Saku,usuda,197, Japan
Matsuyama, Ehime
Recruiting
Quizartinib or Placebo Plus Chemotherapy in Newly Diagnosed Patients With FLT3-ITD Negative AML
This is a clinical trial to compare the effect of quizartinib versus placebo (administered with standard induction and consolidation chemotherapy, then administered as maintenance therapy for up to 36 cycles) on the primary endpoint of overall survival (OS) in adult patients with newly diagnosed FMS-like tyrosine kinase 3 (FLT3)-internal tandem duplication (ITD) negative acute myeloid leukemia (AML). Participants will be tested for FLT3-ITD mutation status in a central laboratory using a validated assay.
Phase
3Span
293 weeksSponsor
Daiichi SankyoMatsuyama
Recruiting
Matsuyama, Ehime
Recruiting
ONO-4538 Phase II Rollover Study (ONO-4538-98)
Phase
2Span
329 weeksSponsor
Ono Pharmaceutical Co. LtdMatsuyama, Ehime
Recruiting
Initial Attack on Latent Metastasis Using TAS-102 for ct DNA Identified Colorectal Cancer Patients After Curative Resection
Phase
3Span
182 weeksSponsor
National Cancer Center Hospital EastMatsuyama, Ehime
Recruiting
A Study of First-Line Olomorasib (LY3537982) and Pembrolizumab With or Without Chemotherapy in Patients With Advanced KRAS G12C-Mutant Non-small Cell Lung Cancer
Dose Optimization, Part A, and Part B are randomized. Safety Lead-In for Part B is single arm, non-randomized.
Phase
3Span
306 weeksSponsor
Eli Lilly and CompanyMatsuyama, Ehime
Recruiting
A Study of LY3556050 in Adult Participants With Diabetic Peripheral Neuropathic Pain
Phase
2Span
95 weeksSponsor
Eli Lilly and CompanyMatsuyama, Ehime
Recruiting
Matsuyama, Ehime
Recruiting
Matsuyama, Ehime
Recruiting
Savolitinib Plus Osimertinib Versus Platinum-based Doublet Chemotherapy in Participants With Non-Small Cell Lung Cancer Who Have Progressed on Osimertinib Treatment
This is a multicentre, Phase III, randomised, open-label study to investigate the efficacy and safety of savolitinib administered orally in combination with osimertinib versus platinum-based doublet chemotherapy in participants with EGFR mutated, MET-overexpressed and/or amplified, locally advanced or metastatic NSCLC who have progressed on first- or second-line treatment with osimertinib as the most recent therapy. Approximately 324 participants with EGFR mutated, MET-overexpressed and/or amplified, locally advanced or metastatic NSCLC will be randomly assigned to study intervention with 1:1 ratio. Patients will be treated until either objective progression of disease (PD) by Response Evaluation Criteria in Solid Tumours 1.1 (RECIST 1.1) is assessed by the investigator, unacceptable toxicity occurs, consent is withdrawn, or another discontinuation criterion is met.
Phase
3Span
229 weeksSponsor
AstraZenecaMatsuyama
Recruiting