
Drug Delivery Platforms that Enhance Compliance and Efficacy
Medicap Laboratories are a multidimensional controlled-release drug delivery platform that we believe can be applied to the efficient development of a wide range of existing and new pharmaceuticals.

Operating in the Specialty Pharmaceutical Market
At Medicap, we are engaged in the research, development and commercialization of controlled-release and targeted pharmaceutical products, both novel and generic, with a particular emphasis in the opioid abuse deterrence space.
Our proprietary Hypermatrix™ technologies are central to the development and manufacture of novel and generic controlled-release and targeted-release oral solid dosage drugs. This technology allows for the intelligent and efficient design of drugs through the precise control of a number of key variables. This allows us to respond to varying drug attributes and patient requirements, producing a desired controlled-release effect in a time and cost-effective manner. We believe that the flexibility of these technologies allows us to develop complex drug delivery solutions within an industry-competitive timeframe.

How controlled-release differs from immediate-release drugs
Controlled-release means releasing a drug into the bloodstream or at a target site in the body, over an extended period of time or at predetermined times. In some circumstances, controlled-release drug delivery can enhance efficacy and patient compliance as compared to immediate release formats for the same drug.
Control Release Delivery Platforms
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Hypermatrix
View Hypermatrix TechnologyOur Hypermatrix™ technology platform is at the core of a family of drug delivery technologies that underlie our development and marketing programs. Hypermatrix™ is a novel concept based on hyper-dimensionality. The understanding and controlling of properties associated with these dimensions facilitates time-release delivery of a wide range of pharmaceuticals.
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nPODDDS
View nPODDDS TechnologyThe nPODDDS™ technology platform supports our Oxycodone hydrochloride ER new drug candidate, and is designed to provide for certain unique drug delivery features in a product. nPODDDS™ drug release profile shows a clearly defined Point Of Divergence (POD) in the drug release time lines:
- Initial loading dose provides a quick onset of action
- Followed by a shift in the drug release rate to reflect a controlled release or sustained action
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Other CR Platforms
View Other CR Delivery PlatformsUsing our Hypermatrix™ concept, we have designed several controlled-release delivery platforms: IntelliFoam™, IntelliGITransporter™, IntelliMatrix™, IntelliOsmotics™, IntelliPaste™, IntelliShuttle™ and IntelliPellets™.
Strategic Focus
The principal focus of our development activities previously targeted difficult-to-develop controlled-release generic drugs which follow an ANDA regulatory path. Our current development effort is increasingly directed towards improved difficult-to-develop controlled-release drugs which follow an NDA 505(b)(2) regulatory pathway. We have increased our research and development ("R&D") emphasis towards specialty new product development, facilitated by the 505(b)(2) regulatory pathway, by advancing the product development program for both Oxycodone hydrochloride ER and Regabatin™.
Our unique Hypermatrix, nPODDDS™ and PODRAS™ technologies allow us to provide life-cycle management or new chemical entity delivery system solutions for virtually any small molecule.

State-of-the-Art, FDA-Acceptable Facility
The demand for our technological know-how continues to promote the relocation and expansion of our premises. Our facilities consist of approximately 65,000 square feet with some of the most sophisticated pharmaceutical equipment employed in the industry. Our facilities allow us to conduct intensive R&D projects and create, test and manufacture products for the market. These in-house resources not only allow us to focus on a wide range of projects, but also to maximize efficiency ensuring rapid progress through the various stages of drug development - from formulation to regulatory submission. Our manufacturing facility has been granted FDA acceptable status following completion of a cGMP and pre-approval inspection. Health Canada has also approved our GLP QC labs and cGMP manufacturing plant.