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Translation strategy for the qualification of drug-induced vascular injury biomarkers.
Bendjama, Kaïdre; Guionaud, Silvia; Aras, Gulfidan; Arber, Nadir; Badimon, Lina; Bamberger, Uwe; Bratfalean, Dorina; Brott, David; David, Maayan; Doessegger, Lucette; Firat, Hüseyin; Gallas, Jean-François; Gautier, Jean-Charles; Hoffmann, Peter; Kraus, Sarah; Padro, Teresa; Saadoun, David; Szczesny, Piotr; Thomann, Peter; Vilahur, Gemma; Lawton, Michael; Cacoub, Patrice.
Afiliación
  • Bendjama K; Firalis SAS, Biomarker R&D, Huningue, France.
  • Guionaud S; Shire, Basingstoke, UK.
  • Aras G; Firalis SAS, Biomarker R&D, Huningue, France.
  • Arber N; Integrated Cancer Prevention Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
  • Badimon L; Cardiovascular Research Center, CSIC-ICCC, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Bamberger U; Boehringer Ingelheim Pharma GmbH & Co. KG Nonclinical Drug Safety Biberach/Riss, Germany.
  • Bratfalean D; Firalis SAS, Biomarker R&D, Huningue, France.
  • Brott D; AstraZeneca Pharmaceuticals, Translational Patient Safety and Enabling Sciences, Wilmington, Delaware, USA.
  • David M; Integrated Cancer Prevention Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
  • Doessegger L; F. Hoffmann-La Roche AG, Basel, Switzerland.
  • Firat H; Firalis SAS, Biomarker R&D, Huningue, France.
  • Gallas JF; Sanofi R&D, Montpellier, France.
  • Gautier JC; Sanofi R&D, Vitry-sur-Seine, France.
  • Hoffmann P; Novartis Pharmaceuticals Corporation, Preclinical safety, East Hanover, New Jersey, USA.
  • Kraus S; Integrated Cancer Prevention Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
  • Padro T; Cardiovascular Research Center, CSIC-ICCC, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Saadoun D; Assistance Publique-Hôpitaux de Paris (AP-HP), Groupe Hospitalier Pitié-Salpêtrière, Department of Internal Medicine and Clinical Immunology, F-75013, Paris, France; Département Hospitalo-Universitaire I2B, UPMC Univ Paris 06, F-75005, Paris, France; INSERM UMR 7211, F-75005, Paris, France; INSERM,
  • Szczesny P; F. Hoffmann-La Roche AG, Basel, Switzerland.
  • Thomann P; Firalis SAS, Biomarker R&D, Huningue, France.
  • Vilahur G; Cardiovascular Research Center, CSIC-ICCC, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
  • Lawton M; Pfizer Worldwide Research & Development, Drug Safety Research & Development, Groton, Connecticut, USA michael.lawton@pfizer.com.
  • Cacoub P; Assistance Publique-Hôpitaux de Paris (AP-HP), Groupe Hospitalier Pitié-Salpêtrière, Department of Internal Medicine and Clinical Immunology, F-75013, Paris, France; Département Hospitalo-Universitaire I2B, UPMC Univ Paris 06, F-75005, Paris, France; INSERM UMR 7211, F-75005, Paris, France; INSERM,
Toxicol Pathol ; 42(4): 658-71, 2014 Jun.
Article en En | MEDLINE | ID: mdl-24771082
ABSTRACT
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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Biomarcadores / Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos / Lesiones del Sistema Vascular Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: America do norte / Europa Idioma: En Revista: Toxicol Pathol Año: 2014 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Biomarcadores / Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos / Lesiones del Sistema Vascular Tipo de estudio: Prognostic_studies Límite: Humans País/Región como asunto: America do norte / Europa Idioma: En Revista: Toxicol Pathol Año: 2014 Tipo del documento: Article País de afiliación: Francia