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Cybin has reported positive Phase 2 data for its lead candidate CYB003, showing breakthrough efficacy with over 70% remission rates at 12 months after just two doses in major depressive disorder. The program has received FDA Breakthrough Therapy Designation and is now enrolling patients in a multinational Phase 3 trial. The company’s second asset, CYB004—a deuterated DMT compound—is being evaluated in a Phase 2 study for generalized anxiety disorder. Both programs are supported by an extensive intellectual property portfolio with more than 80 granted patents and over 220 pending applications.
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