Core Insights - Climb Bio, Inc. has initiated a Phase 2 trial of budoprutug for Primary Membranous Nephropathy (pMN) and expects to advance its clinical programs significantly in 2026 [1][2] - The company has strengthened its leadership team with key appointments to enhance operational capabilities [1][11] - Financial results indicate a cash position that is expected to sustain operations through 2027, allowing for continued development of its clinical pipeline [1][8] Budoprutug Program Updates - The Phase 2 trial, named 'PrisMN,' has been initiated in multiple countries, focusing on safety, pharmacokinetics, and preliminary efficacy [5] - A Phase 1 trial of a subcutaneous formulation of budoprutug is ongoing, with initial data expected in H1 2026 [1][5] - Ongoing trials for budoprutug in Immune Thrombocytopenia (ITP) and Systemic Lupus Erythematosus (SLE) are expected to yield initial data in H2 2026 [1][5] CLYM116 Program Updates - CLYM116, targeting the APRIL pathway for IgA nephropathy, has received regulatory clearance for a Phase 1 trial, with dosing anticipated by year-end 2025 [1][6] - Initial data from the CLYM116 trial is expected in mid-2026, following a recent R&D Spotlight Webcast that highlighted its differentiation from first-generation therapies [6][2] Financial Performance - As of September 30, 2025, the company reported cash, cash equivalents, and marketable securities totaling $175.8 million, expected to fund operations through 2027 [1][11] - Research and Development (R&D) expenses for Q3 2025 were $9.1 million, an increase from $6.2 million in Q3 2024, while General and Administrative (G&A) expenses were $5.8 million, slightly up from $5.5 million in the prior year [8][11]
Climb Bio Reports Third Quarter 2025 Financial Results and Provides Business Updates