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210507s2023 xx |||||o 00| ||eng c |
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|a (DE-627)CTG004733541
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|a (UBBS_Klinische_Studien_WHO)EUCTR2016-003473-17-GB
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|a (UBBS_Klinische_Studien_WHO)CC-90001-IPF-001
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|a DE-627
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|a eng
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|a Investigation to Efficacy and Safety of CC-90001 in patients with Idiopathic Pulmonary Fibrosis
|b A Phase 2, 24-Week Randomized, Double-blind, Placebo-ControlledMulticenter Study, With an 80-Week Active Treatment Extension, toEvaluate the Efficacy and Safety of CC-90001 in Subjects with IdiopathicPulmonary Fibrosis
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|c 2023
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|a Text
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|a WHO International Clinical Trials Registry Platform (https://www.who.int/ictrp/en/), First posted: 24-02-2017, Last updated: 2023-06-29
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|a Medical Condition: IDIOPATHIC PULMONARY FIBROSIS MedDRA version: 20.0Level: LLTClassification code 10067761Term: Exacerbation of idiopathic pulmonary fibrosisSystem Organ Class: 100000004855;Therapeutic area: Diseases [C] - Respiratory Tract Diseases [C08]
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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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|a 610
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|i Enthalten in
|t WHO International Clinical Trials Registry Platform
|g (2023) vom: 21. Juni
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|g year:2023
|g day:21
|g month:06
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|u https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2016-003473-17
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