Appili Therapeutics Reports Financial and Operational Results for First Quarter of Fiscal Year 2024

Rhea-AI Summary

Appili Therapeutics Inc. announces Q1 2024 financial and operational results. They secured $7.3 million in funding for their ATI-1701 vaccine from the Defense Threat Reduction Agency and USAFA. They also obtained a US patent for their Metronidazole formulation. FDA established a PDUFA action date for ATI-1501 on September 23, 2023.

FDA established a PDUFA action date for ATI-1501 of September 23, 2023

Government funding committed to enable Appili to advance its biodefense vaccine candidate ATI-1701 towards an IND

HALIFAX, Nova Scotia--(BUSINESS WIRE)-- Appili Therapeutics Inc. (TSX:APLI; OTCQB: APLIF) (the “Company” or “Appili”), a biopharmaceutical company focused on drug development for infectious diseases and biodefense products, today announced its financial and operational results for the first quarter of its fiscal year 2024, which ended on June 30, 2023. All figures are stated in Canadian dollars unless otherwise stated.

"During this quarter, we executed an agreement with United States Air Force Academy (“USAFA”) for an initial amount of US$7.3million in funding from the Defense Threat Reduction Agency and USAFA for our ATI-1701 vaccine, a crucial defense against Tularemia, which is a top-priority biothreat. Our partnership with USAFA and the recent agreement execution will enable us to advance this program towards an Investigational New Drug (“IND”),” said Don Cilla, Pharm.D., M.B.A., President and Chief Executive Officer of Appili Therapeutics. "Additionally, securing US patent coverage through at least 2039 for ATI-1501, our Metronidazole formulation, is a significant milestone leading up to the anticipated FDA Prescription Drug User Fee (“PDUFA”) date on September 23, 2023. We look forward to receiving milestone payments and royalties from our partner, Saptalis Pharmaceuticals LLC ("Saptalis”), in the coming quarters based on their submission and commercialization plans. These achievements are expected to position us with the required resources to continue to make progress in advancing our infectious disease assets."

Operational Highlights

On May 5, 2023, Appili executed an initial cooperative agreement with USAFA the previously announced funding of the ATI-1701 program. This agreement provides the first stage of funding from the previously announced US$14 million award from the U.S. Department of Defense (“DOD”). This initial funding, in the amount of US$7.3 million, will be used to kick-off ATI-1701 early-stage development and regulatory activities. As the initial activities progress, Appili will submit proposals to USAFA for additional tranches of funding to continue development through IND submission. Under the terms of its agreement with USAFA, Appili will be reimbursed for direct costs and labour associated with budgeted program activities, plus will recover a portion of its overhead costs.

On May 24, 2023, the United States Patent and Trademark Office published patent claims for ATI-1501, Appili’s liquid oral reformulation of the antibiotic metronidazole, under the U.S. Application No. 18/072,154, covering the composition and preparation methods. The patent extends protection for this formulation through 2039.

Appili completed the technology transfer of ATI-1801, a treatment for cutaneous leishmaniasis, to the Company’s contract manufacturing organization. Appili plans to request a meeting with the U.S. Food and Drug Administration (“FDA”) later this year to discuss the previously generated Phase 3 data and agree on the necessary registration package to support a New Drug Application (“NDA”) submission, which the Company expects will include available nonclinical, manufacturing, and clinical data generated to date. To complete the remaining development work, Appili expects to pursue non-dilutive funding and partnership opportunities with NGOs and government agencies which share the Company’s focus on tropical diseases.

Appili is actively evaluating the eligibility of ATI-1801 for a priority review voucher (“PRV”) which, if confirmed, would make ATI-1801 the second program at Appili that is potentially PRV eligible, joining ATI-1701.

Upcoming Milestones

• The FDA established a PDUFA action date for ATI-1501 of September 23, 2023.

• Appili expects to receive milestone payments for ATI-1501 in calendar Q3 2023 and Q4 2023 based on Saptalis’ NDA submission and commercialization plans.

• Appili expects to receive first payments from USAFA for ATI-1701 in the coming weeks

Annual Financial Results

The Company prepares its financial statements in accordance with IFRS as issued by the International Accounting Standard Board and Part I of Chartered Professional Accountants of Canada Handbook–Accounting. All figures are stated in Canadian dollars unless otherwise stated.

