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MedEdge MEA > News > Collaborations > AbbVie acquires Nimble Therapeutics to advance autoimmune and psoriasis treatments
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AbbVie acquires Nimble Therapeutics to advance autoimmune and psoriasis treatments

ME Desk
ME Desk
Published: December 24, 2024
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2 Min Read
Nimble Therapeutics
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December 2024- AbbVie and Nimble Therapeutics announced a definitive agreement under which AbbVie will acquire Nimble, including its lead asset, an investigational oral peptide IL23R inhibitor in preclinical development for the treatment of psoriasis and a pipeline of other novel oral peptide candidates with potential across several autoimmune diseases. Additionally, AbbVie will acquire Nimble’s peptide synthesis, screening, and optimization platform, which uses proprietary technology to help drive rapid discovery and optimization of peptide candidates for a range of targets.

“The addition of Nimble’s pipeline to AbbVie’s existing pipeline, combined with our deep clinical and translational expertise in immunology, represents an important growth opportunity,” said Jonathon Sedgwick, Ph.D., senior vice president and global head of discovery research, AbbVie. “Together, AbbVie and Nimble have the potential to help address the significant unmet medical need for people living with autoimmune diseases.”

Also Read : AbbVie Awards Scholarships to 45 Students with Chronic Diseases

“Nimble Therapeutics is committed to transforming the discovery of oral peptide-based medicines. With AbbVie’s world-class expertise in developing and commercializing medicines on a global scale, Nimble’s novel oral therapies will be well-positioned to reach more people living with autoimmune diseases,” said Jigar Patel, Ph.D., founder and chief executive officer, Nimble Therapeutics.

Nimble’s preclinical-stage IL23R inhibitor is an investigational oral therapy for the treatment of psoriasis and inflammatory bowel disease (IBD). IL23R is a clinically validated therapeutic target in certain autoimmune diseases and a major contributing factor to psoriasis and IBD pathogenesis and progression through increased inflammation and amplified immune responses.

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