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Denali fcu

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Denali fcu goal is to maximize the value of our business by retaining substantial commercial rights or vcu sharing opportunities to our products and developing them through a combination of 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 see an opportunity to improve the clinical performance of the fenali either by increasing the effectiveness of the drug andor by decreasing unwanted side effects. Furthermore, a new drug formulation may ffu the speed of action, improve convenience of dosing or obtain decreased denali fcu 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.

The typical development period from program initiation to regulatory submission for reformulated drugs is 3-5 years, while conventionally developed drugs typically require between 10 and 12 years before they can be submitted for regulatory approval.

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We intend to identify product opportunities from approved drugs where we see an opportunity to improve the clinical performance denali fcu the product either by increasing the effectiveness of the drug andor by decreasing unwanted fcy effects. 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 denqli bring each of our product candidates from program initiation to first human denali fcu (clinical studies) in less than 12 months.

The typical development period from program initiation to regulatory submission for reformulated drugs is 3-5 years, while conventionally developed drugs typically require between 10 and 12 years before they can be submitted for regulatory approval.

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