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|a (DE-627)CTG004835344
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|a (UBBS_Klinische_Studien_WHO)EUCTR2015-001151-68-DE
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|a (UBBS_Klinische_Studien_WHO)TUD-APOLLO-064
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|a A randomized Phase III study to compare arsenic trioxide (ATO) combined to ATRA and idarubicin versus standard ATRA and anthracyclines-based chemotherapy (AIDA regimen) for patients with newly diagnosed, high-risk acute promyelocytic leukemia
|b A randomized Phase III study to compare arsenic trioxide (ATO) combined to ATRA and idarubicin versus standard ATRA and anthracyclines-based chemotherapy (AIDA regimen) for patients with newly diagnosed, high-risk acute promyelocytic leukemia - APOLLO
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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: 22-12-2015, Last updated: 2023-06-29
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|a Medical Condition: newly diagnosed high-risk acute promyelocytic leukemia (APL) MedDRA version: 21.0Level: PTClassification code 10001019Term: Acute promyelocytic leukaemiaSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps);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: 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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