BLASOLUTIONINJECTION
Approved
Feb 2025
Lifecycle
Growth
Competitive Pressure
30/100
Data completeness
2/8 — Basic
IRA Negotiated
MERILOG (insulin aspart-szjj) by Sanofi is insulin, including insulin aspart products is the regulation of glucose metabolism. First approved in 2025.
Drug data last refreshed 9h ago · AI intelligence enriched 1w ago
AI summarySynthesized from FDA + DailyMed + ClinicalTrials.gov data
MERILOG (insulin aspart-szjj) is a rapid-acting insulin analog approved by the FDA on February 14, 2025, as a Sanofi biosimilar referencing insulin aspart. It regulates blood glucose by stimulating peripheral glucose uptake in muscle and fat while inhibiting hepatic glucose production, making it suitable for diabetes management in patients requiring insulin therapy.
Growth
Early-stage growth product with significant price compression (76% reduction post-IRA negotiation); biosimilar entry suggests moderate team scaling for market penetration.
Mechanism of Action
insulin, including insulin aspart products is the regulation of glucose metabolism. Insulin and its analogs lower blood glucose by stimulating peripheral glucose uptake, especially by skeletal muscle and fat, and by inhibiting hepatic glucose production. Insulin inhibits lipolysis and proteolysis,…
Pharmacologic Class:
Insulin Analog
Indications
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
Career Relevance
MERILOG offers early-stage career exposure in biosimilar commercialization within a high-volume therapeutic category. Growth is constrained by price compression and biosimilar competition, making this a stable but modest-growth opportunity suited for professionals building expertise in insulin market dynamics and payer negotiation.
Brand Manager
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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.