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Bardet-Biedl Syndrome

Laurence-Moon-Bardet-Biedl syndromeLaurence-Moon syndrome
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Clinical Trials

This information is provided by ClinicalTrials.gov

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Displaying 1-4 of 4 results.
Clinical Registry Investigating Bardet-Biedl Syndrome
Status: Recruiting
Last Changed: Feb 19, 2020
First Received: Dec 31, 2014
Disease(s): Bardet-Biedl Syndrome
Locations: Marshfield Clinic Research Foundation, Marshfield, Wisconsin, United States
Setmelanotide Phase 2 Treatment Trial in Patients With Rare Genetic Disorders of Obesity
Status: Recruiting
Last Changed: Jun 16, 2020
First Received: Jan 06, 2017
Disease(s): Pro-opiomelanocortin (POMC) Deficiency Obesity (Heterozygous or Epigenetic), Leptin Receptor Deficiency Obesity, Bardet-Biedl Syndrome, Alstrom Syndrome, Smith-Magenis Syndrome
Intervention(s): Setmelanotide
Locations: Synexus Clinical Research US, Inc. - Simon Williamson Clinic, PC, Birmingham, Alabama, United States
Synexus Clinical Research US, Inc. - Phoenix Southeast, Chandler, Arizona, United States
Synexus Clinical Research US, Inc. - Central Arizona Medical Associates, PC, Mesa, Arizona, United States
Honor Health Research Institute, Scottsdale, Arizona, United States
Axis Clinical Trials-Downtown, Los Angeles, California, United States
... and 42 other locations.
Inherited Retinal Degenerative Disease Registry
Status: Recruiting
Last Changed: Dec 13, 2018
First Received: May 06, 2015
Disease(s): Eye Diseases Hereditary, Retinal Disease, Achromatopsia, Bardet-Biedl Syndrome, Bassen-Kornzweig Syndrome, Batten Disease, Best Disease, Choroidal Dystrophy, Choroideremia, Cone Dystrophy, Cone-Rod Dystrophy, Congenital Stationary Night Blindness, Enhanced S-Cone Syndrome, Fundus Albipunctatus, Goldmann-Favre Syndrome, Gyrate Atrophy, Juvenile Macular Degeneration, Kearns-Sayre Syndrome, Leber Congenital Amaurosis, Refsum Syndrome, Retinitis Pigmentosa, Retinitis Punctata Albescens, Retinoschisis, Rod-Cone Dystrophy, Rod Dystrophy, Rod Monochromacy, Stargardt Disease, Usher Syndrome
Locations: Foundation Fighting Blindness, Columbia, Maryland, United States
UAB HRFD Core Center: Core A: The Hepato/Renal Fibrocystic Diseases Translational Resource
Status: Recruiting
Last Changed: Oct 25, 2019
First Received: Jul 26, 2011
Disease(s): Hepato/Renal Fibrocystic Disease, Autosomal Recessive Polycystic Kidney Disease, Joubert Syndrome, Bardet Biedl Syndrome, Meckel-Gruber Syndrome, Congenital Hepatic Fibrosis, Caroli Syndrome, Oro-Facial-Digital Syndrome Type I, Nephronophthisis, Glomerulocystic Kidney Disease
Locations: Children's National Health System, Washington, District of Columbia, United States