Guide La fiebre del carbón (Nuevos Tiempos) (Spanish Edition)

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Review by the Competent Authority or Ethics Committee in the country concerned. EU Clinical Trials Register. Search tools. Select Date Range: to. Select Rare Disease:. IMP with orphan designation in the indication. Orphan Designation Number:. Results Status: Trials with results Trials without results. Clear advanced search filters. Date on which this record was first entered in the EudraCT database:. Title of the trial for lay people, in easily understood, i. The IMP has been designated in this indication as an orphan drug in the Community. Committee on Advanced therapies CAT has issued a classification for this product.

Combination product that includes a device, but does not involve an Advanced Therapy.

Clinical Trials Register

AML is cancer of myeloid line of blood cells characterized by rapid growth of abnormal white blood cells that accumulate in bone marrow and interfere with production of normal blood cells. To determine the safety and tolerability of gilteritinib after HCT. To compare overall survival OS , non-relapse mortality NRM and event-free survival EFS where events include relapse, death, stopping therapy and administration of donor lymphocyte infusion DLI or new therapy for suspicion of disease in participants treated with gilteritinib as maintenance therapy after HCT compared to those treated with placebo.

Vease synopsis del protocolo. Subject is suitable candidate for HCT and has an acceptable source of allogeneic donor stem cells, as defined per institutional practice allogeneic HCT for any donor source [matched sibling, unrelated donor URD , mismatched URD, related haploidentical, or umbilical cord blood] and any graft source [umbilical cord, BM, peripheral blood PB ], and any conditioning [myeloablative conditioning MAC , reduced intensity conditioning RIC , or non-myeloablative conditioning NMA ] will be permitted.

Clinical Trials Register

Subject is legal adult by local regulation at the time of signing ICF 4. Subject has not received more than 2 cycles of induction chemotherapy to achieve CR1. RBC and platelet transfusion independence is not required. The maximum time allowed from establishment of CR1 to registration is 12 months. Subject must meet the following criteria as indicated on the clinical laboratory tests: a. Serum potassium and magnesium greater than the institutional lower limit of normal LLN.


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For all Registration Inclusion Criteria, see protocol. Combination product that includes a device, but does not involve an Advanced Therapy. AML is cancer of myeloid line of blood cells characterized by rapid growth of abnormal white blood cells that accumulate in bone marrow and interfere with production of normal blood cells. To determine the safety and tolerability of gilteritinib after HCT. To compare overall survival OS , non-relapse mortality NRM and event-free survival EFS where events include relapse, death, stopping therapy and administration of donor lymphocyte infusion DLI or new therapy for suspicion of disease in participants treated with gilteritinib as maintenance therapy after HCT compared to those treated with placebo.

Vease synopsis del protocolo. Subject is suitable candidate for HCT and has an acceptable source of allogeneic donor stem cells, as defined per institutional practice allogeneic HCT for any donor source [matched sibling, unrelated donor URD , mismatched URD, related haploidentical, or umbilical cord blood] and any graft source [umbilical cord, BM, peripheral blood PB ], and any conditioning [myeloablative conditioning MAC , reduced intensity conditioning RIC , or non-myeloablative conditioning NMA ] will be permitted.

Subject has not received more than 2 cycles of induction chemotherapy to achieve CR1. RBC and platelet transfusion independence is not required. The maximum time allowed from establishment of CR1 to registration is 12 months.

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Subject must meet the following criteria as indicated on the clinical laboratory tests: a. Serum potassium and magnesium greater than the institutional lower limit of normal LLN.

For all Registration Inclusion Criteria, see protocol. El sujeto debe cumplir los siguientes criterios en las determinaciones de laboratorio: a. Participant has had a prior allogeneic transplant. Participant requires treatment with concomitant drugs that are strong inducers of CYP3A4. If the problem continues, please let us know and we'll try to help. An unexpected error occurred.

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Read e-book La fiebre del carbón (Nuevos Tiempos) (Spanish Edition)

El ensayo de bioluminiscencia de ATP. Dentro de lo etc. Durante este proceso, los protones son "bombeados" en el espacio del intermembrane de mitocondrias. Juntos, el ciclo TCA y etc.

Get PDF La fiebre del carbón (Nuevos Tiempos) (Spanish Edition)

Puesto que la cantidad de luminiscencia producida es directamente proporcional a la cantidad de ATP, es un buen indicador de viabilidad celular y el metabolismo. Ahora que usted entiende los principios de la prueba de bioluminiscencia de ATP, vamos a esbozar un protocolo general. A subscription to J o VE is required to view this content. You will only be able to see the first 20 seconds. To learn more about our GDPR policies click here.

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