BLASUBCUTANEOUSSOLUTION
Approved
Aug 2020
Lifecycle
Peak
Competitive Pressure
30/100
Clinical Trials
3
Data completeness
3/8 — Basic
Drug data last refreshed 23m ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
SOGROYA (somapacitan-beco) is a long-acting human growth hormone (hGH) analog developed by Novo Nordisk for the treatment of growth hormone deficiency in children and adults. It is administered as a subcutaneous injection and represents a cytokine-based therapeutic approach to hormone replacement.
$0.163MPart D
PeakProduct is in peak commercial phase with modest Medicare Part D penetration; brand team likely focused on market expansion and patient access optimization.
Mechanism of Action
Mechanism of action data is being enriched from DailyMed and FDA sources. Check back soon for updated drug intelligence.
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Clinical Trials (3)
Special Use-results Surveillance on Long Term Use of Sogroya® in Children With Short Stature Due to Growth Hormone Deficiency Where Epiphysial Discs Are Not Closed
Started Oct 2023
200 enrolled
Growth Hormone Deficiency in Children
A Study to Follow Patients With Adult Growth Hormone Deficiency (AGHD) Treated With Sogroya® for Long Term Safety Information
Started Feb 2023
400 enrolled
Adult Growth Hormone Deficiency
Post-Marketing Surveillance (Special Use-results Surveillance on Long-term Use) With Sogroya®
Started Feb 2022
200 enrolled
Adult Growth Hormone Deficiency
Career Relevance
SOGROYA offers career opportunities in a peak-stage specialty pharmaceutical product within endocrinology, a traditionally stable therapeutic area. Working on this brand involves managing a niche but growing patient population with focus on payer education, patient convenience narratives, and long-term market expansion.
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Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.