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Our goal is to maximize the value of our business by retaining substantial commercial rights or profit sharing opportunities to our products and developing them through a combination new carlisle federal in-house clinical development and out-licensing of both early- and late-stage programs.

We intend to identify product opportunities from approved drugs where we new carlisle federal an opportunity to improve the clinical performance of the product either by increasing the effectiveness of feeeral drug andor by decreasing unwanted side carlislr. Furthermore, a new drug formulation may accelerate the speed of action, improve convenience of dosing or obtain decreased food interaction with absorption.

The MeltDose technology has allowed us to bring each of our product candidates from program initiation to first human dose (clinical studies) in less than 12 months.

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We intend to identify product opportunities from approved drugs where we see an opportunity to improve the clinical performance of the product either by increasing the effectiveness of the drug andor by decreasing unwanted side effects.

Furthermore, a new drug formulation may accelerate the speed of action, improve convenience of dosing or obtain decreased food interaction with absorption. New carlisle federal MeltDose technology has allowed us to bring each of our product candidates from program initiation to first human dose (clinical studies) in less than 12 months. The typical development period from program initiation to regulatory submission for reformulated drugs nw 3-5 years, while conventionally developed drugs typically require new carlisle federal 10 and 12 years before they can be submitted for regulatory approval.

To attain this goal, we are creating value-added formulations of several approved and marketed drugs in a number of important therapeutic areas. We federral to develop these improved formulations internally as well as in collaboration with existing and future partners.

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