TAK
Takeda Pharmaceutical Company Limited · Healthcare · Drug Manufacturers - Specialty & Generic
At close
$14.88
−$0.30 (−1.98%) Close
Pre-market $15.18 +$0.30 (+2.02%) 9:11 PM ET
Prev close $15.18
Open $15.20
Day high $15.59
Day low $14.86
Volume 911
Avg vol 3,047,897
Mkt cap
$47.96B
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)
−27% (Below avg)
Vol/Avg: 0.73×
RSI
24.06 (Oversold)
Oversold (<30)
MACD momentum
Intraday
-0.00 (Weak)
MACD: -0.01 Signal: -0.00
Short-Term
-0.06 (Weak)
MACD: -0.35 Signal: -0.29
Long-Term
-0.06 (Weak)
MACD: -0.55 Signal: -0.49
Intraday trend score 37.94

Latest news

TAK 12 articles Positive: 7 Neutral: 4 Negative: 1
Neutral GlobeNewswire Inc. • Ascentage Pharma Group International
Ascentage Pharma Presents Data on Olverembatinib in CML-LBP and Ph+ BCP-ALL at ASCO 2026

Ascentage Pharma announced Phase Ib study results showing olverembatinib combined with blinatumomab demonstrated encouraging clinical activity in patients with relapsed/refractory Ph+ BCP-ALL or CML-LBP, with 91% achieving complete response and manageable safety profile. The company presented six studies across three key assets at the 2026 ASCO Annual Meeting, marking its ninth consecutive appearance.

TAK AAPG olverembatinib blinatumomab chronic myeloid leukemia acute lymphoblastic leukemia Phase Ib study ASCO 2026
Sentiment note

Takeda is mentioned as having signed an exclusive option agreement for olverembatinib's global rights outside of Greater China. While this represents a potential partnership opportunity, the article provides no information about Takeda's specific involvement or impact from these clinical results.

Neutral GlobeNewswire Inc. • Ascentage Pharma Group International
Ascentage Pharma Presents Updated Clinical Data for Olverembatinib as Second-Line Therapy in CML-CP at ASCO 2026

Ascentage Pharma presented updated clinical data at ASCO 2026 showing olverembatinib achieved a 91.3% complete cytogenetic response rate and 60.9% major molecular response rate at cycle 24 in CML-CP patients as second-line therapy. The drug demonstrated a stable safety profile with no new safety signals, supporting its potential role in treating patients who failed first-line TKI therapy.

TAK IVBIY AAPG olverembatinib CML-CP second-line therapy BCR-ABL1 inhibitor ASCO 2026
Sentiment note

Takeda is mentioned as having signed an exclusive option agreement for olverembatinib's global rights outside of China. This represents a potential partnership opportunity but no specific developments or outcomes are reported in this article.

Positive GlobeNewswire Inc. • Researchandmarkets.Com
Tacrolimus Market Research Report 2026: Key Growth Drivers, Challenges, Future Opportunities, and Regulatory Landscape 2025-2035

The global tacrolimus market is projected to grow from USD 7.3 billion in 2025 to USD 12.7 billion by 2035 at a CAGR of 5.6%, driven by rising organ transplant procedures and increasing autoimmune disease prevalence. Injectable formulations and hospital settings dominate the market, with North America accounting for 40.4% of the market share. Key players are investing in R&D for improved formulations and expanding into emerging markets.

ALPMY NVS PFE ABT tacrolimus market immunosuppressive therapy organ transplant autoimmune disorders
Sentiment note

Major pharmaceutical company positioned to capitalize on market growth driven by increasing organ transplants and autoimmune disease treatment demand.

Negative Benzinga • Vandana Singh
Jury Hits Takeda With $885 Million Antitrust Verdict

A Massachusetts jury awarded $884.9 million in damages against Takeda Pharmaceutical in an antitrust case related to its constipation drug Amitiza. The verdict stems from allegations that a 2014 settlement agreement between Takeda, Sucampo Pharmaceuticals, and Par Pharmaceutical delayed generic competition. The damages will automatically triple under U.S. antitrust law once judgment is entered. Takeda plans to appeal, defending the settlement as compliant with pharmaceutical patent dispute regulations.

TAK antitrust verdict Amitiza damages settlement agreement generic competition pharmaceutical litigation treble damages
Sentiment note

The company faces a substantial $884.9 million jury verdict that will triple to approximately $2.65 billion under antitrust law. This represents significant financial liability and legal risk, though the company plans to appeal. The verdict reflects a court finding that the company's settlement agreement violated antitrust laws.

Positive GlobeNewswire Inc. • Delveinsight
Global Stem Cell Therapy Market Set to Flourish at a CAGR of ~11% by 2034 Owing to the Technological Advancements and Favorable Regulations | DelveInsight

The global stem cell therapy market is projected to grow from USD 21.9 billion in 2025 to USD 58.5 billion by 2034, driven by technological advancements, favorable regulations, and rising demand for regenerative medicine treatments for chronic diseases. North America leads the market with 48.87% share, while Asia-Pacific emerges as a key growth engine with recent approvals of iPSC-based therapies in Japan.

VCEL TAK SMDPY stem cell therapy regenerative medicine market growth iPSC therapies clinical trials
Sentiment note

Listed as a key company in the expanding stem cell therapy market with strong growth projections and increasing clinical trial activity

Positive GlobeNewswire Inc. • Delveinsight
IgA Nephropathy Market Forecast to 2036: Novel Therapies and Key Growth Drivers Fuel Expansion | DelveInsight

The IgA Nephropathy (IgAN) market is projected to grow at 18.6% CAGR through 2036, driven by rising disease prevalence, improved diagnostics, and a robust pipeline of novel immunotherapies. The market was valued at $1.5 billion in 2025, with recent FDA approvals including VOYXACT and multiple late-stage candidates from major pharmaceutical companies expected to reshape disease management.

VRTX BIIB VERA AZN IgA Nephropathy immunotherapy monoclonal antibodies BAFF/APRIL inhibitors
Sentiment note

TAK-079 (mezagitamab) targeting CD38-expressing plasma cells with launch anticipated 2027-2029. Positioned as competitive plasma cell-directed therapy for sustained disease control.

Positive GlobeNewswire Inc. • Delveinsight
Polycythemia Vera Market Set for Transformation: Key 9 Companies Expected to Enter by 2036 | DelveInsight

The polycythemia vera market is expected to expand significantly by 2036, growing at 8.9% CAGR from a 2025 valuation of approximately USD 2 billion. Nine major pharmaceutical companies are advancing next-generation therapies in various clinical development stages, with rusfertide from Protagonist Therapeutics and Takeda expected to be the first new entrant to market this year, potentially reshaping the treatment paradigm beyond current standard therapies like JAKAFI, BESREMi, and PEGASYS.

PTGX TAK MRK IONS polycythemia vera market expansion clinical trials hepcidin modulators
Sentiment note

Co-developing rusfertide with Protagonist, expected to capture significant market share as the first new therapy entering the polycythemia vera market with strong clinical trial results.

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.

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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