Lilly Wakes Up Sleep Market With $6.3B Centessa Buy To Challenge Takeda

31 Mar 2026
·
Deals
Clinical ResultPhase 3AcquisitionPhase 1Phase 2
iStock, Besiki Kavtaradze In the buyout, Eli Lilly picks up Centessa Pharmaceuticals’ lead asset cleminorexton, which could go toe-to-toe with Takeda’s oveporexton, currently under FDA review with a decision expected in the third quarter. Looking to further expand its expertise beyond the cardiometabolic and neurology arenas, Eli Lilly is taking over Centessa Pharmaceuticals and its pipeline of sleep disorder drugs—a move that could put the pharma in direct competition with Takeda. Under the terms of the acquisition agreement, announced Tuesday morning , Lilly will snap up Centessa for $38 per share or $6.3 billion upfront. The pharma has also offered a contingent value right that entitles stockholders to $9 more per share if the deal hits certain milestones, including one of two FDA approvals before a certain period of time lapses. This contingent offer could add $1.5 billion more to the total buyout value. Lilly and Centessa expect to close the transaction in the third quarter of 2026. The boards of directors of both companies have approved the deal. At the heart of the acquisition agreement is Centessa’s lead asset cleminorexton, an oral orexin receptor 2 (OX2R) agonist being trialed for narcolepsy type 1, narcolepsy type 2 and idiopathic hypersomnia. Orexin is a key neuropeptide that regulates the sleep-wake cycle, according to the biotech’s website , in turn promoting wakefulness. Drugs that activate this pathway could help address excessive daytime sleepiness as well as improve attention, cognition and fatigue. In April 2025, Centessa released Phase 1 data showing that a 5-mg oral dose of cleminorexton delayed sleep by an average of 37.9 minutes compared to 15.3 minutes in placebo recipients, resulting in a “statistically significant” treatment effect of 22.6 minutes, the biotech said at the time. This readout “reinforces ORX750 as a potentially best-in-class OX2R agonistOX2R agonist relative to competitors,” Leerink analysts wrote an April 7, 2025 note. Neuroscience Centessa’s Narcolepsy Drug Shows ‘Compelling’ Effect in Early Study Analysts at BMO Capital Markets said Centessa’s orexin receptor agonistorexin receptor agonist has “best-in-class” potential for narcolepsy, putting the company in a strong position in the $15 billion market. April 7, 2025 · 2 min read · Tristan Manalac Read more With the Centessa pickup, Lilly will go toe-to-toe with Takeda, which is far ahead in the narcolepsy race with its late-stage oveporexton, also an OX2R agonistOX2R agonist. In July 2025, Takeda announced that oveporexton significantly improved excessive daytime sleepiness, attention, quality of life, functioning and cataplexy in two Phase 3 studies. The FDA accepted Takeda’s approval submission for the candidate last month, with a decision out in the third quarter of this year. Also in the narcolepsy game is Alkermes, which in November last year announced that its own OX2R agonistOX2R agonist alixorexton aced Phase 2 and would move into late-stage development. The drug improved wakefulness and eased daytime sleepiness in patients with narcolepsy type 2, according to results presented at the time. Neuroscience Alkermes Pushes Narcolepsy Program to Phase III With ‘Highly Competitive’ Mid-Stage Data Alixorexton’s Phase II performance sets it up for late-stage success, according to analysts at Truist Securities. Alkermes expects to launch a global late-stage program early next year for narcolepsy type 2. November 13, 2025 · 2 min read · Tristan Manalac Read more Aside from cleminorexton, Lilly will also come into possession of Centessa’s broader pipeline of OX2R agonistsOX2R agonists, which includes additional preclinical assets with therapeutic potential “across a broader range of neurological, neurodegenerative, and neuropsychiatric conditions,” the pharma said Tuesday.
The content of the article does not represent any opinions of Synapse and its affiliated companies. If there is any copyright infringement or error, please contact us, and we will deal with it within 24 hours.