Cybin Inc. provided a corporate update, emphasizing the ongoing progress of its clinical pipeline and positive shifts in the regulatory landscape for psychedelic therapeutics. Patient dosing is currently underway in the Phase 3 CYB003 PARADIGM program for Major Depressive Disorder (MDD).
The company has strengthened its commercialization and manufacturing capabilities through strategic partnerships with Osmind and Thermo Fisher Scientific. These collaborations are designed to accelerate the development pathway and prepare for potential market entry.
Cybin highlighted positive regulatory signals from U.S. Health and Human Services (HHS) and FDA officials, alongside bipartisan congressional support. These developments suggest an improved forward regulatory environment, which could expedite regulatory pathways and reduce overall risk across Cybin’s clinical-stage portfolio.
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