Synthesis and detention of Schedule I drugs - Psilocybin, Psilocin and other derived tryptamines
Cultivation of Psilocybe mushrooms and extraction of tryptamines
Positive opinion for the initiation of safety and efficacy testing
This combination of authorizations are unique in Europe and will allow Sintalica to pursue its full research and development and clinical program at the University's laboratory and related facilities.
Sintalica's approach to psychedelic drug discovery focuses on minimizing hallucinogenic effects while enhancing the psychedelic molecule's strong anti-inflammatory properties.
The company's research and drug development program is focused on neurodegenerative disorders, including SCI-Induced Chronic Neuropathic Pain (Spinal Cord Injury), Fibromyalgia, and Inflammation.
Sintalica has filed three provisional patents for proprietary psychedelic molecules with claims of improved stability, efficacy and bioavailability.
The molecules are being produced in the University's state-of-the-art laboratories, and will be tested for safety and efficacy toward target indications.
Sintalica has an exclusive research partnership with leading Italian research institutes, including the University of Messina and the University of Niccolò Cusano of Rome.
Sintalica's scientific team comprises world-leading scientists in chemistry, pharmacology, biotechnology and neurodegenerative diseases.
Sintalica Bioscience is a Canadian drug discovery company operating through its Italian subsidiary focused on using psychedelics to create breakthrough treatments for neuroinflammatory disorders.
Sintalica has filed three provisional patents for proprietary psychedelic molecules with improved stability and safety profiles, reduced hallucinogenic effects, and enhanced bioavailability.
Sintalica has exclusive partnerships with the University of Messina and the University of Niccolò Cusano, providing access to research facilities, including laboratories, a polyclinic hospital, and a team of world-leading scientists.
Merck's sotatercept gains priority review for PAH treatment
Antibe gains approval for otenaproxesul PK/PD study
Calliditas Therapeutics' setanaxib receives US FDA orphan drug designation
Everads Therapy signs license, collaboration and supply agreement with Kriya Therapeutics
IDEAYA Biosciences' IDE161 receives US FDA fast track designation
YS Biopharma enrols first subject in Phase three PIKA Rabies Vaccine clinical trial
Armata Pharmaceuticals doses first patient in Phase 2a of AP-SA02 diSArm study
Melt Pharmaceuticals enters exclusive agreement with Catalent for Zydis fast-dissolve tech
EXACT Therapeutics' ACTIVATE trial shows promise in enhancing chemotherapy efficacy
Sanofi granted Priority Review for EoE treatment in young children
Pierre Fabre Laboratories signs long-term collaboration with Vernalis (R&D)
BioArctic and Eisai secure approval for LEQEMBI infusion in Japan for Alzheimer's disease treatment