Interim Results

Syntopix Group plc 19 April 2007 For immediate release 19 April 2007 SYNTOPIX GROUP PLC ('Syntopix' or 'the Group') Interim results for the six months ended 31 January 2007 Syntopix Group plc, the company focused on the discovery and development of drugs for the topical treatment of dermatological diseases, today announces its interim results for the six months ended 31 January 2007. Operational highlights Good progress with lead candidate development programme: • MHRA approval to conduct first Phase I clinical trial; • Clinical Research Organisation appointed; and • Formulations of other compounds initiated for further human use studies. Continued development of the pipeline: • Compound library now contains over 1,000 compounds for screening; and • Growing patent portfolio which is continually being evaluated. Financial highlights • Cash balance at 31 January 2007 of £2.5m (31 January 2006 - £323,000); • Tight overhead cost control; and • Development programme costs in line with budget. Commenting on today's announcement, Dr Rod Adams, Chairman, said: 'I am delighted to report that significant progress in the first half in the development of our pipeline has produced real momentum in our business in the current half. We have successfully made the transition from a preclinical to a clinical stage company and look forward to reporting on further progress with our pipeline in due course.' ENDS For further information please contact: Syntopix Group plc 0845 125 9204 Stephen Jones, Chief Executive Officer Darren Bamforth, Group Finance Director KBC Peel Hunt Ltd 020 7418 8900 Megan MacIntyre Buchanan Communications 020 7466 5000 Mark Court/Mary-Jane Johnson/Catherine Breen Joint statement from the Chairman and Chief Executive Officer We are pleased to report the interim result for the six months to 31 January 2007. Since our last annual report, we have refined our licensing strategy and now believe that Phase I clinical data, not Phase II, should provide sufficient interest to our potential licensing partners. This approach has been validated in discussions with two large multinational dermatological companies. Our modified strategy has several benefits, most notably that we can screen more compounds faster in human use studies, to the extent that we are now six months ahead of our original schedule. Therefore, we plan to enter potential licensing discussions earlier than originally planned. Lead candidate development programme In January 2007 we announced that the Group had entered into an agreement with a Clinical Research Organisation in preparation for the start of the Group's first Phase I clinical trial. We received approval in February 2007 from an independent Ethics Committee to conduct our first Phase I clinical study which is due to start imminently. We have developed formulations which will be used in the trials to determine the ability of SYN 0017 (an antioxidant present in foods and cosmetics), SYN 0401 (an antifungal present in personal healthcare products), and a combination of SYN 0017 and SYN 0016 (an oxidising agent present in pharmaceutical preparations) to inhibit Propionibacterium acnes (P. acnes) when applied to healthy volunteers. In addition to the Phase I clinical trial, we are also intending to conduct a second human use study. Formulations of SYN 0126 (a compound currently used in a wide variety of cosmetic preparations), and a combination of SYN 0126 with SYN 0091(a bacteriostatic agent used in soap and cosmetics) are being prepared for this study to start in the third quarter of 2007, with results in the fourth quarter. Another human use study this year will start in the fourth quarter of 2007, and is likely to be a Phase I clinical study. The compounds to be tested will depend in some part on the results of the first study, but it is intended to test at least one new compound in this study. By the end of 2007 the Group will have completed several human use studies, and it is our intention to seek licensing partners for any compound(s) which show a positive outcome in a human use study. Over the past six months we have generated significant interest in these studies, and we believe a licensing agreement will follow a successful outcome. Pipeline The Group continues its research activities to generate further potential synergistic combinations. We are