Scancell Holdings plc, („Scancell‟ or the „Company‟) the developer of novel immunotherapies for the
treatment of cancer, was informed on 11 July 2013 that one of the three patients recruited into the higher 8mg dose study of SCIB1 will no longer be eligible for evaluation due to delivery of an incomplete dose of SCIB1 following a fault with the electroporation device for that patient. Scancell will recruit a replacement patient as soon as possible in order to complete the initial phase of the 8mg study which is to assess the safety and immune response produced by the 8mg dose prior to expanding the study to include a further ten patients as planned. The initial part of the study is now expected to be completed early next year.
The higher 8mg dose SCIB1 study has been implemented for two reasons:
Richard Goodfellow, Joint CEO of Scancell, said:
“With the higher dose study underway, we are now looking to recruit a new patient to ensure adequate
safety and immune response data ahead of the extended trial of SCIB1 in patients with tumour load. We
firmly believe that the data we gain from this additional trial will add further value to SCIB1 and the
ImmunoBody® platform and look forward to reporting the results in due course.”
For Further Information:
Scancell Holdings Plc
Dr Richard Goodfellow, Joint CEO
Professor Lindy Durrant, Joint CEO
+ 44 (0) 74 2323 0 497
Cenkos Securities: +44 (0) 20 7397 8900
FTI Consulting +44 (0) 20 7831 3113
Scancell is developing novel immunotherapies for the treatment of cancer based on its ImmunoBody®
and Moditope™ technology platforms. Scancell‟s first ImmunoBody®, SCIB1 is being developed for the
treatment of melanoma and is in Phase 1/2 clinical trials. Preliminary evidence from Part 1 of the study
showing that SCIB1 produced an immune response which might be associated with clinical benefit in
patients with malignant melanoma was released in December 2012.
Scancell‟s ImmunoBody® vaccines target dendritic cells and stimulate both parts of the cellular immune
system; the helper cell system where inflammation is stimulated at the tumour site; and the cytotoxic Tlymphocyte or CTL response where immune system cells are primed to recognise and kill specific cells.
Scancell has also identified and patented a series of modified epitopes that stimulate the production of
killer CD4 T cells that destroy tumours without toxicity. The Directors believe that the Moditope™ platform could play a major role in the development of safe and effective cancer immunotherapies in the future.
Holloway says generating clinical data's a big focus for them in the near-term.
''Over the next two years we expect to see clinical readouts from two of our programmes - SCIB1 and Modi-1''.
''We'll be extending our pipeline particularly around Moditope with the Modi-3 programme, if we're successful with the grand challenge''.
''Then it's around looking at technical partnerships that will allow us to de-risk our developments''.
Thu, 15 Feb 2018 12:38:00
Dutch group ISA Pharmaceutical will incorporate its Amplivant technology into Modi-1, the first cancer treatment candidate being developed on the platform
Thu, 15 Feb 2018 15:00:00
Immuno-therapy SCIB1, which is expected to progress into Phase II clinical trials in the second-half of the year, was the focus of a peer-reviewed paper in OncoImmunology
Mon, 12 Feb 2018 11:50:00