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<item>
  <title>Medivir Announces Phase 2b 24-week Interim Results of TMC435 in Treatment-na&#239;ve Patients Chronically Infected with Genotype-1 Hepatitis C Virus</title>
  <pubDate>Mon, 12 Jul 2010 11:56:00 +0200</pubDate>
  <description>Potent and consistent antiviral efficacy was demonstrated at 24-week end-of-treatment and in interim SVR4 and SVR12 results. There were no clinically relevant differences between TMC435 treatment groups and placebo for adverse events.</description>
  <guid>http://www.mynewsdesk.com/se/pressroom/medivir/pressrelease/view/medivir-announces-phase-2b-24-week-interim-results-of-tmc435-in-treatment-naive-patients-chronically-infected-with-genotype-1-hepatitis-c-virus-438991</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/medivir/pressrelease/view/medivir-announces-phase-2b-24-week-interim-results-of-tmc435-in-treatment-naive-patients-chronically-infected-with-genotype-1-hepatitis-c-virus-438991</link>
  <dc:creator>Medivir AB</dc:creator>
</item>
<item>
  <title>Medivir offentligg&#246;r fas 2b 24 veckors interimsresultat f&#246;r TMC435 i behandlingsnaiva patienter med kronisk hepatit C av genotyp 1</title>
  <pubDate>Mon, 12 Jul 2010 11:46:00 +0200</pubDate>
  <description>Potent och varaktig antiviral effekt uppvisades efter 24 veckors behandling (EoT) samt fyra respektive tolv veckor efter avslutad behandling (SVR4 och SVR12). Det fanns inga kliniskt relevanta skillnader mellan de grupper som behandlades med TMC435 och de som behandlades med placebo n&#228;r det g&#228;ller biverkningar.</description>
  <guid>http://www.mynewsdesk.com/se/pressroom/medivir/pressrelease/view/medivir-offentliggoer-fas-2b-24-veckors-interimsresultat-foer-tmc435-i-behandlingsnaiva-patienter-med-kronisk-hepatit-c-av-genotyp-1-438972</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/medivir/pressrelease/view/medivir-offentliggoer-fas-2b-24-veckors-interimsresultat-foer-tmc435-i-behandlingsnaiva-patienter-med-kronisk-hepatit-c-av-genotyp-1-438972</link>
  <dc:creator>Medivir AB</dc:creator>
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<item>
  <title>APL l&#228;mnar Apoteket AB</title>
  <pubDate>Thu, 01 Jul 2010 08:58:53 +0200</pubDate>
  <description>APL l&#228;mnar Apoteket AB f&#246;r att bli ett direkt&#228;gt bolag av staten.fr&#229;n den 30 juni.
Frikopplingen av APL g&#246;rs eftersom den som driver apotek inte samtidigt kan vara l&#228;kemedelstillverkare.
APLs VD Eva Sj&#246;kvist Saers ser f&#246;r&#228;ndringen som en mycket bra l&#246;sning f&#246;r att APL &#228;ven forts&#228;ttningsvis ska kunna tillverka extemporel&#228;kemdel och utveckla veksamheten som ett kontraktsf&#246;retag.</description>
  <guid>http://www.mynewsdesk.com/se/view/pressrelease/apl-laemnar-apoteket-ab-432920</guid>
  <link>http://www.mynewsdesk.com/se/view/pressrelease/apl-laemnar-apoteket-ab-432920</link>
  <dc:creator>APL</dc:creator>
</item>
<item>
  <title>PHARMALINK AB CLOSES DEAL WITH GRIFOLS SA FOR THE ACQUISITION OF THE XEPOL&#174; PROGRAMME FOR THE TREATMENT OF POST-POLIO SYNDROME</title>
  <pubDate>Wed, 30 Jun 2010 10:55:17 +0200</pubDate>
  <description></description>
  <guid>http://www.mynewsdesk.com/se/view/pressrelease/pharmalink-ab-closes-deal-with-grifols-sa-for-the-acquisition-of-the-xepol-programme-for-the-treatment-of-post-polio-syndrome-432355</guid>
