Genincode PLC (AIM: GENI) announced interim results showing 15% revenue growth to £1.6m, with full-year guidance of around 25% to £3.3m, improved gross margins of 53%, and a tightly managed loss of £2m with £2.4m in cash reserves, as the company advances its strategy in precision genetics for cardiovascular disease prevention and cancer risk assessment. The group is scaling its polygenic risk score (PRS) tests in cardiovascular medicine, with US clinical adoption accelerating as active ordering sites doubled from 20 to 40 clinics in H1 and are on track to exceed 60 by year-end, supported by Medicare reimbursement for Cardio InCode and ongoing FDA de novo review, with additional clinical data to be submitted in early 2026. Management confirmed advanced negotiations with potential US and international commercial partners, which could enable large-scale distribution. In the UK, Genincode continues to support the NHS’s 10-year prevention plan for heart disease, having delivered over 3,000 tests and identified hundreds of high-risk patients, although the company is pushing for faster adoption; in Europe, steady growth is being delivered across Spain, Italy, and Germany. Beyond cardiovascular, the company’s ROCA test for ovarian cancer surveillance has gained traction, with NHS trust adoption and international demand, marking it as the only globally approved test in this space, while ThromboInCode is due to launch in the UK and US within months, expanding the portfolio. Supported by a strong IP position, globally recognised publications, and harmonised AI-driven systems across the US, UK, and EU, Genincode is positioned to capitalise on its 17 years of development in polygenic testing, with upcoming landmark papers expected to reinforce its leadership in genetic risk assessment. Looking ahead, management emphasised revenue acceleration, margin expansion, and the medium-term objective of achieving breakeven, with growth underpinned by strategic partnerships, regulatory milestones, and international market expansion.