no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
1 |
Assessment of benefits and risks in development of targeted therapies for cancer – The view of regulatory authorities
|
Pignatti, Francesco |
|
2015 |
9 |
5 |
p. 1034-1041 8 p. |
article |
2 |
Biomarker validation and testing
|
Hayes, Daniel F. |
|
2015 |
9 |
5 |
p. 960-966 7 p. |
article |
3 |
Bringing in health technology assessment and cost-effectiveness considerations at an early stage of drug development
|
Jönsson, Bengt |
|
2015 |
9 |
5 |
p. 1025-1033 9 p. |
article |
4 |
Cancer chemoprevention: Much has been done, but there is still much to do. State of the art and possible new approaches
|
Serrano, Davide |
|
2015 |
9 |
5 |
p. 1008-1017 10 p. |
article |
5 |
Early phase clinical trials to identify optimal dosing and safety
|
Cook, Natalie |
|
2015 |
9 |
5 |
p. 997-1007 11 p. |
article |
6 |
Editorial Board
|
|
|
2015 |
9 |
5 |
p. ii- 1 p. |
article |
7 |
Emerging uses of patient generated health data in clinical research
|
Wood, William A. |
|
2015 |
9 |
5 |
p. 1018-1024 7 p. |
article |
8 |
Hurdles on the road to personalized medicine
|
Tursz, Thomas |
|
2015 |
9 |
5 |
p. 935-939 5 p. |
article |
9 |
Innovative clinical trials for development of personalized cancer medicine
|
Mendelsohn, John |
|
2015 |
9 |
5 |
p. 933-934 2 p. |
article |
10 |
Next-generation clinical trials: Novel strategies to address the challenge of tumor molecular heterogeneity
|
Catenacci, Daniel V.T. |
|
2015 |
9 |
5 |
p. 967-996 30 p. |
article |
11 |
Optimal design of trials to demonstrate the utility of genomically-guided therapy: Putting Precision Cancer Medicine to the test
|
Dienstmann, Rodrigo |
|
2015 |
9 |
5 |
p. 940-950 11 p. |
article |
12 |
The Brave New World of clinical cancer research: Adaptive biomarker-driven trials integrating clinical practice with clinical research
|
Berry, Donald A. |
|
2015 |
9 |
5 |
p. 951-959 9 p. |
article |