Cybin(CYBN) - 2026 Q2 - Earnings Call Transcript

Financial Data and Key Metrics Changes - Cash-based operating expenses for Q2 2026 totaled $28.5 million, up from $18.2 million in the same period last year, indicating a significant increase in operational costs [17] - Net loss for Q2 2026 was $33.7 million, compared to a net loss of $41.9 million in the same period last year, showing an improvement in financial performance [17] - Cash flows used in operating activities were $34.5 million for Q2 2026, compared to $19.1 million in the same period last year, reflecting increased operational spending [17] - The company ended the quarter with cash, cash equivalents, and investments of $83.8 million [17] Business Line Data and Key Metrics Changes - CYB003, a proprietary deuterated psilocin analog, is in phase 3 studies for major depressive disorder, while CYB004, a deuterated dimethyltryptamine program, is in phase 2 for generalized anxiety disorder [5][8] - The phase 3 CYB003 program has received breakthrough therapy designation and has been granted additional clearances to commence a second phase 3 study in new geographies [5] - Enrollment for the phase 2 CYB004 study has been completed, with top-line data expected in the first calendar quarter of 2026 [9] Market Data and Key Metrics Changes - The phase 3 study for CYB003 targets approximately 330 participants across about 60 clinical sites globally, indicating a broad market reach [8] - The design of the studies aims to reflect real-world clinical populations, allowing for concomitant antidepressants or anxiolytics [9] Company Strategy and Development Direction - The company is focused on patient-centered care, rigorous science, and clear communication, with an emphasis on operational efficiency and scalability in clinical settings [3][4] - The capital plan is aligned with advancing programs towards major data readouts, following a recent financing of $175 million [4][14] - The strategy includes making therapies practical for clinics, with predictable session scheduling and minimal infrastructure requirements [11][12] Management's Comments on Operating Environment and Future Outlook - Management emphasized a conservative regulatory posture and disciplined capital deployment to navigate upcoming data events [20] - The company is preparing for scale with a model built for clinical reality, aiming to deliver clean data on time [20] - The CEO search is active, and the company is focused on maintaining operational stability during the transition [19][20] Other Important Information - The company has strengthened its capital position through a registered direct offering, which provides flexibility to execute its plans [14] - The repayment of $20 million in convertible debt to High Trail was completed, with a 10% prepayment penalty [61] Q&A Session Summary Question: What would give confidence to move forward with CYB004 into phase 3? - Management is looking for directional data and trends in separation between the two arms of the study, with statistical significance being a bonus [24][25] Question: What is the minimum durability threshold needed to compete with Spravato for CYB003? - A minimum of 12 weeks of maintained effects is expected, with hopes for better durability based on phase 2 data showing effects lasting up to a year [30][31] Question: What is the operational status of the Approach trial and site activations? - Enrollment for CYB003 is on track to complete by mid-next year, with top-line data expected by the end of next year [34][35] Question: What engagement has occurred with payers regarding CYB003 and CYB004? - Preliminary market research has begun, but it is still early for detailed payer engagement [38] Question: What criteria were used for selecting clinical trial sites for the Approach trial? - A mix of experienced and less experienced sites were chosen, focusing on those with a proven track record in delivering high-quality data [44][45] Question: What is the status of the preclinical CYB005 program? - Preclinical profiling studies are ongoing, with no specific updates available yet [46] Question: How important is patient compliance with background antidepressant use in the pivotal trial for CYB003? - Patients are required to remain on their background antidepressant medication during the treatment period [69]