scholarly journals Pharmacogenetics in drug development

2005 ◽  
Vol 360 (1460) ◽  
pp. 1579-1588 ◽  
Author(s):  
Alun D McCarthy ◽  
James L Kennedy ◽  
Lefkos T Middleton

Over the last two decades, identification of polymorphisms that influence human diseases has begun to have an impact on the provision of medical care. The promise of genetics lies in its ability to provide insights into an individual's susceptibility to disease, the likely nature of the disease and the most appropriate therapy. For much of its history, pharmacogenetics (PGx—the use of genetic information to impact drug choice) has been limited to comparatively simple phenotypes such as plasma drug levels. Progress in genetics technologies has broadened the scope of PGx efficacy and safety studies that can be implemented, impacting on a broad spectrum of drug discovery and development activities. Recent PGx data show the ability of this approach to generate information that can be applied to dose selection, efficacy determination and safety issues. This in turn will lead to significant opportunities to affect both the approach to clinical development and the probability of success—the latter being an important aspect for pharmaceutical companies and for the patients who will benefit from these new medicines.

1996 ◽  
Vol 6 (1) ◽  
pp. 21-25 ◽  
Author(s):  
O.V. Angelov ◽  
A.G. Wiese ◽  
D.D. Tang-Liu ◽  
A.A. Acheampong ◽  
I.M. Ismail ◽  
...  

Brimonidine is a selective α2-adrenergic agonist developed for lowering intraocular pressure in glaucoma patients. Since brimonidine will be used in long-term theraphy, the safety of this drug is an important feature for its clinical success. Brimonidine has been evaluated in a number of safety studies using doses much greater than those in humans. In this paper chronic and carcinogenicity studies are presented. The results of the 6-month ocular/systemic study in rabbits and the 1-year ocular/systemic study in monkeys with 0.2, 0.5, and 0.8% brimonidine ophthalmic formulations showed no ocular or organ toxicity. The highest concentration of 0.8% used in rabbits and monkeys resulted in plasma drug concentrations of 95 (Cmax) and 10 (C2hr) times, respectively, higher than those seen in humans following topical dosing. Dose-related transient exaggerated pharmacologic effects of sedation were observed in the 1-year oral study in monkeys without any organ toxicity. The dose that elicited an apparent pharmacologic effect produced a plasma drug concentration that was approximately 115 times higher than that in humans. In 2-year carcinogenicity studies in mice and rats using doses that produced plasma concentrations 77 and 118 times, respectively, higher than those seen in humans, no oncogenic effect was observed. Based on the extensive safety research on brimonidine, it was concluded that this drug has an excellent safety profile.


2014 ◽  
Vol 15 (13) ◽  
pp. 1943-1953 ◽  
Author(s):  
Maria Rosaria Anna Muscatello ◽  
Antonio Bruno ◽  
Paolo Micali Bellinghieri ◽  
Gianluca Pandolfo ◽  
Rocco Antonio Zoccali

EP Europace ◽  
2017 ◽  
Vol 19 (suppl_3) ◽  
pp. iii141-iii141
Author(s):  
S. Bjork ◽  
E. Ojala ◽  
T. Nordstrom ◽  
E. Kankuri ◽  
E. Mervaala

2001 ◽  
Vol 75 (1) ◽  
pp. 115-124 ◽  
Author(s):  
Osmond J D’Cruz ◽  
Seang H Yiv ◽  
Barbara Waurzyniak ◽  
Fatih M Uckun

2013 ◽  
Vol 19 (3) ◽  
Author(s):  
Dianne Nicol ◽  
Johnathon Liddicoat ◽  
Christine Critchley

The orthodox business model of many drug discovery and development companies centres on adding value to early-stage discoveries prior to engaging with large pharmaceutical companies to bring products to market. Anecdotal observations suggest some companies are moving to a ‘virtual’ business model - instead of employing in-house scientists, a skeletal management team runs the company and out-sources all research and development. This article presents a novel method to determine whether companies are virtual, based on author bylines in peer-reviewed journal articles. Applying this method to Australian companies in this sector, the size of the cohort identified as virtual was much larger than anticipated, around 52%. The accuracy of this method has been verified statistically using interview data. This article discusses the value and limitations of this method, positing that it can be used to analyse industry and policy implications that may result from widespread adoption of the virtual model


Neurology ◽  
2012 ◽  
Vol 78 (Meeting Abstracts 1) ◽  
pp. P06.073-P06.073
Author(s):  
F. Sacca ◽  
A. Marsili ◽  
A. Brunetti ◽  
R. Carbone ◽  
G. De Michele ◽  
...  

2011 ◽  
Vol 30 (3) ◽  
pp. 272-286 ◽  
Author(s):  
R. Dustan Sarazan ◽  
Scott Mittelstadt ◽  
Brian Guth ◽  
John Koerner ◽  
Joanne Zhang ◽  
...  

There are several recent examples where clinically significant, safety-related, drug effects on hemodynamics or cardiac function were not apparent until large clinical trials were completed or the drugs entered the consumer market. Such late-stage safety issues can have significant impact on patient health and consumer confidence, as well as ramifications for the regulatory, pharmaceutical, and financial communities. This manuscript provides recommendations that evolved from a 2009 HESI workshop on the need for improved translation of nonclinical cardiovascular effects to the clinical arena. The authors conclude that expanded and improved efforts to perform sensitive yet specific evaluations of functional cardiovascular parameters in nonclinical studies will allow pharmaceutical companies to identify suspect drugs early in the discovery and development process while allowing promising drugs to proceed into clinical development.


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