The net loss and comprehensive loss of $1.5 million or $0.01 loss per share for the three months ended June 30, 2023, was $0.8 million lower than the net loss and comprehensive loss of $2.3 million or $0.03 loss per share during the three months ended June 30, 2022. This relates mainly to an increase in government assistance of $0.8 million, an increase of $0.3 million in foreign exchange gains and a decrease in general and administrative expenses by $0.2 million. These decreases were offset by an increase in research and development expenses of $0.2 million, an increase in financing costs of $0.2 million and an increase in business development of $0.1 million.

As of June 30, 2023, the Company had cash of $0.5 million, compared to $2.5 million on March 31, 2023. In addition, the Company is dependent in large part on receiving the US$14 million DOD funding for the development of ATI-1701 in a timely manner. Due to delays in reimbursement for previously submitted invoices in the near term, Appili entered into a definitive agreement with respect to an unsecured $300,000 bridge loan from Bloom Burton & Co. Inc. For further details, please refer to the Company’s management’s discussion and analysis (the “MD&A”) for the first quarter of the 2024 fiscal year.

As of August 11, 2023, the Company had 121,266,120 issued and outstanding Common Shares, 7,842,000 stock options, and 58,247,879 warrants outstanding.

This press release should be read in conjunction with the Company’s unaudited interim condensed financial statements for the first quarter of the 2024 fiscal year and the related MD&A, copies of which are available under the Company’s profile on SEDAR+ at www.sedarplus.ca.

About Appili Therapeutics

Appili Therapeutics is a biopharmaceutical company that is purposefully built, portfolio-driven, and people-focused to fulfill its mission of solving life-threatening infectious diseases. By systematically identifying urgent infections with unmet needs, Appili’s goal is to strategically develop a pipeline of novel therapies to prevent deaths and improve lives. The Company is currently advancing a diverse range of anti-infectives, including a vaccine candidate to eliminate a serious biological weapon threat, a topical antiparasitic for the treatment of a disfiguring disease, and a novel easy to use, liquid oral formulation targeting parasitic and anaerobic infections. Led by a proven management team, Appili is at the epicenter of the global fight against infection. For more information, visit www.AppiliTherapeutics.com.

Forward looking statements

This news release contains “forward-looking statements”, including with respect to the funding commitment from USAFA and expected timing of invoice payment, further anticipated milestones and the timing thereof, the Company’s development plans with respect to ATI-1501, ATI-1701 and ATI-1801, the anticipated PDUFA timing for ATI-1501, the timing of any milestone and/or royalty payments in respect of ATI-1501, potential PRV eligibility for ATI-1701 and ATI-1801 and the Company’s expectations with respect to its ability to operate as a going concern and satisfy its ongoing working capital requirements. Wherever possible, words such as “may,” “would,” “could,” “should,” “will,” “anticipate,” “believe,” “plan,” “expect,” “intend,” “estimate,” “potential for” and similar expressions have been used to identify these forward-looking statements. These forward-looking statements reflect the current expectations of the Company’s management for future growth, results of operations, performance and business prospects and opportunities and involve significant known and unknown risks, uncertainties and assumptions, including, without limitation, those listed in the annual information form of the Company dated June 22, 2023, and the other filings made by the Company with the Canadian securities regulatory authorities (which may be viewed at www.sedarplus.ca). Should one or more of these risks or uncertainties materialize or should assumptions underlying the forward-looking statements prove incorrect, actual results, performance or achievements may vary materially from those expressed or implied by the forward-looking statements contained in this news release. These factors should be considered carefully, and prospective investors should not place undue reliance on the forward-looking statements. The Company disclaims any intention or obligation to revise forward-looking statements whether as a result of new information, future developments or otherwise, except as required by law.

View source version on businesswire.com: https://www.businesswire.com/news/home/20230811690167/en/

Media:

Jenna McNeil, Communications Manager

Appili Therapeutics

E: Info@AppiliTherapeutics.com

Investor Relations:

Don Cilla, President and CEO

Appili Therapeutics

E: Info@AppiliTherapeutics.com

Source: Appili Therapeutics Inc.

FAQ

What is the funding amount Appili secured for their ATI-1701 vaccine?

Appili secured $7.3 million in funding for their ATI-1701 vaccine.

What is the significance of the US patent coverage for ATI-1501?

The US patent coverage for ATI-1501 extends through at least 2039.

What is the PDUFA action date for ATI-1501?

The PDUFA action date for ATI-1501 is September 23, 2023.