語系:
繁體中文
English
說明(常見問題)
登入
回首頁
切換:
標籤
|
MARC模式
|
ISBD
Biopharmaceutical applied statistics...
~
Chen, Ding-Geng.
Biopharmaceutical applied statistics symposium.. Volume 1,. Design of clinical trials
紀錄類型:
書目-語言資料,印刷品 : Monograph/item
正題名/作者:
Biopharmaceutical applied statistics symposium./ edited by Karl E. Peace, Ding-Geng Chen, Sandeep Menon.
其他作者:
Peace, Karl E.
出版者:
Singapore :Springer Singapore : : 2018.,
面頁冊數:
xiv, 409 p. :ill., digital ; : 24 cm.;
Contained By:
Springer eBooks
標題:
Drugs - Congresses. - Testing -
電子資源:
https://doi.org/10.1007/978-981-10-7829-3
ISBN:
9789811078293
Biopharmaceutical applied statistics symposium.. Volume 1,. Design of clinical trials
Biopharmaceutical applied statistics symposium.
Volume 1,Design of clinical trials[electronic resource] /edited by Karl E. Peace, Ding-Geng Chen, Sandeep Menon. - Singapore :Springer Singapore :2018. - xiv, 409 p. :ill., digital ;24 cm. - ICSA book series in statistics,2199-0980. - ICSA book series in statistics..
1. A Statistical Approach to Clinical Trial Simulations -- 2. Comparison of Statistical Analysis Methods Using Modeling and Simulation for Optimal Protocol Design -- 3. Adaptive Trial Design in Clinical Research -- 4. Best Practices and Recommendations for Trial Simulations Within the Context of Designing Adaptive Clinical Trials -- 5. Designing and Analyzing Recurrent Event Data Trials -- 6. Bayesian Methodologies for Response-Adaptive Allocation -- 7. Addressing High Placebo Response in Neuroscience Clinical Trials -- 8. Phase I Cancer Clinical Trial Design: Single and Combination Agents -- 9. Sample Size and Power for the Mixed Linear Model -- 10. Crossover Designs -- 11. Data monitoring: Structure for Clinical Trials and Sequential Monitoring Procedures -- 12. Design and Data Analysis of Multiregional Clinical Trials (MRCT) - Theory and Practice -- 13. Multiregional Clinical Trials (MRCT) -- 14. Adaptive Group-Sequential Multi-regional Outcome Studies in Vaccines -- 15. Development and validation of Patient-reported Outcomes -- 16. Interim Analysis of Survival Trials: Group Sequential Analyses and Conditional Power.
This BASS book Series publishes selected high-quality papers reflecting recent advances in the design and biostatistical analysis of biopharmaceutical experiments - particularly biopharmaceutical clinical trials. The papers were selected from invited presentations at the Biopharmaceutical Applied Statistics Symposium (BASS), which was founded by the first Editor in 1994 and has since become the premier international conference in biopharmaceutical statistics. The primary aims of the BASS are: 1) to raise funding to support graduate students in biostatistics programs, and 2) to provide an opportunity for professionals engaged in pharmaceutical drug research and development to share insights into solving the problems they encounter. The BASS book series is initially divided into three volumes addressing: 1) Design of Clinical Trials; 2) Biostatistical Analysis of Clinical Trials; and 3) Pharmaceutical Applications. This book is the first of the 3-vol ume book series. The topics covered include: A Statistical Approach to Clinical Trial Simulations, Comparison of Statistical Analysis Methods Using Modeling and Simulation for Optimal Protocol Design, Adaptive Trial Design in Clinical Research, Best Practices and Recommendations for Trial Simulations in the Context of Designing Adaptive Clinical Trials, Designing and Analyzing Recurrent Event Data Trials, Bayesian Methodologies for Response-Adaptive Allocation, Addressing High Placebo Response in Neuroscience Clinical Trials, Phase I Cancer Clinical Trial Design: Single and Combination Agents, Sample Size and Power for the Mixed Linear Model, Crossover Designs in Clinical Trials, Data Monitoring: Structure for Clinical Trials and Sequential Monitoring Procedures, Design and Data Analysis for Multiregional Clinical Trials - Theory and Practice, Adaptive Group-Sequential Multi-regional Outcome Studies in Vaccines, Development and Validation of Patient-reported Outcomes, Interim Analysis of Survival Trials: Group Sequential Analyses, and Conditional Power - A Non-proportional Hazards Perspective.
ISBN: 9789811078293
Standard No.: 10.1007/978-981-10-7829-3doiSubjects--Topical Terms:
1208725
Drugs
--Testing--Congresses.
LC Class. No.: RS189 / .B567 2018
Dewey Class. No.: 617.040287
Biopharmaceutical applied statistics symposium.. Volume 1,. Design of clinical trials
LDR
:04342nam a2200349 a 4500
001
928623
003
DE-He213
005
20190304134716.0
006
m d
007
cr nn 008maaau
008
190626s2018 si s 0 eng d
020
$a
9789811078293
$q
(electronic bk.)
