TAK
Takeda Pharmaceutical Company Limited · Healthcare · Drug Manufacturers - Specialty & Generic
Last
$17.83
+$0.04 (+0.25%) 4:00 PM ET
After hours $17.47 −$0.36 (−1.99%) 5:28 AM ET
Prev close $17.78
Open $17.87
Day high $17.97
Day low $17.80
Volume 2,398,779
Avg vol 2,917,343
Mkt cap
$56.17B
Sector
Healthcare
AI report sections
TAK
Takeda Pharmaceutical Company Limited
Takeda’s ADR trades near the top of its 52-week range with solid 3–12 month price appreciation and price action currently above key moving averages. Technical indicators and pattern signals point to an ongoing upward bias with recent bullish breakout characteristics, though the elevated short volume ratio introduces heightened short-term positioning risk. Fundamental and valuation detail is limited in the available data, so the current view is driven primarily by price behavior, liquidity, and sentiment indicators.
AI summarized at 12:17 AM ET, 2026-04-01
AI summary scores
INTRADAY: 63 SWING: 72 LONG: 69
Volume vs average
Intraday (cumulative)
−22% (Below avg)
Vol/Avg: 0.78×
RSI
43.33 (Neutral)
Neutral (40–60)
MACD momentum
Intraday
+0.00 (Strong)
MACD: -0.00 Signal: -0.00
Short-Term
-0.08 (Weak)
MACD: -0.04 Signal: 0.05
Long-Term
-0.08 (Weak)
MACD: 0.20 Signal: 0.28
Intraday trend score 38.24

Latest news

TAK 12 articles Positive: 5 Neutral: 6 Negative: 1
Neutral GlobeNewswire Inc. • Delveinsight
Non-Small Cell Lung Cancer Clinical Trial Race Intensifies as 100+ Companies Competing in Therapeutic Segment Worldwide | DelveInsight

Over 100 pharmaceutical companies are competing to develop 120+ pipeline drugs for non-small cell lung cancer (NSCLC), with approximately 30+ drugs in late-stage development. The competitive landscape is driven by precision oncology advances, including next-generation targeted agents and immunotherapy combinations. Recent FDA approvals and designations highlight innovation in treating EGFR-mutated, ALK-positive, and other biomarker-selected NSCLC populations.

PFE ABBV BNTX MRK non-small cell lung cancer NSCLC clinical trials pipeline drugs
Sentiment note

Takeda is mentioned as an active player in NSCLC drug development but no specific pipeline updates or clinical data are provided in the article.

Positive GlobeNewswire Inc. • Delveinsight
The Psoriasis Clinical Trial Pipeline Boom as 90+ Companies are in the Race for Better Treatments | DelveInsight

Over 90 pharmaceutical companies are actively developing more than 100 pipeline psoriasis drugs across various clinical stages. Key players including Takeda, Can-Fite BioPharma, Oruka Therapeutics, and others are advancing promising therapies with novel mechanisms of action such as TYK2 inhibitors and IL-23 inhibitors. Recent developments include positive Phase III results from Alumis and Takeda, and regulatory progress from multiple companies, indicating robust innovation in the psoriasis treatment landscape.

CANF ORKA ALMS TAK psoriasis clinical trials pipeline drugs TYK2 inhibitors
Sentiment note

Announced positive topline results from Phase III trials of zasocitinib (TAK-279) for moderate-to-severe plaque psoriasis in December 2025, demonstrating clinical efficacy and advancement toward potential market approval.

Positive GlobeNewswire Inc. • Delveinsight
Eosinophilic Esophagitis Market in the US to Grow at 13.2% CAGR During the Forecast Period (2026–2036) Owing to the Emergence of Drug Classes Such as TSLP Inhibitors, Glucocorticoid Receptor Agonists, and Immunomodulators | DelveInsight

The US eosinophilic esophagitis market is projected to grow at 13.2% CAGR through 2036, driven by increased disease awareness, standardized diagnostics, and high relapse rates. The market was valued at $647 million in 2025, with emerging therapies from major pharmaceutical companies expected to transform the treatment landscape, including TSLP inhibitors, glucocorticoid receptor agonists, and immunomodulators.

