Monday, June 1, 2015

BRIEF-Interim data support safety and efficacy of Pharming Group's RUCONEST

<span id="midArticle_start"/> Pharming Group NV :

<span id="midArticle_0"/>* Announces interim results from the ongoing phase IIpediatric clinical trial of RUCONEST

<span id="midArticle_1"/> <span class="first-article-divide"/>* Interim data from ongoing pediatric clinical trial andresults from a clinical immunology study support safety andefficacy of RUCONEST

<span id="midArticle_2"/> <span class="second-article-divide"/>* Several abstracts presented demonstrate Pharming's ongoingcommitment to advance innovative science in HereditaryAngioedema (HAE)

<span id="midArticle_3"/> <span class="third-article-divide"/>* "These data add to our clinical database andpost-marketing experience that demonstrate a very low risk ofallergy with rhC1INH exposure" - Chief Operating officerSource text for Eikon: Further company coverage: (Gdynia Newsroom)

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