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Start of phase II trial

5 Jul 2006 07:00

Immupharma PLC05 July 2006 For Immediate Release 5 July 2006 ImmuPharma IPP- 201101 treatment for Lupus enters Phase II - First patients dosed - - Results expected before end of 2006 - ImmuPharma PLC (LSE:IMM), the specialist drug discovery and development company,announced today that its IPP-201101 treatment for Lupus, a chronic,life-threatening autoimmune disease, has entered into Phase II clinical trials.The first group of Lupus patients in the study have already been given the drug. This European Phase II study in Lupus patients is a proof of concept, doseranging, safety and efficacy study. The efficacy will be assessed usingappropriate surrogate markers that are involved in the disease and biomarkersrelated to mechanism of action of IPP-201101. Results from this short durationstudy, expected by year end, will be of great value in preparation of pivotalPhase III studies. This follows on from the announcement in May of the successful completion of aplacebo-controlled phase I study involving 24 healthy volunteers to assess itssafety and tolerability. The preliminary safety report confirmed that the drugwas safe and well-tolerated. Commenting on the announcement, Dimitri Dimitriou, Chief Executive Officer,said: "We are delighted to have continued our progress. Entering phase II withour lead drug candidate for Lupus marks an exciting time for the company, makingImmuPharma and its assets attractive for potential corporate deals with majorpharmaceutical and biotech companies." Richard Warr, Executive Chairman, added: "We believe IPP-201101 has blockbuster potential but more importantly, combinedwith very low marketing costs and low cost of goods, makes it an attractivecandidate for licensing. The interest we have seen to-date from big pharmacompanies is encouraging." For further information please contact: ImmuPharma PLC: TelephoneRichard Warr, Executive Chairman: +44 20 7152 4080Dimitri Dimitriou, Chief Executive Officer: +44 20 7152 4080Dr Robert Zimmer, President & Chief Scientific Officer: +33 389 32 76 50 Buchanan Communications:Lisa Baderoon: + 44 20 7466 5000Rebecca Skye Dietrich : + 44 20 7466 5000 Notes to Editors: About ImmuPharma ImmuPharma PLC is a drug discovery and development company headquartered inLondon, UK and quoted on AIM of the London Stock Exchange (LSE:IMM). It hasresearch operations in France (ImmuPharma (France) SA) and Switzerland(ImmuPharma AG). ImmuPharma is dedicated to the development of novel drugs,largely based on peptide therapeutics, to treat serious medical conditions suchas autoimmune diseases characterised by: o blockbuster potential in niche markets o low promotional costs in few specialised physicians and centres and o lower risk of drug development and lower development costs ImmuPharma is a currently developing drug candidates for three different medicalconditions, each of which would represent a significant breakthrough in itsfield. The furthest advanced drug candidate targets Lupus, a disease for whichthere is currently no cure or specific treatment. The other two address moderateto severe pain (such as that experienced by cancer sufferers and post-operativepatients), and MRSA and similar severe hospital-acquired resistant infections. All three have significant sales potential as well as low marketing costs and arelatively low risk of development failure. One or more have the potential to befast-tracked by the US Food and Drug Administration according to "Guidance forIndustry: Fast Track Drug Development Programs - Designation, Development andApplication Review" issued July 2004 and could therefore obtain their marketauthorization by 2010. Key to the potential success of ImmuPharma is its unique collaborative agreementwith Centre National de la Recherche Scientifique, France's scientific researchinstitution. This agreement grants ImmuPharma worldwide exclusive rights toexploit certain key discoveries. In addition to its three leading drug candidates, ImmuPharma has a drugdevelopment pipeline using its rights to a virtual chemical library of hundredsof thousands of molecules as well as an innovative technology for convertingpeptides to drug candidates. ImmuPharma has the option to commercialise its assets itself or to license themto other pharmaceutical companies at an earlier stage. The products Treatment of Lupus (IPP-201101) Lupus is a chronic, life-threatening autoimmune disease where the immune systemattacks healthy cells. There is currently no cure and existing medications onlytreat the symptoms. By selectively modulating the aberrant T-cells in Lupus,ImmuPharma's drug candidate has the potential to produce remission of thedisease in a substantial proportion of patients. Based on independent forecasts, the value of ImmuPharma's Lupus drug isestimated to be "substantial" with peak annual sales forecast to generate inexcess of $4 billion. Severe pain relief (IPP-102199) ImmuPharma is developing a compound for relieving moderate to severe pain, suchas experienced by cancer sufferers and post-surgical patients. Most existingtreatments are derived from the opiate morphine and have serious side effectsassociated with a morphine-like mechanism of action. ImmuPharma's new approachis based on met-enkephalin, one of the body's internal analgesics. IPP-102199 isbeing developed to have major advantages over morphine such as longer painrelief duration and reduced side effects. The market for chronic opioids in theUS currently exceeds $3.5 billion and is growing by more than 10 to 20 per centa year. Antibiotic for MRSA and similar highly resistant infections (IPP-203101) This