Focus: Ipsen is a mid-size biopharmaceutical company headquartered in Tianjin, China, with 1,001–5,000 employees specializing in small molecules and biologics across oncology, endocrinology, neurology, and gastroenterology. The company generates 73% of revenue from its flagship product AURYXIA (ferric citrate), indicating heavy reliance on a single asset.
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Automated analysis based on publicly available data (FDA, SEC, ClinicalTrials.gov). May be incomplete or delayed. This score does not reflect insider knowledge and should not be used as the sole basis for investment or employment decisions.
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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.
Generated by Claude from Ipsen's SEC filings, pipeline programs, hiring velocity, FDA actions, and WARN data. Inference, not editorial — verify before quoting.
Flagship product accounting for 73% of company revenue; approaching patent cliff in July 2030 creates material revenue headwind.
Second-largest revenue contributor; somatostatin analog with established clinical use; LOE timeline not disclosed but likely approaching.
ANDA generic product post-LOE; minimal revenue contribution.
Rare disease therapeutic with extended LOE runway (November 2041); Phase 3 ongoing in biliary atresia signals growth potential.
Approved competitor to Botox; recent dual Phase 3 migraine wins (July 2026) position product for label expansion and revenue growth.
Nanoparticle oncology asset with extended patent protection (October 2036); modest current revenue.
ANDA NSAID generic; minimal strategic value post-LOE.
BLA biologic for rare pediatric growth disorder; narrow indication limits revenue scale.
First-in-class retinoid for rare genetic bone disorder; Phase 2 expansion signals label extension ambition; LOE June 2037.
PPAR agonist for rare liver disease; Phase 3 study underway; LOE March 2037; expansion potential in NASH/fibrosis space.
2 discontinued, 1 duplicate formulations not shown
Ipsen delivers excellent H1 2026 results and upgrades its full-year guidance - GlobeNewswire
Ipsen delivers excellent H1 2026 results and upgrades its full-year guidance GlobeNewswire
Ipsen delivers excellent H1 2026 results and upgrades its full-year guidance - GlobeNewswire
Ipsen delivers excellent H1 2026 results and upgrades its full-year guidance GlobeNewswire
Ipsen Names Catherine Bradley as Its Audit Committee Chair - Stock Titan
Ipsen Names Catherine Bradley as Its Audit Committee Chair Stock Titan
Ipsen’s Bylvay fails Phase III trial in biliary atresia - The Pharma Letter
Ipsen’s Bylvay fails Phase III trial in biliary atresia The Pharma Letter
Another setback for Ipsen's Albireo portfolio as Bylvay flunks phase 3 trial - Fierce Pharma
Another setback for Ipsen's Albireo portfolio as Bylvay flunks phase 3 trial Fierce Pharma
Ipsen Drug Misses Goal in Late-Stage Trial for Rare Liver Disease - WSJ
Ipsen Drug Misses Goal in Late-Stage Trial for Rare Liver Disease WSJ
Showing 6 of 10 news items
No open positions listed yet. Check their careers page directly.
Based on last 4 crawl cycles
Source: USCIS H-1B Employer Data Hub
Recent peer-reviewed publications with author affiliations at this company
Burden of primary biliary cholangitis on the Italian National Health Service: retrospective analysis from an administrative database.
Effect of an Integrated Postdischarge Care Program for Older Patients After Hip Fracture Discharged to the Community: A Multicenter Cohort Study.
Showing 5 of 10 publications
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