Cabaletta Bio reported its Q3 2024 financial results, highlighting the ongoing clinical execution with 40 U.S. clinical sites actively recruiting patients for the RESET clinical trial program for CABA-201. The company is preparing to present clinical data from the RESET-Myositis™, RESET-SLE™ and RESET-SSc™ trials at ACR Convergence 2024. Cabaletta expects its cash, cash equivalents and short-term investments to fund its operating plan into the first half of 2026.
Clinical data from the RESET-Myositis™ and RESET-SLE™ trials, along with initial clinical data from the RESET-SSc™ trial, to be presented at ACR Convergence 2024.
16 patients enrolled with 10 patients dosed as of November 12 across the RESET™ clinical development program; 40 U.S. clinical sites actively recruiting patients.
Data permitting, anticipate meeting with the FDA in 2025 regarding potential registrational program designs for CABA-201.
Clinical development expanding efficiently into Europe with EMA CTA authorization for CABA-201 received in lupus; Gerwin Winter appointed as Senior VP and Head of International.
Cabaletta Bio expects that its cash, cash equivalents and short-term investments as of September 30, 2024, will enable it to fund its operating plan into the first half of 2026.