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Interval Estimation of the 50% Effective Time in Small Sample Assay Data

Alternatives to Animal Testing and Experimentation, 2022-08, Vol.27 (1), p.36-36

2022

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敏感肌に対するリポポリサッカライドの有効性: バリア機能の改善

日本化粧品技術者会誌, 2021/12/20, Vol.55(4), pp.338-345

2021

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Effectiveness of Lipopolysaccharide for Sensitive Skin: Improvement of Barrier Function

Journal of Society of Cosmetic Chemists of Japan, 2021/12/20, Vol.55(4), pp.338-345

2021

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Application of gamma process to two-agent combinations with delayed toxicity

Communications in statistics. Simulation and computation, 2021-01, Vol.50 (1), p.153-163

2021

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Response to tocilizumab and work productivity in patients with rheumatoid arthritis: 2-year follow-up of FIRST ACT-SC study

Modern rheumatology, 2021, Vol.31 (1), p.42-52

2021

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Utility-Based Interim Decision Rule Planning in Adaptive Population Selection Designs With Survival Endpoints

Statistics in biopharmaceutical research, 2020-07, Vol.12 (3), p.360-368

2020

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Performance of randomization-based causal methods with and without integrating external data sources for adjusting overall survival in case of extensive treatment switches in placebo-controlled randomized oncology phase 3 trials

Journal of biopharmaceutical statistics, 2020-03, Vol.30 (2), p.377-401

2020

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Risk factors for paraaortic lymph-node recurrence in colorectal cancer

Annals of Cancer Research and Therapy, 2019/07/30, Vol.27(2), pp.52-56

2019

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Phase III randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage III colon cancer: final results of the JFMC37-0801 study

British journal of cancer, 2019-04, Vol.120 (7), p.689-696

2019

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Dose individualization and variable selection by using the Bayesian lasso in early phase dose finding trials

Journal of the Royal Statistical Society Series C: Applied Statistics, 2019-02, Vol.68 (2), p.445-460

2019

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Two-stage approach based on zone and dose findings for two-agent combination Phase I/II trials

Journal of biopharmaceutical statistics, 2018-11, Vol.28 (6), p.1025-1037

2018

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A Bayesian hierarchal modeling approach to shortening phase I/II trials of anticancer drug combinations

Pharmaceutical statistics : the journal of the pharmaceutical industry, 2018-11, Vol.17 (6), p.750-760

2018

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Effect of subcutaneous tocilizumab treatment on work/housework status in biologic-naïve rheumatoid arthritis patients using inverse probability of treatment weighting: FIRST ACT-SC study

Arthritis research & therapy, 2018-07, Vol.20 (1), p.151-151, Article 151

2018

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Sample size determination for the current strategy in oncology Phase 3 trials that tests progression-free survival and overall survival in a two-stage design framework

Journal of biopharmaceutical statistics, 2018-07, Vol.28 (4), p.589-611

2018

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Risk Factors for Peritoneal Recurrence in Stage II to III Colon Cancer

Diseases of the colon & rectum, 2018-07, Vol.61 (7), p.803-808

2018

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Clinical Signatures of Mucinous and Poorly Differentiated Subtypes of Colorectal Adenocarcinomas by a Propensity Score Analysis of an Independent Patient Database from Three Phase III Trials

Diseases of the colon & rectum, 2018-04, Vol.61 (4), p.461-471

2018

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Statistical analysis for toxicity studies

Journal of Toxicologic Pathology, 2018, Vol.31 (1), p.15-22

Chikuma Hamada

2018

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Questionnaire Survey From the Viewpoint of Concordance in Patient and Physician Satisfaction Concerning Hypertensive Treatment in Elderly Patients　― Patients Voice Study

Circulation Journal, 2018/03/23, Vol.82(4), pp.1051-1061

2018

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Statistical analysis for toxicity studies

Journal of Toxicologic Pathology, 2018, Vol.31(1), pp.15-22

Hamada, Chikuma

2018

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Development and validation of a prognostic nomogram for colorectal cancer after radical resection based on individual patient data from three large-scale phase III trials

Oncotarget, 2017-11, Vol.8 (58), p.99150-99160

2017

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Adaptive phase I/II clinical trials for drug combination assessment in oncology using the outcomes of each cycle

