Climb Bio (CLYM) Q2 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q2 2026 earnings summary
6 Aug, 2026Executive summary
Focused on developing therapeutics for immune-mediated diseases, with lead candidates budoprutug (anti-CD19 mAb) and CLYM116 (anti-APRIL mAb) in clinical development for nephrology and autoimmune indications.
Achieved key milestones for budoprutug and CLYM116, advancing four ongoing trials and preparing for a Phase 2 trial in IgA nephropathy in Q3 2026.
Multiple ongoing Phase 1 and 2 trials for budoprutug in primary membranous nephropathy (pMN), immune thrombocytopenia (ITP), and systemic lupus erythematosus (SLE); CLYM116 in Phase 1 for IgA nephropathy.
Presented initial Phase 1 safety data for CLYM116 and Phase 1b data for budoprutug, both showing favorable safety and efficacy signals.
No product revenue to date; operations funded by equity offerings and private placements.
Financial highlights
Cash, cash equivalents, and marketable securities totaled $239.2 million as of June 30, 2026, up from $160.7 million at year-end 2025.
Net loss was $13.5 million for Q2 2026 and $27.2 million for the six months ended June 30, 2026, compared to $8.7 million and $29.4 million for the same periods in 2025.
Research and development expenses increased to $9.7 million in Q2 2026 (up $3.1 million year-over-year), while general and administrative expenses rose to $5.6 million (up $1.5 million year-over-year).
Net cash used in operating activities was $24.9 million for the first half of 2026; net cash provided by financing activities was $103.7 million, primarily from a private placement.
Other income, net, was $1.9 million for Q2 2026, slightly down from $2.0 million in Q2 2025.
Outlook and guidance
Cash runway expected to fund operations into the second half of 2028, but future capital raises will be needed to support ongoing development and potential commercialization.
Initial data from ongoing clinical trials for budoprutug and CLYM116 expected in late 2026 and 2027.
Plan to initiate a multiple-dose study of subcutaneous budoprutug in autoimmune patients, with data expected in 2027.
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