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TYO:4502

17 stories mentioning TYO:4502Updated 3d ago

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Asia

Dr. Reddy's Enters Agreement to Bring Takeda's Dengue Vaccine to India

Dr. Reddy's Laboratories (BOM:500124, NSE:DRREDDY) signed a marketing and distribution agreement with Takeda Biopharmaceuticals India to bring the Qdenga dengue vaccine to India, according to a same-day filing with the bourse.Dr. Reddy's will handle private market sales, while Takeda Biopharmaceuticals, a unit of Japan-listed Takeda Pharmaceutical (TYO:4502), will manufacture, import and oversee public market distribution.The agreement follows Indian regulators' July clearance of Qdenga for individuals aged 4 to 60, making it the country's first approved dengue vaccine, the company said.Dr. Reddy's shares were last up around 2% in recent trade.

BOM:500124NSE:DRREDDYTYO:4502
Asia

U.S. FDA Grants Priority Review to Takeda Pharmaceutical's Zasocitinib NDA for Plaque Psoriasis

The U.S. Food and Drug Administration (FDA) accepted Takeda Pharmaceutical's (TYO:4502) new drug application (NDA) for zasocitinib under priority review for adults with moderate‑to‑severe plaque psoriasis, according to a Monday filing with the Japanese bourse.The application is supported by Phase III LATITUDE PsO 3001 and 3002 trials, which met all primary and ranked secondary endpoints. About 70% of patients achieved clear or nearly clear skin by Week 16, with improvements seen from Week 4 and sustained through Week 52, the filing said.Shares of Takeda Pharmaceutical added over 1% at market close.

TYO:4502
Asia

Takeda Pharmaceutical Wins US Approval for New PV Treatment MIMRYLO

Takeda Pharmaceutical (TYO:4502) has secured U.S. approval for MIMRYLO, a new once-weekly injectable medicine for adults with polycythemia vera, a rare blood disorder that causes the body to produce too many red blood cells.Clinical trial data showed nearly 77% of patients responded to the treatment, which helped control red blood cell levels and reduced the need for blood removal procedures, while also improving fatigue.The most common side effects were injection-site reactions and anemia, according to a Tokyo bourse filing on Friday.The approval offers a fresh approach for the estimated 90,000 Americans living with the condition, many of whom struggle to manage their symptoms with existing options.

TYO:4502
Asia

Takeda's Orzeryful Approved in Japan as First Treatment Targeting Narcolepsy Type 1

Takeda Pharmaceutical (TYO:4502) has secured Japanese regulatory approval for Orzeryful, a first-of-its-kind pill that tackles the underlying cause of narcolepsy type 1(NT1).The approval, granted by Japan's Ministry of Health, Labour and Welfare, is based on global Phase 3 studies demonstrating statistically significant improvements across the full range of NT1 symptoms.Takeda is proceeding with launch preparations and expects to make ORZEYFUL available as soon as possible, according to a statement on Monday.Narcolepsy type 1 is a rare, chronic neurological disorder that can severely disrupt daily life, affecting work, education and social interactions.Despite its impact, lack of awareness and the complexity of symptoms often lead to misdiagnoses, with patients waiting more than 10 years on average for a correct diagnosis.This marks the third major approval for ORZEYFUL worldwide, following earlier clearances in China and the United States, where the drug is still awaiting final scheduling review by the U.S. Drug Enforcement Administration.

TYO:4502
Asia

Takeda Wins FDA Approval for First-in-Class Narcolepsy Treatment ORZEYFUL

Takeda Pharmaceutical (TYO:4502) has secured U.S. FDA approval for ORZEYFUL (oveporexton), an oral orexin receptor 2 agonist, as the first treatment to holistically address narcolepsy type 1, according to a statement on Thursday.The rare neurological disorder, which affects an estimated 120,000 Americans, is driven by orexin deficiency and causes excessive daytime sleepiness, cataplexy, cognitive issues and disrupted nighttime sleep.The approval introduces a new class of medicine for NT1, potentially redefining disease management and patient outcomes, according to principal investigator Dr. Emmanuel Mignot.Shares of Takeda rose nearly 2% in recent trade.

TYO:4502
Asia

Market Chatter: Takeda Pharmaceutical Seeks India's Backing for Landmark Dengue Shot

Takeda (TYO:4502) aims to include its dengue shot in India's state immunization program after local regulators approved it, Nikkei Asia reported Wednesday, citing head of intercontinental markets Mahender Nayak.The newly approved shot, Qdenga, works against the mosquito-borne illness and covers all four viral strains, the news daily said.Nayak said Takeda's strategic focus is on securing national program status to maximize public access, the publication said.(Market Chatter news is derived from conversations with market professionals globally. This information is believed to be from reliable sources but may include rumor and speculation. Accuracy is not guaranteed.)

