Focus: Takeda is a Tokyo-based multinational pharmaceutical company with 49,000 employees specializing in small molecules and enzymes across gastroenterology, rare diseases, neuroscience, and oncology. It is one of the world's largest pharmaceutical companies by headcount and revenue scale.
Profile data last refreshed 7h ago · AI intelligence enriched 3mo ago
Hot — 1146 jobs added in 30d
Net +664 (1146 new, 482 removed). Aggressive expansion phase.
5 recent layoff filings (12 mo) — 637 affected
Source: state DOL filings via Big Local News
Takeda offers a stable Big Pharma foundation with strong current franchises and global reach, but the looming patent cliff (2028–2029) combined with recent layoffs signal near-term restructuring risk; best suited for candidates seeking established-market expertise rather than long-term growth trajectory.
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.
Takeda's largest single revenue contributor (26% of revenue), providing a stable cash stream until patent expiry in 2032.
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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 Takeda's SEC filings, pipeline programs, hiring velocity, FDA actions, and WARN data. Inference, not editorial — verify before quoting.
Second-largest revenue driver; faces patent cliff in 2029, exposing the company to significant revenue erosion in the medium term.
Established neuroscience franchise supporting revenue, though lifecycle stage and patent data indicate no defined expiration in dataset.
Oncology franchise with patent protection until 2033, contributing meaningfully to specialty pharma positioning.
Recent FDA expansion approval for intravenous formulation (June 2026) positions this GI franchise as a growth driver; 16.99M shares granted June 2026 suggest company confidence.
GI market mainstay with patent protection until 2032, contributing to Takeda's gastroenterology portfolio depth.
GI-focused product facing patent expiration in 2028, making it a near-term cliff risk requiring pipeline replacement.
Rare disease franchise supporting niche indication; lifecycle and patent data indicate no defined expiration in dataset.
43 discontinued, 19 duplicate formulations not shown
+16 more products with revenue data
Should FDA Approval Of MIMRYLO Reshape How Investors View Takeda Pharmaceutical’s (TSE:4502) Rare-Disease Strategy? - simplywall.st
Should FDA Approval Of MIMRYLO Reshape How Investors View Takeda Pharmaceutical’s (TSE:4502) Rare-Disease Strategy? simplywall.st
First-in-Class Takeda, Protagonist Drug Lands FDA Approval in Rare Blood Disorder - MedCity News
First-in-Class Takeda, Protagonist Drug Lands FDA Approval in Rare Blood Disorder MedCity News
Takeda Secures FDA Approval For First-In-Class Blood Cancer Drug - Benzinga
Takeda Secures FDA Approval For First-In-Class Blood Cancer Drug Benzinga
FDA OKs Takeda, Protagonist drug for rare blood cancer - BioPharma Dive
FDA OKs Takeda, Protagonist drug for rare blood cancer BioPharma Dive
Takeda Pharmaceutical Company Limited (TAK) Peer Comparison – Compare with Others - valueresearchonline.com
Takeda Pharmaceutical Company Limited (TAK) Peer Comparison – Compare with Others valueresearchonline.com
Takeda receives US FDA approval of Mimrylo - The Pharma Letter
Takeda receives US FDA approval of Mimrylo The Pharma Letter
Showing 6 of 10 news items
Based on last 4 crawl cycles
Source: USCIS H-1B Employer Data Hub
Recent peer-reviewed publications with author affiliations at this company
Analysis of healthcare resource utilization before and after initiation of maribavir for cytomegalovirus treatment.
Bleeding rates, healthcare utilization, and costs among patients with hemophilia a without inhibitors treated with concomitant octocog alfa or extended half-life factor VIII while on emicizumab prophylaxis.
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Source: state DOL filings, aggregated via Big Local News
Cambridge-based R&D roles face significant attrition risk; restructuring appears tied to pipeline deprioritization ahead of patent cliffs; candidates should clarify program viability and site stability during interviews.
Showing 5 of 10 publications
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