OUR 1-2-3 TRANSDERMAL FEASIBILITY PROGRAM
Have a clinical stage asset? A commercially approved product? At Corium Innovations, we’re ready to tailor a rapid, smart-priced feasibility program to test the technical viability of producing a multi-day delivery transdermal system for your drug.
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As the market leader in advanced transdermal drug delivery and polymer science, we’ll use our expertise in both formulation and process to produce working prototypes based on our flexible Corplex® 7-day technology.
We’ll subject them to skin-flux models to predict overall drug absorption and drug uptake duration. Plus, perform abbreviated physical and chemical testing on the prototypes. And summarize the findings in a concise development report—including our professional recommendations. All in just 60 days.
Here’s how it works:
Stage 1 PAPER SCREENING
- Assess key drug properties
- Determine partner/patient clinical demand
- Model potential for skin irritation
- Score quantitative likelihood of formulation success
Completion time: 1-2 weeks
Stage 2 SOLUBILITY STUDY
- Determine drug solubility in multiple GRAS excipients and process aids
- Determine gross compatibility of multiple adhesive mixes
- Map prototype formulation from combined results
Completion time: 2-3 weeks
Stage 3 SKIN FLUX TESTING
- Produce 3-5 patch prototypes
- Run skin flux testing (N=3) on all test patch systems
- Perform physical + chemical testing of the systems
- Issue report of generated data and recommendations
Completion time: 3-4 weeks
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For more information
contact: Kevin Ostrander MS, MBA
Chief Business Officer
Corium
INNOVATIONS
at a glance
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Founded in 1999
Transdermal/oral thin film experts
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FDA/DEA
registered facilities
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Rx and OTC
manufacturing