  <link>http://www.mynewsdesk.com/se/view/pressrelease/pharmalink-ab-closes-deal-with-grifols-sa-for-the-acquisition-of-the-xepol-programme-for-the-treatment-of-post-polio-syndrome-432355</link>
  <dc:creator>Pharmalink AB </dc:creator>
</item>
<item>
  <title>Ny ledning till PledPharma </title>
  <pubDate>Thu, 24 Jun 2010 09:40:35 +0200</pubDate>
  <description>Jacques N&#228;sstr&#246;m har utsetts till VD och Michaela Johansson till CFO i bolaget. PledPharma kommer att utv&#228;rdera olika alternativ f&#246;r att finansiera fortsatta studier efter de positiva fas II-resultaten som presenterades idag.</description>
  <guid>http://www.mynewsdesk.com/se/pressroom/acceleratorab/pressrelease/view/ny-ledning-till-pledpharma-429609</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/acceleratorab/pressrelease/view/ny-ledning-till-pledpharma-429609</link>
  <dc:creator>Accelerator Nordic AB</dc:creator>
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<item>
  <title>PledPharma reports positive results from cancer study</title>
  <pubDate>Thu, 24 Jun 2010 09:37:28 +0200</pubDate>
  <description>No serious side effects of the chemotherapy were observed in the patients who received PP-095 (mangafodipir), while several serious side effects (grades 3 and 4 on the 4-point NCI-CTCAE scale) were observed in the patients who received placebo.</description>
  <guid>http://www.mynewsdesk.com/se/pressroom/acceleratorab/pressrelease/view/pledpharma-reports-positive-results-from-cancer-study-429607</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/acceleratorab/pressrelease/view/pledpharma-reports-positive-results-from-cancer-study-429607</link>
  <dc:creator>Accelerator Nordic AB</dc:creator>
</item>
<item>
  <title>PledPharma rapporterar positiva resultat fr&#229;n cancerstudie</title>
  <pubDate>Thu, 24 Jun 2010 09:27:28 +0200</pubDate>
  <description>Inga allvarliga biverkningar av cellgiftsbehandlingen s&#229;gs hos de patienter som fick PP-095 (mangafodipir), medan flera allvarliga biverkningar (grad 3 och 4 p&#229; den 4-gradiga s.k. NCI-CTCAE skalan) s&#229;gs hos de patienter som fick placebo. </description>
  <guid>http://www.mynewsdesk.com/se/pressroom/acceleratorab/pressrelease/view/pledpharma-rapporterar-positiva-resultat-fraan-cancerstudie-429601</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/acceleratorab/pressrelease/view/pledpharma-rapporterar-positiva-resultat-fraan-cancerstudie-429601</link>
  <dc:creator>Accelerator Nordic AB</dc:creator>
</item>
<item>
  <title>GlaxoSmithKline enters agreement with Medivir for exclusive rights to cold sore treatment Xerclear&#8482; </title>
  <pubDate>Wed, 23 Jun 2010 08:30:00 +0200</pubDate>
  <description>GlaxoSmithKline (GSK) and Medivir (STO: MVIR-B) today announced an exclusive agreement for the commercialization of cold sore treatment, Xerclear&#8482; (acyclovir and hydrocortisone) for non-prescription use (OTC) in key global markets. Xerclear&#8482; is the first and only topical herpes labialis (cold sores) treatment clinically proven to help prevent cold sore lesions appearing. </description>
  <guid>http://www.mynewsdesk.com/se/pressroom/medivir/pressrelease/view/glaxosmithkline-enters-agreement-with-medivir-for-exclusive-rights-to-cold-sore-treatment-xercleartm-428692</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/medivir/pressrelease/view/glaxosmithkline-enters-agreement-with-medivir-for-exclusive-rights-to-cold-sore-treatment-xercleartm-428692</link>
  <dc:creator>Medivir AB</dc:creator>
</item>
<item>
