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28 July, 2025 |
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Max Gelman and Ryan Cross are in Toronto this week, covering the Alzheimer's Association International Conference. Their first piece examines the latest data for Roche’s next-generation Alzheimer’s disease treatment. Be sure to check it out. |
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Jaimy Lee |
Deputy Editor, Endpoints News
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by Ryan Cross, Max Gelman
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TORONTO — Three years after a disappointing clinical failure cast doubts on Roche’s future in Alzheimer’s disease, the company is going all in on a sequel program. And early data suggest it might be the most potent amyloid-clearing drug yet. In a packed room at the Alzheimer’s Association International
Conference in Toronto on Sunday, Roche revealed the latest cut of data from its closely-watched Phase 1/2 study of trontinemab, an amyloid-targeting antibody designed to latch onto receptors that yank it across the protective blood-brain barrier. Unlike its failed predecessor gantenerumab, which only slowly and modestly reduced amyloid plaques over two years, trontinemab practically eliminated amyloid in just
seven months. One patient died from a brain hemorrhage early in their treatment, causing Roche to tighten its criteria last year to exclude participants who are susceptible to the fatal side effect. |
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by Lei Lei Wu
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Adaptimmune is selling three cell therapy assets, including its sarcoma therapy Tecelra, to US WorldMeds for $55 million in cash after announcing plans earlier this year to further cut costs and seek “strategic options.” The company also disclosed Monday morning that it is laying off 62% of its workforce, and several executives are leaving. Adaptimmune’s stock ADAP fell about 65% Monday morning when markets opened. Despite winning FDA approval for Tecelra in August, the company’s shares have dropped 90% over the last 12 months. “Given the financial situation of the company, it is clear that securing the right strategic option was critical to maximize value for all of our
stakeholders and importantly ensure our patients continue to receive Tecelra,” Adaptimmune CEO Adrian Rawcliffe said in a statement. |
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by Kyle LaHucik
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A California biotech working in a hot but risky area of schizophrenia and Alzheimer's drug development has secured the third-largest private funding round of 2025 so far. MapLight Therapeutics said Monday morning
it corralled $372.5 million in a Series D raise from Forbion, Goldman Sachs Alternatives' life sciences team, Sanofi, Novo Holdings and others. Sanofi previously bought another Alzheimer's biotech, Vigil Neuroscience, for $470 million. MapLight is in Phase 2 testing in schizophrenia and Alzheimer's disease psychosis with a candidate codenamed ML-007C-MA. The experimental oral medicine is a fixed-dosed
combination of an M1/M4 muscarinic agonist that is co-formulated with a peripherally acting anticholinergic to tamp down on "peripheral cholinergic side effects," the company said. |
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by Kyle LaHucik
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Bavarian Nordic could forge an approximately $3 billion buyout in the coming weeks as private equity firms circling the company have come forward on potential deal terms. Large investment firms Nordic Capital and Permira have set up a private company called Innosera, with the goal of making an all-cash takeover offer for the Danish vaccine
maker within four weeks, according to a Monday release. The firms plan to offer 233 Danish krone ($36.4) per share, which is a 21% premium to the Copenhagen-based company's closing price on July 23, when market rumors began circulating about a potential buyout. Bavarian Nordic confirmed the deal discussions shortly after. The offer follows "intense nego&sh |
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