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New Programme

21 Jul 2005 07:00

VASTox plc21 July 2005 For immediate release 21 July 2005 VASTox plc ("VASTox" or "the Company") Initiation of a new proprietary programme Oxford, UK: 21 July 2005 - VASTox plc (AIM: VOX), the drug discovery andservices business, is pleased to announce today that it has initiated a new drugdiscovery programme focused on the treatment of Spinal Muscular Atrophy (SMA), agenetic neuromuscular disease. This is VASTox's third proprietary programmealongside Duchenne Muscular Dystrophy and Tuberculosis. SMA affects 50,000 people worldwide and is a degenerative disease causing lossof motor neurons in the spinal cord resulting in muscle atrophy. There arevarious forms of the disease with onset from infancy to adulthood. SMA is themost severe genetic disease in children under the age of two and there iscurrently no cure or adequate treatment for the condition. VASTox has unique and unparalleled expertise in this disease area through itsscientific founders and scientific advisory board. Professor Kay Davies CBE,FRS, and Dr Marcel van den Heuvel are both leading authorities on neuromusculardiseases working out of the Medical Research Council Functional Genetics Unit,University of Oxford. Professor Kay Davies is a scientific founder of VASTox, and Dr van den Heuveljoined the company's scientific advisory board in March 2005. Dr van den Heuvelis recognised as an expert on SMA having dedicated his research to the area forthe last four years. Utilising its in-house synergy between chemistry and biology the company isdeveloping a chemical genomic screen using Drosophila flies based on Dr van denHeuvel's research. This screen will be used to identify promising compoundsfrom VASTox's proprietary neuromuscular chemical library and advance these intonovel drugs to treat SMA. Dr Steven Lee, CEO of VASTox, said: "Initiation of this programme marks an exciting milestone for VASTox because thescientific rationale predominantly comes not from one of the original foundingscientists but from a scientific advisor who was recruited post-IPO. VASTox isbuilding on our expertise in Duchenne Muscular Dystrophy, confirming ourcommitment to finding cures for neuromuscular diseases. By leveraging ourgenomics platform, our world-leading academic advisors, and our chemistryskills, we have an opportunity to make significant progress in treating thisdisease - for the benefit of patients." For more information please contact: VASTox plcSteven Lee, Chief Executive Officer 01235 443 901 07766 913 898 Buchanan CommunicationsMark Court / Mary-Jane Johnson 020 7466 5000 Notes for Editors: About VASTox plc VASTox is a chemical genomics technology company that provides services to thepharmaceutical industry and discovers and develops proprietary novel drugs. Thecompany's technology platform aims to use high volume, high content screeningusing zebrafish and fruitflies to provide a high level of predictability of theefficacy and toxicity of potential drug compounds in humans which has thepotential to dramatically decrease the time and cost of drug discovery anddevelopment. VASTox was formed in January 2003, from the University of Oxford,by some of the UK's foremost scientists who have taken a highly creativeapproach to the problems involved in drug discovery and who have a proven recordin delivering technological excellence. The company listed on the London StockExchange AIM in October 2004. About Spinal Muscular Atrophy (SMA) Spinal Muscular Atrophy affects 50,000 people worldwide and is a degenerativedisease causing loss of motor neurons in the spinal cord resulting in muscleatrophy. Patients progressively lose the ability to walk, sit and, eventually,move. The most severe form, known as type I, reduces life expectancy to lessthan two years. SMA is a genetic disease caused by a defect in a single gene(SMN1). SMN protein is critical to the survival and health of motor neurons.Without this protein, nerve cells atrophy, shrink and eventually die, resultingin the observed muscle weakness. This information is provided by RNS The company news service from the London Stock Exchange
