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TYO:4502

11 stories mentioning TYO:4502Updated 2d ago

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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.(covers equity, commodity and economic research from major banks and research firms in North America, Asia and Europe. Research providers may contact us here: https://finwires.com/en/contact)

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.(covers equity, commodity and economic research from major banks and research firms in North America, Asia and Europe. Research providers may contact us here: https://finwires.com/en/contact)

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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