By setting the regulatory-approved protocol for a suite of first-in-human studies on BIA 10-2474 against the subsequent French investigations, we highlight six key design and statistical issues which reinforce recommendations by a Royal Statistical Society Working Party which were made in the aftermath of cytokine release storm in six healthy volunteers in the UK in 2006. The 6 issues are dose determination, availability of pharmacokinetic results, dosing interval, stopping rules, appraisal by safety committee, and clear algorithm required if combining approvals for single and multiple ascending dose studies.SS’s work was funded by the European Union's FP7 programme grant number 602552 for the IDEAL project
Purpose: Recent France clinical trial with the drug coded, B1A10-2474, turned out to be a safety fai...
Serum parameters as indicators for the efficacy of therapeutic drugs are currently in the focus of i...
AIM: The primary aim of this study was to explore the safety profile of biologic treatments in Behçe...
By setting the regulatory-approved protocol for a suite of first-in-human studies on BIA 10-2474 aga...
In March 2006 a first-in-man trial took place using healthy volunteers involving the use of monoclo...
International audienceThe presentation and discussion of the BIAL/Biotrial case below is based on pu...
OBJECTIVES: The introduction of biological therapies for the treatment of rheumatic diseases has dra...
Background: Pharmacoepidemiological (PE) research should provide consistent, reliable and reproducib...
International audiencePurpose: In the frame of the QA program of RENEB, an inter-laboratory comparis...
International audienceAimsFollowing the serious adverse events that occurred in January 2016 during ...
BACKGROUND: Observational pharmacoepidemiological (PE) studies on drug safety have produced discrepa...
BACKGROUND: Observational pharmacoepidemiological (PE) studies on drug safety have produced discrepa...
Serum parameters as indicators for the efficacy of therapeutic drugs are currently in the focus of i...
Introduction: The quantity and quality of data for determining the dose and treatment schedule of me...
BACKGROUND: Observational pharmacoepidemiological (PE) studies on drug safety have produced discrepa...
Purpose: Recent France clinical trial with the drug coded, B1A10-2474, turned out to be a safety fai...
Serum parameters as indicators for the efficacy of therapeutic drugs are currently in the focus of i...
AIM: The primary aim of this study was to explore the safety profile of biologic treatments in Behçe...
By setting the regulatory-approved protocol for a suite of first-in-human studies on BIA 10-2474 aga...
In March 2006 a first-in-man trial took place using healthy volunteers involving the use of monoclo...
International audienceThe presentation and discussion of the BIAL/Biotrial case below is based on pu...
OBJECTIVES: The introduction of biological therapies for the treatment of rheumatic diseases has dra...
Background: Pharmacoepidemiological (PE) research should provide consistent, reliable and reproducib...
International audiencePurpose: In the frame of the QA program of RENEB, an inter-laboratory comparis...
International audienceAimsFollowing the serious adverse events that occurred in January 2016 during ...
BACKGROUND: Observational pharmacoepidemiological (PE) studies on drug safety have produced discrepa...
BACKGROUND: Observational pharmacoepidemiological (PE) studies on drug safety have produced discrepa...
Serum parameters as indicators for the efficacy of therapeutic drugs are currently in the focus of i...
Introduction: The quantity and quality of data for determining the dose and treatment schedule of me...
BACKGROUND: Observational pharmacoepidemiological (PE) studies on drug safety have produced discrepa...
Purpose: Recent France clinical trial with the drug coded, B1A10-2474, turned out to be a safety fai...
Serum parameters as indicators for the efficacy of therapeutic drugs are currently in the focus of i...
AIM: The primary aim of this study was to explore the safety profile of biologic treatments in Behçe...