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Trial Match

Clinical trials test new treatments โ€” sometimes the newest options available for a disease. Find trials that are recruiting now, near you. Open one to see its eligibility rules as simple questions to go through with your doctor.

Know your stage or your test results (such as EGFR, HER2 or BRCA)? Match trials to your own profile - nothing you type is saved.

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30 recruiting trials

for Rare Diseases

Nephrotic Syndrome Study Network NCT01209000n/a44 sites๐Ÿ“ Los Angeles๐Ÿ“ Palo Alto๐Ÿ“ San Francisco University of Michigan ยท Tests: Kidney Biopsy Assessing Pulmonary Changes in HSCT NCT07823036Phase 1, Phase 21 site๐Ÿ“ Cincinnati Children's Hospital Medical Center, Cincinnati ยท Tests: Hyperpolarized 129 Xenon Identification of the Molecular and/or Pathophysiological Bases of Rare Diseases of Genetic Origin (or Rare Forms of Frequent Diseases Suspected of Being of Genetic Origin). NCT03287193n/a1 site๐Ÿ“ Dijon Centre Hospitalier Universitaire Dijon ยท Tests: Blood and/or tissue sampling, high-throughput sequencing Caregiving Networks Across Disease Context and the Life Course NCT05007990n/a1 site๐Ÿ“ Bethesda National Human Genome Research Institute (NHGRI) Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford NCT01793168n/a1 site๐Ÿ“ Sioux Falls Sanford Health Diagnostic Research in Patients With Rare Diseases -Solving the Unsolved Rare Diseases NCT04024774n/a1 site๐Ÿ“ Dijon Centre Hospitalier Universitaire Dijon ยท Tests: Biological samples, Genetic test Performance Indicators and Impact on the Care Pathway of Sequencing on the SeqOIA and AURAGEN (Seqogen) Platforms for Oncology Patients NCT07147465n/a3 sites๐Ÿ“ Lyon๐Ÿ“ Paris๐Ÿ“ Paris Assistance Publique - Hรดpitaux de Paris Rare Kidney Stone Consortium Patient Registry NCT00588562n/a4 sites๐Ÿ“ Rochester๐Ÿ“ Rochester๐Ÿ“ New York Mayo Clinic Transcriptomic Analysis of Fibroblasts and Blood in Patients With Rare Diseases NCT07075107NA1 site๐Ÿ“ Marseille Assistance Publique Hopitaux De Marseille ยท Tests: Blood collection, skin biopsy RegistRare: a Retro-prospective Registry of Rare Primary Headaches in Italian Tertiary Headache Centres NCT03416114n/a1 site๐Ÿ“ Florence Silvia Benemei Functional Study to Indentify Genetic Etiology of Rare Diseases - ORIGIN NCT05499091NA1 site๐Ÿ“ Angers University Hospital, Angers ยท Tests: Skin biopsy, blood sample, urine sample Rheopheresis as Adjuvant Treatment of Calciphylaxis NCT04654000NA29 sites๐Ÿ“ Angers๐Ÿ“ Arras๐Ÿ“ Auxerre University Hospital, Lille ยท Tests: Rheopheresis procedure, Sham-apheresis The Freiburg Registry on SpontanEous IntercrAnial Hypotension (SIH) & Post-duraL Puncture Headache (PDPH) NCT06711731n/a1 site๐Ÿ“ Freiburg im Breisgau University Hospital Freiburg UW Undiagnosed Genetic Diseases Program NCT04586075n/a1 site๐Ÿ“ Madison University of Wisconsin, Madison ยท Tests: Trio Whole Genome Sequencing and Participant-Specific Research Self-questionnaire in Osteoporosis NCT07067827n/a1 site๐Ÿ“ Quรฉbec CHU de Quebec-Universite Laval ยท Tests: Self-administered questionnaire, Family tree DETERMINE Trial Treatment Arm 01: Alectinib in Adult, Paediatric and Teenage/Young Adult Patients With ALK Positive Cancers NCT05770037Phase 2, Phase 327 sites๐Ÿ“ Belfast๐Ÿ“ Birmingham๐Ÿ“ Birmingham Cancer Research UK ยท Tests: Alectinib Vascular Disease Discovery Protocol NCT03538639n/a1 site๐Ÿ“ Bethesda National Heart, Lung, and Blood Institute (NHLBI) DETERMINE Trial Treatment Arm 02: Atezolizumab in Adult, Paediatric and Teenage/Young Adult Patients With Cancers With High Tumour Mutational Burden (TMB) or Microsatellite Instability-high (MSI-high) or Proven Constitutional Mismatch Repair Deficiency (CMMRD) Disposition NCT05770102Phase 2, Phase 327 sites๐Ÿ“ Belfast๐Ÿ“ Birmingham๐Ÿ“ Birmingham Cancer Research UK ยท Tests: Atezolizumab A Multi-Center Natural History of Urothelial Cancer and Rare Genitourinary Tract Malignancies NCT04923178n/a1 site๐Ÿ“ Bethesda National Cancer Institute (NCI) The KidneyCARE (Community Access to Research Equity) Study NCT05497518n/a1 site๐Ÿ“ Danville Tufts Medical Center ยท Tests: Observational study - registry The Efficacy and Safety of PEGylated GH for the Treatment of Short Stature in Chinese Children-GLOBE Reg NCT06037473n/a1 site๐Ÿ“ Beijing Beijing Children's Hospital ยท Tests: Polyethylene glycol recombinant human growth hormone injection Genomic Profiling of Genetic and Rare Diseases NCT06926127NA1 site๐Ÿ“ Rome Fondazione Policlinico Universitario Agostino Gemelli IRCCS ยท Tests: Whole Exome Sequencing (WES) The Relationship Between Functional Independence and Family Well-being in Children With Rare Genetic Disorders NCT07348926n/a1 site๐Ÿ“ Istanbul BahรงeลŸehir University The Sarcoma Biology and Outcome Project NCT04758325n/a1 site๐Ÿ“ Heidelberg Prof. Dr. Richard F Schlenk Genetics of Inherited Eye Disease NCT02471287n/a1 site๐Ÿ“ Bethesda National Eye Institute (NEI) Understanding of Rare Inflammatory Arthritis in Comparison to Classical Inflammatory Arthritis : Tissular Observations and Immune Infiltrate Characterization : the UTOPIC Project NCT07302074NA2 sites๐Ÿ“ Bordeaux๐Ÿ“ Brest University Hospital, Brest ยท Tests: Biopsy Clinical Characteristics and Analysis of Pituitary Complex and Rare Diseases NCT06435195n/a1 site๐Ÿ“ Beijing Peking Union Medical College Hospital ยท Tests: Surgical Removal, Biopsy Collection of Blood and Skin Samples From Patients With Primary Mitochondrial Diseases and Healthy Volunteers NCT06474104n/a1 site๐Ÿ“ Ramat Gan Minovia Therapeutics Ltd. Firmonertinib Combined With Definitive Radiotherapy in Stage III Unresectable EGFR Uncommon Mutant Pulmonary Adenocarcinoma NCT07314216Phase 21 site๐Ÿ“ Changsha Hunan Cancer Hospital ยท Tests: Firmonertinib, Definitive Thoracic Radiotherapy Clinical Trial in Patients With Barth Syndrome- 4TAZPower NCT07531251Phase 43 sites๐Ÿ“ Needham๐Ÿ“ Calgary๐Ÿ“ Bristol Stealth BioTherapeutics Inc. ยท Tests: Elamipretide, Placebo
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