Date   Source Headline
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11th Feb 202010:00 amGNWAIM Delisting Reminder
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27th Jan 20207:00 amGNWExercise of Restricted Stock Units
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20th Jan 20202:15 pmGNWHolding(s) in Company
20th Jan 20202:15 pmGNWHolding(s) in Company
15th Jan 202012:15 pmGNWNotification of Transactions of Persons Discharging Managerial Responsibilities
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31st Dec 20199:00 amGNWHolding(s) in Company
30th Dec 20197:00 amGNWHolding(s) in Company
24th Dec 20198:30 amGNWCompletion of $50 million Fundraising and Directorate Change
24th Dec 20197:01 amGNWAward of Share Options
24th Dec 20197:00 amGNWExercise of Restricted Stock Units
23rd Dec 201912:00 pmGNWResult of General Meeting
19th Dec 20197:00 amGNWTimetable Update
17th Dec 201912:00 pmGNWSummit Therapeutics Reports Financial Results and Operational Progress for the Third Quarter and Nine Months Ended 31 October 2019
16th Dec 20192:15 pmGNWNotice of Q3 Results
6th Dec 201912:00 pmGNWSummit Announces a Proposed Subscription and Placing to Raise approximately $50.0 Million and Notice of General Meeting
6th Nov 201912:00 pmGNWSummit Therapeutics to Participate in Panel Sessions at the World Antimicrobial Resistance Congress
4th Nov 201912:00 pmGNWSummit Therapeutics Recognises C. difficile Awareness Month
16th Oct 201912:00 pmGNWSummit Therapeutics to Present at the 2019 BIO Investor Forum
11th Oct 201912:01 pmGNWDirectorate change
11th Oct 201912:00 pmGNWHalf-year report
10th Oct 20192:30 pmGNWNotice of Results
7th Oct 201912:00 pmGNWSummit Therapeutics Reports New Data from Phase 2 Clinical Trial Connecting Ridinilazole’s Microbiome Preservation to Improved Clinical Outcomes for Patients with C. difficile Infection
3rd Oct 201912:00 pmGNWSummit Therapeutics Reports Ridinilazole Significantly Improved Short and Longer-Term Quality of Life Measures in Patients with C. difficile Infection Compared to Standard of Care
3rd Oct 20197:00 amGNWBlock Listing Six Month Review
1st Oct 20192:05 pmRNSSecond Price Monitoring Extn
1st Oct 20192:00 pmRNSPrice Monitoring Extension
25th Sep 201912:00 pmGNWSummit Therapeutics to Host R&D Day 7 October 2019
24th Sep 201912:00 pmGNWSummit Therapeutics to Present Data from Phase 2 Clinical Trial of Ridinilazole at ID Week 2019
18th Sep 20197:00 amGNWSummit Announces Publication of Editorial in Future Microbiology Advocating for Innovation in Antibiotic Development to Drive Stewardship Focus on Improving Patient Outcomes
5th Sep 201912:00 pmGNWSummit Presented In Vivo Proof of Concept Data for Targeted Enterobacteriaceae Antibiotics at ASM/ESCMID Conference
4th Sep 201912:00 pmGNWSummit Therapeutics to Participate in Upcoming Investor Conferences
1st Aug 201912:00 pmGNWSummit Therapeutics to Present at the Canaccord Genuity Growth Conference
17th Jul 201912:00 pmGNWSummit Highlighted Potential of SMT-571 to Combat the Rising Global Health Threat of Gonorrhoea at STI & HIV World Congress
9th Jul 201912:00 pmGNWSummit’s DDS-04 Enterobacteriaceae Programme Demonstrates In Vivo Efficacy in Sepsis and Pneumonia
20th Jun 201912:00 pmGNWSummit to Present on Pipeline and Strategy for its New Classes of Antibiotics at ASM Microbe 2019
19th Jun 201912:00 pmGNWResult of AGM
18th Jun 201912:00 pmGNWIncreased BARDA Award and Option Exercise
12th Jun 201912:00 pmGNWSummit Therapeutics Reports Financial Results and Operational Progress for the First Quarter Ended 30 April 2019
5th Jun 20192:00 pmGNWNotice of First Quarter Results
14th May 20195:30 pmGNWUK Annual Report and Notice of AGM
29th Apr 201912:30 pmGNWBlock Listing Interim Review
24th Apr 20194:20 pmGNWExercise of Restricted Stock Units
15th Apr 20197:00 amGNWSummit Presents In Vivo Proof of Concept Data for New Mechanism Antibiotics Targeting Enterobacteriaceae in Oral Session at ECCMID 2019

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