Stock Markets March 31, 2026

Alkermes Jumps After Lilly Announces Acquisition of Centessa; Deal Includes Up to $47 Per Share

Market reaction lifts Alkermes stock as Eli Lilly agrees to buy Centessa with contingent payments tied to FDA approvals

By Nina Shah ALKS LLY CNTA
Alkermes Jumps After Lilly Announces Acquisition of Centessa; Deal Includes Up to $47 Per Share
ALKS LLY CNTA

Alkermes shares surged 13% after Eli Lilly disclosed plans to acquire Centessa Pharmaceuticals. The transaction will pay $38.00 in cash per Centessa share plus one non-transferable contingent value right (CVR) with up to $9.00 of additional potential consideration, making the total possible payment $47.00 per share. The upfront cash values Centessa at roughly $6.3 billion, with the CVR adding up to about $1.5 billion in contingent equity value. Centessa’s lead candidate, cleminorexton, has shown Phase 2a results in multiple sleep disorders; the CVR payouts depend on specific U.S. FDA approvals within stated timeframes.

Key Points

  • Alkermes stock rose 13% after Eli Lilly announced it would acquire Centessa Pharmaceuticals.
  • Lilly will pay $38.00 in cash per Centessa share plus one non-transferable CVR that could add up to $9.00, making total potential consideration $47.00 per share; upfront cash implies about $6.3 billion in aggregate equity value and the CVR up to about $1.5 billion.
  • Centessa’s lead candidate, cleminorexton, has Phase 2a results in narcolepsy type 1, narcolepsy type 2, and idiopathic hypersomnia; the CVR payments are contingent on specified U.S. FDA approvals within defined timeframes.

Alkermes (NASDAQ:ALKS) shares climbed about 13% Tuesday after Eli Lilly (NYSE:LLY) announced an agreement to acquire Centessa Pharmaceuticals (NASDAQ:CNTA). The deal terms specify an immediate cash payment of $38.00 per Centessa share plus one non-transferrable contingent value right - a CVR - that could deliver up to an additional $9.00, for maximum potential consideration of $47.00 per share.

The upfront cash component equates to an aggregate equity value for Centessa of approximately $6.3 billion. The CVR, contingent on future regulatory milestones, represents an additional potential aggregate equity value of roughly $1.5 billion.

Centessa’s clinical focus is a portfolio of orexin receptor 2 - OX2R - agonists aimed at modulating the neurobiological system that governs the sleep-wake cycle. Its lead investigational therapy, cleminorexton, has produced results in Phase 2a studies across narcolepsy type 1, narcolepsy type 2, and idiopathic hypersomnia.

The structure and timing of the CVR payments are explicitly linked to U.S. Food and Drug Administration approvals. There are three possible milestone payments per CVR:

  • $2.00 if cleminorexton or ORX142 receives U.S. FDA approval for narcolepsy type 2 treatment prior to the fifth anniversary of the transaction closing;
  • $5.00 if a U.S. FDA approval is obtained for idiopathic hypersomnia within that same five-year post-closing period; and
  • $2.00 upon the first U.S. FDA approval for any indication occurring prior to January 1, 2030.

Beyond cleminorexton, Centessa’s OX2R agonist program includes additional assets that are in clinical and preclinical stages. The company notes potential applicability of these assets across a range of conditions, specifically neurological, neurodegenerative, and neuropsychiatric disorders.

The market reaction that lifted Alkermes shares followed Lilly’s disclosure of the acquisition terms and the contingent payment schedule tied to regulatory milestones. The transaction values and the CVR mechanics were provided as part of Lilly’s announcement of the agreement to acquire all issued and to be issued share capital of Centessa.

Risks

  • Regulatory approval risk - CVR payouts depend on U.S. FDA approvals for cleminorexton or ORX142 and for idiopathic hypersomnia within specified windows, creating uncertainty for the contingent payments. - Impacts pharmaceutical and biotech sectors.
  • Development-stage risk - Centessa’s portfolio includes clinical and preclinical assets, meaning outcomes remain uncertain and dependent on future trials and regulatory review. - Impacts biotech R&D investment and clinical-stage companies.
  • Timing conditions risk - Several CVR milestones are tied to specific deadlines (the fifth anniversary of closing and January 1, 2030), so even if approvals occur, timing could affect whether payments are triggered. - Impacts transaction valuation for shareholders and potential cash flow timing for the acquiring company.

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