🧪 UPDATED DAILY FROM CLINICALTRIALS.GOVSynced Apr 1

Find Clinical Trials for Your Rare Disease

9+ recruiting trials across all rare diseases. Filter by phase, location, and condition.

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Showing 9 of 9 recruiting trials for “benign-concentric-annular-macular-dystrophy”

Phase 1, PHASE2RecruitingNCT07185256 ↗

Safety and Tolerability of Subretinally Injected OPGx-BEST1 in Patients With Best Vitelliform Macular Dystrophy (BVMD) or Autosomal-Recessive Bestrophinopathy (ARB)

🏥 Opus Genetics, Inc📍 4 sites📅 Started Sep 2025View details ↗
RecruitingNCT07125040 ↗

Characterization of the Natural History of LAMA2-RD and Identification of Novel Disease Biomarkers

🏥 Università Vita-Salute San Raffaele📍 1 site📅 Started Jul 2025View details ↗
RecruitingNCT06503367 ↗

Observation Study in Patients Age 0-5 Years With LAMA2-related Congenital Muscular Dystrophy

👨‍⚕️ Anne M Connolly, MD, Nationwide Childrens Hospital📍 14 sites📅 Started May 2025View details ↗
RecruitingNCT06805474 ↗

A Prospective Observational Study to Assess the Reliability and Validity of the MLSDT

👨‍⚕️ Samuel Barone, MD, Nanoscope Therapeutics Inc.📍 1 site📅 Started Jan 2025View details ↗
RecruitingNCT06354790 ↗

Natural History Study of Children With LAMA2-related Dystrophies

🏥 Institut de Myologie, France📍 4 sites📅 Started Dec 2024View details ↗
RecruitingNCT06924125 ↗

Spanish Natural History Study for LAMA2 Muscular Dystrophy

🏥 Hospital Universitari Vall d'Hebron Research Institute📍 1 site📅 Started Jul 2021View details ↗
RecruitingNCT05809635 ↗

Study of BEST1 Vitelliform Macular Dystrophy

👨‍⚕️ Stephen H Tsang, MD, PhD, Columbia University📍 3 sites📅 Started Mar 2021View details ↗
RecruitingNCT01403402 ↗

Congenital Muscle Disease Study of Patient and Family Reported Medical Information

👨‍⚕️ Gustavo Dziewczapolski, PhD, CureCMD, CMDIR📍 1 site📅 Started Sep 2009View details ↗
RecruitingNCT00138931 ↗

Genetics of Cardiovascular and Neuromuscular Disease

👨‍⚕️ Elizabeth McNally, MD PhD, University of Chicago📍 1 site📅 Started Sep 1996View details ↗

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