Focus: Recordati is a mid-cap specialty pharmaceutical company headquartered in France with 1,001–5,000 employees, focused on small-molecule manufacturing across oncology, rare diseases, endocrinology, cardiovascular, and hematology. The company is public and generates 67% of revenue from its flagship product ISTURISA.
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Generated by Claude from Recordati's SEC filings, pipeline programs, hiring velocity, FDA actions, and WARN data. Inference, not editorial — verify before quoting.
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.
Blockbuster-scale rare-disease drug; 11β-hydroxylase inhibitor generating 67% of company revenue with 9-year patent runway.
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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.
Second-largest product; CPS1 activator for urea-cycle disorders facing patent expiration in ~2 years.
Methylating agent for cysteine metabolism; mature rare-disease product with modest revenue.
Ophthalmologic cystine-depleting agent; niche rare-disease indication with long-term market position.
Somatostatin receptor agonist facing patent cliff in 7 months; modest revenue but active pipeline expansion into prolactin tumors.
First-in-class complement inhibitor (BLA) for rare hematologic disease; growth potential as awareness expands.
Lead-chelating agent for pediatric toxicology; minimal revenue, regulatory niche product.
Legacy antiepileptic; no reported Part D spending, likely post-patent generic or discontinued.
Nucleic-acid synthesis inhibitor (ANDA); post-LOE generic chemotherapy with minimal branded revenue.
Duplicate ANDA entry for dactinomycin; post-LOE generic status indicates commodity oncology product.
7 discontinued, 5 duplicate formulations not shown
EU greenlights Recordati deal under streamlined merger scrutiny - The Brussels Times
EU greenlights Recordati deal under streamlined merger scrutiny The Brussels Times
EU greenlights Recordati deal under streamlined merger scrutiny - The Brussels Times
EU greenlights Recordati deal under streamlined merger scrutiny The Brussels Times
8-K Filing: IONIS PHARMACEUTICALS INC (IONS) (CIK 0000874015) — 8-K
8-K
IONS Out-Licenses ex-U.S. Rights for Rare Neurology Drug to Recordati - Yahoo Finance
IONS Out-Licenses ex-U.S. Rights for Rare Neurology Drug to Recordati Yahoo Finance
Ionis grants Recordati rights to zilganersen for Alexander disease - Pharmaceutical Technology
Ionis grants Recordati rights to zilganersen for Alexander disease Pharmaceutical Technology
IONS Out-Licenses ex-U.S. Rights for Rare Neurology Drug to Recordati - Zacks Investment Research
IONS Out-Licenses ex-U.S. Rights for Rare Neurology Drug to Recordati Zacks Investment Research
Showing 6 of 10 news items
No open positions listed yet. Check their careers page directly.
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Upgrade to Pro — $25/moRecent peer-reviewed publications with author affiliations at this company
Cost-effectiveness of pasireotide long-acting release in acromegaly: a systematic literature review and methodology assessment.
Impact of Osilodrostat on Health-Related Quality of Life in Cushing's Disease: Analysis of Patient-Reported Outcomes From the Phase III LINC 3 and LINC 4 Clinical Trials.
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Showing 5 of 10 publications