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.

संबंधित लेख

Scientists in a lab celebrating conditional approval of iPS cell products for treating Parkinson's and heart disease.
AI द्वारा उत्पन्न छवि

Health ministry panel conditionally approves iPS cell products

AI द्वारा रिपोर्ट किया गया AI द्वारा उत्पन्न छवि

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.

दिल्ली हाई कोर्ट ने 12 जनवरी को एक फैसले में जायडस लाइफसाइंसेज को वैश्विक दवा कंपनी ब्रिस्टल मायर्स-स्क्विब के कैंसर ड्रग नivolumab का बायोसिमिलर वर्जन बनाने और बेचने की अनुमति दी है। यह फैसला भारत में कैंसर मरीजों के लिए सस्ती इम्यूनोथेरेपी उपचारों का रास्ता खोल सकता है। नivolumab कई प्रकार के कैंसर के खिलाफ प्रभावी है और इसका पेटेंट मई 2026 में समाप्त हो रहा है।

AI द्वारा रिपोर्ट किया गया

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.

अमेरिकी खाद्य एवं औषधि प्रशासन (एफडीए) ने थैलेसीमिया वाले वयस्कों में एनीमिया के इलाज के लिए मितापिवाट (एक्वेस्मे ब्रांड नाम से) को मंजूरी दे दी है, जो लाल रक्त कोशिकाओं की ऊर्जा सुधारकर काम करता है। यह गोली नियमित रक्त आधान की आवश्यकता वाले और न वाले दोनों रोगियों के लिए ली जा सकती है। विशेषज्ञों का कहना है कि यह भारत जैसे देशों में रोग प्रबंधन को बदल सकता है जहां थैलेसीमिया का बोझ अधिक है।

AI द्वारा रिपोर्ट किया गया

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.

AI द्वारा रिपोर्ट किया गया तथ्य-जाँच किया गया

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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