Aimmune Therapeutics, Inc. (Nasdaq:AIMT), a biopharmaceutical company developing CODIT™ (Characterized Oral Desensitization ImmunoTherapy) treatments for life-threatening food allergies, today announced that it will present Phase 2 clinical data on AR101, its investigational biologic oral immunotherapy for desensitization of patients with peanut allergy, and host corporate forums at:
Details for Aimmune Presentations at FAAM, October 13-15, 2016, in Rome
Aimmune will host an Industry Satellite Symposium titled “Peanut Allergy Oral Immunotherapy: Exploring the Needs of Peanut-Allergic Patients and Their Families” on Friday, October 14, 12:45-1:45 PM, at the Plenary Hall (Medici Visconti), and will feature:
Details for Aimmune Presentations at ACAAI, November 10-14, 2016, in San Francisco
Aimmune will host a Corporate Forum titled “Peanut Oral Immunotherapy: Thresholds of Eliciting Dose, Clinical and Immune Response from AR101 Phase 2 Clinical Trials, and Treatment Optimization Through Early Intervention” on Friday, November 11.
Additional details will be available closer to the time of the meeting.
About Aimmune Therapeutics
Aimmune Therapeutics, Inc., is a clinical-stage biopharmaceutical company developing treatments for life-threatening food allergies. The company’s Characterized Oral Desensitization ImmunoTherapy (CODIT™) system, an approach to oral immunotherapy (OIT), uses rigorously characterized biologic product candidates with gradual, controlled up-dosing protocols to obtain clinically meaningful desensitization to food allergens. Aimmune’s first CODIT product, AR101 for the treatment of peanut allergy, has received the FDA’s Breakthrough Therapy Designation for the desensitization of peanut-allergic patients 4-17 years of age and is currently being evaluated in Phase 3 clinical trials. For more information, please see www.aimmune.com.
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Last updated on: 11/10/2016
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