Exhibit 99.1

Aimmune Therapeutics Announces Third Quarter 2018 Financial Results and Recent Corporate Highlights

BRISBANE, California, November 8, 2018 – Aimmune Therapeutics, Inc. (Nasdaq: AIMT), a biopharmaceutical company developing treatments for life-threatening food allergies, today announced financial results for the quarter and nine months ended September 30, 2018. As of September 30, 2018, cash, cash equivalents and investments totaled $255.2 million.

Aimmune also announced that the safety profile of AR101 demonstrated in its recently completed Phase 3 RAMSES trial was consistent with the safety profile observed in its previously reported pivotal Phase 3 PALISADE trial in peanut-allergic children and teens, ages 4-17. Approximately 80% of participants treated with AR101 completed each trial. There were no serious adverse events related to treatment with AR101 in the RAMSES study.    

RAMSES was a double-blind, placebo-controlled safety study, which enrolled 506 peanut-allergic children and teens, ages 4-17 years, in the United States. The study monitored treatment-emergent adverse events during the initial six-month up-dosing period. As this was a safety study, there were no oral food challenges at entry or exit.

“We are very pleased that RAMSES further confirms the favorable safety profile of AR101,” said Jayson Dallas, M.D., President and CEO of Aimmune. “The BLA submission is our top priority now and remains on track for December. We will have a robust data package on approximately 1,200 patients treated with AR101. PALISADE is the core of our BLA, having shown the potential for AR101 to reduce the frequency and severity of allergic reactions due to accidental ingestion of peanut.

“Our goal is to provide families of peanut-allergic children and teens the certainty and convenience of a once-daily, oral medication for desensitization. We believe the clinical data on AR101 support that goal, and we look forward to sharing our plans in December for making AR101 available to the peanut-allergic community, assuming approval.”  

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Third Quarter and Recent Highlights

Third Quarter Financial Results

For the quarter and nine months ended September 30, 2018, net loss was $51.7 million and $153.8 million, respectively, compared to net loss of $31.8 million and $90.2 million for the comparable periods in 2017.

On a per share basis, net loss for the quarter and nine months ended September 30, 2018, was $0.89 and $2.72, respectively, compared to net loss per share of $0.63 and $1.79 for the comparable periods in 2017. The weighted average shares outstanding for the quarter and nine months ended September 30, 2018, was 58.3 million and 56.6 million, respectively, compared to 50.5 million and 50.3 million shares for the comparable periods in 2017. In the first quarter of 2018, the Company completed an underwritten public offering with net proceeds of $190.4 million through the sale and issuance of an aggregate of 6,325,000 shares of common stock.

Research and development expenses for the quarter and nine months ended September 30, 2018, were $31.7 million and $100.4 million, respectively, compared to $21.1 million and $60.7 million for the comparable periods in 2017. The increase was primarily due to higher costs from the progression of certain AR101 clinical trials and higher contract manufacturing costs to support clinical development and regulatory activities.

General and administrative expenses for the quarter and nine months ended September 30, 2018, were $21.3 million and $56.5 million, respectively, compared to $11.2 million and $31.0 million for the comparable periods in 2017. The increase was primarily due to additional employee-related costs and external professional services as Aimmune continues to build its infrastructure to support the development and potential commercialization of AR101. Stock-based compensation expense also increased primarily due to the expansion and extension of our long-term commercial supply agreement with Golden Peanut Company and modification of certain executives’ stock options resulting from their planned separation.

Cash, cash equivalents, and investments totaled $255.2 million at September 30, 2018, compared to $182.4 million at December 31, 2017. The increase primarily reflects net cash proceeds of $190.4 million received as of September 30, 2018, from the sale of common stock, partially off-set by cash used in operating activities of $117.6 million and cash used for purchase of plant and equipment of $8.3 million.

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Anticipated Upcoming Milestones

About Aimmune Therapeutics

Aimmune Therapeutics, Inc., is a biopharmaceutical company developing 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 plans to submit regulatory filings for marketing approval of AR101 in the United States and Europe based on data from the pivotal Phase 3 PALISADE clinical trial of AR101, which in 4-17 year-old subjects met all its primary and secondary endpoints, and additional ongoing and completed AR101 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 potential benefits of AR101; Aimmune’s expectations for the ARTEMIS and ARC004 trials, including the expected timing of data readouts and data cuts for these trials; Aimmune’s expectations on regulatory submissions for marketing approval of AR101 in the United States and Europe, including the timing of these submissions; Aimmune’s expectations regarding the potential commercial launch of AR101, including the timing of a potential approval of AR101 in

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the United States; Aimmune’s expectations regarding the timing of initiating additional clinical trials for AR101, including ARC005; Aimmune’s expectations on the timing of submitting an IND and initiating Phase 2 clinical trials for AR201 in egg allergy and AR301 in walnut allergy; 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; Aimmune’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; Aimmune’s reliance on third parties for the manufacture of its product candidates; possible regulatory developments in the United States and foreign countries; and Aimmune’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, 2018. 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 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.

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Contacts:

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