BRIEF-Gilead Says European Commission Grants Conditional Marketing Authorization For Veklury (Rem... - 1 minute read
July 3 (Reuters) - Gilead Sciences Inc:
* EUROPEAN COMMISSION GRANTS CONDITIONAL MARKETING AUTHORIZATION FOR GILEAD’S VEKLURY® (REMDESIVIR) FOR THE TREATMENT OF COVID-19
* GILEAD SCIENCES - UNDER AUTHORIZATION, VEKLURY IS INDICATED FOR TREATMENT OF COVID-19 IN ADULTS AND ADOLESCENTS WITH PNEUMONIA REQUIRING SUPPLEMENTAL OXYGEN
* GILEAD SCIENCES INC - CONDITIONAL MARKETING AUTHORIZATION IN EUROPE FOR VEKLURY (REMDESIVIR) IS INITIALLY VALID FOR ONE YEAR Source text for Eikon: Further company coverage:
Source: Reuters
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* EUROPEAN COMMISSION GRANTS CONDITIONAL MARKETING AUTHORIZATION FOR GILEAD’S VEKLURY® (REMDESIVIR) FOR THE TREATMENT OF COVID-19
* GILEAD SCIENCES - UNDER AUTHORIZATION, VEKLURY IS INDICATED FOR TREATMENT OF COVID-19 IN ADULTS AND ADOLESCENTS WITH PNEUMONIA REQUIRING SUPPLEMENTAL OXYGEN
* GILEAD SCIENCES INC - CONDITIONAL MARKETING AUTHORIZATION IN EUROPE FOR VEKLURY (REMDESIVIR) IS INITIALLY VALID FOR ONE YEAR Source text for Eikon: Further company coverage:
Source: Reuters
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