AZN AMGN DBVT EPRX eosinophilic esophagitis EoE market TSLP inhibitors emerging therapies
Sentiment note

Markets Budesonide oral suspension (EOHILIA), approved in US 2024 for EoE patients aged ≥11 years. Established approved therapy captures market share in the growing EoE treatment segment.

Positive GlobeNewswire Inc. • Researchandmarkets.Com
Crohn's Disease Eight-Market Drug Forecast and Market Analysis Report 2025-2026: Novel MOAs Will Provide Market Shifts Throughout the Forecast Period to 2032

The Crohn's Disease therapeutics market across eight major markets is projected to grow from $9.5 billion to $13.8 billion by 2032 at a CAGR of 3.9%, driven by approvals of 8 pipeline, generic, and biosimilar therapies. Novel mechanisms of action and emerging treatments will reshape the competitive landscape, with key opportunities in strategic licensing and partnerships.

ABBV TAK JNJ LLY Crohn's Disease drug market forecast pipeline drugs biosimilars
Sentiment note

Featured as a major competitor in the CD market with potential to capitalize on the projected $9.5B to $13.8B market expansion through 2032.

Neutral Benzinga • Vandana Singh
Takeda Exits Dementia Drug Partnership With Denali Therapeutics - Here's Why

Takeda Pharmaceutical has terminated its collaboration with Denali Therapeutics on DNL593, a progranulin replacement therapy for frontotemporal dementia. The decision is strategic and not related to safety or efficacy concerns. Denali regains full ownership and control of the therapy, with plans to report Phase 1/2 trial results by end of 2026. Denali shares fell 3.73% on the news.

DNLI TAK dementia drug partnership termination DNL593 progranulin replacement therapy frontotemporal dementia Phase 1/2 trial
Sentiment note

Stock declined 2.64%, but the exit appears to be a strategic business decision rather than driven by safety or efficacy issues. The termination allows Takeda to reallocate resources, though the modest stock decline suggests limited market impact from this partnership dissolution.

Negative Benzinga • Vandana Singh
What's Going On With Eli Lilly On Monday?

Eli Lilly announced a $3 billion investment in China over the next decade, with its obesity drug Mounjaro added to China's state health insurance reimbursement list. However, the company faces a setback as the U.S. Supreme Court allowed a multibillion-dollar class action lawsuit to proceed against Eli Lilly and Takeda Pharmaceutical regarding inadequate risk disclosures for the diabetes drug Actos. LLY shares were up 0.75% at $913.46.

LLY TAK AAPL China expansion GLP-1 obesity drugs Mounjaro Actos litigation pharmaceutical regulation
Sentiment note

Named as co-defendant in the Supreme Court-approved Actos class action lawsuit involving allegations of inadequate risk disclosures for bladder cancer risks. This represents material litigation exposure and legal liability.

Positive GlobeNewswire Inc. • Researchandmarkets.Com
Feiba VH (Takeda Pharmaceuticals) Market Research Report 2026: Epidemiology, Pipeline Analysis, Trends, Strategies, & Forecasts, 2020-2025, 2025-2030F, 2035F

A market research report projects growth in the Feiba VH market through 2035, driven by increasing hemophilia diagnoses, rising healthcare expenditure, expanding surgical procedures, and personalized hemophilia management. North America leads the market while Asia-Pacific is expected to experience the fastest growth. Tariffs are influencing costs but encouraging domestic investment in coagulation therapies.

TAK Feiba VH hemophilia bypassing agents market growth healthcare expenditure specialty centers Asia-Pacific
Sentiment note

Takeda is the primary manufacturer of Feiba VH with North America as the largest market in 2025. The report projects market growth driven by multiple factors including rising healthcare spending, increased surgical procedures, and expanding access to specialty centers, which should benefit the company's market position and revenue.

Neutral Benzinga • Vandana Singh
Takeda Shares Down After Entyvio Shows Strong Results In Ulcerative Colitis Trial In Children, Shows Potential To Address Treatment Gaps

Takeda Pharmaceutical's stock declined 0.64% despite positive Phase 3 trial results for Entyvio (vedolizumab) in pediatric ulcerative colitis patients. The KEPLER trial showed 47.3% of participants achieved clinical remission at week 54, with additional positive secondary endpoints. Technical analysis shows mixed momentum with neutral RSI but bearish MACD signals.

