Aquestive Therapeutics Advances Anaphylm™ Research at AAAAI 2025
Aquestive Therapeutics Unveils Promising Data on Anaphylm
In a significant announcement, Aquestive Therapeutics, Inc. (NASDAQ: AQST) has highlighted new findings regarding their innovative product, Anaphylm, an epinephrine sublingual film. This research is expected to be presented at the renowned AAAAI Annual Meeting, which is a pivotal event for allergy and immunology professionals.
Key Findings from Anaphylm Studies
The latest data emerging from this research demonstrates that Anaphylm maintains its stability and potency even in extreme environmental conditions. It addresses critical concerns for those at risk of severe allergic reactions, ensuring effectiveness in various situations, be it heat, cold, or humid conditions.
Enhanced Drug Absorption
One of the standout results showcases that dosing with Anaphylm allows for consistent absorption of epinephrine without compromising safety or pharmacodynamic parameters. This indicates that patients can rely on Anaphylm for effective treatment during emergencies.
Rapid Symptom Resolution
Moreover, the studies revealed a remarkable median symptom resolution time of just 12 minutes for those treated with Anaphylm, compared to an alarming 74 minutes for untreated individuals. This highlights the potential of Anaphylm to provide swift relief from symptoms associated with anaphylaxis and angioedema.
Upcoming Presentations at AAAAI 2025
Aquestive is set to showcase various presentations that will delve deeper into the outstanding performance of Anaphylm. Details of some notable posters include:
Poster Presentation Highlights
Title: Durability of Anaphylm under Real-World Use
Poster Number: 304
Author: Steve Wargacki, PhD
Time: Saturday, Mar. 1, 9:45 am – 10:45 am PT
Title: Stability of Anaphylm Under Extreme Conditions
Poster Number: 305
Author: Steve Wargacki, PhD
Time: Saturday, Mar. 1, 9:45 am – 10:45 am PT
Title: Pharmacokinetic and Pharmacodynamic Responses
Poster Number: 312
Author: Carl N. Kraus, MD
Time: Saturday, Mar. 1, 9:45 am – 10:45 am PT
Title: Oral Anaphylm Symptom Intervention Study: Outcomes
Poster Number: L18
Author: Carl N. Kraus, MD
Time: Saturday, Mar. 1, 9:45 am – 10:45 am PT
The Impact of Anaphylm on Patient Care
Aquestive Therapeutics is committed to enhancing patient care through innovative solutions. Anaphylm is engineered to provide a convenient and effective means of delivering epinephrine. Its compact size and easy-to-use format is tailored to meet the needs of individuals facing life-threatening allergic reactions.
About Aquestive Therapeutics
Aquestive is a pioneering pharmaceutical company focused on advancing medicines that significantly improve patient quality of life. With a proven record of developing novel therapeutics, they have commercialized several products that cater to complex medical needs. Anaphylm stands as a testament to their dedication to create accessible healthcare solutions.
Future Developments in Anaphylm
As Aquestive moves forward, the anticipated next steps include regulatory discussions regarding the FDA approval process. The successful launch of Anaphylm could dramatically alter the landscape of emergency treatment for anaphylaxis.
Frequently Asked Questions
What is Anaphylm?
Anaphylm is an epinephrine sublingual film designed for rapid administration in emergency situations related to severe allergic reactions.
How does Anaphylm compare to traditional epinephrine injections?
Anaphylm is intended to be more accessible and easier to use, eliminating the need for injections, which can be intimidating for many patients.
What were the main outcomes from the Anaphylm studies?
The studies showed significant stability under various conditions and rapid symptom resolution when Anaphylm was administered.
When and where will the findings be presented?
Aquestive will present their findings at the 2025 AAAAI Annual Meeting, scheduled from February 28 to March 3 in San Diego.
Is Anaphylm approved for public use?
Anaphylm is currently a product candidate under investigation and awaits FDA approval for public use.
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