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|a (DE-627)WHO007539525
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|a (UBBS_Klinische_Studien_WHO)EUCTR2020-005979-12-GR
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|a (UBBS_Klinische_Studien_WHO)2020-005979-12-ES
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|a Efficacy and safety of XAV-19 for the treatment of moderate COVID-19
|b An international, placebo-controlled, double-blind, randomized clinical trial to evaluate the efficacy and safety of 150 mg XAV-19 infusion, in patients with moderate COVID-19: the EUROXAV study - EUROXAV Study
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|c 2021
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|a WHO International Clinical Trials Registry Platform (https://www.who.int/ictrp/en/), First posted: 08-02-2021, Last updated: 2022-11-24
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|a Medical Condition: Moderate COVID-19 MedDRA version: 23.1Level: PTClassification code 10084460Term: COVID-19 treatmentSystem Organ Class: 10042613 - Surgical and medical procedures;Therapeutic area: Diseases [C] - Virus Diseases [C02]
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|a Study Type: Interventional
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|a Phase: Phase 2
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|a Recruitment Status: Authorised-recruitment may be ongoing or finished
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