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Re Sativex Update

15 Nov 2005 07:02

GW Pharmaceuticals PLC15 November 2005 Embargoed until 0700 15 November 2005 GW Pharmaceuticals plc ("GW" or "the Company") UK Named Patient Prescribing for Sativex(R) GW announces that it has been informed by the Home Office that the DrugsMinister, Paul Goggins, has confirmed that Sativex(R) oromucosal spray, itscannabis-based medicine, may be imported from Canada to satisfy its prescriptionto individual patients in the UK as an unlicensed medicine. This development isin response to enquiries from a number of UK doctors and individual patients whohave been in contact with the Home Office to request access to Sativex. In accordance with the Medicines Act, a medicine which has yet to be licensed inthe UK may be prescribed and supplied in response to an unsolicited request tofulfil the special needs of an individual patient under a physician's directpersonal responsibility. The basis on which Sativex may be imported, therefore,is the clinical judgement of doctors in relation to specific nominated patients. This development follows the approval of Sativex by Health Canada in April 2005.The medicine has been available on prescription in Canada since late June. More recently, the Medicines and Healthcare products Regulatory Agency (MHRA)has issued to GW a Wholesale Dealer's (Importation from non-EU countries)Licence, and has not objected to the importation of Sativex under theregulations for importation of medicines unlicensed in the UK. Sativex will remain a Schedule 1 controlled drug in the UK in line with statedgovernment policy. This means that the prescribing of Sativex can only bepermitted under Home Office licence. The Home Office will therefore bedeveloping a licensing regime to fit these circumstances. GW expects to discussthe implementation practicalities with the Home Office over the coming weeks. Clearance for supply on an unlicensed basis does not affect GW's plans to seekfull regulatory approval from the MHRA for Sativex in the UK. The Company iscurrently conducting a number of further Phase III trials and is still planningto submit an application for Marketing Authorisation to the MHRA during 2006.Only after such an approval is granted can the product be promoted in the UK. - Ends- GW Pharmaceuticals plc + 44 (0)1980 557000Dr Geoffrey Guy, ChairmanJustin Gover, Managing DirectorMark Rogerson, Press and PR + 44 (0)7885 638810 Weber Shandwick Square Mile + 44 (0)20 7067 0700Kevin Smith/Yvonne Alexander About GW Pharmaceuticals plcGW Pharmaceuticals plc is licensed by the UK Home Office to undertake apharmaceutical research and development program to develop non-smokedcannabis-based prescription medicines. GW's shares are publicly traded on AiM, amarket on the London Stock Exchange. Full details of GW and the company's research programme can be found atwww.gwpharm.com. This news release may contain forward-looking statements that reflect GW'scurrent expectations regarding future events, including the clinical developmentand regulatory clearance of its products. Forward-looking statements involverisks and uncertainties. Actual events could differ materially from thoseprojected herein and depend on a number of factors, including (inter alia), thesuccess of GW's research strategies, the applicability of the discoveries madetherein, the successful and timely completion of clinical studies, includingwith respect to Sativex and GW's other products, the uncertainties related tothe regulatory process, and the acceptance of Sativex and other products byconsumers and medical professionals. This information is provided by RNS The company news service from the London Stock Exchange
Date   Source Headline
10th May 20134:24 pmRNSHolding(s) in Company
9th May 20133:40 pmRNSTotal Voting Rights
8th May 20138:00 amRNSClosing of Initial Public Offering on Nasdaq
7th May 20137:00 amRNSSativex Commercialization Approval in Italy
1st May 20135:47 pmRNSPricing of U.S. Initial Public Offering
22nd Apr 20137:00 amRNSUS Patent Allowance for SATIVEX Formulation Spray
18th Apr 20132:23 pmRNSAmendment to Registration Statement for NASDAQ
12th Apr 201310:31 amRNSResults of General Meeting
10th Apr 20137:00 amRNSSativex moved to Schedule 4 of UK Drugs Act
3rd Apr 20137:00 amRNSNew US Patent Allowance for Delivery of SATIVEX
22nd Mar 20132:35 pmRNSPosting of Shareholder Circular
19th Mar 20132:46 pmRNSAppoints Stephen Schultz VP of Investor Relations
19th Mar 20131:10 pmRNSUpdate on Sativex in Germany
19th Mar 20131:01 pmRNSFiling for listing on NASDAQ
19th Feb 20133:16 pmRNSDirectorate Change
19th Feb 20139:30 amRNSBlocklisting Interim Review
4th Dec 201210:04 amRNSDirector/PDMR Shareholding
30th Nov 20122:54 pmRNSDirector/PDMR Shareholding
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22nd Nov 201211:31 amRNSNotice of Results
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1st Oct 20127:00 amRNSAppointment of Chief Operating Officer
13th Sep 20127:00 amRNSPublication of New Epilepsy Data
20th Aug 201212:14 pmRNSDirector/PDMR Shareholding
17th Aug 20124:04 pmRNSBlocklisting Interim Review
22nd Jun 20127:00 amRNSGerman GBA establishes positive benefit of Sativex
13th Jun 201210:19 amRNSDirector/PDMR Shareholding
6th Jun 20124:03 pmRNSDirector/PDMR Shareholding
23rd May 20123:56 pmRNSDirector/PDMR Shareholding
22nd May 20127:00 amRNSThird Cancer Pain Trial Commences
22nd May 20127:00 amRNSInterim Results
8th May 20127:00 amRNSSuccessful completion of MRP for Sativex
26th Apr 201211:00 amRNSNotice of Results
23rd Apr 20127:00 amRNSSativex phase IIb pain trial results publication
16th Apr 20127:00 amRNSAlmirall Milestone
5th Apr 20127:00 amRNSBoard Changes
2nd Apr 20122:31 pmRNSDirector/PDMR Shareholding
30th Mar 20121:57 pmRNSDirector/PDMR Shareholding
15th Mar 20127:00 amRNSGW and Almirall Strengthen Strategic Collaboration
8th Mar 20127:00 amRNSAppointment of Professor Vincenzo Di Marzo
17th Feb 20127:00 amRNSBlocklisting Interim Review
7th Feb 20127:00 amRNSSATIVEX® Regulatory Approval Received in Austria
25th Jan 20121:46 pmRNSResult of AGM
11th Jan 201211:43 amRNSHolding(s) in Company
11th Jan 201211:42 amRNSHolding(s) in Company
28th Dec 201110:39 amRNSDirector/PDMR Shareholding
22nd Dec 20117:00 amRNSSativex Approval in Sweden

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