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Weather Update

BCM Family Medicine on Kirby is without electrical power. Patients with appointments on Tuesday at this location will be moved to Baylor Medicine on the McNair Campus:  7200 Cambridge St, 7th floor, Suite 7B. Patients will be contacted. For questions, call 713-798-7700.

Search for Clinical Trials

Background Smith-Magenis Syndrome (SMS) is a genetic syndrome caused by mutations in the RAI1 gene or deletions of the 17p11.2 chromosome.…
  • Autism
  • Diabetes
  • Digestive System
  • Endocrinology
  • Genetic and Rare Diseases - Observational and Gene Discovery
  • Genetic and Rare Diseases - Treatment
  • Nutrition
  • Obesity and Metabolism
  • Pediatrics
  • Psychiatry and Behavior
An Open-Label Dose-Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of mRNA-3745 in Participants with…
  • Genetic and Rare Diseases - Treatment
Introduction: The melanocortin-4 receptor (MC4R) pathway is the principal regulator of mammalian energy balance and body weight. Originating in the…
  • Endocrinology
  • Genetic and Rare Diseases - Treatment
  • Pediatrics
RM-493-034: A 2-Stage (Open-Label Run-In Followed by Randomized Withdrawal), Double-Blind, Placebo-Controlled, Phase 2 Study of Setmelanotide In…
  • Genetic and Rare Diseases - Treatment
  • Endocrinology
  • Pediatrics
  • Obesity and Metabolism
Long Term Extension Trial Of Setmelanotide (RM-493) For Patients Who Have Completed A Trial Of Setmelanotide For The Treatment Of Obesity Associated…
  • Geriatrics
  • Genetic and Rare Diseases - Treatment
  • Endocrinology
  • Obesity and Metabolism
  • Nutrition
  • Digestive System
  • Diabetes
The goal of this study is to establish a database of pediatric patients with early-onset obesity who have been phenotypically well-characterized…
  • Growth and Development
  • Genetic and Rare Diseases - Treatment
  • Genetic and Rare Diseases - Observational and Gene Discovery
  • Endocrinology
  • Pediatrics
  • Obesity and Metabolism
  • Nutrition
  • Diabetes
Recruitment for a study to learn about the experiences and perspectives of children with dystonia and their caregivers to learn what you think about…
  • Genetic and Rare Diseases - Treatment
  • Pediatrics
A study on natural history and molecular mechanisms of neurodevelopmental and neuropsychiatric disorders, including EBF3-related Hypotonia, Ataxia,…
  • Brain/Spinal Cord/Nervous System
  • Genetic and Rare Diseases - Observational and Gene Discovery
  • Genetic and Rare Diseases - Treatment
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