  <title>GlaxoSmithKline ing&#229;r avtal med Medivir om ensamr&#228;tt att marknadsf&#246;ra Xerclear&#8482; mot muns&#229;r </title>
  <pubDate>Wed, 23 Jun 2010 08:30:00 +0200</pubDate>
  <description>GlaxoSmithKline (GSK) och Medivir (STO: MVIR-B) meddelade i dag att man ing&#229;tt ett exklusivt marknadsf&#246;ringsavtal om receptfri f&#246;rs&#228;ljning av muns&#229;rsl&#228;kemedlet Xerclear&#8482; p&#229; viktiga globala marknader. Xerclear&#8482; &#228;r den f&#246;rsta och enda topikala behandlingen av l&#228;ppherpes (muns&#229;r) som kliniskt visat sig kunna f&#246;rhindra uppkomsten av muns&#229;r. 1)</description>
  <guid>http://www.mynewsdesk.com/se/pressroom/medivir/pressrelease/view/glaxosmithkline-ingaar-avtal-med-medivir-om-ensamraett-att-marknadsfoera-xercleartm-mot-munsaar-428706</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/medivir/pressrelease/view/glaxosmithkline-ingaar-avtal-med-medivir-om-ensamraett-att-marknadsfoera-xercleartm-mot-munsaar-428706</link>
  <dc:creator>Medivir AB</dc:creator>
</item>
<item>
  <title>Corline signs exclusive license and supply agreement with major US medical device manufacturer</title>
  <pubDate>Tue, 22 Jun 2010 15:05:41 +0200</pubDate>
  <description>Swedish company Corline Systems AB, a maker and distributor of CHS, a unique heparin coating technology for use on Medical Devices and for Regenerative Medicine, today announced that it has signed an agreement exclusively licensing its technology within a specified Field-of-Use to one of the major US medical device manufacturers. 
</description>
  <guid>http://www.mynewsdesk.com/se/view/pressrelease/corline-signs-exclusive-license-and-supply-agreement-with-major-us-medical-device-manufacturer-428719</guid>
  <link>http://www.mynewsdesk.com/se/view/pressrelease/corline-signs-exclusive-license-and-supply-agreement-with-major-us-medical-device-manufacturer-428719</link>
  <dc:creator>Corline Systems AB</dc:creator>
</item>
<item>
  <title>B&#228;ttre livskvalitet med ny orphan drug f&#246;r Addisons sjukdom</title>
  <pubDate>Tue, 22 Jun 2010 06:30:00 +0200</pubDate>
  <description>Det svenska l&#228;kemedelsf&#246;retaget DuoCort Pharmas nya mer fysiologiska behandling f&#246;r binjurebarksvikt f&#246;rb&#228;ttrar patienternas livskvalitet. F&#246;retaget har ocks&#229; tagit fram metoder f&#246;r att optimera doseringen vilket ocks&#229; bidrar till att p&#229; sikt f&#246;rb&#228;ttra behandlingen. DuoCort Pharma presenterar dessa nya data fr&#229;n sin fas II/III studie vid den 92:a &#229;rliga kongressen ENDO i San Diego, USA. </description>
  <guid>http://www.mynewsdesk.com/se/pressroom/duocort/pressrelease/view/baettre-livskvalitet-med-ny-orphan-drug-foer-addisons-sjukdom-426739</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/duocort/pressrelease/view/baettre-livskvalitet-med-ny-orphan-drug-foer-addisons-sjukdom-426739</link>
  <dc:creator>DuoCort</dc:creator>
</item>
<item>
  <title>Better quality of life with new orphan drug for Addison&#180;s disease</title>
  <pubDate>Mon, 21 Jun 2010 18:00:00 +0200</pubDate>
  <description>DuoCort Pharma&#180;s new physiological treatment for adrenal insufficiency improves patients&#8217; quality of life. The company has also developed methods to optimize the dosage regimen which also contributes to an improvement in therapy over time. The Swedish pharmaceutical company presents this new data from its phase II/III trial at the 92nd annual ENDO congress in San Diego today.   



