BRISBANE, Calif.--(BUSINESS WIRE)--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 four upcoming investor conferences in May and June:
Event: Bank of America Merrill Lynch Healthcare Conference
Date:
May 16, 2018
Presentation Time: 1:40 p.m. Pacific Time
Location:
Las Vegas
Presenter: Stephen Dilly, M.B.B.S., Ph.D.,
Chief Executive Officer
Event: Jefferies Global Healthcare Conference
Date: June
5, 2018
Presentation Time: 3:30 p.m. Eastern Time
Location:
New York
Presenter: Stephen Dilly, M.B.B.S., Ph.D., Chief
Executive Officer
Event: Nasdaq 38th Investor Conference
Date: June 12,
2018
Presentation Time: 8:00 a.m. British Summer Time
Location:
London
Presenter: Eric Bjerkholt, Chief Financial Officer
Event: JMP Securities Life Sciences Conference
Date: June
20, 2018
Presentation Time: 1:00 p.m. Eastern Time
Location:
New York
Presenter: 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 for at least 30 days following each webcast.
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™) approach is intended to achieve meaningful levels of protection by desensitizing patients with defined, precise amounts of key allergens. Aimmune’s first investigational biologic product, AR101, which uses CODIT™ 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.
This press release concerns a product that is under clinical investigation and that has not yet been approved for marketing by the U.S. Food and Drug Administration (FDA) or the European Medicines Agency (EMA). It is currently limited to investigational use, and no representation is made as to its safety or effectiveness for the purposes for which it is being investigated.