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Zelluna (ZLNA) investor relations material
Zelluna Q2 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
IND/CTA filing for lead program ZEMA-41/ZI-MA4-1 is on track for H2 2025, with first human data or patient dosing expected in H1 2026.
Completed key preclinical investigations and initiated GMP manufacturing of clinical material in July 2025.
Business combination completed in Q1 2025, streamlining operations and securing funding for clinical readiness.
Platform leverages off-the-shelf, scalable TCR-NK technology targeting solid tumors, with strong support from clinical experts and regulatory engagement.
Strategic positioning is reinforced by recent high-value deals in the cell therapy sector, highlighting strong market appetite for early-stage, off-the-shelf therapies.
Financial highlights
Cash position at end of Q2 2025 was NOK 76 million (USD 7 million), providing runway into Q2 2026.
Q2 2025 EBIT/operating expenses were negative NOK 38 million; year-to-date EBIT/operating expenses negative NOK 68 million.
Q2 2025 net loss/profit before tax was negative NOK 38 million; year-to-date net loss/profit before tax negative NOK 66 million.
Operating cash flow for Q2 2025 was negative NOK 59 million, mainly due to working capital changes and one-off manufacturing investments.
Cash burn rate is expected to decrease significantly after Q2 2025.
Outlook and guidance
Financial runway expected to cover key R&D and clinical milestones through Q2 2026.
IND/CTA submission for ZEMA-41/ZI-MA4-1 is on schedule for H2 2025, with initial clinical data anticipated in 2026.
Anticipates significant reduction in cash burn as R&D activities wind down and workforce reductions take effect.
Decision on first clinical trial location (US or Europe) pending further regulatory feedback.
Actively pursuing partnering opportunities for the TCR-NK platform.
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