US FDA Approves Initiation of ViroMed’s VM202 for Phase III Clinical Study of … – Business Wire (press release) | Leaders in Pharmaceutical Business Intelligence (LPBI) Group

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US FDA Approves Initiation of ViroMed’s VM202 for Phase III Clinical Study of … – Business Wire (press release)

September 5, 2015 by 2012pharmaceutical

ViroMed received an approval from the US FDA to launch a pivotal Phase III clinical trial utilizing VM202, a proprietary DNA based biopharmaceutical.

Sourced through Scoop.it from: www.businesswire.com

See on Scoop.it – Cardiovascular Disease: PHARMACO-THERAPY

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