Published in Vaccine Weekly, December 29th, 2010
"This open-label phase II study was conducted to evaluate the safety of the new formulation in patients with unresectable stage IIIA/IIIB NSCLC. Twenty-two patients received L-BLP25 1000 mu g every week for 8 weeks plus best supportive care....
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Source: Vaccine Weekly (2010-12-29)
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