Breakdown | |||||
TTM | Mar 2024 | Mar 2023 | Mar 2022 | Mar 2021 | Mar 2020 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
0.00 | 0.00 | 0.00 | 0.00 | 864.00K | 0.00 | Gross Profit |
-280.00K | -424.00K | -251.00K | -168.00K | 200.00K | 0.00 | EBIT |
-45.51M | -78.84M | -54.94M | -63.60M | -30.46M | -1.95M | EBITDA |
-134.69M | -78.58M | -47.24M | -63.67M | -32.17M | 9.60K | Net Income Common Stockholders |
-103.90M | -78.08M | -47.49M | -67.63M | -32.22M | -1.94M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
136.29M | 208.99M | 16.63M | 64.03M | 1.54M | 1.54M | Total Assets |
253.55M | 302.02M | 53.90M | 92.11M | 1.71M | 1.71M | Total Debt |
0.00 | 291.00K | 0.00 | 0.00 | 0.00 | 0.00 | Net Debt |
-136.29M | -208.70M | -16.63M | -64.03M | -1.54M | -1.54M | Total Liabilities |
13.31M | 10.10M | 5.66M | 5.99M | 263.00K | 263.00K | Stockholders Equity |
240.24M | 291.93M | 48.23M | 86.12M | 1.45M | 1.45M |
Cash Flow | Free Cash Flow | ||||
-101.99M | -69.62M | -50.74M | -19.26M | -19.26M | ― | Operating Cash Flow |
-100.89M | -68.91M | -47.43M | -19.03M | -19.03M | ― | Investing Cash Flow |
-1.10M | 6.92M | -3.31M | -1.19M | -1.19M | ― | Financing Cash Flow |
190.08M | 254.51M | 13.56M | 35.78M | 82.72M | ― |
Cybin has launched strategic clinical site partnerships to accelerate its PARADIGM program, a multinational Phase 3 initiative evaluating CYB003 for treating major depressive disorder. This program includes multiple studies across over 40 sites in the U.S. and Europe, with a significant addressable market of over 300 million people. With a robust drug development team and Breakthrough Therapy Designation from the FDA, Cybin aims to shift depression treatment towards more intermittent therapies rather than daily dosing.
Cybin announced the launch of its first strategic partnership agreement with Segal Trials to support its multinational pivotal Phase 3 program for CYB003, designed to treat Major Depressive Disorder. This collaboration aims to enhance trial efficiency and performance, with the potential to expedite the approval process, while enrolling approximately 550 patients across more than 40 clinical sites in the U.S. and Europe.
Cybin Inc. announced significant achievements in 2024, including successful Phase 2 results for its CYB003 drug, demonstrating a breakthrough in treating major depressive disorder. The company received FDA Breakthrough Therapy Designation for CYB003 and initiated a multinational pivotal Phase 3 program. Looking forward to 2025, Cybin anticipates advancing its clinical pipeline with key milestones, including topline efficacy data for CYB004 in generalized anxiety disorder and further progress in its Phase 3 program.