TYO:4502
Asia

Takeda Pharmaceutical Profit Drops 9% in Fiscal Q1

Takeda Pharmaceutical (TYO:4502) profit attributable to owners of the parent fell 8.9% to 113.2 billion yen for the fiscal first quarter, from 124.2 billion yen a year earlier.The pharmaceutical company's earnings per share slipped to 70.54 yen from 78.23 yen a year ago, according to a Tokyo bourse filing on Thursday.Revenue increased 10.2% to 1.220 trillion yen for the three months ended June 30, from 1.107 trillion yen.For the fiscal year ending March 31, 2027, the company expects an attributable profit of 166.0 billion yen, EPS of 104.26 yen and revenue of 4.640 trillion yen.Takeda expects to pay interim and year-end dividends of 102.00 yen per share each for the current fiscal year.

TYO:4502
Research

SBI Securities Starts Takeda Pharmaceutical at Neutral with 5,400 Yen Price Target

Takeda Pharmaceutical (TYO:4502) has an average rating of overweight and mean price target of 6,264.50 yen, according to analysts polled by FactSet.

TYO:4502
Research

China Merchants Starts Takeda Pharmaceutical at Buy with 6,600 Yen Price Target

Takeda Pharmaceutical (TYO:4502) has an average rating of overweight and mean price target of 6,264.50 yen, according to analysts polled by FactSet.

TYO:4502
Asia

Update: India Approves Takeda's Dengue Vaccine QDENGA

(Updates to reflect Takeda's official announcement)India's drug regulator has approved Takeda's QDENGA, marking the first dengue vaccine authorized in the country, the company said in an emailed press release to.The approval comes as dengue cases in India have surged 11-fold over the past two decades, addressing a critical public health need.With the India approval, QDENGA is now cleared in 43 countries, with more than 32 million doses distributed globally via public and private programs to date, the company said.

TYO:4502
Asia

Market Chatter: India Approves Takeda's Dengue Vaccine QDENGA

India's drug regulator has approved Takeda's QDENGA, marking the first dengue vaccine authorized in the country, Bloomberg News reported on Monday.The approval comes as dengue cases in India have surged 11-fold over the past two decades, addressing a critical public health need, the news wire said.Takeda is partnering with Biological E to expand manufacturing, aiming to produce 50 million doses annually in India as part of the company's global target of 100 million doses per year by 2030, the publication said.Takeda did not immediately respond to' request for comment.(Market Chatter news is derived from conversations with market professionals globally. This information is believed to be from reliable sources but may include rumor and speculation. Accuracy is not guaranteed.)

TYO:4502
Asia

Takeda Pharmaceutical Completes Share Issuance, Disposal Under Incentive Plan

Takeda Pharmaceutical (TYO:4502) said it has completed the issuance of new shares and disposal of treasury stock under its long-term incentive plan, according to a Wednesday filing.The company said the incentive plan for group employees outside Japan follows a partial forfeiture of rights granted to previously planned allottees.The company issued 16.9 million ordinary shares totaling 85.2 billion yen, comprising 10.8 million newly issued shares and 6.1 million treasury shares, down from the proposed 85.8 billion yen worth of shares.The allotments covered 10,477 employees of Takeda and its subsidiaries, compared with the originally planned 10,557 recipients.

TYO:4502
Asia

Insilico Medicine Strikes Drug Discovery Deal With Japan's Takeda Pharmaceutical

Insilico Medicine (HKG:3696) struck a drug discovery deal with Japan's Takeda Pharmaceutical (TYO:4502) that could net the company up to $600 million.In a Hong Kong bourse filing Thursday, Insilico Medicine said it will use its artificial intelligence-powered Pharma.AI platform to advance drug candidates across multiple therapeutic areas for Takeda.Insilico said the deal is valued at $600 million after accounting for the $60 million project initiation fee plus milestone payments. The company will also receive royalties on sales of commercialized drugs.

HKG:3696TYO:4502
Asia

Takeda Pharmaceutical to Issue 17 Million Shares Under Employee Incentive Plan

Takeda Pharmaceutical (TYO:4502) will issue nearly 17 million ordinary shares at 5,050 yen each for a total of 85.8 billion yen.The shares will be allocated to 10,557 employees of Takeda and its subsidiaries under the company's Long-Term Incentive Plan, according to a Tokyo bourse filing on Wednesday.The incentive grants are restricted stock units that vest annually over three years and performance stock units that vest after a three-fiscal-year evaluation based on achievement of performance goals.

