Progress in RAMSES, ARTEMIS and ARC004 Phase 3 AR101 StudiesAimmune anticipates milestones in its additional Phase 3 studies of AR101 throughout 2018. The RAMSES (ARC007) trial, taking place in the United States and Canada and designed to illuminate real-world patient and allergist experiences with AR101, exceeded enrollment projections. Aimmune expects data from RAMSES in the second half of 2018. The ARTEMIS (ARC010) trial, a dedicated European study of AR101, is on track to complete enrollment in the first quarter of 2018, and Aimmune expects data from ARTEMIS in early 2019. To support regulatory filings, Aimmune also plans a data readout from the PALISADE follow-on trial, ARC004, in the third quarter of 2018. Plans for AR101 Regulatory Filings Aimmune continues to expect to file a Biologics License Application (BLA) for AR101 with the U.S. Food and Drug Administration (FDA) at the end of 2018. Soon afterward, the company plans to begin a similar process in Europe, with the intention of filing a Marketing Authorisation Application (MAA) with the European Medicines Agency (EMA) in the first half of 2019. Additional Peanut Allergy Trials and Food Allergy Programs Aimmune's 2018 plans also include the initiation of the ARC005 clinical trial of AR101 for peanut allergy in young children ages 6-48 months, and the initiation, with Regeneron and Sanofi, of a Phase 2 clinical trial of AR101 and adjunctive dupilumab. Aimmune also expects to file an investigational new drug application (IND) for its egg allergy program in 2018 and continue work toward filing an IND for walnut allergy in 2019. Financial Outlook Aimmune ended 2017 in a strong financial position with approximately $182 million in cash, cash equivalents and investments as of December 31, 2017. About Aimmune's AR101 Phase 3 Development Program AR101 is an investigational biologic currently in Phase 3 clinical trials for the treatment of peanut allergy. AR101 has received U.S. Food and Drug Administration (FDA) Fast Track Designation, as well as FDA Breakthrough Therapy Designation for peanut allergy patients ages 4-17. Aimmune has completed its pivotal Phase 3 clinical trial of AR101, PALISADE ( Peanut Allergy Oral Immunotherapy Study of AR101 for Desensitization in Children and Adults), which enrolled 554 subjects ages 4-49 in the United States, Canada, and eight countries in Europe. Aimmune's open-label follow-on study to PALISADE, ARC004, which allowed eligible PALISADE AR101 subjects to roll over to additional maintenance therapy and PALISADE placebo subjects to cross over to AR101 treatment, has completed enrollment and is ongoing. Aimmune's real-world experience safety trial of AR101, RAMSES ( Real-World AR101 Market- Supporting Experience Study in Peanut Allergic Children Ages 4-17 Years), taking place in the United States and Canada, has competed enrollment. Aimmune's European Phase 3 efficacy trial of AR101, ARTEMIS ( AR101 Trial in Europe Measuring Oral Immunotherapy Success), designed with a higher efficacy bar and a shorter maintenance period than in PALISADE, remains open to enrollment. Aimmune expects to file a BLA with the FDA based on data from the PALISADE, ARC004, and RAMSES trials and an MAA with the EMA based on data from the PALISADE, ARC004, RAMSES and ARTEMIS trials. About Aimmune Therapeutics Aimmune Therapeutics, Inc., is a clinical-stage biopharmaceutical company developing treatments for potentially 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 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 and is currently being evaluated in Phase 3 clinical trials. For more information, please see www.aimmune.com. Forward-Looking Statements Statements contained in this press release regarding matters that are not historical facts are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. Such statements include, but are not limited to, statements regarding: Aimmune's expectations regarding the availability of topline data from the PALISADE trial of AR101 in February 2018 and additional data in March 2018 at AAAAI-WAO; Aimmune's expectations regarding its RAMSES, ARTEMIS and ARC004 trials of AR101, including the timing of the completion of such trials and the availability of data from such trials; Aimmune's ability to develop and advance additional product candidates into and successfully complete clinical trials; Aimmune's expectations regarding the timing of potential regulatory filings; Aimmune's expectations regarding the potential benefits of AR101; and Aimmune's expectations regarding potential applications of the CODIT™ approach to treating life-threatening food allergies. Risks and uncertainties that contribute to the uncertain nature of the forward-looking statements include: the expectation that Aimmune will need additional funds to finance its operations; the company's ability to initiate and/or complete clinical trials; the unpredictability of the regulatory process; the possibility that the results of early clinical trials may not be predictive of future results; the possibility that Aimmune's clinical trials will not be successful; Aimmune's dependence on the success of AR101; possible regulatory developments in the United States and foreign countries; and the company's ability to attract and retain senior management personnel. These and other risks and uncertainties are described more fully in Aimmune's most recent filings with the Securities and Exchange Commission, including its Quarterly Report on Form 10-Q for the quarter ended September 30, 2017. All forward-looking statements contained in this press release speak only as of the date on which they were made. Aimmune undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.
This press release concerns a product that is under clinical investigation and that has not yet been approved for marketing by the FDA or the 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.