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Jacobio Pharmaceuticals Group (1167) investor relations material
Jacobio Pharmaceuticals Group H1 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Revenue reached RMB45.7 million for the six months ended June 30, 2025, driven by a milestone payment from the Allist Licensing Agreement, compared to nil in the prior year period.
Loss for the period narrowed significantly to RMB59.0 million from RMB169.1 million year-over-year, reflecting reduced R&D and administrative expenses.
Achieved NMPA market approval and launch of glecirasib for ≥2L NSCLC in China in May 2025, with strong clinical efficacy and safety data published.
Advanced a diversified oncology pipeline, including pan-KRAS, SHP2, BET, Aurora kinase A, p53 Y220C, iADC, and tADC programs, with global and China-based trials ongoing.
Entered a licensing agreement with Allist for commercialization and clinical development of glecirasib and sitneprotafib in Greater China, triggering milestone revenue.
Financial highlights
Revenue increased to RMB45.7 million from nil, attributable to the Allist Licensing Agreement milestone.
R&D expenses decreased 47.3% year-over-year to RMB93.2 million, mainly due to Allist funding pivotal trials.
Administrative expenses fell 12.4% to RMB18.6 million, reflecting cost controls and efficiency gains.
Net loss for the period was RMB59.0 million, a substantial improvement from RMB169.1 million in the prior year; adjusted loss was RMB56.7 million.
Gross profit reached RMB45.7 million, with no cost of revenue recognized.
Outlook and guidance
Focus on expanding the KRAS and iADC pipelines, leveraging allosteric inhibitor and iADC platforms for global leadership in oncology.
Continued investment in R&D and strategic collaborations to maximize clinical and commercial value.
Anticipated completion of key Phase I/II trials and further regulatory submissions in 2026.
Expects to utilize remaining IPO proceeds by end of 2025, with resource reallocation to early-stage drug discovery and development.
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