Angle Regulatory News (AGL)

ANGLE plc

("ANGLE" or "the Company")

PATIENT DATA SHOWS "UNPRECEDENTED SENSITIVITY AND SPECIFICITY" FOR PARSORTIX OVARIAN CANCER CLINICAL APPLICATION

ANGLE plc (AIM: AGL OTCQX: ANPCY), the specialist medtech company, is delighted to announce that the Medical University of Vienna, one of its key opinion leaders, has reported highly convincing patient data in support of the use of ANGLE's Parsortix system in the detection of ovarian cancer.

The Medical University of Vienna will now lead, in collaboration with ANGLE, a clinical study of the use of the Parsortix system as a clinical application in the routine detection and treatment of ovarian cancer patients. The multi-centre clinical study will be in collaboration with other members of the European Network for Translational Research in Ovarian Cancer (EUTROC) and the Tumour Bank Ovarian Cancer Network (TOC) from Austria, Belgium, Germany and UK. It is expected to take 18 months to complete. Assuming the clinical study confirms the recent patient study results then ANGLE will be able to make clinical sales of the Parsortix system to help inform detection of ovarian cancer and clinical decision-making in its treatment.

The patient study was undertaken under ANGLE's collaboration agreement with the Ludwig Boltzmann Cluster 'Translational Oncology' led by the head of the interdisciplinary Molecular Oncology Group at the Medical University of Vienna, Professor Robert Zeillinger. The study utilised RNA markers developed in Vienna to analyse the cells harvested by ANGLE's Parsortix system.

The Vienna team has worked for many years with a wide range of CTC systems, both those commercially available from ANGLE's competitors and new technologies under development including commercial and academic systems. Due to lack of suitable cell surface markers, antibody-based systems are ineffective for ovarian cancer. The best result that has been obtained to date with other non-antibody based systems is a CTC detection sensitivity level of 24.5% (i.e. capturing CTCs from only one quarter of ovarian cancer patients).

Against this context, Dr Eva Obermayr, Principal Investigator at the Medical University of Vienna describes the results with ANGLE's Parsortix system as "sensational" and offering "unprecedented sensitivity and specificity". The results indicated a sensitivity of 90% for primary epithelial ovarian cancer at a specificity of 100%. Epithelial ovarian cancer (also known as ovarian carcinoma) is the most common ovarian cancer and accounts for some 90% of cases.

If these results are repeated in a prospective clinical study, Professor Zeillinger believes that ANGLE's Parsortix system together with the proprietary RNA marker panel could be adopted in clinical practice to help inform clinical decision-making for ovarian cancer patients in:

· Detection of cancer in high risk or genetically pre-disposed patients (detection)

· Monitoring therapy and selection of therapies in treatment of ovarian cancer patients (therapy monitoring)

· Monitoring of ovarian cancer patients in remission for early detection of relapse (remission monitoring)

ANGLE estimates that the ovarian cancer sales potential available for the Parsortix system in the European and United States markets would be in excess of £300 million per annum.

Annually 239,000 women are diagnosed with ovarian cancer worldwide. There is a high mortality rate and 152,000 die from it each year. Ovarian cancer is commonly known as the silent killer due to its lack of symptoms in its earlier stages. It is frequently diagnosed late in which case the UK five year survival rate is only 3.5% for Stage IV and 18.6% for Stage III at diagnosis (Source: Cancer Research UK Ovarian Cancer survival statistics). In contrast where it is diagnosed at Stage I, the UK five year survival rates are much higher at 90%. As a result there is an acute medical need for improved ovarian cancer detection.

Ovarian cancer surgery is highly complex and maximal tumour removal has a very strong impact on survival. Women with the diagnosis or a strong indication of ovarian cancer can be referred for surgery to specialists in gynaecologic oncology. The consequence is a significantly better outcome compared to the situation when surgery is performed by a general gynaecologist and cancer is diagnosed at this point. There would therefore be great clinical benefit if it were possible to know in advance of surgery if an abnormal pelvic mass is malignant.

A common approach is to use a blood test for the biomarker CA-125 for detection of epithelial ovarian cancer, either alone or in combination with another marker HE4. However the quoted sensitivity for CA-125 is only 63% (i.e. 37% of cancers are missed as false negatives) and as a result it is not considered effective.

