The Citizens Life Sciences Conference 2026
Logotype for Aquestive Therapeutics Inc

Aquestive Therapeutics (AQST) The Citizens Life Sciences Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for Aquestive Therapeutics Inc

The Citizens Life Sciences Conference 2026 summary

10 Mar, 2026

Regulatory update and next steps

  • Received a Complete Response Letter (CRL) from the FDA for Anaphylm, primarily focused on human factors related to product handling and administration, not clinical deficiencies.

  • Required to rerun a human factors validation study and conduct an additional pharmacokinetic (PK) study, both considered efficient in terms of time and cost.

  • Plan to resubmit the NDA in the third quarter, with all protocols and CROs in place and a Type A meeting scheduled to confirm study details.

  • Improvements include simplifying packaging and adding clearer instructions to address FDA concerns.

  • Success in the human factors study is qualitatively assessed, aiming for a threshold of around 90% correct use.

Market landscape and product positioning

  • The market for anaphylaxis treatments is growing, with robust auto-injector sales and a new nasal spray competitor increasing awareness.

  • Needle-free alternatives address significant unmet needs, as many patients delay or avoid using injectable epinephrine due to form factor and convenience.

  • The company is expanding its sales force and medical affairs presence, focusing on education and engagement with the allergy community.

  • Believes its film-based product offers a more compelling alternative to both auto-injectors and nasal sprays.

  • Payer engagement is a key focus to ensure successful market access.

Launch preparation and financial position

  • Medical affairs is prioritizing conference presence, publications, and outreach to prescribers to build trust and awareness.

  • Ended the year with $120 million in cash, with additional financing secured and sufficient funds to support launch preparations and ongoing studies.

  • Expect to end the year with $70 million in cash, not including potential out-licensing or additional capital.

  • Confident in readiness for commercial launch, with all rights to Anaphylm retained and another product, Libervant, potentially available for out-licensing next year.

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