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210507s2023 xx |||||o 00| ||eng c |
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|a (DE-627)CTG006157319
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|a (UBBS_Klinische_Studien_WHO)EUCTR2016-000297-38-GB
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|a (UBBS_Klinische_Studien_WHO)CL1-68587-003
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|a (UBBS_Klinische_Studien_WHO)NCT02735083
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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 evaluate the long-term safety of patients with advanced lymphoid malignancies who have been previously administered with UCART19 or ALLO-501
|b Long-term follow-up study of patients who have previously been exposed to UCART19 / ALLO-501 (allogeneic engineered T-cells expressing a lentiviral-based anti-CD19 chimeric antigen receptor)
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|c 2023
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|a Text
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|a Computermedien
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|a WHO International Clinical Trials Registry Platform (https://www.who.int/ictrp/en/), First posted: 15-04-2016, Last updated: 2023-06-29
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|a Medical Condition: Advanced lymphoid malignancies MedDRA version: 21.0Level: LLTClassification code 10060390Term: Leukaemia lymphoblastic acuteSystem Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps) MedDRA version: 21.1Level: PTClassification code 10008958Term: Chronic lymphocytic 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 1
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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:2016-000297-38
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