Somatrogon

Somatrogon, sold under the brand name Ngenla, is a medication for the treatment of growth hormone deficiency.[1][4] Somatrogon is a glycosylated protein constructed from human growth hormone and a small part of human chorionic gonadotropin which is appended to both the N-terminal and C-terminal.[4]

Somatrogon
Clinical data
Trade namesNgenla
Other namesMOD-4023
Pregnancy
category
Routes of
administration		Subcutaneous injection
ATC code
Legal status
Legal status
Identifiers
CAS Number
DrugBank
UNII
KEGG

The most common side effects include reactions at the site of injection, headache, and fever.[3]

Somatrogon was approved for medical use in Australia in November 2021,[1] and in the European Union in February 2022.[3]

Society and culture

On 16 December 2021, the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion, recommending the granting of a marketing authorization for the medicinal product Ngenla, intended for the treatment of growth hormone deficiency (GHD) in children and adolescents from three years of age.[5] The applicant for this medicinal product is Pfizer Europe MA EEIG.[5] Somatrogon was approved for medical use in the European Union in February 2022.[3]

Names

Somatrogon is the international nonproprietary name (INN).[6]

References
  1. "Ngenla". Therapeutic Goods Administration (TGA). 13 December 2021. Retrieved 28 December 2021.
  2. "Summary Basis of Decision (SBD) for Ngenla". Health Canada. 23 October 2014. Retrieved 29 May 2022.
  3. "Ngenla EPAR". European Medicines Agency. 14 December 2021. Retrieved 2 March 2022. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  4. "Pfizer and OPKO Announce Extension of U.S. FDA Review of Biologics License Application of Somatrogon for Pediatric Growth Hormone Deficiency" (Press release). Opko Health. 24 September 2021. Retrieved 18 December 2021 – via GlobeNewswire.
  5. "Ngenla: Pending EC decision". European Medicines Agency (EMA). 16 December 2021. Retrieved 18 December 2021. Text was copied from this source which is copyright European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  6. World Health Organization (2017). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 77". WHO Drug Information. 31 (1). hdl:10665/330984.

Further reading
  • "Somatrogon". Drug Information Portal. U.S. National Library of Medicine.


This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.