A Phase 1 trial of pf‑03084014 in patients with advanced solid tumor malignancy and t‑cell acute lymphoblastic leukemia/lymphoblastic lymphoma

Mise à jour : Il y a 4 ans
Référence : EUCTR2010-022036-36

Femme et Homme

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Extrait

Phase 1a Primary Objectives 1. To determine the maximum tolerated dose (MTD) of PF-03084014 when administered twice daily for 21 days alone in patients with advanced malignancies (encompassing advanced solid tumors and relapsed or refractory T-ALL/LBL). Phase 1b Primary Objectives 1. To determine the MTD of PF-03084014 when administered twice daily for 21 days in combination with dexamethasone given once daily on Day 1 to Day 3 and Day 11 to Day 13 of each cycle in patients with advanced malignancies (encompassing advanced solid tumors and relapsed or refractory T-ALL/LBL).


Critère d'inclusion

  • advanced solid tumor malignancies or relapsed or refractory acute T-cell lymphoblastic leukemia/lymphoblastic lymphoma (T-ALL/LBL)

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