
Endocrinologist

No OPD information available
Allan-Herndon-Dudley Syndrome
Childhood Hypophosphatasia (HPP)
Nephrocalcinosis
Rickets
Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED)
Autoimmune Polyglandular Syndrome Type 2
Becker Muscular Dystrophy
Calcinosis
Cystic Fibrosis
Duchenne Muscular Dystrophy
Peter J. Simm is a male medical professional who helps people with different health conditions like Allan-Herndon-Dudley Syndrome, Childhood Hypophosphatasia, Nephrocalcinosis, Rickets, and more. He specializes in treating various diseases such as Becker Muscular Dystrophy, Calcinosis, Cystic Fibrosis, and Duchenne Muscular Dystrophy.
Peter J. Simm uses special skills and treatments to care for his patients. He communicates with patients in a way that makes them feel comfortable and safe. Patients trust him because he listens to their concerns and explains things clearly.
Peter J. Simm stays updated with the latest medical knowledge and research to provide the best care for his patients. He works closely with other medical professionals to share information and improve patient outcomes. His relationships with colleagues are strong, and they collaborate to give the best possible care.
Peter J. Simm's work has had a positive impact on many patients' lives. His research on X-Linked Hypophosphataemia and Burosumab has been published in the Journal of Pediatrics and Child Health. He has also conducted clinical trials like the study on daily oral LUM-201 for children with Idiopathic Growth Hormone Deficiency, which has been completed successfully.
Overall, Peter J. Simm is a dedicated and knowledgeable medical professional who uses his expertise to help patients with various health conditions. His commitment to staying updated with the latest research and working collaboratively with colleagues ensures that his patients receive the best possible care.
Enrollment Status: Completed
Published: October 15, 2024
Intervention Type: Drug
Study Drug:
Study Phase: Phase 2