</description>
  <guid>http://www.mynewsdesk.com/us/pressroom/duocort/pressrelease/view/better-quality-of-life-with-new-orphan-drug-for-addison-s-disease-426752</guid>
  <link>http://www.mynewsdesk.com/us/pressroom/duocort/pressrelease/view/better-quality-of-life-with-new-orphan-drug-for-addison-s-disease-426752</link>
  <dc:creator>DuoCort</dc:creator>
</item>
<item>
  <title>Doxa sluter distributionsavtal f&#246;r den svenska marknaden</title>
  <pubDate>Mon, 21 Jun 2010 10:20:38 +0200</pubDate>
  <description>Doxa har slutit ett exklusivt distribut&#246;rsavtal med AB Nordenta (inom Lifco-koncernen) f&#246;r bolagets f&#246;rsta marknadslanserade produkt, dentalcementet Ceramir&#174; Crown &amp; Bridge.</description>
  <guid>http://www.mynewsdesk.com/se/view/pressrelease/doxa-sluter-distributionsavtal-foer-den-svenska-marknaden-427737</guid>
  <link>http://www.mynewsdesk.com/se/view/pressrelease/doxa-sluter-distributionsavtal-foer-den-svenska-marknaden-427737</link>
  <dc:creator>Doxa AB</dc:creator>
</item>
<item>
  <title>Laccure tar in 10,8 miljoner f&#246;r att f&#228;rdigutveckla sin produkt f&#246;r bakteriell vaginos </title>
  <pubDate>Mon, 21 Jun 2010 06:30:00 +0200</pubDate>
  <description>Laccure AB, tar in 10,8 miljoner i en nyemission f&#246;r att slutf&#246;ra utvecklingen av en ny produkt f&#246;r kvinnor med bakteriell vaginos.  Bakteriell vaginos drabbar 10-30% av alla kvinnor. Idag finns ingen anv&#228;ndarv&#228;nlig produkt p&#229; marknaden som samtidigt &#228;r effektiv och s&#228;ker. </description>
  <guid>http://www.mynewsdesk.com/se/pressroom/puls/pressrelease/view/laccure-tar-in-10-8-miljoner-foer-att-faerdigutveckla-sin-produkt-foer-bakteriell-vaginos-426079</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/puls/pressrelease/view/laccure-tar-in-10-8-miljoner-foer-att-faerdigutveckla-sin-produkt-foer-bakteriell-vaginos-426079</link>
  <dc:creator>P.U.L.S. AB</dc:creator>
</item>
<item>
  <title>MOBERG DERMA ING&#197;R DISTRIBUTIONSAVTAL P&#197; YTTERLIGARE 8 MARKNADER F&#214;R EMTRIX&#8482;</title>
  <pubDate>Fri, 18 Jun 2010 09:53:43 +0200</pubDate>
  <description>Moberg Derma AB meddelar idag att man ing&#229;tt ett distributionsavtal f&#246;r &#229;tta l&#228;nder i Mellan&#246;stern. Avtalet g&#228;ller Moberg Dermas nagelprodukt Emtrix&#8482; &#8211; en ny behandling av missf&#228;rgade och skadade naglar t ex orsakat av nagelsvamp eller nagelpsoriasis. </description>
  <guid>http://www.mynewsdesk.com/se/view/pressrelease/moberg-derma-ingaar-distributionsavtal-paa-ytterligare-8-marknader-foer-emtrixtm-426847</guid>
  <link>http://www.mynewsdesk.com/se/view/pressrelease/moberg-derma-ingaar-distributionsavtal-paa-ytterligare-8-marknader-foer-emtrixtm-426847</link>
  <dc:creator>Moberg Derma AB</dc:creator>
</item>
<item>
  <title>DuoCort ans&#246;ker om europeiskt marknadsgodk&#228;nnande f&#246;r sin orphan drug</title>
  <pubDate>Thu, 17 Jun 2010 06:30:00 +0200</pubDate>
  <description>Det svenska l&#228;kemedelsf&#246;retaget DuoCort Pharma tar ytterligare ett steg n&#228;rmare marknaden genom att ans&#246;ka om marknadsgodk&#228;nnande inom EU f&#246;r sin nya behandling f&#246;r den ovanliga och livshotande sjukdomen binjurebarksvikt, ofta kallad Addisons sjukdom. </description>
  <guid>http://www.mynewsdesk.com/se/pressroom/duocort/pressrelease/view/duocort-ansoeker-om-europeiskt-marknadsgodkaennande-foer-sin-orphan-drug-425533</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/duocort/pressrelease/view/duocort-ansoeker-om-europeiskt-marknadsgodkaennande-foer-sin-orphan-drug-425533</link>
