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Biovica International (BIOVIC) investor relations material
Biovica International Q2 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
DiviTum, a blood-based test for monitoring breast cancer treatment efficacy, is FDA-cleared, CE-marked, included in Medicare, and has demonstrated strong clinical value, with new studies confirming its utility in metastatic breast cancer.
The product targets both metastatic and early breast cancer, with market potential in the hundreds of millions of dollars, and is offered as a service in the U.S. and as kits in other markets.
Clinical trials, collaborations with leading academic centers, and commercial agreements with major US cancer centers underpin commercialization and expansion.
Rights and directed share issues in August raised SEK 122.3 million before costs, significantly strengthening liquidity.
The Board has suspended financial targets due to sales delays and pipeline unpredictability, but aims for positive cash flow by 2027.
Financial highlights
Q2 sales reached SEK 2.7 million, up 16% year-over-year; year-to-date sales were SEK 5.3 million, up 31%.
U.S. IVD business grew 47% and pharma business 24% in Q2; research test business nearly doubled.
Operating loss for Q2 was SEK -14,964 thousand, improved from SEK -19,753 thousand year-over-year.
Cash and cash equivalents at period end were SEK 100.6 million, up from SEK 61.9 million.
Equity ratio at 89% versus 80% last year.
Outlook and guidance
Ambition to achieve cash flow positivity in 2027 remains, though timing is now expected later in the year due to partnership delays.
No specific revenue targets provided; updates will follow after closing key agreements.
Pharma Services pipeline is strong, with SEK 25–28 million in contracts over the next three years and expected record revenues in coming quarters.
U.S. clinical sales growth has flattened but is expected to rebound with new client bill agreements and adjuvant product rollouts.
Sales targets for FY 2025/26 and 2026/27 withdrawn due to delays in US clinical study and sales pipeline maturation.
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