London · Delayed Price · Currency is GBP · Price in GBX Scancell Holdings Earnings Call Transcripts
Fiscal Year 2026
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Lead asset iSCIB1+ achieved 74% PFS at 16 months in melanoma, with FDA phase III clearance and strong patent protection. Cash runway extends into H2 2026, with multiple financing and partnering options under evaluation. Blockbuster market potential and diversified pipeline support long-term growth.
Fiscal Year 2025
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Phase II SCOPE study of iSCIB1+ in advanced melanoma showed a 74% PFS at 16 months and strong disease control, with favorable safety and robust T cell responses. Regulatory agencies support phase III plans, and commercialization is targeted for late 2029.
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Strong clinical results for iSCIB1+ in advanced melanoma and robust financial position support late-stage development, with regulatory and partnership discussions underway. Cash runway extends into 2026, and milestone payments from Genmab are anticipated within 12 months.
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Phase II data for iSCIB1+ in advanced melanoma showed a 68.6% response rate and 69% PFS at 22 months, outperforming standard of care by 20%. Safety was excellent, and a biomarker enables precise patient selection for phase III. Strong commercial and regulatory prospects highlighted.
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Significant progress continues in clinical and corporate strategy, with SCOPE study data on track for July and year-end, and the launch of GlyMab Therapeutics to unlock antibody portfolio value. Financial position is strong, with ongoing partnerships and regulatory planning supporting future growth.
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Lead immunotherapy and antibody assets are advancing with strong clinical data, strategic partnerships, and a robust financial position. Multiple value inflection points are expected in 2025, with regulatory and partnering strategies in place to maximize shareholder value.
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Strong clinical efficacy and safety data in melanoma and head and neck cancer, new licensing and financing deals, and a robust cash position support continued development and business development activities through 2026.
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SCOPE and ModiFY studies show strong clinical progress, with SCOPE achieving 80% disease control and 72% tumor reduction in late-stage melanoma. Recent £11.3M financing extends cash runway into 2026, supporting multiple data readouts in 2025.