Pharmaceutical statistics : the journal of the pharmaceutical industry, 2017-11, Vol.16 (6), p.433-444

2017

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Japanese Society for Biopharmaceutical Statistics (JSBS) and Japan Activity for Improvement of Cardiovascular Evaluation by Telemetry system (J-ICET)_ECG Group Collaboration Project: Proposal of Standard Statistical Analysis Method of Monkey Telemetry Study for Cardiovascular Risk Assessment

Journal of pharmacological and toxicological methods, 2017-11, Vol.88, p.183-183

2017

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Clinical impact of tumor location on the colon cancer survival and recurrence: analyses of pooled data from three large phase III randomized clinical trials

Cancer medicine (Malden, MA), 2017-11, Vol.6 (11), p.2523-2530

2017

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Adaptive Seamless Design for Establishing Pharmacokinetic and Efficacy Equivalence in Developing Biosimilars

Therapeutic innovation & regulatory science, 2017-11, Vol.51 (6), p.761-769

2017

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Exploratory double-blind, parallel-group, placebo-controlled extension study of edaravone (MCI-186) in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2017-10, Vol.18 (sup1), p.20-31

2017

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Interval Estimation of the 50% Effective Time in Small Sample Assay Data

敏感肌に対するリポポリサッカライドの有効性: バリア機能の改善

Effectiveness of Lipopolysaccharide for Sensitive Skin: Improvement of Barrier Function

Application of gamma process to two-agent combinations with delayed toxicity

Response to tocilizumab and work productivity in patients with rheumatoid arthritis: 2-year follow-up of FIRST ACT-SC study

Utility-Based Interim Decision Rule Planning in Adaptive Population Selection Designs With Survival Endpoints

Performance of randomization-based causal methods with and without integrating external data sources for adjusting overall survival in case of extensive treatment switches in placebo-controlled randomized oncology phase 3 trials

Risk factors for paraaortic lymph-node recurrence in colorectal cancer

Phase III randomised trial comparing 6 vs. 12-month of capecitabine as adjuvant chemotherapy for patients with stage III colon cancer: final results of the JFMC37-0801 study

Dose individualization and variable selection by using the Bayesian lasso in early phase dose finding trials

Two-stage approach based on zone and dose findings for two-agent combination Phase I/II trials

A Bayesian hierarchal modeling approach to shortening phase I/II trials of anticancer drug combinations

Effect of subcutaneous tocilizumab treatment on work/housework status in biologic-naïve rheumatoid arthritis patients using inverse probability of treatment weighting: FIRST ACT-SC study

Sample size determination for the current strategy in oncology Phase 3 trials that tests progression-free survival and overall survival in a two-stage design framework

Risk Factors for Peritoneal Recurrence in Stage II to III Colon Cancer

Clinical Signatures of Mucinous and Poorly Differentiated Subtypes of Colorectal Adenocarcinomas by a Propensity Score Analysis of an Independent Patient Database from Three Phase III Trials

Statistical analysis for toxicity studies

Questionnaire Survey From the Viewpoint of Concordance in Patient and Physician Satisfaction Concerning Hypertensive Treatment in Elderly Patients　― Patients Voice Study

Statistical analysis for toxicity studies

Development and validation of a prognostic nomogram for colorectal cancer after radical resection based on individual patient data from three large-scale phase III trials

Adaptive phase I/II clinical trials for drug combination assessment in oncology using the outcomes of each cycle

Japanese Society for Biopharmaceutical Statistics (JSBS) and Japan Activity for Improvement of Cardiovascular Evaluation by Telemetry system (J-ICET)_ECG Group Collaboration Project: Proposal of Standard Statistical Analysis Method of Monkey Telemetry Study for Cardiovascular Risk Assessment

Clinical impact of tumor location on the colon cancer survival and recurrence: analyses of pooled data from three large phase III randomized clinical trials

Adaptive Seamless Design for Establishing Pharmacokinetic and Efficacy Equivalence in Developing Biosimilars

Exploratory double-blind, parallel-group, placebo-controlled extension study of edaravone (MCI-186) in amyotrophic lateral sclerosis

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