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Galecto (GLTO) investor relations material
Galecto Q2 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Focus shifted to oncology and severe liver diseases, prioritizing GB3226 and GB1211 after a strategic review and asset acquisition from Bridge Medicines in October 2024.
GB3226, a dual ENL-YEATS and FLT3 inhibitor for AML, is advancing toward IND submission in Q1 2026, with initial clinical data expected in 2027.
Preclinical data show GB3226 efficacy as monotherapy and in combination, outperforming current FLT3 and menin inhibitors.
GB1211 continues in an investigator-initiated Phase 2 trial for metastatic melanoma and HNSCC, with promising early results in combination with checkpoint inhibitors.
Substantial additional capital will be required to advance clinical programs and maintain operations.
Financial highlights
Net loss for Q2 2025 was $3.4 million, or $(2.60) per share, improved from $5.3 million, or $(4.92) per share, year-over-year.
Operating expenses for Q2 2025 decreased 39% year-over-year to $3.4 million, reflecting lower R&D and G&A costs.
Research and development expenses for the quarter fell to $1.5 million from $1.8 million year-over-year, mainly due to reduced personnel and consulting costs.
General and administrative expenses for Q2 2025 were $2.0 million, down from $2.8 million in Q2 2024, driven by lower personnel and legal costs.
No restructuring costs in 2025; prior year included $1.0 million in such expenses.
Outlook and guidance
Existing cash of $10.2 million as of June 30, 2025, is expected to fund preclinical development and IND submission for GB3226 into 2026.
Additional funding is required for clinical development and to continue as a going concern beyond the next 12 months.
If unable to secure funding, may need to reduce spending, delay or eliminate programs, or consider liquidation.
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