Cedar Clinical Research selected as clinical research site for Cybin's Phase 3 Study of CYB003
With the Phase 2 trial data, the U.S. Food and Drug Administration ("FDA") granted CYB003 breakthrough therapy designation, potentially shortening the drug development timeline.
- With the Phase 2 trial data, the U.S. Food and Drug Administration ("FDA") granted CYB003 breakthrough therapy designation, potentially shortening the drug development timeline.
- The Phase 3 trial for CYB003 is planned to commence enrollment mid-2024 and focus on its safety and efficacy.
- "The Phase 2 results from the CYB003 trials were impressive and demonstrated the potential for treating a serious condition that affects over 20 million Americans," said Dr. Thielking.
- To learn more about enrolling in the CYB003 Phase 3 Trial, please visit this link .