Biomarkers as drug development tools: discovery, validation, qualification and use

2018 ◽  
Vol 14 (6) ◽  
pp. 354-362 ◽  
Author(s):  
Virginia B. Kraus
2021 ◽  
pp. 153537022110021
Author(s):  
John-Michael Sauer ◽  
Amy C Porter

Safety biomarkers are important drug development tools, both preclinically and clinically. It is a straightforward process to correlate the performance of nonclinical safety biomarkers with histopathology, and ideally, the biomarker is useful in all species commonly used in safety assessment. In clinical validation studies, where histopathology is not feasible, safety biomarkers are compared to the response of standard biomarkers and/or to clinical adjudication. Worldwide, regulatory agencies have put in place processes to qualify biomarkers to provide confidence in the manner of use and interpretation of biomarker data in drug development studies. This paper describes currently qualified safety biomarkers which can be utilized to monitor for nephrotoxicity and cardiotoxicity and ongoing projects to qualify safety biomarkers for liver, skeletal muscle, and vascular injury. In many cases, the development and use of these critical drug development tools is dependent upon partnerships and the precompetitive sharing of data to support qualification efforts.


2020 ◽  
Vol 16 (S9) ◽  
Author(s):  
Klaus Romero ◽  
Nathan J. Hanan ◽  
Sudhir Sivakumaran ◽  
Vikram Sinha ◽  
Samantha Budd Haeberlein ◽  
...  

2018 ◽  
Vol 6 (2) ◽  
pp. 1-7
Author(s):  
Garima Kshatriya ◽  
Dilip G. Maheshwari

Drug Development Tools are methods, materials, or measures that have the potential to facilitate drug development. USFDA has specified three major drug development tools and has also given the guidelines recommending their qualification which would expedite the drug development process. This qualification would ensure better understanding of drug targets and long term safety outcomes. Regulatory authorities of Europe, Japan & India have also focused on developing a formal qualification process of drug development tools though most of it follows USFDA.


2018 ◽  
Vol 151 ◽  
pp. 291-306 ◽  
Author(s):  
Stephen P. Arnerić ◽  
Volker D. Kern ◽  
Diane T. Stephenson

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