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210507s2021 xx |||||o 00| ||eng c |
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|a (DE-627)CTG006141765
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|a (UBBS_Klinische_Studien_WHO)EUCTR2020-001782-37-SK
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|a (UBBS_Klinische_Studien_WHO)P?-COV-III-20
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|a DE-627
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|a A multi-centre, adaptive, randomized, double-blind, placebo-controlled comparative clinical study of the safety and efficacy of 12 mg Polyoxidonium®, lyophilizate solution for injections (NPO Petrovax Pharm LLC, Russia) in patients with coronavirus disease (COVID-19).
|b A multi-centre, adaptive, randomized, double-blind, placebo-controlled comparative clinical trial of the safety and efficacy of 12 mg Polyoxidonium®, lyophilizate solution for injections (NPO Petrovax Pharm LLC, Russia), in patients with coronavirus disease (COVID-19)
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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: 15-06-2020, Last updated: 2022-11-24
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|a Medical Condition: MedDRA version: 21.1Level: PTClassification code 10035737Term: Pneumonia viralSystem Organ Class: 10021881 - Infections and infestations;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: Not yet recruiting
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|a 610
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|t WHO International Clinical Trials Registry Platform
|g (2021) vom: 07. Juni
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|g year:2021
|g day:07
|g month:06
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