10 October
Avacta Group plc
("Avacta" or "the Group" or "the Company")
Avacta to Unveil Pipeline Expansion and Novel, Next-Generational Targeted Cancer Therapy Programs at 2024 EORTC-NCI-AACR Symposium
LONDON, UK, 10 OCT 2024, Avacta Group plc (AIM: AVCT), a life sciences company developing innovative, targeted cancer treatments, today announced that the Company will present new preclinical data on two breakthroughs in the pre|CISION platform in poster sessions at the 2024 EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics in Barcelona, Spain from 23-25 October 2024. Together, the presentations advance the utility of our pre|CISION drug delivery platform technology, which delivers highly potent warheads directly to the tumor microenvironment while minimizing exposure in normal tissues, thus allowing dosing to be optimized to deliver the best outcomes for patients.
The first advance in the pre|CISION platform is the design and preclinical analysis of the Company's newest development candidate, AVA6103, a novel, potent peptide drug conjugate (PDC) that FAP-enables the most potent Topoisomerase I inhibitor in clinical testing, via the pre|CISION technology with tumor-specific delivery of the warhead to induce DNA damage and drive cancer cell death. AVA6103 is a Generation Two pre|CISION PDC in the Avacta pipeline.
The second advance in the pre|CISION platform is the first description of a novel class of engineered biotherapeutics, called Affirmer® Drug Conjugates, that are dual-targeting and have the potential to offer a delivery mechanism with greater specificity than the PDC, thus potentially unlocking the patient populations with low expression of FAP in the tumor. This program is a Generation Three pre|CISION medicine and utilizes the same release mechanism in the pre|CISION platform. Based on this, the Affimer drug conjugates have the potential to not only increase the specificity of delivery but to also minimize systemic exposure to the warhead.
AVA6103: FAP-enabled PDC Targeting Topoisomerase I to the Tumor Microenvironment
Avacta discovered AVA6103 using its pre|CISION platform technology and structure-based drug design. AVA6103 incorporates a dipeptide that is specifically cleaved by Fibroblast Activation Protein a (FAP), which is overexpressed on the surface of cancer associated fibroblasts. AVA6103 consists of a highly potent Topoisomerase I warhead that is covalently linked to a dipeptide containing a cleaving sequence susceptible to hydrolysis by FAP, but which is resistant to hydrolysis by mammalian peptidases. The high selectivity of the pre|CISION substrate to FAP results in release of the topoisomerase inhibitor warhead only in the tumor microenvironment, which could potentially reduce systemic exposure and enable greater tolerability. Avacta will present in vivo data that demonstrates the ability to target and accumulate the active warhead in the tumor microenvironment, resulting in tumor growth inhibition with AVA6103.
Details of the poster are as follows:
- Abstract Title: The novel peptide drug conjugate AVA6103 is a FAP-enabled pre|CISION medicine which targets Topoisomerase I to the tumor microenvironment via FAP cleavage
- Session Title: Antibody Drug Conjugate Therapeutics
- Session Date: October 24, 2024
Affirmer® Drug Conjugates: New Class of Engineered Biotherapeutics Targeting FAP to Deliver Powerful Warheads to the Tumor Microenvironment
Avacta has created Affimer® Drug Conjugates (AFFDCs) as a novel class of engineering biotherapeutics that incorporate a topoisomerase inhibitor for delivery specifically in the tumor microenvironment. AFFDCs are designed with several key advantages over monoclonal antibodies, including significant smaller size, tumor penetration, tunable binding affinity to specific cancer targets and the ability to be dimerized. Avacta will present data supporting that exposure of tumor cell line or fibroblast cell co-cultures to AFFDCs results in drug cleavage, release of the warhead and tumor cell kill as a bystander function.
Details of the poster presentations are as follows:
- Abstract Title: Affimer® Drug Conjugates targeting Fibroblast Activation Protein a deliver highly toxic warheads to the tumor microenvironment by leveraging the pre|CISION release mechanism
- Session Title: Antibody Drug Conjugate Therapeutics
- Session Date and Time: October 24, 2024
-Ends-
For further information from Avacta Group plc, please contact:
| Avacta Group plc Michael Vinegrad, Group Communications Director | Tel: +44 (0) 1904 21 7070 https://avacta.com/ (https://avacta.com/) |
| Peel Hunt (Nomad and Broker) James Steel / Chris Golden / Patrick Birkholm | www.peelhunt.com (http://www.peelhunt.com/) |
| ICR Consilium Mary-Jane Elliott / Jessica Hodgson / Sukaina Virji | avacta@consilium-comms.com (mailto:avacta@consilium-comms.com) |
About Avacta Group plc - https://avacta.com/
Avacta Group is a UK-based life sciences company focused on improving healthcare outcomes through targeted cancer treatments and diagnostics.
Avacta Therapeutics: a clinical stage oncology biotech division that is harnessing the proprietary pre|CISION platform technology to develop novel, highly targeted cancer drugs.
The pre|CISION platform is a highly specific substrate for fibroblast activation protein (FAP) which is upregulated in most solid tumors compared with healthy tissues. The pre|CISION platform harnesses this tumor specific protease to cleave pre|CISION peptide drug conjugates and pre|CISION antibody/Affimer® drug conjugates in the tumor microenvironment, thus releasing active payload in the tumor and reducing systemic exposure and toxicity, allowing dosing to be optimized to deliver the best outcomes for patients.
The lead pre|CISION program AVA6000, a peptide drug conjugate form of doxorubicin, is in Phase 1 studies. It has shown an improvement in safety and tolerability in clinical trials to date compared with standard doxorubicin and preliminary signs of clinical activity in multiple patients.
Avacta Diagnostics focuses on supporting healthcare professionals and broadening access to diagnostics.
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