screening combinations of compounds, and now have over 1,000 in our library. Approximately 30% of these show sufficient antimicrobial activity against P. acnes and/or Staphylococcus aureus to indicate suitability for topical use. Our intellectual property portfolio continues to grow: Syntopix has a patent portfolio that currently comprises nine patent applications. Each application is continually re-evaluated for commercial relevance, and in the last twelve months we have filed a new application every six to eight weeks. Financial summary During the six months to 31 January 2007 the Group's focus has been the continuation of our lead candidate development programme through pre-clinical development and into clinical trials, with the intention of achieving future revenue streams through milestone payments and licensing deals with third parties. The development programme is proceeding in line with our expectations and the expenditure of £491,000 on Research and Development activity for the six months ended 31 January 2007 is within our budget. During the period the Group received European grant income of £20,000 which has mitigated some of the costs of maintaining our patent portfolio, and we anticipate further grant receipts during the forthcoming months. Additionally the Group has benefited from the receipt of R&D tax credits which has reduced the overall expenditure on our programme. Administrative overheads are running at a comparable rate to those incurred in the year ended 31 July 2006 and are closely controlled. The Group benefits from its association with the University of Bradford and the purpose built microbiology laboratory facilities at the University's Institute of Pharmaceutical Innovation are provided to Syntopix at significantly reduced rates. Cash balances at 31 January 2007 were £2,501,993 (31 January 2006 : £323,396). The Group's financial strategy continues to be to monitor costs carefully during the period until licensing deals can be achieved and revenues can begin to be generated. The Group periodically conducts small research consultancy projects, and whilst not significant in the period ended 31 January 2007, a number of revenue generating projects are currently in progress. This is the first period in which we are required to comply with FRS 20 - 'Share Based Payments'. Under this accounting standard we are required to calculate the fair value of share options issued. This means that the loss for the six months to 31 January 2007 has been increased by £52,546 (six months to 31 January 2006: loss increased by £410) and the loss for the year ended 31 July 2006 has been increased by £16,832. Outlook We are very pleased with progress to date. Preparatory work undertaken since the flotation and during the first half of the year has delivered real momentum in the business and we look forward to the future with confidence. Dr Rod Adams Dr Stephen Jones Chairman Chief Executive Officer 18 April 2007 18 April 2007 Consolidated profit and loss account for the six months ended 31 January 2007 Six months Six months Year ended ended ended 31 January 31 January 31 July 2007 2006 2006 Restated Restated £ £ £ TURNOVER 2,500 16,800 31,914 Research and development costs (490,763) (169,078) (493,645) Administrative expenses (356,355) (130,331) (608,982) Other operating income 20,000 2,949 2,949 OPERATING LOSS (824,618) (279,660) (1,067,764) Interest receivable 55,123 6,796 53,993 Interest payable (937) (17) (76) LOSS ON ORDINARY ACTIVITIES BEFORE TAXATION (770,432) (272,881) (1,013,847) Taxation 92,207 35,352 86,169 LOSS FOR THE FINANCIAL PERIOD (678,225) (237,529) (927,678) LOSS PER SHARE Basic and diluted (11.9p) (8.8p) (22.0p) All Group activities relate to continuing operations. Statement of total recognised gains and losses £ £ £ Loss for the period (678,225) (237,529) (927,678) Total recognised gains and losses relating to the period (678,225) (237,529) (927,678) Prior year adjustment (see note 2) (16,832) - - Total recognised gains and losses since the last annual report (695,057) (237,529) (927,678) Consolidated balance sheet as at 31 January 2007 31 January 31 January 31 July 2007 2006 2006 Restated Restated £ £ £ FIXED ASSETS Tangible assets 117,470 102,702 121,041 CURRENT ASSETS Debtors 179,368 73,668 123,976 Cash at bank and in hand 2,501,993 323,396 3,247,430 2,681,361 