Aptar’s Intranasal Delivery System Used in Phase II Clinical Study for Investigational SPONTAN® Nasal Spray
Supporting advancement of complex intranasal therapies through clinical development
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Aptar’s Intranasal Delivery System Utilized in Phase II Clinical Study of SPONTAN® Nasal Spray
Aptar Pharma’s nasal spray platform is a multidose delivery system designed to deliver accurate and consistent dosing of prescription drug products administered via the nose, supporting reliable intranasal administration throughout clinical development.
This collaboration, supported by Aptar Pharma companies Nanopharm and Noble, helps reinforce Aptar Pharma’s position as a trusted partner in advancing complex intranasal therapies through robust delivery platforms and deep regulatory and technical expertise. Nanopharm developed and optimized the formulation to support the intended product profile, supported by analytical services demonstrating drug product and device performance alongside stability, while Noble is delivering end‑to‑end human factors and risk management support to enhance regulatory readiness and validate usability.
About Aptar
Aptar is a global leader in drug delivery, dosing and protection technologies, and consumer product dispensing. Aptar partners with the world’s top healthcare and consumer brands to deliver medicines and create exceptional user experiences. Serving diverse markets, from pharmaceutical to beauty to food and beverage, Aptar combines market expertise with proprietary design, engineering and science to develop innovative solutions that help improve lives worldwide. Headquartered in
About
This press release contains forward-looking statements, including regarding the use of Aptar Pharma’s intranasal spray platform in third-party intranasal clinical development activities and the potential role of such platform in supporting pharmaceutical development programs. Forward-looking statements generally can be identified by the fact that they do not relate strictly to historical or current facts and by use of words such as “expects,” “anticipates,” “believes,” “estimates,” “future,” “potential,” “continues” and other similar expressions or future or conditional verbs such as “will,” “should,” “would” and “could” are intended to identify such forward-looking statements. Forward-looking statements are made pursuant to the safe harbor provisions of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934 and are based on our beliefs as well as assumptions made by and information currently available to us. Accordingly, our actual results or other events may differ materially from those expressed or implied in such forward-looking statements due to known or unknown risks and uncertainties that exist in our operations and business environment including, but not limited to: risks related to clinical development activities conducted by third parties; development and commercialization risks; customer adoption; regulatory requirements and compliance; and competition, including technological advances. For additional information on these and other risks and uncertainties, please see our filings with the Securities and Exchange Commission, including the discussion under “Risk Factors” and “Management’s Discussion and Analysis of Financial Condition and Results of Operations” in our Form 10-K and Form 10-Qs. We undertake no obligation to update publicly any forward-looking statements, whether as a result of new information, future events or otherwise, except as required by law.
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