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20 April, 2026 |
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When a deal gets announced, it's always a fun exercise to look at which early investors stand to benefit. In the case of Lilly's $3.25B acquisition of Kelonia, that's looking like a 45-times return for Venrock, which put $20 million into the in vivo CAR-T developer. Not too shabby for a company that almost ran out of money while looking for its next round of investors. Read the full story here. |
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Lydia Ramsey Pflanzer |
Deputy Editor, Endpoints News
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by Max Bayer
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Over the weekend, President Donald Trump endorsed the potential of psychedelic treatments and vowed to expedite their research and development as remedies for severe mental health conditions, a seminal moment for a field long shunned by the US government. But how impactful his latest executive
order is, and whether it actually benefits a therapeutic class trying to break into mainstream prescribing, remains to be seen. The announcement Saturday sent the world of psychedelics ablaze, in a good way, with companies and researchers heralding Trump’s actions as a breakthrough. The executive order directs the FDA to hasten review of psychedelic drug applications using the Commissioner’s National Priority Voucher (CNPV) and to work with the Drug Enforcement Administration to allow eligible patients to receive the drugs under the Right to Try law. | |
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by Drew Armstrong, Kyle LaHucik
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The investor Venrock will make $900 million on a relatively small $20 million investment into Kelonia Therapeutics, which on Monday agreed to sell itself to Eli Lilly in a $3.25 billion upfront deal. Venrock's return — 45 times its initial investment — could grow substantially larger if the deal pays out more of its full value, a spokesperson for the VC firm told Endpoints News. As part of its acquisition of Boston-based Kelonia, Lilly could pay out as much as $3.75 billion more if Kelonia's in vivo CAR-T programs hit certain milestones. If those later payments also come in, Venrock's total return could rise to 100 times its initial investment, the spokesperson said. | |
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Lord Patrick Vallance, the UK's Minister for Science, Research and Innovation, speaking at Boehringer Ingelheim's Monday event announcing its AI facility in King's Cross (Credit: Boehringer Ingelheim) |
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by Anna Brown
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LONDON – Boehringer Ingelheim is growing its artificial intelligence arm to the UK by building a new hub in central London and investing £150 million over the next 10 years. The AI hub will be in the Knowledge Quarter in King’s Cross, which is also home to AI units for other drugmakers like BioNTech and Novo Nordisk. The area is also a key location for companies like OpenAI, Google, Meta and BenevolentAI. Once complete, the German drugmaker’s AI hub will focus on very early
disease biology, Nicola Richmond, Boehringer’s head of AI and machine learning, told Endpoints News in an interview. “The vision is that we build AI foundational capabilities that help our scientists better understand disease,” she added. | |
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by Nicole DeFeudis
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Novartis has axed two late-stage programs in cancer-related blood clots after observing “inferior efficacy” in a clinical trial. The move marks a setback for a candidate that Novartis out-licensed in 2019, then paid $925 million upfront to get back in 2025. Novartis is still pursuing the drug, abelacimab, for its lead indication: atrial fibrillation. Abelacimab is part of a new class of anticoagulants called factor XI inhibitors, which are designed to prevent blood clots while reducing the bleeding risks associated with traditional blood thinners. The drug was in three Phase 3 trials, two of which were focused on cancer-related thrombosis. | |
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