TYO:4502
Innovent Biologics Secures Up to $10.5 Billion Pfizer Oncology Deal
US Markets

Innovent Biologics Secures Up to $10.5 Billion Pfizer Oncology Deal

Chinese biopharmaceutical company Innovent Biologics (HKG:1801) has secured an oncology licensing deal with New York-based pharmaceutical giant Pfizer that could potentially be worth up to $10.5 billion.Innovent will receive a $650 million upfront payment and is eligible for up to $9.85 billion in development, regulatory and commercial milestone payments, according to a joint release on Thursday.The company is also entitled to up to "double-digit" royalties on net sales of each approved product.The deal covers 12 early-stage and de novo cancer drug programs from Innovent's pipeline, spanning antibody-drug conjugates (ADCs) with novel payloads and multi-specific antibodies with immune-engaging features, according to the release.Eight of the 12 programs originated by Innovent's early-stage programs, while the remaining four are Pfizer-proposed discovery programs.Under the terms of the deal, Innovent will carry out Phase 1 clinical trials of these programs before Pfizer takes over global development."This agreement brings together best-in-industry expertise of Pfizer and Innovent to advance novel cancer medicines to patients at a global scale," said Dr. Hui Zhou, Chief R&D Officer (Oncology Pipeline) of Innovent."By leveraging both companies' complementary resources, we can develop our early-stage oncology pipeline with greater speed and impact to help bring innovative therapies to patients more efficiently worldwide."For Innovent, the agreement further bolsters its presence in the biopharmaceutical market. The company said it has launched 18 products in the market, has five assets in Phase III or pivotal clinical trials and 14 more molecules in early clinical stage.The company has partnered with over 30 global healthcare companies, including Eli Lilly, Roche, Takeda, Sanofi, Incyte, LG Chem (KRX:051910) and MD Anderson Cancer Center."This collaboration brings together two highly complementary engines of innovation with a shared ambition to move faster, go further and deliver truly transformative medicines to patients who are waiting," said Jeff Legos, Chief Oncology Officer, Pfizer.The deal with Pfizer is subject to regulatory approvals.The agreement marks Innovent's latest billion-dollar licensing deal with a multinational pharma company after striking a license and collaboration deal with Japan's Takeda Pharmaceutical (TYO:4502) in December 2025.As part of that deal, Innovent licensed two late-stage cancer drug candidates, IBI363 and IBI343, to Takeda, and granted an option over early-stage asset IBI3001. The agreement included an upfront payment of about $1.2 billion.The deal also saw Innovent issuing about 6.9 million new shares to Takeda at HK$112.56 each. The shares represent roughly 0.4% of Innovent's enlarged share capital and generated net proceeds of about HK$777 million.Innovent's shares jumped 6% in early-morning trade in Hong Kong on Friday.

HKG:1801KRX:051910TYO:4502
Asia

US Jury Orders Takeda to Pay $885 Million in AMITIZA Antitrust Case; Takeda Plans Appeal

A U.S. jury has returned a verdict against Takeda Pharmaceutical (TYO:4502) in the AMITIZA antitrust litigation, awarding plaintiffs $884.9 million in single damages, with portions subject to automatic trebling under U.S. antitrust law.The case consolidates claims from wholesalers, retailers, and end payors, who alleged that a 2014 patent settlement between Takeda, Sucampo, and Par Pharmaceutical was anticompetitive, according to a statement on Tuesday.Takeda maintains the settlement was reached through proper arms-length negotiation under the Hatch-Waxman framework and allowed Par to launch an authorized generic years before patents expired.The company has stated it will vigorously pursue post-trial motions and an appeal, citing evidentiary and legal errors during the trial.While the verdict is not yet enforceable, Takeda is assessing the financial provision for its fiscal 2025 statements but does not expect a material impact on its fiscal 2026 core financial forecast.

TYO:4502
Asia

Veritas In Silico and Takeda Mutually Terminate mRNA-Targeted Drug Research Collaboration

Veritas In Silico (TYO:130A) and Takeda Pharmaceutical (TYO:4502) have mutually agreed to terminate their collaborative drug discovery research on mRNA-targeted small-molecule drugs, effective immediately.Although the research has produced some results since the agreement began in June 2023, the parties will now discuss and consider potential future applications of the findings gained from the collaboration, according to a Tokyo bourse filing on the same day.Veritas In Silico expects the termination's impact on its business performance to be limited, with no change to its earnings forecast for the fiscal year ending December, and will promptly disclose any material developments if they arise.

TYO:130ATYO:4502

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