Aimmune inks license deal and makes investment in Xencor

5 February 2020
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Hot on the heels of US regulatory approval of its Palforzia (Peanut [Arachis hypogaea] allergen powder-dnfp), the first approved treatment for patients with peanut allergy, Aimmune Therapeutics (Nasdaq: AIMT) today announced it has obtained an exclusive worldwide license to develop and commercialize the investigational humanized monoclonal antibody XmAb 7195 from  Californian monoclonal antibody specialist Xencor (Nasdaq: XNCR).

News of the deal saw Aimmune’s shares rise 9.3% to $32.11 shortly after markets opened, while Xencor gained just 3% to $35.27.

XmAb7195, which has been renamed AIMab7195, was originally developed by Xencor for the treatment of allergic asthma. It uses three distinct mechanisms of action to reduce blood serum IgE and suppress IgE-producing cells. Aimmune initially plans to develop AIMab7195 as an adjunctive treatment with select Characterized Oral Desensitized ImmunoTherapy (CODIT) programs, including Palforzia, to explore treatment outcomes in patients with food allergies.

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