  <dc:creator>DuoCort</dc:creator>
</item>
<item>
  <title>Adenovir Pharma tar in 6,1 miljoner f&#246;r utveckling av &#246;gonl&#228;kemedel</title>
  <pubDate>Tue, 15 Jun 2010 06:30:00 +0200</pubDate>
  <description>Adenovir Pharma AB tar in 6,1 miljoner kronor via nyemission f&#246;r att finansiera fortsatt utveckling av ett nytt l&#228;kemedel f&#246;r behandling av smittsamma &#246;goninfektioner. Dessa infektioner orsakas av virus och drabbar &#229;rligen ett stort antal m&#228;nniskor. Idag finns inte n&#229;gon effektiv behandling f&#246;r dessa ytterst sm&#228;rtsamma och smittsamma infektioner i &#246;gonen. </description>
  <guid>http://www.mynewsdesk.com/se/pressroom/puls/pressrelease/view/adenovir-pharma-tar-in-6-1-miljoner-foer-utveckling-av-oegonlaekemedel-424731</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/puls/pressrelease/view/adenovir-pharma-tar-in-6-1-miljoner-foer-utveckling-av-oegonlaekemedel-424731</link>
  <dc:creator>P.U.L.S. AB</dc:creator>
</item>
<item>
  <title>Ny arbetande styrelseordf&#246;rande i inkubatorn PULS  </title>
  <pubDate>Fri, 11 Jun 2010 06:30:00 +0200</pubDate>
  <description>Den privata inkubatorn PULS st&#228;rker sin organisation ytterligare med Clas Runnberg som ny arbetande styrelseordf&#246;rande samt Mats Ardevall som CFO. Ytterligare en ny partner och tv&#229; associate partners ansluter sig ocks&#229; till det befintliga partnerskapet och breddar d&#228;rmed kompetensbasen ytterligare. </description>
  <guid>http://www.mynewsdesk.com/se/pressroom/puls/pressrelease/view/ny-arbetande-styrelseordfoerande-i-inkubatorn-puls-423256</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/puls/pressrelease/view/ny-arbetande-styrelseordfoerande-i-inkubatorn-puls-423256</link>
  <dc:creator>P.U.L.S. AB</dc:creator>
</item>
<item>
  <title>Unitech Pharma tillverkar ytterligare GMP material &#229;t Aprea </title>
  <pubDate>Tue, 08 Jun 2010 16:25:00 +0200</pubDate>
  <description>Unitech Pharma f&#229;r fortsatt f&#246;rtroende att tillverka Apreas l&#228;kemedelskandidat APR-246 enligt h&#246;gt st&#228;llda GMP-krav. </description>
  <guid>http://www.mynewsdesk.com/se/pressroom/unitech-pharma/pressrelease/view/unitech-pharma-tillverkar-ytterligare-gmp-material-aat-aprea-421820</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/unitech-pharma/pressrelease/view/unitech-pharma-tillverkar-ytterligare-gmp-material-aat-aprea-421820</link>
  <dc:creator>UniTech Pharma </dc:creator>
</item>
<item>
  <title>Unitech Pharma produces additional GMP materials for Aprea </title>
  <pubDate>Tue, 08 Jun 2010 16:21:00 +0200</pubDate>
  <description>Unitech Pharma AB announces today that it will provide Aprea AB with additional GMP manufacturing of APR-246. APR-246 is Aprea&#8217;s first candidate drug which is undergoing a Phase I clinical study for refractory hematological malignancies and prostate cancer patients in Sweden.</description>
  <guid>http://www.mynewsdesk.com/se/pressroom/unitech-pharma/pressrelease/view/unitech-pharma-produces-additional-gmp-materials-for-aprea-421815</guid>
  <link>http://www.mynewsdesk.com/se/pressroom/unitech-pharma/pressrelease/view/unitech-pharma-produces-additional-gmp-materials-for-aprea-421815</link>
  <dc:creator>UniTech Pharma </dc:creator>
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