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Elicera Therapeutics (ELIC) investor relations material
Elicera Therapeutics Q2 2025 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.
Executive summary
Operating loss for Q2 2025 improved to SEK -2.9M from SEK -5.8M year-over-year, with a similar trend for the half-year period, reflecting increased grants and reduced costs.
Four out of six patients in the first two CARMA study cohorts achieved complete metabolic response, with no serious adverse events reported.
ELC-100 received Orphan Drug Designation in the U.S. for pancreatic neuroendocrine tumors.
Successful warrant program and share issue raised SEK 22M, extending capitalization until mid-2027.
Financial highlights
Q2 2025 operating loss: SEK -2,892,341 (Q2 2024: -5,841,409); H1 2025: SEK -10,961,745 (H1 2024: -11,274,831).
Loss for Q2 2025: SEK -2,732,070 (Q2 2024: -5,622,779); H1 2025: SEK -10,745,532 (H1 2024: -10,992,456).
Cash flow from operating activities H1 2025: SEK -6,736,135 (H1 2024: -16,997,666).
Cash and cash equivalents at period end: SEK 39,661,563 (H1 2024: 32,864,607).
Earnings per share H1 2025: SEK -0.25 (H1 2024: -0.39).
Outlook and guidance
Capitalization is projected to last until mid-2027, supporting completion of the CARMA study.
Final reporting for the ELC-100 Phase I/IIa study is postponed to year-end 2025 due to a database transition.
Continued focus on securing funding and partnerships for preclinical programs, especially ELC-401 for glioblastoma.
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