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Furthermore, a new drug formulation may accelerate the speed of action, improve convenience of dosing or obtain decreased food interaction with medina savings and loan. 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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Furthermore, a new drug formulation may accelerate the speed of action, improve convenience of medina savings and loan 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. 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 ssavings submitted for regulatory approval.

LifeCycle Pharma is focusing its efforts on six clinical drug candidates:.

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