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BioWorld - Saturday, June 13, 2026
Home » Newsletters » BioWorld

BioWorld

Dec. 30, 2024

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Antibody-drug conjugate

Ideaya, Hengrui join hands in $1B deal for phase I ADC targeting DLL3

In a deal worth up to $1 billion, Ideaya Biosciences Inc. is in-licensing Jiangsu Hengrui Pharmaceuticals Co. Ltd.’s SHR-4849, a phase I DLL3-targeting opo-I-payload antibody-drug conjugate (ADC). Under terms of the deal, San Francisco-based Ideaya will develop and commercialize SHR-4849 worldwide outside of greater China, and Shanghai-based Hengrui is eligible to receive up to $1.04 billion that includes a $75 million up-front fee, $200 million in development and regulatory milestone payments, and commercial success-based milestone payments. Hengrui is also eligible to receive royalties on net sales outside of greater China. Read More
Head and neck anatomy

Pick Pyxis in head and neck despite pullback on ADC phase I?

Though Pyxis Oncology Inc.’s preliminary phase I data with antibody-drug conjugate (ADC) PYX-201 in solid tumors were characterized as positive, findings sent the Boston-based firm’s stock (NASDAQ:PYXS) into a tailspin. Shares dropped from $3.82 to $2.01 between Nov. 20 and the morning of Nov. 21, even as experts along with Wall Street agreed that the compound shows particular promise in head and neck squamous cell carcinoma – a space where developers aplenty remain busy. Read More
EU flags at EC building

New year, new five-year mandate, to make Europe more competitive

As 2025 gets underway, a new European Commission will start work on its new five-year mandate, with plans for multiple pieces of legislation that have implications for biotech and pharma – and the life sciences industry more broadly – due to be put forward. Read More

Biontech’s $1.26B vaccine royalty settlement clears path forward

Biontech SE agreed to pay up to nearly $1.26 billion in two separate settlements to resolve royalty disputes with the U.S. NIH and the University of Pennsylvania related to the COVID-19 vaccine the company partnered with Pfizer Inc. Read More
Year in review 2024 - Asia deals and innovation

Major 2024 licensing deals confirm Asia’s ascent from copier to innovator

From local drug discovery to global innovation, economic uncertainty is taking a toll on China’s innovative biotech system, forcing local companies to weather unpredictable storms, investors said during the Chinabio Partnering Forum in Shanghai in September. Read More
Hepatitis B virus rendering

Ausperbio bags $73M series B for hep B-targeting RNA therapy

Ausperbio Therapeutics Inc. raised $110 million from two financing rounds in 2024 to advance its lead antisense oligonucleotide candidate as a functional cure for chronic hepatitis B. Read More
Clinical-trial-syringe-and-pills1.png

November's phase III successes; Syros, Cassava tumble on misses

In November 2024, BioWorld tracked 180 clinical trial updates, down from 219 in October and 252 in September but up from 92 in August. The month included 13 successful phase III outcomes and five trial failures. Read More

Year in review 2024: firsts

Approvals and other breakthroughs in 2024. Read More

ICYMI: Week in review, Dec. 23-27, 2024

A quick look back at top stories. Read More

Biggest gainers and losers for Dec. 23-27, 2024

The top 10 biopharma stock gainers and losers for the week. Read More

Financings for Dec. 30, 2024

Biopharmas raising money in public or private financings, including: Northwest, Tscan, Vor. Read More

In the clinic for Dec. 30, 2024

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Assembly, Viracta. Read More

Other news to note for Dec. 30, 2024

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Avenacy, Exicure, GPCR Therapeutics, Hyloris, Viracta, Wuxi Apptec. Read More

Regulatory actions for Dec. 30, 2024

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Argenx, Beigene, Takeda. Read More

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