLI-E-0002 or Study DNLI-E-0007 — Enrolling by invitation
• Study of Bictegravir/Lenacapavir in Children and Adolescents With HIV-1 — Running, not enrolling
• A Pilot Study of SurVaxM in Children Progressive or Relapsed Medulloblastoma, High Grade Glioma, Ependymoma and Newly Diagnosed Diffuse Intrinsic Pontine Glioma — Running, not enrolling
• An Observational Study Comparing Delandistrogene Moxeparvovec (ELEVIDYS) With Standard of Care in Participants With Duchenne Muscular Dystrophy — Enrolling by invitation
• Post-trial Access Program of Idursulfase-IT Along With Elaprase in Children With Hunter Syndrome — Available (expanded access)
• A Study of Soticlestat in Adults and Children With Rare Epilepsies — Stopped early
• A Study to Evaluate Long-Term Safety, Tolerability, & Efficacy of BMN 111 in Children With Achondroplasia (ACH) — Running, not enrolling
• An Extension Study to Evaluate the Efficacy and Safety of BMN 111 in Children With Achondroplasia — Running, not enrolling
• Retrospective Analysis of Prismaflex HF20 Set Versus ppCRRT Registry — Completed
• A Study of Avapritinib in Pediatric Patients With Solid Tumors Dependent on KIT or PDGFRA Signaling — Completed
• A Study of Gene Therapy for Classic Congenital Adrenal Hyperplasia (CAH) — Running, not enrolling
• A Study of ELAPRASE in Treatment-naïve Participants With Hunter Syndrome (Mucopolysaccharidosis [MPS] II) — Withdrawn before enrolling
• Study of SRP-4045 (Casimersen) and SRP-4053 (Golodirsen) in Participants With Duchenne Muscular Dystrophy (DMD) — Completed
• A Study of Ponatinib With Chemotherapy in Children, Teenagers, and Adults With Philadelphia Chromosome-Positive Acute Lymphoblastic Leukemia — Stopped early
• An Open-Label Extension Trial to Assess the Long-Term Safety of ZX008 (Fenfluramine Hydrochloride HCl) Oral Solution in Children and Young Adults With Dravet Syndrome — Completed
• A Study to Evaluate Safety and Effectiveness of mRNA-1273 COVID-19 Vaccine in Healthy Children Between 6 Months of Age and Less Than 12 Years of Age — Completed
• Efficacy and Safety of QGE031 (Ligelizumab) in Patients With Peanut Allergy — Stopped early
• A Study in Adolescents and Adults With Eosinophilic Esophagitis (EoE) Measuring Histologic Response and Determine if Reduction in Dysphagia is Achieved — Completed
• Study to Assess the Efficacy and Safety of Viltolarsen in Ambulant Boys With DMD (RACER53) — Completed
• EZH2 Inhibitor Tazemetostat in Pediatric Subjects With Relapsed or Refractory INI1-Negative Tumors or Synovial Sarcoma — Completed
• Tamoxifen Therapy for Myotubular Myopathy — Stopped early
• An Extension Study to Evaluate Casimersen or Golodirsen in Patients With Duchenne Muscular Dystrophy — Stopped early
• A Clinical Trial to Evaluate the Safety and Efficacy of BMN 111 in Infants and Young Children With Achondroplasia — Completed
• Posoleucel (ALVR105) for the Treatment of Adenovirus Infection in Pediatric and Adult Participants Receiving Standard of Care Following Allogeneic Hematopoietic Cell Transplantation — Stopped early
• A Study of Pomalidomide Monotherapy for Children and Young Adults With Recurrent or Progressive Primary Brain Tumors — Completed