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Appili Therapeutics and Colleagues Publish Manuscript Demonstrating Efficacy of ATI-1701 Tularemia Vaccine

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Appili Therapeutics (OTC:APLIF) has published significant findings in the journal Vaccine demonstrating the effectiveness of ATI-1701, their biodefense vaccine candidate against tularemia. The study showed 100% survival rates in rats challenged with aerosolized F. tularensis SCHU S4, even at doses exceeding 10,000 times the median lethal dose.

The vaccine demonstrated up to 100% protection in cynomolgus macaques, with reduced disease severity and improved outcomes. ATI-1701, being developed in partnership with the U.S. Department of Defense, represents a first-in-class vaccine candidate for tularemia prevention, addressing an unmet need as there are currently no approved vaccines in major global markets.

Appili Therapeutics (OTC:APLIF) ha pubblicato risultati importanti sulla rivista Vaccine, dimostrando l'efficacia di ATI-1701, il loro candidato vaccino biodefensivo contro la tularemia. Lo studio ha evidenziato un tasso di sopravvivenza del 100% in ratti esposti ad aerosol di F. tularensis SCHU S4, anche a dosi superiori di oltre 10.000 volte la dose letale mediana.

Il vaccino ha mostrato fino a un 100% di protezione nei macachi cynomolgus, con una riduzione della gravità della malattia e un miglioramento degli esiti. ATI-1701, sviluppato in collaborazione con il Dipartimento della Difesa degli Stati Uniti, rappresenta un candidato vaccinale innovativo per la prevenzione della tularemia, rispondendo a un bisogno non soddisfatto dato che attualmente non esistono vaccini approvati nei principali mercati globali.

Appili Therapeutics (OTC:APLIF) ha publicado hallazgos significativos en la revista Vaccine que demuestran la eficacia de ATI-1701, su candidato a vacuna de biodefensa contra la tularemia. El estudio mostró una tasa de supervivencia del 100% en ratas expuestas a aerosol de F. tularensis SCHU S4, incluso con dosis que superan 10,000 veces la dosis letal media.

La vacuna demostró hasta un 100% de protección en macacos cínomolgus, con una reducción en la gravedad de la enfermedad y mejores resultados. ATI-1701, desarrollado en asociación con el Departamento de Defensa de EE.UU., representa un candidato vacunal pionero para la prevención de la tularemia, cubriendo una necesidad no satisfecha ya que actualmente no existen vacunas aprobadas en los principales mercados globales.

Appili Therapeutics (OTC:APLIF)� 학술지 Vaccine� 그들� 생물방어 백신 후보물질� ATI-1701� 효과� 입증하는 중요� 연구 결과� 발표했습니다. 연구에서� F. tularensis SCHU S4 에어로졸� 노출� 쥐에� 100% 생존�� 보였으며, 이는 중간 치사량의 10,000배가 넘는 용량에서� 나타났습니다.

� 백신은 사이노몰구스 원숭이에� 최대 100% 보호 효과� 보였으며, 질병� 중증� 감소와 치료 결과 개선� 확인했습니다. ATI-1701은 � 국방부와 협력하여 개발 중인 최초� 클래� 백신 후보�, 현재 주요 글로벌 시장에서 승인� 백신� 없어 충족되지 않은 수요� 해결합니�.

Appili Therapeutics (OTC:APLIF) a publié des résultats significatifs dans la revue Vaccine, démontrant l'efficacité de ATI-1701, leur candidat vaccin de biodéfense contre la tularémie. L'étude a montré un taux de survie de 100% chez des rats exposés à un aérosol de F. tularensis SCHU S4, même à des doses supérieures à 10 000 fois la dose létale médiane.

Le vaccin a démontré jusqu'à 100% de protection chez les macaques cynomolgus, avec une réduction de la gravité de la maladie et une amélioration des résultats. Développé en partenariat avec le Département de la Défense des États-Unis, ATI-1701 représente un candidat vaccin innovant pour la prévention de la tularémie, répondant à un besoin non satisfait car il n'existe actuellement aucun vaccin approuvé sur les principaux marchés mondiaux.

Appili Therapeutics (OTC:APLIF) hat bedeutende Ergebnisse in der Fachzeitschrift Vaccine veröffentlicht, die die Wirksamkeit von ATI-1701, ihrem Biodefense-Impfstoffkandidaten gegen Tularemie, belegen. Die Studie zeigte eine 100% Überlebensrate bei Ratten, die mit aerosolisiertem F. tularensis SCHU S4 exponiert wurden, selbst bei Dosen, die das 10.000-fache der medianen Letaldosis übersteigen.

Der Impfstoff zeigte bis zu 100% Schutz bei Cynomolgus-Makaken mit reduzierter Krankheitsintensität und verbesserten Ergebnissen. ATI-1701, das in Partnerschaft mit dem US-Verteidigungsministerium entwickelt wird, stellt einen neuartigen Impfstoffkandidaten zur Prävention von Tularemie dar und erfüllt einen ungedeckten Bedarf, da derzeit keine zugelassenen Impfstoffe auf den wichtigsten globalen Märkten verfügbar sind.