Vermillion, a US Nasdaq listed company, has developed OVA1, an alternative epithelial ovarian cancer test that integrates biomarker measurement in blood and a software algorithm, which is FDA authorised and the company is now beginning to commercialise. The Medicare reimbursement level for OVA1 is $516. The company estimate that, in the United States alone, there are some 200,000 patients with abnormal pelvic masses where surgery is undertaken, which may be investigated with OVA1 (of which 22,000 will have ovarian cancer) suggesting a United States market for a specific segment of the larger detection market of in excess of $100m per annum. There is a substantially larger patient population in the United States of some 750,000 per annum if all abnormal pelvic masses are investigated. Vermillion quotes a sensitivity of 93% and specificity of 43% for OVA1 and indicates that this is a considerable improvement over CA-125.

If the clinical study confirms the patient data announced today then ANGLE's Parsortix system has the potential to substantially out-perform the current standard of care in ovarian cancer, particularly in relation to specificity (i.e. if a person does not have the disease how often will the test be negative).

The group at the Medical University of Vienna believes that the exceptionally good results with the Parsortix system are explained by the high purity of the Parsortix harvest (very low numbers of leukocytes) combined with the sensitivity of their RNA markers.

Professor Robert Zeillinger, Head of the Molecular Oncology Group at the Medical University of Vienna, commented:

"Using ANGLE's Parsortix system with a panel of ovarian carcinoma-specific RNA markers, we were able to detect and analyse CTCs in 90% of patient samples at a specificity of 100%. This is an unprecedented test performance and we will be immediately moving to a clinical study to validate the use of this system in the detection and treatment of ovarian cancer patients. We will also be preparing a high impact publication on these results for discussion with our colleagues in ovarian cancer worldwide."

ANGLE Founder and Chief Executive, Andrew Newland, commented:

"These are highly encouraging results for the use of the Parsortix system. There is a very strong medical need in ovarian cancer for earlier detection and monitoring of patients and we hope our Parsortix system will be able to really make a difference. Commercially ovarian cancer is a substantial but tightly defined market where there is little competition. It is an ideal first clinical market for ANGLE to progress. We will be focusing our resources to deliver this opportunity as quickly as possible. Today's announcement marks the start of ANGLE moving into the clinical phase."

For further information:

For Frequently Used Terms, please see the Company's website on http://www.angleplc.com/the-parsortix-system/glossary/

Notes for editors

About ANGLE plc www.angleplc.com

ANGLE is a specialist medtech company commercialising a disruptive platform technology that can capture cells circulating in blood, such as cancer cells, even when they are as rare in number as one cell in one billion blood cells, and harvest the cells for analysis.

ANGLE's cell separation technology is called the Parsortix system and it enables a liquid biopsy (simple blood test) to be used to provide the cells of interest. Parsortix is the subject of two granted US patents and three extensive families of patents being progressed worldwide. The system is based on a microfluidic device that captures cells based on a combination of their size and compressibility. The Parsortix system is established with strong positive evaluations from leading cancer research centres and is working with these cancer centres to demonstrate key applications. Parsortix has a CE Mark for Europe and FDA authorisation is in process for the US.

The analysis of the cells that can be harvested from patient blood with ANGLE's Parsortix system has the potential to help deliver personalised cancer care offering profound improvements in clinical and health economic outcomes in the treatment and diagnosis of various forms of cancer.

The increase in cancer to a 1 in 3 lifetime incidence is set to drive a multi $billion clinical market. The Parsortix system is designed to be compatible with existing major medtech analytical platforms and to act as a companion diagnostic for major pharma in helping to identify patients that will benefit from a particular drug and then monitoring the drug's effectiveness.

Now that the Parsortix system has been developed, ANGLE is focused on its commercialisation in the market.

ANGLE has established formal collaborations with world-class cancer centres and is working with these cancer centres to demonstrate key applications for its Parsortix non-invasive cancer diagnostic system as a liquid biopsy. Details are available here http://www.angleplc.com/the-company/collaborators/

As well as cancer, the Parsortix technology has the potential for deployment with several other important cell types in the future.

ANGLE began trading on the AIM market of the London Stock Exchange in March 2004 under the ticker symbol AGL. For further information please visit: www.angleplc.com.