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Scancell Holdings (SCLP) investor relations material
Scancell Holdings H2 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Advanced melanoma Phase 3 trial of iSCIB1+ planned for Q4 2026, following FDA IND clearance and fast track designation and UK MHRA authorization.
Proposed Neuphoria merger and related financing could fund development plans, but completion depends on shareholder, regulatory and other conditions.
Financial highlights
FY2026 revenue was £nil vs £4.7m in FY2025; R&D expenses fell to £12.0m from £14.7m, mainly due to lower manufacturing costs.
Operating loss widened to £17.4m from £15.0m; net loss was £17.9m vs £12.3m, with no £1.8m convertible-note modification gain recorded in FY2026.
Cash and cash equivalents were £5.3m at 30 April 2026 vs £16.9m a year earlier; net cash used in operating activities was £10.8m.
Outlook and guidance
Phase 3 iSCIB1+ trial targeting ~550 patients with unresectable Stage IIIB or IV melanoma is expected to start in Q4 2026; further Phase 2 SCOPE PFS data expected in H1 2027.
A randomized neoadjuvant/adjuvant iSCIB1+ Phase 2 trial is intended for H1 2027, subject to financing and regulatory clearance.
Further ModiFY data for HNSCC and RCC are expected later in 2026.
- iSCIB1+ shows strong efficacy in advanced melanoma, with phase III and commercial expansion underway.SCLP
H.C. Wainwright 28th Annual Global Investment Conference - iSCIB1+ delivers robust efficacy in melanoma with a defined path to approval and major market potential.SCLP
Corporate presentation - Strong clinical progress and partnerships set up multiple value drivers and milestones for 2025.SCLP
Investor update - SCOPE study advances with strong early results as GlyMab spinout drives strategic momentum.SCLP
Status update - iSCIB1+ plus checkpoint inhibitors achieved 69% response and 69% PFS at 22 months in melanoma.SCLP
Study update - iSCIB1+ achieved 74% PFS at 16 months, surpassing standard care and supporting phase III plans.SCLP
Study update - Lead cancer vaccines deliver strong interim results; cash runway secured to H2 2026.SCLP
H1 2025 - iSCIB1+ shows robust melanoma efficacy, supporting pipeline growth and solid cash runway.SCLP
H2 2025 - iSCIB1+ achieved 74% PFS in melanoma; Phase 3 trial and key data readouts expected in 2026.SCLP
H1 2026
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