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WHO004913035 |
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DE-627 |
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210507s2021 xx |||||o 00| ||eng c |
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|a (DE-627)WHO004913035
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|a (UBBS_Klinische_Studien_WHO)EUCTR2015-004725-13-DE
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|a (UBBS_Klinische_Studien_WHO)SHP620-303
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|a (UBBS_Klinische_Studien_WHO)NCT02931539
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|a DE-627
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|e rakwb
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|a eng
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|a A study to determine how safe and effective maribavir versus standard of care is in treating cytomegalovirus in transplant patients
|b A Phase 3, Multicenter, Randomized, Open-label, Active-controlled Study to Assess the Efficacy and Safety of Maribavir Treatment Compared to Investigator-assigned Treatment in Transplant Recipients with Cytomegalovirus (CMV) Infections that are Refractory or Resistant to Treatment with Ganciclovir, Valganciclovir, Foscarnet, or Cidofovir.
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|c 2021
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|a Text
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|2 rdacontent
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|a Computermedien
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|2 rdamedia
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|a Online-Ressource
|b cr
|2 rdacarrier
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|a WHO International Clinical Trials Registry Platform (https://www.who.int/ictrp/en/), First posted: 21-12-2016, Last updated: 2022-11-24
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|a Medical Condition: CMV infections resistant or refractory in transplant patients MedDRA version: 20.0Level: LLTClassification code 10021819Term: Infection in marrow transplant recipientsSystem Organ Class: 100000004862 MedDRA version: 20.0Level: LLTClassification code 10021829Term: Infection in solid organ transplant recipientsSystem Organ Class: 100000004862;Therapeutic area: Diseases [C] - Virus Diseases [C02]
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|a Study Type: Interventional
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|a Phase: Phase 3
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|a Recruitment Status: Not yet recruiting
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|a 610
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|i Enthalten in
|t WHO International Clinical Trials Registry Platform
|g (2021) vom: 14. Juni
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|g year:2021
|g day:14
|g month:06
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|u https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2015-004725-13
|z kostenfrei
|3 Volltext
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|a GBV_CTG
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|a SSG-OLC-PHA
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|a AR
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|j 2021
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|c 06
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