is a novel antibiotic to counter the effects of MRSA and other severehospital-acquired, resistant infections which affect some two million people inthe US, according to the US Centers for Disease Control and Prevention.ImmuPharma's drug candidate is targeted at disrupting the membrane potential ofMRSA and other bacterial strains. It is hoped this novel approach will reducetheir potential to become resistant. Key management Richard Warr, MA, Executive Chairman, has 20 years experience in investmentbanking and the capital markets. He was previously a director of ABN Amro;director and head of European sales and marketing at Credit Lyonnais; executivedirector at Dresdner Kleinwort Benson Securities Ltd; and head of Europeanequity distribution at Swiss Bank Corporation. He has extensive experience incorporate and governmental equity capital market transactions. Dimitri F Dimitriou, MSc, Chief Executive Officer, has over 20 years experiencein the pharmaceutical and biotech industry. He was senior director, worldwidebusiness development, at GlaxoSmithKline, where his responsibilities includedlicensing deals, alliances and collaborations on a worldwide basis. Dr Robert Zimmer, MD, PhD, Chief Scientific Officer and head of R&D, began hiscareer with Roche in Basle, where he was responsible for numerous Phase Istudies. In 1990 he joined JAGO in Basle and, on its acquisition by SkyePharma,became director and head of research and development at SkyePharma. Hisexpertise includes managerial experience in multifunctional research anddevelopment and the assessment of technologies with multi-nationalpharmaceutical companies. Paddy Walker-Taylor, FCA, MCT Chief Financial Officer, was previously financedirector of Sir Robert McAlpine Ltd. He was involved in the AIM float of ISGGroup, in which McAlpine had a minority shareholding. Previously he had held anumber of key financial positions including finance director of Woolworths plcand treasurer of Marks & Spencer. Douglas Paterson, MA, FCA, senior Non-Executive Director, has been a charteredaccountant for 37 years and was a senior audit partner at Coopers & Lybrand (nowPricewaterhouseCoopers) for 22 years. He currently holds a number ofnon-executive directorships, including Close Brothers Group plc and GoldmanSachs International Bank. Anthony Johnson, B Pharm, MSc, Non-Executive Director, has over 30 yearsexperience in the pharmaceutical industry, focused on the scientific aspects ofdeal making, support during competitive analysis, technical due diligence andinput in development strategy. He was formerly senior director of scientificlicensing at SmithKline Beecham (now GlaxoSmithKline). Collaboration with Centre National de la Recherche Scientifique (CNRS) ImmuPharma has important collaboration arrangements with Centre National de laRecherche Scientifique, France's scientific research institution, including aresearch collaboration agreement relating to the therapeutic use of peptides andpeptide derivatives. ImmuPharma has been granted the worldwide exclusive rightsto exploit all discoveries made under this agreement. ImmuPharma will co-own therelevant intellectual property with CNRS which will share in the revenuegenerated by ImmuPharma from exploiting CNRS' licensed and co-owned rights. This information is provided by RNS The company news service from the London Stock Exchange
Date   Source Headline
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19th May 20107:00 amRNSPreliminary Results
8th Apr 20109:26 amRNSBest Drug Development Company in Europe Award
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3rd Dec 20097:00 amRNSR&D Symposium at the CNRS in Paris
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19th Oct 200910:31 amRNS'Best Technology 2009' Award at the AIM Awards
9th Oct 200910:14 amRNSAppointment of Joint Broker
29th Sep 20097:00 amRNSInterim Results
21st Sep 20099:55 amRNS8th Annual Bio Investor Forum
17th Sep 20097:00 amRNSJMP Healthcare Focus Conference
24th Jul 200912:12 pmRNSResult of AGM
23rd Jul 20094:17 pmRNSDirectors' Dealings
30th Jun 20097:00 amRNSAnnual Report and Accounts
24th Jun 20097:00 amRNSPreliminary Results
17th Jun 20097:00 amRNSPiper Jaffray Europe Conference
23rd Mar 20097:00 amRNSDirectors' Dealings
4th Feb 200912:32 pmRNSShare Options
2nd Feb 20092:33 pmRNSCephalon license exercise
30th Jan 20097:00 amRNSSuccessful trial results
22nd Dec 200812:00 pmRNSfurther instalment of grant
25th Nov 20087:00 amRNSOption Agreement with Cephalon
12th Nov 20087:00 amRNSGrant Award
21st Oct 20089:31 amRNSPatents Granted
17th Oct 20084:22 pmRNSAdditional Listing and Total Voting Rights
25th Sep 20087:00 amRNSInterim Results
5th Aug 20083:44 pmRNSAGM Result
10th Jul 20087:00 amRNSSecond Placing
2nd Jul 20087:30 amRNSToxicology study
2nd Jul 20087:00 amRNSFund Raising
30th Jun 20083:00 pmRNSAnnual Report and Accounts
20th May 20087:00 amRNSPre-clinical Data
13th May 20086:00 amRNSTrademark Approval
8th May 20087:00 amRNSPreliminary Results
26th Feb 20087:00 amRNSPhase IIb Trial of IPP-201101
8th Jan 20087:00 amRNSNovel Drug Candidate
18th Dec 200712:51 pmRNSDirectors' Dealings
6th Dec 20077:01 amRNSInitiation of Phase IIb trial
16th Nov 200712:28 pmRNSAppointment of Nomad
28th Sep 20077:02 amRNSInterim Results
22nd Aug 20077:00 amRNSCompound Discovery
20th Aug 200710:17 amRNSAIM Rule 26
13th Aug 20074:17 pmRNSDirectors' Dealing
6th Aug 20072:40 pmRNSGrant of Options
10th Jul 20077:01 amRNSPivotal phase II/III trial
13th Jun 20072:00 pmRNSAGM and Board Update
1st May 20077:02 amRNSPreliminary Results
27th Apr 20074:02 pmRNSBoard Appointment
15th Feb 20077:01 amRNSAppointment of adviser

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