Takeda Pharmaceutical Company Limited · Healthcare · Drug Manufacturers - Specialty & Generic
Scores & Status Key
AI Summary Scores: Intraday / Swing / Long scores are synthesized from multi-factor analysis for each timeframe. They summarize current conditions discussed in the report and do not constitute trading recommendations.
Intraday Trend Score: A 0–100 composite from the Trend Explorer™ analytics engine used for ranking and comparison. It describes current conditions and is not a forecast.
Trend Status: A rules-based label (Bullish / Mixed / Bearish) derived from signal confluence (trend structure, momentum, and positioning). It indicates alignment, not expected return.
Last
$18.24
+$0.26 (+1.44%) 4:00 PM ET
After hours$18.48
+$0.24 (+1.32%) 10:37 PM ET
Prev closePrevC$17.98
OpenOpen$18.15
Day highHigh$18.40
Day lowLow$18.15
VolumeVol1,881,631
Avg volAvgVol3,311,199
On chart
Interval
Intervals apply to 1D & 5D.
Intervals apply to 1D & 5D.
Scale: Linear
Overlays
Panels
Style
Scale: Linear
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Tickers only (no ^ indexes). Add up to 5.
Mkt cap
$57.42B
Sector
Healthcare
AI report sections
MIXED
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:63SWING:72LONG:69
Volume vs average
Intraday (cumulative)
−8% (Below avg)
Vol/Avg: 0.92×
RSI
57.93(Neutral)
Neutral (40–60)
0255075100
MACD momentum
Intraday
+0.00 (Strong)
MACD: 0.00 Signal: 0.00
Short-Term
-0.02 (Weak)
MACD: 0.32 Signal: 0.34
Long-Term
+0.01 (Strong)
MACD: 0.59 Signal: 0.57
Intraday trend score
61.24
LOW55.24HIGH75.24
Latest news
TAK•12 articles•Positive: 6Neutral: 5Negative: 1
NeutralZacks Investment Research• Zacks.Com
If You Invested $1000 in Halozyme Therapeutics a Decade Ago, This is How Much It'd Be Worth Now
A $1,000 investment in Halozyme Therapeutics made in September 2016 would be worth $10,866.33 as of September 1, 2026, representing a 986.63% gain. The biopharmaceutical company's success is driven by its ENHANZE drug delivery technology licensed to major pharma partners like Roche, Takeda, J&J, and AbbVie, generating royalties that comprise over 55% of revenues. While strong demand for partnered drugs and new collaboration deals support growth, biosimilar competition for blockbuster drugs and dependence on partner revenues present risks.
Fabry Disease Treatment Market 2026-2031 - Growth Driven by Increasing Adoption of Enzyme Replacement Therapy
The global Fabry disease treatment market is projected to grow from USD 2.63 billion in 2025 to USD 4.09 billion by 2031, with a CAGR of 7.63%. Growth is driven by expanded screening identifying more patients, advances in gene and mRNA therapies, and sustained enzyme replacement therapy demand. However, high treatment costs remain a significant barrier to patient access, particularly in emerging markets. Asia-Pacific is expected to record the fastest growth at 8.28% CAGR.
Major player in the Fabry disease treatment market with established therapies, well-positioned to capture market share as prevalence increases and treatment adoption expands globally.
NeutralGlobeNewswire Inc.• Ascentage Pharma Group International
Ascentage Pharma Chairman and CEO Dr. Dajun Yang Named to The Medicine Maker Power List 2026
Dr. Dajun Yang, Chairman and CEO of Ascentage Pharma, has been recognized in The Medicine Maker Power List 2026, ranking No. 3 in the Small Molecules category. The recognition highlights the company's achievements in advancing innovative cancer therapies, including the commercialization of olverembatinib and lisaftoclax, with multiple global Phase III clinical trials underway.
Mentioned as a global partnership partner with Ascentage Pharma, but no specific details about the partnership or its impact are provided in the article.
PositiveGlobeNewswire Inc.• Healthcare Foresights
[Latest] Global Botulinum Toxin in Urology Market Size/Share Worth USD 1.98 Billion by 2035 at a 6.08% CAGR: Healthcare Foresights (Analysis, Outlook, Leaders, Report, Trends, Forecast, Segmentation, Growth Rate, Value, SWOT Analysis)
The global botulinum toxin in urology market is projected to grow from USD 1.1 billion in 2025 to USD 1.98 billion by 2035, at a CAGR of 6.08%. Growth is driven by increasing prevalence of urological disorders, aging populations, preference for minimally invasive treatments, and advancements in injection techniques. OnabotulinumtoxinA (Botox) leads the market, with overactive bladder being the largest application segment.
Parent company of Shire, a listed key player in the expanding botulinum toxin in urology market.
NeutralGlobeNewswire Inc.• Researchandmarkets.Com
Clinical Stage Partnering Terms and Agreements in Pharmaceuticals and Biotechnology 2020-2026 | Benchmark More Than 1,800 Biopharma Deals with Various Indexes
ResearchAndMarkets.com released a comprehensive report analyzing over 1,859 clinical-stage pharmaceutical and biotechnology partnership deals announced since 2020. The report provides detailed financial terms, deal structures, contract documents, and insights into negotiation dynamics for clinical-stage drug development collaborations, serving as a benchmarking resource for biopharma dealmakers.
Included as a featured company in the clinical-stage partnerships analysis, indicating active collaboration involvement, but no specific deal information is provided.
PositiveGlobeNewswire Inc.• Sns Insider
Autoimmune Disease Therapeutics Market Size to Reach USD 137.85 Billion by 2035 as Biologics and Precision Medicine Drive Growth | SNS Insider
The global autoimmune disease therapeutics market is projected to grow from USD 80.54 billion in 2025 to USD 137.85 billion by 2035, with a CAGR of 5.52%. Growth is driven by rising prevalence of autoimmune diseases, adoption of biologics, JAK inhibitors, monoclonal antibodies, and precision medicine technologies. North America leads with 39.96% market share, while Asia-Pacific shows the fastest growth at 6.28% CAGR.
Leading market player with presence in autoimmune disease therapeutics, positioned to capture market growth from increasing prevalence and treatment adoption.
PositiveBenzinga• Vandana Singh
Takeda AI-Drug Shows Superior Skin Clearance Against Bristol-Myers' Med
Takeda Pharmaceutical's AI-developed drug zasocitinib demonstrated statistical superiority over Bristol-Myers Squibb's deucravacitinib in a Phase 3 head-to-head trial for plaque psoriasis treatment. Zasocitinib achieved over 35% complete skin clearance (PASI 100) at week 16, more than 2.5 times the response rate of the competitor drug. The company plans to submit a New Drug Application to the FDA this fiscal year, with peak annual sales potential of $3-6 billion.
Takeda's AI-developed drug demonstrated superior efficacy compared to competitor's established treatment in head-to-head trial, with significantly higher skin clearance rates and potential $3-6 billion peak annual sales. Positive trial results support regulatory approval pathway.
NeutralGlobeNewswire 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.
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.
NeutralGlobeNewswire 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.
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.
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.
Major pharmaceutical company positioned to capitalize on market growth driven by increasing organ transplants and autoimmune disease treatment demand.
NegativeBenzinga• 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.
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.
PositiveGlobeNewswire 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.
Listed as a key company in the expanding stem cell therapy market with strong growth projections and increasing clinical trial activity
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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