Growth Hormone Deficiency – Executive Insights – Growth hormone deficiency: Executive Insights (US)
Growth hormone deficiency (GHD) is characterized by slow growth or absence of growth, short stature, and absent or delayed sexual development. Accurately testing for GHD is challenging and often cumbersome. Recombinant human growth hormone (rhGH) has been the mainstay treatment for GHD since 1985. The current landscape for rhGH therapy is very competitive; several products are approved, and only a few agents are in late-phase clinical trials. Each of the products in development aims to improve the frequency of dosing, thereby reducing the burden on patients.
Questions answered
- What is the prevalence of GHD? How are U.S. GHD patients managed?
- What are the key areas of unmet need and opportunities in the treatment of GHD?
- Which therapies are in late-phase development for GHD? What is the potential impact of new launches, and how will these therapies affect future opportunity in the treatment of GHD?
- What are the key drivers of, and limitations on, the market today and in the future?
Product description
Executive Insights provides indication-specific market intelligence withworld-class epidemiology and keen insight into current treatment paradigms, biotherapeutic pipelines, key clinical unmet needs, and competitive landscapes, supported by primary and secondary research. This solution provides succinct insights to any biopharma function or business professional looking to quickly grasp a new indication of interest.
Geography: United States
Primary research: Three KOL interviews from March 2023
Key companies covered: Novo Nordisk, Eli Lilly, Roche / Genentech, Pfizer, Sandoz, Merck KGaA, Ferring, Ascendis Pharma, Lumos Pharma
Key drugs covered: Norditropin, Genotropin / Genotropin MiniQuick, Omnitrope, Humatrope, Nutropin, Saizen, Zomacton, Skytrofa, Somapacitan (Sogroya), Somatrogon (Ngenla), Ibutamoren mesylate (LUM 201)
Sayani Datta, M.Sc., Manager – Cardiovascular, Metabolic, Renal, and Hematologic (CMRH) Disorders. At Clarivate, Sayani’s primary areas of focus are nonalcoholic steatohepatitis (NASH) and pulmonary hypertension (PH). Previously, she was an associate consultant with IQVIA. She has worked on diverse types of custom and syndicated research projects in several therapeutic areas and has experience in sales- and epidemiology-based forecasting, commercial opportunity assessments, and market tracking and intelligence. She is an M.Sc. in biotechnology from the University of Leeds and gained exposure to life sciences research and development working as a postgraduate research intern.
Anuhya V., M.Pharm., is a research associate on the Cardiovascular, Metabolic, Renal, and Hematological Disorders team at Clarivate. She conducts extensive secondary market research for a variety of CMRH indications, including pulmonary hypertension (PH), nonalcoholic steatohepatitis (NASH), and heart failure (e.g., HFrEF, HFpEF). She holds a master’s degree in general pharmacy from BITS Pilani in India and a bachelor’s degree in pharmacy from G. Pulla Reddy College of Pharmacy, which is affiliated with Osmania University, in Hyderabad, India.