Scancell Holdings Plc Update on SCOPE trial (0436A)
17 Januar 2024 - 2:46PM
UK Regulatory
TIDMSCLP
RNS Number : 0436A
Scancell Holdings Plc
17 January 2024
17 January 2024
This announcement contains inside information for the purposes
of Article 7 of the UK version of Regulation (EU) No 596/2014 which
is part of UK law by virtue of the European Union (Withdrawal) Act
2018, as amended ("MAR"). Upon the publication of this announcement
via a Regulatory Information Service, this inside information is
now considered to be in the public domain.
Scancell Holdings plc
("Scancell" or the "Company")
Update on SCOPE trial
MHRA approval to add a third cohort using iSCIB1+ to the SCOPE
trial
Scancell Holdings plc (AIM: SCLP), the developer of novel
immunotherapies for the treatment of cancer and infectious disease,
announces today that following further discussions with the
Medicines and Healthcare products Regulatory Agency (MHRA), it has
now received approval to add a third cohort to the SCOPE trial.
This cohort will recruit 43 advanced unresectable melanoma patients
who will receive i SCIB1 + with doublet therapy, consisting of
ipilimumab (Yervoy(R)) plus nivolumab (Opdivo(R)).
iSCIB1+ is a modified version of SCIB1 developed using
Scancell's AvidiMab(R) platform to enhance its potency compared to
SCIB1 and gives 15 years of extended patent protection. iSCIB1+
also includes additional melanoma-specific epitopes so it has the
potential to be effective in a broader patient population beyond
the 40% of patients with the tissue type treatable with SCIB1,
where treatment is HLA dependent.
Exceptional results from the first 13 patients receiving SCIB1
in the ongoing SCOPE trial, with an objective response rate of 85%,
indicate a high probability of success in this cohort which should
complete in Q2 2024. Recruitment into the iSCIB1+ cohort is
expected to be complete by the end of Q2 2024, with early data
expected in Q3 2024.
The results from these SCIB1 and iSCIB1+ cohorts, administered
in combination with doublet therapy, will enable the Company to
make a data-led decision regarding initiation of a randomised Phase
2/3 adapted registration programme in patients with unresectable
melanoma, which represents a potential $1.5 billion per annum
market. The Phase 2 part of the adapted trial is anticipated to
take 18 months, with the potential to generate attractive licensing
opportunities.
Prof Lindy Durrant, Chief Executive Officer, Scancell,
commented: "Thanks to the excellent work done by the Scancell team,
working hand in hand with a responsive MHRA, we are pleased to
report today that we have received approval to include a third
cohort of patients in the SCOPE trial who will now receive iSCIB1+
in combination with doublet checkpoints. We anticipate that iSCIB1+
will be as effective as SCIB1 and, with its potentially increased
potency and broader patient profile, make it a promising candidate
for registration studies. We look forward to providing further
updates on our progress given the extremely positive results to
date."
-ENDS-
For further information, please contact:
Scancell Holdings plc +44 (0) 20 3709 5700
Professor Lindy Durrant, CEO
Dr Jean-Michel Cosséry, Non-Executive Chairman
Stifel Nicolaus Europe Limited (Nominated Adviser
and Joint Broker) +44 (0) 20 7710 7600
Nicholas Moore/Samira Essebiyea/William Palmer-Brown
(Healthcare Investment Banking)
Nick Adams/Nick Harland (Corporate Broking)
WG Partners LLP (Joint Broker) +44 (0) 20 3705 9330
David Wilson/Claes Spang/Sathesh Nadarajah/Erland
Sternby
Panmure Gordon (UK) Limited (Joint Broker) +44 (0) 20 7886 2500
Freddy Crossley/Emma Earl (Corporate Finance)
Rupert Dearden (Corporate Broking)
ICR Consilium +44 (0) 20 3709 5700
Mary-Jane Elliott/Matthew Neal/Chris Welsh scancell@consilium-comms.com
About Scancell
Scancell is a clinical stage biopharmaceutical company that is
leveraging its proprietary research, built up over many years of
studying the human adaptive immune system, to generate novel
medicines to treat significant unmet needs in cancer and infectious
disease. The Company is building a pipeline of innovative products
by utilising its four technology platforms: Moditope (R) and
ImmunoBody (R) for vaccines and GlyMab(R) and AvidiMab (R) for
antibodies.
Adaptive immune responses include antibodies and T cells (CD4
and CD8), both of which can recognise damaged or infected cells. In
order to destroy such cancerous or infected cells, Scancell uses
either vaccines to induce immune responses or monoclonal antibodies
(mAbs) to redirect immune cells or drugs. The Company's unique
approach is that its innovative products target modifications of
proteins and lipids. For the vaccines (Moditope (R) and ImmunoBody
(R) ) this includes citrullination and homocitrullination of
proteins, whereas its mAb portfolio targets glycans or sugars that
are added onto proteins and / or lipids (GlyMab(R) ) or enhances
the potency of antibodies and their ability to directly kill tumour
cells (AvidiMab (R) ).
For further information about Scancell, please visit:
https://www.scancell.co.uk/
This announcement contains inside information for the purposes
of Article 7 of Regulation (EU) 596/2014 (MAR).
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