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Lytix Biopharma (LYTIX) investor relations material
Lytix Biopharma Q4 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Entered a decisive new phase with strong clinical data, especially for ruxotemitide and LTX-401, and expanded commercialization opportunities.
Interim NeoLIPA study in melanoma showed 44% pathological complete response and 55% major pathological response among first 9 patients, shaping future development and regulatory strategy.
Partnership with Verrica Pharmaceuticals advanced, with promising immune-response data in basal cell carcinoma and preparations for pivotal Phase III trial.
NOK 77.3 million raised in January 2026 via private placement and subsequent offering, strengthening the balance sheet for key milestones.
Leadership and board enhanced to support late-stage execution and commercial readiness.
Financial highlights
Q4 2025 operating expenses were NOK 21.2 million, down from NOK 33 million year-over-year, mainly due to reduced R&D activity.
Cash and short-term investments at Q4 2025 end were NOK 72 million, with NOK 77.3 million raised post-quarter.
Total liabilities at Q4 2025 were NOK 20 million, down from NOK 39 million year-over-year.
Loss for Q4 2025 was NOK 18.7 million, improved from NOK 31.9 million in Q4 2024.
Cash flow from operations was negative NOK 29.5 million in H2 2025, an improvement from negative NOK 33.1 million in H2 2024.
Outlook and guidance
Well-capitalized into mid-2027, supporting clinical and partnering milestones, with focus on pivotal studies and commercialization.
NeoLIPA topline results expected in H2 2026; pivotal study for ruxotemitide in preparation.
LTX-401 clinical entry targeted for 2027, with ongoing evaluation of strategic development opportunities.
Actively pursuing capital raising and pharma partnerships to fund pivotal studies.
Expectation of continued disciplined execution, targeted investment, and strategic collaboration.
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