020
$a
9789811078286
$q
(paper)
024
7
$a
10.1007/978-981-10-7829-3
$2
doi
035
$a
978-981-10-7829-3
040
$a
GP
$c
GP
041
0
$a
eng
050
4
$a
RS189
$b
.B567 2018
072
7
$a
PBT
$2
bicssc
072
7
$a
MED090000
$2
bisacsh
072
7
$a
PBT
$2
thema
072
7
$a
MBNS
$2
thema
082
0 4
$a
617.040287
$2
23
090
$a
RS189
$b
.B615 2018
245
0 0
$a
Biopharmaceutical applied statistics symposium.
$n
Volume 1,
$p
Design of clinical trials
$h
[electronic resource] /
$c
edited by Karl E. Peace, Ding-Geng Chen, Sandeep Menon.
260
$a
Singapore :
$c
2018.
$b
Springer Singapore :
$b
Imprint: Springer,
300
$a
xiv, 409 p. :
$b
ill., digital ;
$c
24 cm.
490
1
$a
ICSA book series in statistics,
$x
2199-0980
505
0
$a
1. A Statistical Approach to Clinical Trial Simulations -- 2. Comparison of Statistical Analysis Methods Using Modeling and Simulation for Optimal Protocol Design -- 3. Adaptive Trial Design in Clinical Research -- 4. Best Practices and Recommendations for Trial Simulations Within the Context of Designing Adaptive Clinical Trials -- 5. Designing and Analyzing Recurrent Event Data Trials -- 6. Bayesian Methodologies for Response-Adaptive Allocation -- 7. Addressing High Placebo Response in Neuroscience Clinical Trials -- 8. Phase I Cancer Clinical Trial Design: Single and Combination Agents -- 9. Sample Size and Power for the Mixed Linear Model -- 10. Crossover Designs -- 11. Data monitoring: Structure for Clinical Trials and Sequential Monitoring Procedures -- 12. Design and Data Analysis of Multiregional Clinical Trials (MRCT) - Theory and Practice -- 13. Multiregional Clinical Trials (MRCT) -- 14. Adaptive Group-Sequential Multi-regional Outcome Studies in Vaccines -- 15. Development and validation of Patient-reported Outcomes -- 16. Interim Analysis of Survival Trials: Group Sequential Analyses and Conditional Power.
520
$a
This BASS book Series publishes selected high-quality papers reflecting recent advances in the design and biostatistical analysis of biopharmaceutical experiments - particularly biopharmaceutical clinical trials. The papers were selected from invited presentations at the Biopharmaceutical Applied Statistics Symposium (BASS), which was founded by the first Editor in 1994 and has since become the premier international conference in biopharmaceutical statistics. The primary aims of the BASS are: 1) to raise funding to support graduate students in biostatistics programs, and 2) to provide an opportunity for professionals engaged in pharmaceutical drug research and development to share insights into solving the problems they encounter. The BASS book series is initially divided into three volumes addressing: 1) Design of Clinical Trials; 2) Biostatistical Analysis of Clinical Trials; and 3) Pharmaceutical Applications. This book is the first of the 3-vol ume book series. The topics covered include: A Statistical Approach to Clinical Trial Simulations, Comparison of Statistical Analysis Methods Using Modeling and Simulation for Optimal Protocol Design, Adaptive Trial Design in Clinical Research, Best Practices and Recommendations for Trial Simulations in the Context of Designing Adaptive Clinical Trials, Designing and Analyzing Recurrent Event Data Trials, Bayesian Methodologies for Response-Adaptive Allocation, Addressing High Placebo Response in Neuroscience Clinical Trials, Phase I Cancer Clinical Trial Design: Single and Combination Agents, Sample Size and Power for the Mixed Linear Model, Crossover Designs in Clinical Trials, Data Monitoring: Structure for Clinical Trials and Sequential Monitoring Procedures, Design and Data Analysis for Multiregional Clinical Trials - Theory and Practice, Adaptive Group-Sequential Multi-regional Outcome Studies in Vaccines, Development and Validation of Patient-reported Outcomes, Interim Analysis of Survival Trials: Group Sequential Analyses, and Conditional Power - A Non-proportional Hazards Perspective.
650
0
$a
Drugs
$x
Testing
$x
Statistical methods
$v
Congresses.
$3
1208725
650
0
$a
Biopharmaceutics
$v
Congresses.
$3
1208726
650
1 4
$a
Statistics for Life Sciences, Medicine, Health Sciences.
$3
670172
650
2 4
$a
Biostatistics.
$3
783654
700
1
$a
Peace, Karl E.
$3
1132099
700
1
$a
Chen, Ding-Geng.
$3
848229
700
1
$a
Menon, Sandeep.
$3
1208724
710
2
$a
SpringerLink (Online service)
$3
593884
773
0
$t
Springer eBooks
830
0
$a
ICSA book series in statistics.
$3
1067975
856
4 0
$u
https://doi.org/10.1007/978-981-10-7829-3
950
$a
Mathematics and Statistics (Springer-11649)
筆 0 讀者評論
多媒體
評論
新增評論
分享你的心得
Export
取書館別
處理中
...
變更密碼[密碼必須為2種組合(英文和數字)及長度為10碼以上]
登入