397,064 3,371,406 CREDITORS: Amounts falling due within one year (162,556) (172,669) (230,493) NET CURRENT ASSETS 2,518,805 224,395 3,140,913 NET ASSETS 2,636,275 327,097 3,261,954 CAPITAL AND RESERVES Called up share capital 568,398 286,984 568,398 Share premium account 3,379,046 - 3,379,046 Merger reserve 337,935 389,811 337,935 Profit and loss account (1,649,104) (349,696) (1,023,425) EQUITY SHAREHOLDERS' FUNDS 2,636,275 327,097 3,261,954 Consolidated cash flow statement for the six months ended 31 January 2007 Six months Six months Year ended ended ended 31 January 31 January 31 July 2007 2006 2006 Restated Restated £ £ £ Cash outflow from operating activities (873,431) (240,566) (878,390) Returns on investments and servicing of finance 54,186 6,779 53,917 Taxation 86,168 - - Capital expenditure and financial investment (12,360) (109,583) (141,346) CASH OUTFLOW BEFORE FINANCING (745,437) (343,370) (965,819) Financing - 21,343 3,567,826 (DECREASE)/INCREASE IN CASH IN THE PERIOD (745,437) (322,027) 2,602,007 Reconciliation of net cash flow to movement in net funds for the six months ended 31 January 2007 Six months Six months Year ended ended ended 31 January 31 January 31 July 2007 2006 2006 Restated Restated £ £ £ (Decrease)/increase in cash in the period (745,437) (322,027) 2,602,007 Cash outflow from decrease in debt financing - - 62,101 MOVEMENT IN NET FUNDS IN THE PERIOD (745,437) (322,027) 2,664,108 NET FUNDS AT THE BEGINNING OF THE PERIOD 3,247,430 583,322 583,322 NET FUNDS AT THE END OF THE PERIOD 2,501,993 261,295 3,247,430 Reconciliation of operating loss to operating cash flows for the six months ended 31 January 2007 Six months Six months Year ended ended ended 31 January 31 January 31 July 2007 2006 2006 Restated Restated £ £ £ Operating loss (824,618) (279,660) (1,067,764) Depreciation 15,931 6,881 20,305 Share option expense 52,546 410 16,832 (Increase) in debtors (49,354) (31,166) (30,657) (Decrease)/increase in creditors (67,936) 62,969 182,894 Net cash outflow from operating activities (873,431) (240,566) (878,390) Notes to the consolidated interim financial statements 1 The interim financial statements have been prepared in accordance with UK GAAP, using accounting policies and practices consistent with those applied in the 2006 annual reports and accounts with the exception of the application of FRS 20 (see below). The interim statements have neither been reviewed nor audited by the Group's auditors. The financial information contained in this report does not constitute statutory accounts as defined by Section 240 of the Companies Act 1985. The figures for the year ended 31 July 2006 have been extracted from the statutory accounts which have been filed with the Registrar of Companies but have been restated for the impact of FRS 20. The auditors' report for the 2006 accounts was unqualified and did not contain a statement under s237 (2) or (3) of the Companies Act 1985. 2 The adoption of FRS20 - Share Based Payments requires a prior period adjustment to be made. This has reduced retained profits for the year ended 31 July 2006 by £16,832 but has no effect on net assets at that date. FRS 20 is effective for accounting periods beginning on or after 1 January 2006 and must be applied retrospectively to equity settled awards that were granted after 7 November 2002 and had not vested by 1 January 2006. 3 The interim results were approved by the Board of Directors on 18 April 2007. 4 Copies of this interim report are available on the Group's website ' www.syntopix.com' and upon application to Syntopix Group plc, Institute of Pharmaceutical Innovation, University of Bradford, Bradford, BD7 1DP. 5 The calculation of basic and diluted loss per share is based upon the loss after tax divided by the weighted average number of shares in issue during the period. Due to the losses incurred there is no dilutive effect from the issue of share options. Weighted (Loss) average number EPS Basic and diluted loss per share £ of shares (pence) Six months ended 31 January 2007 (678,225) 5,683,981 (11.9) Six months ended 31 January 2006 (237,529) 2,698,544 (8.8) 12 months ended 31 July 2006 (927,678) 4,211,384 (22.0) J D Bamforth Secretary 18 April 2007 This information is provided by RNS The company news service from the London Stock Exchange

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