TAK Takeda Pharmaceutical Entyvio vedolizumab ulcerative colitis Phase 3 trial KEPLER trial clinical remission
Sentiment note

While the company announced strong Phase 3 trial results for Entyvio with 47.3% of pediatric patients achieving clinical remission, the stock declined 0.64% on the news. Technical indicators show mixed signals with neutral RSI (50.00) and bearish MACD (0.10 below signal line of 0.15), suggesting the positive clinical data was offset by profit-taking or broader market concerns, resulting in a neutral overall sentiment.

Positive GlobeNewswire Inc. • Sns Insider
Global Blood Plasma Derivatives Market Size Projected to Reach $104.30 Billion by 2033; Immunoglobulins Drive Robust 9.08% CAGR – SNS Insider

The global blood plasma derivatives market is expected to double from $52.16 billion in 2025 to $104.30 billion by 2033, growing at a 9.08% CAGR. Growth is driven by increasing immune deficiencies, hematological disorders, and neurological conditions, with immunoglobulins representing 41.28% of the market. North America leads with 39.57% market share, while Asia-Pacific is the fastest-growing region at 10.89% CAGR.

TAK GRFS BAX BAYRY blood plasma derivatives immunoglobulins plasma-derived therapies coagulation factors
Sentiment note

Launched innovative HyHub and HyHub Duo devices in the U.S. for plasma-derived immunoglobulin therapy, simplifying treatment and enhancing patient mobility, indicating product innovation and market penetration.

Neutral Benzinga • Vandana Singh
FDA Grants Breakthrough Status To Johnson & Johnson's Cancer Drug For Advanced Head and Neck Cancer

The FDA granted Breakthrough Therapy Designation to Johnson & Johnson's Rybrevant Faspro (amivantamab and hyaluronidase-lpuj) for treating advanced, HPV-unrelated head and neck squamous cell carcinoma in adults. The drug is being evaluated in combination with Merck's Keytruda in an ongoing Phase 3 trial. Additionally, J&J extended its contract with Trellus Health for patient support services through mid-2026.

JNJ MRK ICLR TAK FDA Breakthrough Designation Rybrevant Faspro head and neck cancer amivantamab
Sentiment note

Mentioned as sponsor of immunology and inflammation clinical trials using Trellus's TrialSet platform, but no direct impact on company operations or financials disclosed.

Neutral GlobeNewswire Inc. • Visiongain
Anti-Obesity Drugs Market to Reach US$195.99 Billion by 2036 as GLP-1 Therapies Drive a Structural Shift in Weight Management

The global anti-obesity drugs market is estimated at US$22.52 billion in 2026 and is projected to grow at a CAGR of 24.2% to reach US$195.99 billion by 2036, driven by rising obesity rates, improved clinical efficacy of GLP-1 and multi-agonist therapies, and broader recognition of obesity as a chronic disease. However, US trade tariffs are adding cost pressures to pharmaceutical supply chains.

NVO LLY PFE AMGN anti-obesity drugs GLP-1 therapies chronic disease management pharmaceutical market growth
Sentiment note

Included in competitive landscape without specific details on market positioning or product performance.

Neutral Benzinga • Vandana Singh
Takeda Flags Vyvanse Hit, Lifts 2025 Profit Guidance On Cost Control

Takeda Pharmaceutical reported Q3 2025 adjusted net profit of 235 billion yen ($1.53B), missing EPS expectations of 55 cents at 47 cents. Sales declined to $7.60B, below consensus of $8.53B, primarily due to generic erosion of Vyvanse for ADHD. Despite the Neuroscience revenue drop of 23.6%, the company raised its 2025 profit guidance citing cost discipline and FX tailwinds. Core operating profit jumped 16.1% to 332.4 billion yen.

TAK Takeda Pharmaceutical Q3 2025 earnings Vyvanse generic erosion ADHD drug profit guidance raised cost control Neuroscience revenue decline
Sentiment note

Mixed results with earnings miss (47 cents vs 55 cents expected) and revenue miss ($7.60B vs $8.53B expected), offset by raised 2025 profit guidance due to cost discipline and FX benefits. Significant Vyvanse generic erosion is a headwind, but operational efficiency improvements and strong core operating profit growth (+16.1%) provide some support.

News and sentiment labels describe article tone and are provided for research purposes only. They are not trading recommendations or forecasts.
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