Angle PLC Announces Launch of PD-L1 Test to Support Cancer Studies
- The launch of the Portrait PD-L1 test by ANGLE plc has the potential to streamline patient selection and optimize PD-L1 monitoring for treatment response and disease progression throughout clinical studies.
- The test is designed to address the fundamental flaw in current PD-L1 tests via a simple blood test, providing accurate, repeatable, and precise results for CTC PD-L1 biomarker expression.
- The global PD-1 and PD-L1 immunotherapy market is currently valued at US $36.9 billion per annum, and analysts predict the market to reach US $109.1 billion by 2032.
- None.
ANGLE LAUNCHES PD-L1 TEST TO SUPPORT CANCER THERAPY STUDIES
ANGLE's Portrait PD-L1 test uses CTCs harvested from the Parsortix system to investigate real-time patient PD-L1 status for clinical studies
The test is designed for highly accurate, repeatable, and precise results for CTC PD-L1 biomarker expression
GUILDFORD, UK / ACCESSWIRE / November 9, 2023 / ANGLE plc (AIM:AGL)(OTCQX:ANPCY), a world-leading liquid biopsy company with innovative circulating tumour cell (CTC) diagnostic solutions for use in research, drug development and clinical oncology, is delighted to announce the launch of its Portrait® PD-L1 test for the evaluation of PD-L1 protein expression on CTCs following extensive development and optimisation. The test is provided as a service from ANGLE's Onc-ADaPT® GCP-compliant laboratories and is conducted by an expert team with over 10 years' experience in CTC analysis.
PD-L1 is an immune-related biomarker that can be expressed on the surface of tumour cells across a range of cancer types, and expression of this biomarker enables cancer cells to evade immune response mechanisms that would typically keep abnormal cell growth in check. Consequently, PD-1/PD-L1 inhibitors have emerged as the leading immunotherapy treatment option with over 2,800 active interventional studies in progress involving 430,000 patients.
The output of current tumour tissue-based PD-L1 tests varies considerably, with poor performance often unavoidable due to the elapsed time between tissue biopsy (generally taken at diagnosis and difficult or impossible to repeat) and disease progression (which may be months or years later) when immunotherapies are considered, during which time PD-L1 status can change. ANGLE has developed its immunofluorescence (IF) based test for the determination of PD-L1 status on CTCs to allow real-time assessment of biomarker status, which may address this fundamental flaw in current PD-L1 tests via a simple blood test.
ANGLE's Portrait PD-L1 service is an end-to-end solution using ANGLE's world leading Parsortix CTC technology to deliver:
· minimally invasive liquid biopsy with sample stability up to five days post-blood collection
· biomarker independent harvest of phenotypically diverse CTCs from a simple blood test
· identification and enumeration of CTCs with accurate, precise assessment of PD-L1 status (see https://angleplc.com/onc-adapt-laboratories/portrait-pd-l1/)
· longitudinal monitoring of PD-L1 status over multiple time points including before, during and after the patient receives the treatment.
It is well established that the number of CTCs is prognostic of cancer treatment response, recurrence, and relapse and this has been documented in numerous peer-reviewed publications. It is now evident that changes in CTC numbers and their PD-L1 status can provide an early indication of immunotherapy treatment resistance and progressive disease. Studies have also shown that CTCs isolated from patients with solid cancers and expressing PD-L1 may serve as a clinically actionable biomarker for immunotherapy.
The global PD-1 and PD-L1 immunotherapy market is currently valued at US
ANGLE Founder and Chief Executive, Andrew Newland, commented:
"Whilst immune checkpoint inhibitors have achieved remarkable progress in tumour treatment, the cost of treatment is high and currently the majority of patients fail to respond.
ANGLE's Portrait PD-L1 test provides accurate, repeatable, and precise PD-L1 identification on CTCs and hence has the potential to streamline patient selection and optimise PD-L1 monitoring for treatment response and disease progression throughout clinical studies.
We are now beginning an active promotion of this test to biopharma customers."
For further information:
ANGLE plc | +44 (0) 1483 343434 |
Andrew Newland, Chief Executive Ian Griffiths, Finance Director | |
Berenberg (NOMAD and Joint Broker) Toby Flaux, Ciaran Walsh, Milo Bonser | +44 (0) 20 3207 7800 |
Jefferies (Joint Broker) Thomas Bective, Shaam Vora, Alexander Ind | +44 (0) 20 7029 8000 |
FTI Consulting Simon Conway, Ciara Martin Matthew Ventimiglia (US) | +44 (0) 203 727 1000 +1 (212) 850 5624 |
For Research Use Only. Not for use in diagnostic procedures.
For Frequently Used Terms, please see the Company's website on https://angleplc.com/investor-relations/glossary/
Notes for editors
About ANGLE plc
ANGLE is a world-leading liquid biopsy company with innovative circulating tumour cell (CTC) diagnostic solutions for use in research, drug development and clinical oncology using a simple blood sample. ANGLE's FDA cleared and patent protected circulating tumour cell (CTC) harvesting technology known as the Parsortix® PC1 System enables complete downstream analysis of the sample including whole cell imaging and proteomic analysis and full genomic and transcriptomic molecular analysis.
ANGLE's commercial businesses are focusing on diagnostic products and clinical services. Diagnostic products include the Parsortix® system and associated consumables. The clinical services business is offered through ANGLE's GCP-compliant laboratories. Services include custom made assay development and clinical trial testing for pharma.
Over 80 peer-reviewed publications have demonstrated the performance of the Parsortix system. For more information, visit www.angleplc.com
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SOURCE: ANGLE plc
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