- CEO
- Patrick Alexandre
- Full Time Employees
- 103
- Sector
- Health technology
- Industry
- Medical specialties
- Address
- 6 Rue Pauline Kergomard Dijon BF France 21000
- IPO Date
- Feb 20, 2014
- Business
- Crossject S.A. (Euronext: ALCJ.PA) develops and manufactures needle-free, pre-filled, single-use auto-injectors based on its proprietary ZENEO platform for the rapid delivery of emergency medications via intradermal, subcutaneous, and intramuscular routes; core products in its pipeline include ZEPIZURE (midazolam for status epilepticus, poisoning, and epileptic seizures targeting FDA EUA submission in Q2 2025 and NDA in mid-2026), CJT-L15 (hydrocortisone for acute adrenal insufficiency), CJT-L21 (epinephrine for anaphylactic shock), CJT-L20 (terbutaline for severe asthma), CJT-L11 (sumatriptan for migraine and cluster headache), CJT-L9 (methotrexate for rheumatoid arthritis), and CJT-L16 (naloxone for opioid overdose), all pursuing FDA 505(b)(2) NDA pathways between 2026 and 2028. Founded in 2001 and headquartered in Dijon, France, with manufacturing sites in Dijon and Gray, the company operates primarily in Europe and pursues U.S. commercialization through partnerships, targeting patients and healthcare providers in emergency situations such as epilepsy, allergies, adrenal crises, and overdoses. Recent developments include a €5 million financing completion with Vatel Capital in November 2025, an €11.3 million BARDA funding extension in September 2025 for ZEPIZURE development, a June 2025 €5 million capital increase, a $60 million BARDA contract for ZEPIZURE, U.S. infrastructure expansion with key hires like a Chief Operating Officer and Chief Medical Officer in 2024, geographic commercialization extensions for ZEPIZURE in Europe, a renewed U.S. Department of Defense CRADA in December 2024, and successful ISO/GMP audits confirming manufacturing readiness.