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210507s2023 xx |||||o 00| ||eng c |
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|a (DE-627)CTG004263790
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|a (UBBS_Klinische_Studien_WHO)EUCTR2013-001790-25-DE
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|a (UBBS_Klinische_Studien_WHO)FP01C-13-001
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|a (UBBS_Klinische_Studien_WHO)2013-001790-25-AT
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|a DE-627
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|a eng
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|a A clinical trial for advanced prostatic cancer patients . The study medication will be Leuprolide Mesylate, which will be administered as an injection twice. Both the study doctors and clinical trial participants know which treatment is being administered, there will be only one treatment group.The safety and efficacy of the medicinal product will be tested during the study.
|b An Open-Label, Single-Arm Study of the Safety, Efficacy, and Pharmacokinetic Behavior of Leuprolide Mesylate for Injectable Suspension (LMIS 50 mg) in Subjects with Advanced Prostate Carcinoma
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|c 2023
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|a Text
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|a Computermedien
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|a Online-Ressource
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|a WHO International Clinical Trials Registry Platform (https://www.who.int/ictrp/en/), First posted: 30-06-2014, Last updated: 2023-06-29
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|a Medical Condition: Advanced Prostate Carcinoma MedDRA version: 19.0Level: LLTClassification code 10036921Term: Prostate carcinomaSystem Organ Class: 100000004864;Therapeutic area: Diseases [C] - Cancer [C04]
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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 (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:2013-001790-25
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|a AR
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