Medicine company Eli Lilly and Company (NYSE: LLY) and biopharmaceutical company Morphic Holding Inc (NASDAQ: MORF) on Monday announced a definitive agreement for Lilly to acquire Morphic, a biopharmaceutical firm developing oral integrin therapies for serious chronic diseases.
Morphic's lead program, MORF-057, a selective oral small molecule inhibitor of α4β7 integrin, targets inflammatory bowel disease (IBD) and is undergoing Phase 2 studies in ulcerative colitis and Crohn's disease. Morphic also has a preclinical pipeline for autoimmune diseases, pulmonary hypertensive diseases, fibrotic diseases and cancer.
Lilly will launch a tender offer to purchase all Morphic shares at USD57 per share in cash, totaling approximately USD3.2bn. This represents a 79.0% premium to the closing stock price on 5 July 2024. The transaction, approved by both companies' boards, is expected to close in Q3 2024, subject to customary conditions.
Lilly's financial results will reflect the acquisition as a business combination or asset acquisition per GAAP. Citi and Kirkland & Ellis LLP are advising Lilly, while Centerview Partners LLC, Evercore Group L.L.C. and Fenwick & West LLP are advising Morphic.
With nearly 150-year history of pioneering life-changing medicines, Lilly aims to improve patient outcomes and expand treatment options for IBD with this acquisition.
Biophytis advances sarcopenia treatment with positive Phase 2 results
AstraZeneca secures EU approval for Imfinzi in limited-stage small cell lung cancer
BioSurfaces collaborates with Morphocell Technologies
iOncologi acquires TargImmune Therapeutics
Argent BioPharma announces positive CimetrA Phase IIb clinical trial results
Korro Bio receives FDA orphan drug designation for KRRO-110
SpliceBio doses first patient in Phase 1/2 ASTRA study of SB-007
Third Arc Bio reports first patient dosed in first-in-human study assessing ARC101
Amgen reports positive Phase 3 trial results for UPLIZNA in generalised myasthenia gravis
Celltrion launches STELARA biosimilar STEQEYMA in US market
Merck reports positive Phase 3 Data on HIV treatment DOR/ISL
Cantargia enrolls first patient in leukemia study with nadunolimab
Shilpa Medicare's Nor Ursodeoxycholic Acid Tablets IND receives regulatory approval in India