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- A phase II, single arm, open label, study on the safety, efficacy, pharmacokinetics and pharmacodynamics of quizartinib in combination with chemotherapy and as single-agent after high dose therapy in newly diagnosed pediatric FLT3-ITD positive and NPM1 wild-type AML patients. (A linked-trial of the CHIP-AML22/Master protocol by the NOPHO-DB-SHIP consortium).
A phase II, single arm, open label, study on the safety, efficacy, pharmacokinetics and pharmacodynamics of quizartinib in combination with chemotherapy and as single-agent after high dose therapy in newly diagnosed pediatric FLT3-ITD positive and NPM1 wild-type AML patients. (A linked-trial of the CHIP-AML22/Master protocol by the NOPHO-DB-SHIP consortium).
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PRINCESS MÁXIMA CENTER FOR PEDIATRIC ONCOLOGY B.V.,
Cita
A phase II, single arm, open label, study on the safety, efficacy, pharmacokinetics and pharmacodynamics of quizartinib in combination with chemotherapy and as single-agent after high dose therapy in newly diagnosed pediatric FLT3-ITD positive and NPM1 wild-type AML patients. (A linked-trial of the CHIP-AML22/Master protocol by the NOPHO-DB-SHIP consortium). (CHIP-AML22/Quizartinib). PRINCESS MÁXIMA CENTER FOR PEDIATRIC ONCOLOGY B.V.,. 2024IP:JOSÉ MARÍA FERNÁNDEZ NAVARRO.
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