Ascendia® is a specialty pharmaceutical company dedicated to developing  enhanced formulations of existing drug products, and enabling formulations for pre-clinical and clinical stage drug candidates.  Ascendia provides state-of-the-art formulation development services for poorly water soluble molecules, and cGMP manufacture of clinical trial materials.  Applying its nano-particle technologies and expertise, Ascendia can rapidly assess the feasibility of a broad array of formulation options in order to improve a drug’s bioavailability.  Our technologies include nano-emulsions, amorphous solid dispersions, oral controlled release, self-emulsifying drug delivery systems (SEDDs) and production of nano-particles.  Ascendia provides development and testing services – from pre-formulation through to manufacture of pilot clinical supplies.


We execute rapid, comprehensive, and cost-effective programs for our clients.  We partner with emerging, discovery-stage pharmaceutical companies to provide early-stage formulations; with generic companies that seek enabling technology fort ANDA development projects; and with specialty pharmaceutical companies that need development of new 505(b)(2) products for clinical testing.


Ascendia’s headquarters, laboratories and manufacturing suites are located in central New Jersey, and the company also has a facility in Xiamen, China to serve formulation development needs of the Chinese market.  Ascendia is a privately-held company with a mission to provide customized formulation solutions to salvage difficult compounds and to create advanced medicines to help patients prevail over their disease and enhance their quality of life.

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