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Kusajili – Centralise les essais cliniques mondiaux
Résultat
de votre recherche par promoteur : Astellas Pharma Global Development, Inc
Homme Max 99 ans
Astellas Pharma Global Development, Inc (APGD)
MAJ Il y a 4 ans
A Multinational study, Phase 3, Randomized, Double-blind, and controlled against a Placebo that studies the Efficacy and the Safety of Enzalutamide Plus Androgen Deprivation Therapy (ADT) Versus Placebo Plus ADT in Patients with Metastatic Hormone Sensitive Prostate Cancer (mHSPC)
To determine the benefit of enzalutamide plus ADT as compared to placebo plus ADT as assessed by radiographic progression-free survival (rPFS) based on central review
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unknown
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Femme et Homme Max 99 ans
Astellas Pharma Global Development, Inc (APGD)
MAJ Il y a 4 ans
A Phase 2/3 Multicenter, Open-label, 3-arm, 2-stage Randomized Study of ASP2215 (Gilteritinib), Combination of ASP2215 Plus Azacitidine and Azacitidine Alone in the Treatment of Newly Diagnosed Acute Myeloid Leukemia with FLT3 Mutation in Patients Not Eligible for Intensive Induction Chemotherapy
Determine the efficacy superiority of ASP2215 and/or ASP2215 plus azacitidine versus azacitidine as measured by overall survival (OS).
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unknown
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Femme et Homme Max 99 ans
Astellas Pharma Global Development, Inc (APGD)
MAJ Il y a 4 ans
Effectiveness and safety of gilteritinib (ASP2215) as maintenance treatment (maintain the response achieved during the first course of treatment) for Acute myeloid leukemia patients who are in a first complete remission (no residual leukemia cells in your bone marrow), with mutations in the FLT3 gene compared to placebo given alone. Fenntartó kezelésként alkalmazott gilteritinib (ASP2215) hatásosságának és biztonságosságának vizsgálata első teljes remisszió időszakában levő (tumorsejt nem található a csontvelőben), FLT3 génmutációval rendelkező, akut myeloid leukémiában szenvedő betegek körében, placebóhoz viszonyítva
The primary objective is to compare relapse-free survival (RFS) between subjects with FLT3/ITD AML in first complete remission (CR1) without transplant and who are randomized to receive gilteritinib o...
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unknown
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Femme et Homme Max 99 ans
Astellas Pharma Global Development, Inc (APGD)
MAJ Il y a 4 ans
A Phase II, Multicenter, Open-Label Study Of YM155 Plus Docetaxel in Subjects with Stage III (Unresectable) or Stage IV Melanoma
To evaluate 6-month Progression Free Survival (PFS).
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unknown
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Femme et Homme Max 99 ans
Astellas Pharma Global Development, Inc (APGD)
MAJ Il y a 4 ans
A Phase 3b Randomized, Double-Blind, Placebo Controlled, Parallel Group Study to Evaluate the Safety and Efficacy of Vernakalant Hydrochloride Injection in Patients with Recent Onset Symptomatic Atrial Fibrillation
The primary safety objective of this study is to evaluate the safety of vernakalant injection in subjects with recent onset (AF > 3 hours to less than or equal to 7 days), symptomatic atrial fibrillat...
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Essai clos aux inclusions
Plus d'informations
Femme et Homme Max 99 ans
Astellas Pharma Global Development, Inc (APGD)
MAJ Il y a 4 ans
A clinical study (Phase III) to assess the Evaluate the Protective Efficacy and Safety of a Therapeutic Vaccine, ASP0113, in Cytomegalovirus (CMV)-Seropositive Recipients Undergoing Allogeneic, Hematopoietic Cell Transplant (HCT), when compared against placebo in a randomised, double blind manner
• To evaluate the efficacy of ASP0113 compared with placebo as measured by a primary composite endpoint of overall mortality and CMV end organ disease (EOD) through one year post-transplant. • To eval...
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unknown
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Femme et Homme Max 99 ans
Astellas Pharma Global Development, Inc (APGD)
MAJ Il y a 4 ans
This is a phase 3, open-label, multicenter, randomized study to compare the efficacy and safety of ASP2215 therapy to salvage chemotherapy in FLT3-mutated AML subjects who are refractory to or have relapsed after first-line AML therapy
The primary objective is to determine the clinical benefit of ASP2215 therapy in subjects with FMS-like tyrosine kinase (FLT3) mutated AML who are refractory to or have relapsed after first-line AML t...
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unknown
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Femme et Homme Max 99 ans
Astellas Pharma Global Development, Inc
MAJ Il y a 4 ans
Lintisinib rollover study
The objective of the study is to provide treatment continuation for subjects participating in other Astellas-sponsored studies with linsitinib.
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Essai clos aux inclusions
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