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Pin to quick picksPlethora Solutions Holdings Plc Regulatory News (PLE)

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Clinical Update - PSD508

6 Dec 2007 07:00

Plethora Solutions Holdings PLC06 December 2007 PLETHORA SOLUTIONS HOLDINGS PLC Clinical Update - PSD508 for dysmenorrhoea Phase IIb trial initiated, first patients recruited Plethora Solutions Holdings PLC ("Plethora", AIM: PLE), the specialist developerof products for the treatment and management of urological disorders, is pleasedto announce that the first patients have been recruited into a Phase IIb studyin dysmenorrhoea (period/menstrual pain). PSD508 is a well characterised non-steroidal anti-inflammatory (NSAID) which isadministered intra-vaginally utilising proprietary technology which Plethoralicensed from Metris Therapeutics Limited in 2006. This novel approach has thepotential benefit of allowing women to access a convenient "on-demand" treatmentcontaining an NSAID whilst minimising systemic exposure to the drug. It shouldallow higher doses of drug than might otherwise have been delivered orally; thusproviding rapid, local pain relief and minimal systemic and compliance-limitinggastro-intestinal side effects, which would otherwise be associated withexposure to orally administered NSAIDs. Dysmenorrhoea is a painful, often incapacitating, menstrual cramp which afflictsaround 50% of women of reproductive age and is one of the leading causes ofabsenteeism from work and school. Standard treatments include orallyadministered non-steroidal anti-inflammatory drugs, pain-killers and hormonetherapy to bring about symptomatic relief. Study details The study is a double-blind, placebo-controlled, multiple-dose, crossover proofof concept study which compares the efficacy of vaginally delivered PSD508 tothat of oral NSAID and placebo in relieving menstrual-related pain. This studywill take place across three consecutive menstrual cycles, allowing the trial totake place in the shortest possible time frame. The study will also evaluate thesafety and tolerability of PSD508. Up to 90 women will be recruited in Europe.Regulatory approval for this study has been achieved and the first patientsrecruited. Dr Steven Powell, CEO of Plethora, commented: "Plethora has reported significant progress this quarter. The initiation of thisstudy is a major step in the development of PSD508 and enables us to progressdiscussion with potential partners. In addition, this meets our commitment toinitiate clinical studies with this novel delivery system by end of 2007." -Ends- For further information contact: Plethora Solutions Tel : 020 7269 8630Steven Powell City/Financial Enquiries Tel: 020 7379 5151MaitlandBrian Hudspith/Liz Morley Scientific/Trade Press Enquiries Tel: 020 7861 3838De Facto CommunicationsRichard Anderson About Plethora: Plethora is focused on the development and marketing of products for thetreatment of urological disorders. The Company has products in clinicaldevelopment for the treatment of overactive bladder, stress urinaryincontinence, interstitial cystitis, gynaecological pain, erectile dysfunctionand premature ejaculation. Plethora has a US subsidiary, Timm MedicalTechnologies Inc, which markets products for the treatment of erectiledysfunction (ED) to urology clinics through a national US specialty sales team.The Company is headquartered in the UK and is listed on the London StockExchange (AIM:LSE). Further information is available atwww.plethorasolutions.co.uk. This information is provided by RNS The company news service from the London Stock Exchange
Date   Source Headline
30th Sep 20087:00 amRNSInterim Results
30th Sep 20087:00 amRNSClinical Update - PSD502
11th Aug 20087:00 amRNSBoard Change
21st Jul 20082:20 pmRNSHolding(s) in Company
1st Jul 20087:05 amRNSDirector/PDMR Shareholding
1st Jul 20087:00 amRNSChange of Adviser
27th Jun 20087:00 amRNSBoard Change
23rd Jun 20082:44 pmRNSAGM Statement
19th Jun 20087:00 amRNSClinical Update PSD502 Phase
22nd May 200810:00 amRNSAnnual Report and Accounts
29th Apr 20087:00 amRNSFinal Results
24th Apr 20087:00 amRNSClinical Update - PSD508
21st Apr 200811:13 amRNSNotice of Results
1st Apr 20087:01 amRNSRe $28m Financing
10th Mar 20085:49 pmRNSHolding(s) in Company
5th Feb 20087:00 amRNSClinical Update - PSD506
10th Jan 200810:39 amRNSChange of Registered Office
19th Dec 20077:01 amRNSClinical Update - PSD502
6th Dec 20077:00 amRNSClinical Update - PSD508
29th Nov 20077:01 amRNSClinical Update PSD503
30th Oct 200712:30 pmBUSSciele Pharma and Plethora Solutions Holdings PLC Announce Initiation of Pivotal Phase III Trials for PSD502 for Premature Ejaculation
30th Oct 20077:01 amRNSClinical Update PSD502 Ph III
8th Oct 20077:00 amRNSClinical Update PSD597
26th Sep 20077:02 amRNSInterim Results
25th Sep 20074:55 pmRNSHolding(s) in Company
10th Sep 20079:27 amRNSNotice of Results
6th Sep 20077:01 amRNSClinical Update PSD597
16th Aug 20072:44 pmRNSAIM Rule 26
12th Jul 20077:01 amRNSClinical Update - PSD502
10th Jul 20074:11 pmRNSResult of AGM
2nd Jul 20073:14 pmRNSDirector/PDMR Shareholding
2nd Jul 20077:01 amRNSProduct Update - Invicorp
29th Jun 20071:20 pmRNSTotal Voting Rights
29th Jun 200710:29 amRNSShare Options Award
25th Jun 20077:01 amRNSClinical Update PSD597 for IC
14th Jun 20074:46 pmRNSHolding(s) in Company
14th Jun 20074:39 pmRNSHolding(s) in Company
1st Jun 200710:00 amRNSDirectorate Change
30th May 20077:01 amRNSPreliminary Results
24th May 20071:00 pmBUSSciele Enters Into Exclusive License Agreement with Plethora Solutions Limited to Market PSD502 for the Treatment of Premature Ejaculation
24th May 20077:05 amRNSNotice of Results
24th May 20077:03 amRNSLicensing deal
8th May 20077:02 amRNSProduct Acquisitions
5th Apr 20077:36 amRNSAcquisition
21st Mar 20075:05 pmRNSHolding(s) in Company
21st Mar 20075:05 pmRNSHolding(s) in Company
21st Mar 20075:04 pmRNSHolding(s) in Company
13th Mar 20071:08 pmRNSHolding(s) in Company
12th Mar 20072:16 pmRNSExercise of share options
1st Mar 20077:03 amRNSDirectorate Change

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