Membro del Comitato di Clinical Study Protocol ML 18253 “ A multicenter randomized, controlled study comparing the efficacy and safty of 48 weeks of 40 kD branched pegylated interferon alfa2a (PEGASYS®; Ro 25-8310) versus 96 weeks PEGASYS®, alone or in combination with 100 mg lamivudine for 48 weeks in patients with HbeAg-negative chronic hepatitis B” Sponsor : Roche S.p.A / CRO : Quintiles S.p.A. EudraCT Number: 2004-002985-39(2006 Jan).

Membro del Comitato di Clinical Study Protocol ML 18253 “ A multicenter randomized, controlled study comparing the efficacy and safty of 48 weeks of 40 kD branched pegylated interferon alfa2a (PEGASYS®; Ro 25-8310) versus 96 weeks PEGASYS®, alone or in combination with 100 mg lamivudine for 48 weeks in patients with HbeAg-negative chronic hepatitis B” Sponsor : Roche S.p.A / CRO : Quintiles S.p.A. EudraCT Number: 2004-002985-39

2006

Fondazione Ospedale Maggiore Policlinico
Activity
Membro del Comitato di Clinical Study Protocol ML 18253 “ A multicenter randomized, controlled study comparing the efficacy and safty of 48 weeks of 40 kD branched pegylated interferon alfa2a (PEGASYS®; Ro 25-8310) versus 96 weeks PEGASYS®, alone or in combination with 100 mg lamivudine for 48 weeks in patients with HbeAg-negative chronic hepatitis B” Sponsor : Roche S.p.A / CRO : Quintiles S.p.A. EudraCT Number: 2004-002985-39(2006 Jan).
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/32538
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