BRISBANE, Calif.--(BUSINESS WIRE)--Mar. 5, 2019--
Aimmune Therapeutics, Inc. (Nasdaq: AIMT), a biopharmaceutical company
developing treatments for life-threatening food allergies, today
announced that members of the Aimmune executive management team will
participate in three upcoming investor conferences in March:
Event:Cowen and Company 39th Annual Healthcare
Date:Tuesday, March 12, 2019
Time:8:00 a.m. Eastern Time
Jayson Dallas, M.D., President and Chief Executive Officer
Event:Barclays Global Healthcare Conference
Date:Wednesday, March 13, 2019
Presentation Time:2:05 p.m.
Bjerkholt, Chief Financial Officer, and Andrew Oxtoby, Chief Commercial
Event: 31st Annual ROTH Conference
Date:Monday, March 18, 2019
Presentation Time:1:30 p.m. Pacific
Time/4:30 p.m. Eastern Time
Location:Laguna Niguel, CA
Eric Bjerkholt, Chief Financial Officer
Live webcasts of the presentations will be accessible on the Events page
under the Investor Relations section of the Aimmune website at www.aimmune.com.
Replays of the webcasts will be available following each webcast.
About Aimmune Therapeutics
Aimmune Therapeutics, Inc., is a biopharmaceutical company developing
oral treatments for life-threatening food allergies. The company’s
Characterized Oral Desensitization ImmunoTherapy (CODIT™) approach is
intended to provide meaningful levels of protection against allergic
reactions resulting from accidental exposure to food allergens by
desensitizing patients with defined, precise amounts of key allergens.
Aimmune’s first investigational biologic product using CODIT™, 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. Aimmune’s regulatory filing for marketing approval of
AR101 in the United States (submitted 4Q18) is based on data from the
pivotal Phase 3 PALISADE clinical trial of AR101, which in 4-17 year-old
subjects met its primary and key secondary endpoints, and additional
ongoing and completed AR101 clinical trials. Aimmune expects to file for
marketing approval of AR101 in Europe mid-2019. Aimmune has filed an IND
application for its second product, AR201, for the treatment of egg
allergy and intends to start a randomized Phase 2 clinical trial
mid-2019. For more information, please see www.aimmune.com.
This press release concerns AR101, a product candidate that is under
clinical investigation, and AR201, a product candidate that Aimmune
expects will be under clinical investigation in 2019. Neither AR101 nor
AR201 has been approved for marketing by the FDA or the European
Medicines Agency (EMA). AR101 and AR201 are currently limited to
investigational use, and no representation is made as to their safety or
effectiveness for the purposes for which they are being investigated.
View source version on businesswire.com: https://www.businesswire.com/news/home/20190305005339/en/
Source: Aimmune Therapeutics, Inc.
Laura Hansen, Ph.D., 650-396-3814