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  • Product still in preclinical stage requiring further development and regulatory approvals

Peer-reviewed publication highlights ATI-1701’s robust protection against aerosolized Francisella tularensis exposure in multiple animal models

HALIFAX, Nova Scotia, Aug. 06, 2025 (GLOBE NEWSWIRE) -- Appili Therapeutics Inc. (TSX:APLI; OTCPink: APLIF) (the “Company� or “Appili�), a biopharmaceutical company focused on drug development for infectious diseases and medical countermeasures,today announced a new publication in the journal Vaccine, supporting the efficacy of its biodefense vaccine candidate, ATI-1701. The manuscript, titled, details studies showing robust and durable protection from lethal tularemia exposure in both rat and non-human primate models.

ATI-1701, a live attenuated strain of F. tularensis, is being developed as a first-in-class vaccine to protect against tularemia, a highly contagious and potentially fatal bacterial disease. The publication, co-authored by Dr. Carl Gelhaus, Director of Non-Clinical Research at Appili, and researchers from leading biodefense institutions in the U.S., Canada, and Sweden, highlights key findings from multiple preclinical studies.

“This publication marks a significant milestone in the development of ATI-1701 and adds to the growing body of evidence supporting its protective potential,� said Dr. Carl Gelhaus. “In both rats and cynomolgus macaques, ATI-1701 showed strong immunity against aerosolized F. tularensis SCHU S4 � one of the most virulent strains and most concerning routes of exposure. Protection was dose-dependent, long-lasting, and associated with robust immune responses, including strong antigen-specific antibody titers.�

Key results from the study include:

  • 100% survival in rats challenged with aerosolized SCHU S4 up to one-year post-vaccination, even at challenge doses >10,000x the median lethal dose (LD50).
  • In cynomolgus macaques, ATI-1701 demonstrated up to 100% protection, reduced disease severity, and improved histopathological outcomes.
  • Immunized animals exhibited robust antibody responses, correlating with survival and supporting the vaccine’s immunogenic potential.

This study reinforces ATI-1701’s potential as a leading candidate for tularemia prevention and supports continued development in partnership with the U.S. Department of Defense.

ATI-1701 is the Company’s first-in-class vaccine candidate for the prevention of infection withF. tularensis. Since it is a highly infectious pathogen capable of causing severe illness, medical countermeasures for F. tularensis are a top biodefense priority for governments around the world. There is currently no approved vaccine for the prevention of tularemia in the United States or other major global markets, strengtheningATI-1701’s position as a potentially valuable vaccine urgently needed on the market.

About ATI-1701
ATI-1701 is a novel, live-attenuated vaccine for F. tularensis, which causes tularemia, a Category A pathogen which can be aerosolized and is over 1,000 times more infectious than anthrax. Since it is a highly infectious pathogen capable of causing severe illness, medical counter measures for F. tularensis are a top biodefense priority for the United States and governments around the world. There is currently no approved vaccine for the prevention of tularemia in the United States or other major global markets.

About Appili Therapeutics
Appili Therapeutics is an infectious disease biopharmaceutical company that is purposefully built, portfolio-driven, and people-focused to fulfill its mission of solving life-threatening infections. 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.

Forward looking statements
This news release contains “forward-looking statements�, including with respect to further anticipated milestones and the timing thereof and the Company’s development plans with respect to ATI-1701. 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, the risk that ATI-1701 may never become an approved vaccine for the prevention or treatment of tularemia, and the other risks listed in the annual information form of the Company dated June 25, 2025, and the other filings made by the Company with the Canadian securities regulatory authorities (which may be viewed at www.sedar.com). 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.

Media Contact:
Jenna McNeil, Communications Manager
Appili Therapeutics
E:

Investor Relations Contact:
Don Cilla, President and CEO
Appili Therapeutics
E:


FAQ

What are the key results of Appili Therapeutics' (APLIF) ATI-1701 tularemia vaccine study?

The study showed 100% survival rates in rats challenged with aerosolized F. tularensis SCHU S4, even at doses >10,000x the median lethal dose, and up to 100% protection in cynomolgus macaques with reduced disease severity.

Is there currently an approved vaccine for tularemia in the United States?

No, there is currently no approved vaccine for tularemia prevention in the United States or other major global markets.

Who is Appili Therapeutics (APLIF) partnering with for ATI-1701 development?

Appili Therapeutics is developing ATI-1701 in partnership with the U.S. Department of Defense.

How long does the protection from ATI-1701 vaccine last in animal studies?

The studies demonstrated protection lasting up to one year post-vaccination in rat models.

What makes ATI-1701 significant in the biodefense field?

ATI-1701 is a first-in-class vaccine candidate for tularemia prevention, addressing a top biodefense priority for governments worldwide, with no current approved vaccines available in major markets.
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