Takeda's AI-developed psoriasis pill succeeds in trials

Takeda Pharmaceutical has announced that its AI-assisted oral psoriasis drug zasocitinib proved safe and effective in late-stage trials. The once-daily pill outperformed placebo and the existing therapy apremilast in clearing skin for patients with moderate-to-severe plaque psoriasis. If approved, it would mark one of the first drugs discovered with artificial intelligence.

Takeda Pharmaceutical announced on December 18 that its experimental oral drug zasocitinib, also known as TAK-279, demonstrated safety and efficacy in late-stage clinical trials for moderate-to-severe plaque psoriasis. Patients taking the once-daily pill achieved significantly clearer skin compared to those on placebo or the established treatment apremilast, according to the company's statement. Takeda intends to submit the data to the U.S. Food and Drug Administration and other regulators starting in fiscal year 2026.

The drug's discovery relied heavily on artificial intelligence, with algorithms speeding up the selection of zasocitinib from a vast array of molecules. Jeb Keiper, CEO of Nimbus Therapeutics, which originated the medicine, noted that these algorithms "significantly accelerated the identification" process. In 2023, Takeda acquired zasocitinib from the Boston-based Nimbus for an upfront payment of $4 billion, plus up to $2 billion in potential milestone payments.

This therapy forms part of Takeda's broader plan to mitigate revenue losses from generic competition to its blockbuster ulcerative colitis drug Entyvio. Analyst Stephen Barker at Jefferies Japan estimates that zasocitinib could reach peak sales of $5 billion if expanded to indications like inflammatory bowel disease. The global psoriasis market, valued at $27 billion in 2024, is expected to nearly double to $58 billion by 2032, per Fortune Business Insights. Psoriasis, a chronic autoimmune disorder affecting over 125 million people worldwide, causes itchy, scaly rashes.

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Scientists in a lab celebrating conditional approval of iPS cell products for treating Parkinson's and heart disease.
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Health ministry panel conditionally approves iPS cell products

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A health ministry expert panel has conditionally approved two regenerative medicine products derived from induced pluripotent stem (iPS) cells for treating Parkinson's disease and severe heart disease. This marks a potential world first in commercializing Nobel Prize-winning stem cell technology. The approval, based on small-scale clinical trials confirming safety and presumed efficacy, requires post-market verification within seven years.

A Delhi High Court verdict on January 12 has allowed Indian pharma company Zydus Lifesciences to manufacture and sell a biosimilar version of Bristol Myers-Squibb's cancer drug Nivolumab. This ruling could pave the way for more affordable immunotherapy treatments for cancer patients in India. Nivolumab is effective against various cancers, with its patent set to expire in May 2026.

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Alzheimer's trials are shifting to a multi-target approach inspired by cancer research, even after failures with Novo Nordisk's semaglutide. Only two drugs, Eli Lilly's Kisunla and Eisai and Biogen's Leqembi, are widely approved to slow progression. This evolution treats the brain-wasting disease as a complex system, seeking new ways to halt it amid its global impact.

The US Food and Drug Administration (FDA) has approved mitapivat (brand name Aqvesme) for treating anaemia in adults with thalassaemia, working by improving red blood cell energy. The twice-daily pill can be taken by patients who need regular blood transfusions or those who do not. Experts say it could transform disease management in high-burden countries like India.

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Servier Egypt has launched Tibsovo (ivosidenib), the first targeted therapy available in the country for patients with IDH1-mutated Acute Myeloid Leukemia (AML) and intrahepatic cholangiocarcinoma. The treatment offers a median overall survival of 29.3 months for eligible AML patients and 10.3 months for those with intrahepatic cholangiocarcinoma, according to clinical data. It is approved as a first-line treatment for AML and a second-line option for intrahepatic cholangiocarcinoma.

Cuban President Miguel Díaz-Canel presented preliminary positive results from clinical trials of the biotechnological drug Jusvinza in patients with chronic post-chikungunya arthritis. The studies, started in December 2025, show notable improvements in provinces like Havana and Matanzas. Experts highlight the drug's safety profile and potential to slow inflammation.

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Researchers at Karolinska Institutet report that using a reduced dose of ipilimumab together with nivolumab in immunotherapy for advanced malignant melanoma was associated with better tumor control and fewer serious side effects than the traditional full-dose combination. In a real-world study of nearly 400 patients with advanced, inoperable skin cancer, response rates and survival times were higher in the lower-dose group, according to results published in the Journal of the National Cancer Institute.

 

 

 

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