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Featured researches published by Uwe Bamberger.


Toxicologic Pathology | 2014

Translation Strategy for the Qualification of Drug-induced Vascular Injury Biomarkers

Kaïdre Bendjama; Silvia Guionaud; Gulfidan Aras; Nadir Arber; Lina Badimon; Uwe Bamberger; Dorina Bratfalean; David Brott; Maayan David; Lucette Doessegger; Hüseyin Firat; Jean-François Gallas; Jean-Charles Gautier; Peter Hoffmann; Sarah Kraus; Teresa Padró; David Saadoun; Piotr Szczesny; Peter Thomann; Gemma Vilahur; Michael T. Lawton; Patrice Cacoub

Drug-induced vascular injury (DIVI) is a common preclinical toxicity usually characterized by hemorrhage, vascular endothelial and smooth muscle damage, and inflammation. DIVI findings can cause delays or termination of drug candidates due to low safety margins. The situation is complicated by the absence of sensitive, noninvasive biomarkers for monitoring vascular injury and the uncertain relevance to humans. The Safer And Faster Evidence-based Translation (SAFE-T) consortium is a public–private partnership funded within the European Commission’s Innovative Medicines Initiative (IMI) aiming to accelerate drug development by qualifying biomarkers for drug-induced organ injuries, including DIVI. The group is using patients with vascular diseases that have key histomorphologic features (endothelial damage, smooth muscle damage, and inflammation) in common with those observed in DIVI, and has selected candidate biomarkers associated with these features. Studied populations include healthy volunteers, patients with spontaneous vasculitides and other vascular disorders. Initial results from studies with healthy volunteers and patients with vasculitides show that a panel of biomarkers can successfully discriminate the population groups. The SAFE-T group plans to seek endorsement from health authorities (European Medicines Agency and Food and Drug Administration) to qualify the biomarkers for use in regulatory decision-making processes.


Archive | 1999

FAPalpha-specific antibody with improved producibility

John Edward Park; Pilar Garin-Chesa; Uwe Bamberger; Wolfgang J. Rettig; Olivier Leger; Jose Saldanha


Archive | 2001

ANTIBODI FAP-α-SPESIFIK DENGAN PERBAIKAN KEMAMPUAN PRODUKSI

Edward Park John; Pilar Garin Chesa; Uwe Bamberger; Rettig Wolfgang J; Olivier Leger; William Saldanha Jose


Archive | 1999

ANTIBODY WITH IMPROVED PRODUCIBILITY

John Edward Park; Pilar Garin-Chesa; Uwe Bamberger; Wolfgang J. Rettig; Olivier Leger; Jose Saldanha


Archive | 1999

Antikörper mit verbesserter produzierbarkeit Antibodies with improved reproducibility

Uwe Bamberger; Pilar Garin-Chesa; Olivier Leger; John Edward Park; Wolfgang J. Rettig; Jose Saldanha


Archive | 1999

Antibody with improved production capacity.

Uwe Bamberger; Pilar Garin-Chesa; Olivier Leger; John Edward Park; Wolfgang J. Rettig; Jose Saldanha


Archive | 1999

Antikörper mit verbesserter produzierbarkeit

John Edward Park; Pilar Garin-Chesa; Uwe Bamberger; Wolfgang J. Rettig; Olivier Leger; Jose Saldanha


Archive | 1999

Anticuerpo con capacidad de produccion mejorada.

Uwe Bamberger; Pilar Garin-Chesa; Olivier Leger; John Edward Park; Wolfgang J. Rettig; Jose Saldanha


Archive | 1999

Anticorps alpha specifique fap a aptitude a la production amelioree

Uwe Bamberger; Pilar Garin-Chesa; Olivier Leger; John Edward Park; Wolfgang J. Rettig; Jose Saldanha


Archive | 1998

Fap alpha-spezifischer antikörper mit verbesserter produzierbarkeit

Uwe Bamberger; Pilar Garin-Chesa; Olivier Leger; John Edward Park; Wolfgang J. Rettig; Jose Saldanha

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John Edward Park

Garvan Institute of Medical Research

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Wolfgang J. Rettig

Garvan Institute of Medical Research

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Pilar Garin-Chesa

Research Institute of Molecular Pathology

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Jose Saldanha

Chugai Pharmaceutical Co.

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John Edward Park

Garvan Institute of Medical Research

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Jose Saldanha

Chugai Pharmaceutical Co.

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Pilar Garin-Chesa

Research Institute of Molecular Pathology

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Wolfgang J. Rettig

Garvan Institute of Medical Research

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Maayan David

Tel Aviv Sourasky Medical Center

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