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|a (UBBS_Klinische_Studien_WHO)EUCTR2020-005447-23-NL
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|a (UBBS_Klinische_Studien_WHO)75871
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|a Intravenous imatinib for corona virus-related lung injury.
|b A randomised, double-blind, placebo-controlled study to investigate the safety and efficacy of intravenous imatinib mesilate (Impentri®) in subjects with Acute Respiratory Distress Syndrome induced by COVID-19. - Intravenous imatinib for COVID-19-related ARDS.
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|a WHO International Clinical Trials Registry Platform (https://www.who.int/ictrp/en/), First posted: 28-01-2021, Last updated: 2022-11-24
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|a Medical Condition: COVID-19 related Acute Respiratory Distress Syndrome (ARDS) in mechanically-ventilated patients on the Intensive Care Unit. MedDRA version: 23.0Level: LLTClassification code 10084270Term: SARS-CoV-2 acute respiratory diseaseSystem Organ Class: 100000004862;Therapeutic area: Diseases [C] - Immune System Diseases [C20]
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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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