Scancell Holdings plc (AIM:SCLP)
London
· Delayed Price · Currency is GBP · Price in GBX | Market Cap | 142.69M |
| Revenue (ttm) | 4.71M |
| Net Income (ttm) | -5.51M |
| Shares Out | 1.04B |
| EPS (ttm) | -0.01 |
| PE Ratio | n/a |
| Forward PE | n/a |
| Dividend | n/a |
| Ex-Dividend Date | n/a |
| Volume | 7,534,440 |
| Average Volume | 1,325,117 |
| Open | 13.50 |
| Previous Close | 13.00 |
| Day's Range | 13.48 - 14.06 |
| 52-Week Range | 7.86 - 14.06 |
| Beta | 0.45 |
| RSI | 56.29 |
| Earnings Date | Jan 29, 2026 |
About Scancell Holdings
Scancell Holdings plc, a clinical stage biopharmaceutical company, discovers and develops of immunotherapies for the treatment of cancer in the United Kingdom. Its product candidates include SCIB1/iSCIB1+ that is in Phase II for the treatment of melanoma; and SC134, an antibody for the treatment of small cell lung cancer. It also develops Modi-1, an active peptide immunotherapy that is in phase II clinical trials for the treatment of solid tumors, including renal, head and neck, ovarian and triple negative breast cancers; and Modi-2, which targ... [Read more]
Financial Performance
Financial StatementsNews
Scancell Holdings Earnings Call Transcript: H1 2026
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.
Scancell announces FDA clearance of IND application for global Phase 3 trial of iSCIB1+ in advanced melanoma
Unlocks path towards registrational Phase 3 trial planned to start in 2026 Data from Phase 2 SCOPE trial show iSCIB1+ has potential to redefine standard of care (SoC) iSCIB1+ shows an interim 24%-poin...
Scancell Holdings Transcript: Study update
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.
Scancell Holdings Earnings Call Transcript: H2 2025
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.
Scancell reports Business Update and Financial Results for the Year Ended 30 April 2025
NOTTINGHAM, United Kingdom, Sept. 11, 2025 (GLOBE NEWSWIRE) -- Scancell Holdings plc (AIM: SCLP), the developer of ImmunoBody® and Moditope® active immunotherapies to treat cancer, today announces a b...
Scancell Holdings Transcript: Study update
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.
Scancell reports Phase 2 data showing strongly improved outcomes in Late-Stage Melanoma with its Immunobody® iSCIB1+
SCOPE trial of SCIB1/iSCIB1+ plus standard of care shows excellent results encompassing efficacy, durability, immune responses and safety
Scancell Holdings Transcript: Status update
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.
Scancell Holdings Transcript: Investor update
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.
Scancell Holdings Earnings Call Transcript: H1 2025
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.
Scancell Holdings Earnings Call Transcript: H1 2025
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.
PharmaJet and Scancell Sign Strategic Partnership Agreement for Development and Commercialization of a Needle-free DNA Vaccine for Advanced Melanoma
GOLDEN, Colo.--(BUSINESS WIRE)--PharmaJet and Scancell agreement builds on PharmaJet's strategy to be the best-in-class delivery system for novel DNA and RNA cancer immunotherapies.
PharmaJet Partner, Scancell, Announces Positive Data from the First Stage of its Phase 2 Trial of Advanced Melanoma DNA Vaccine delivered Needle-free
GOLDEN, Colo.--(BUSINESS WIRE)--Positive data announced for first stage of Phase 2 trial for advanced melanoma DNA vaccine delivered by the PharmaJet Stratis needle-free system.