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Pearl Therapeutics Highlights Its Porous Particle Cosuspension Platform, Demonstrating Universal Applicability Across Multiple Drug Classes and Combination Products
Date:5/5/2011

r components over long periods of time; and manufacturability with standard components and equipment. These attributes finally position MDIs to be the simple and universal dosage form that they were designed to be when first introduced over 50 years ago."

"The Pearl cosuspension platform's predictability of drug delivery across various therapeutic classes and product types, and compatibility with conventional manufacturing equipment, should allow product development and commercial-scale production to proceed without loss of time due to complicated iterative development that has traditionally plagued inhalation product development, and without costly investment in new capital equipment or processes. We expect that this will yield significant timeline and economic advantages to Pearl, as well as to potential partners," said Chuck Bramlage, Pearl's chief executive officer.

RDD Europe is taking place from May 3 - 6, 2011 in Berlin, Germany. Information regarding RDD Europe may be found on the congress website at www.rddonline.com. Details of Pearl's presentations are below.

Presentation Date/Time: 10:30 AM, Thursday May 5, 2011
Oral Presentation Title: A New Cosuspension MDI Platform: Scientific Foundations of Mono, Dual and Triple Combination Products
Session: Science in Product Development: Advances in Processing, Formulation and Characterization (Session #3)

Presentation Date/Time:  May 4 and 5, 2011
Poster Title: Development of Mono, Dual and Triple Combination pMDIs without Co-formulation Effect

Presentation Date/Time:  May 4 and 5, 2011
Poster Title: Performance Advantages of Pearl Cosuspension Formulations Technology for Manufacturing of Metered Dose Inhalers

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