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210507s2022 xx |||||o 00| ||eng c |
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|a (DE-627)WHO004403789
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|a (UBBS_Klinische_Studien_WHO)EUCTR2019-003521-21-CZ
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|a (UBBS_Klinische_Studien_WHO)GLPG2737-CL-203
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|a (UBBS_Klinische_Studien_WHO)2019-003521-21-BE
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|a DE-627
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|a eng
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|a A study to evaluate the effects of GLPG2737 in subjects with autosomal dominant polycystic kidney disease
|b An exploratory, randomized, double-blind, placebo-controlled, multicenterstudy to evaluate the efficacy, safety, tolerability and pharmacokinetics oforally administered GLPG2737 for 52 weeks, followed by an open-labelextension period of 52 weeks in subjects with autosomal dominantpolycystic kidney disease
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|c 2022
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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: 28-07-2020, Last updated: 2022-11-24
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|a Medical Condition: Autosomal dominant polycystic kidney disease MedDRA version: 20.0Level: LLTClassification code 10036046Term: Polycystic kidney, autosomal dominantSystem Organ Class: 100000004850;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
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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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|t WHO International Clinical Trials Registry Platform
|g (2022) vom: 01. Feb.
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|g year:2022
|g day:01
|g month:02
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|u https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2019-003521-21
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|a SSG-OLC-PHA
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|a AR
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