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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 ludowici bank developed drugs typically require between 10 and 12 years lkdowici they can be submitted for regulatory approval.

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

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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 ludowici bank drugs typically require between 10 and 12 years before they can be submitted for regulatory approval.

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

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