Pharmaceutical Business review

Therapix signs binding MOU with Swiss pharmaceutical firm to receive License to use formulation for ultralow-dosage administration

The final agreement will be signed, inter alia, subject to the completion of an initial clinical trial in the technology to the satisfaction of Therapix, and the completion of a technology due diligence.

Dr. Elran Haber, Therapix Biosciences’ CEO, stated that "the Company continues to realize its business strategy in the research and development of cannabinoid-based drugs. We believe that the sublingual technology for administrating the active ingredient, will allow us to improve the absorption and shorten the time for receiving the therapeutic effect of THC in the drugs that we develop.

"This unique formulation will expand the Company’s technological ability set, and we believe that it will enable us to provide an improved response in treating the indications on which the Company has chosen to focus, concurrently with the commencement of the clinical trials in H2/2016."

Several days ago, Therapix Biosciences filed an application with the U.S. Food and Drug Administration to approve an "orphan" drug designation for a drug (THX-TS01) developed based on the entourage technology, which combines cannabinoid substances in treating Tourette syndrome.

The application was filed after the completion of the pre-clinical phase and proof-of-concept of the entourage technology and further to the Company’s preparations towards the development of a drug based on the technology in the context of clinical trials in humans.