Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Kirk M Chan-Tack"'
Publikováno v:
Infection Control & Hospital Epidemiology. 41:489-491
Autor:
Kimberly A Struble, Thamban Valappil, Dionne Price, Poonam Mishra, Kirk M Chan-Tack, Jeffrey S. Murray, Debra Birnkrant, Karen Qi, Sarah Connelly
Publikováno v:
Journal of Virus Eradication
Journal of Virus Eradication, Vol 5, Iss 3, Pp 138-144 (2019)
Journal of Virus Eradication, Vol 5, Iss 3, Pp 138-144 (2019)
Objectives Under representation of black subjects in trials of hepatitis C virus (HCV) direct-acting antivirals (DAAs) complicates assessment of differential outcomes for black individuals vs non-black individuals. HCV trials submitted to the Food an
Publikováno v:
The New England journal of medicine. 383(27)
FDA Approval of Remdesivir On October 22, 2020, on the basis of the results of three phase 3 clinical trials, the FDA approved remdesivir for use in adults and pediatric patients (12 years of age o...
Autor:
Patrick R. Harrington, Kimberly A Struble, Kirk M Chan-Tack, Jeffrey S. Murray, Lisa K. Naeger, Sarita D. Boyd, Debra Birnkrant, Takashi E. Komatsu
Publikováno v:
Journal of Viral Hepatitis. 25:969-975
Multiple direct-acting antiviral (DAA)-based regimens are now available for all hepatitis C virus (HCV) genotypes (GTs). Because HCV GT 4, 5 and 6 are less common in the United States (US) and worldwide, relatively small numbers of participants with
Autor:
Kimberly A Struble, Su-Young Choi, David McMillan, Timothy J Bensman, Eric F. Donaldson, Hanan Ghantous, Mark Seaton, Thamban Valappil, Laine Myers, Julian J. O'Rear, Debra Birnkrant, Patrick R. Harrington, Yu Cao, Kirk M Chan-Tack
Publikováno v:
Antiviral Research. 195:105182
The development and approval of brincidofovir for the treatment of smallpox, a disease that was eradicated from the world over 40 years ago, has resulted in the second antiviral approved via the Medical Countermeasure Initiative (MCMi) to combat this
Publikováno v:
The Journal of Clinical Pharmacology. 57:S136-S142
In this review of individual patient expanded-access requests to the Center for Drug Evaluation and Research for the period Fiscal Year 2010 to Fiscal Year 2014, we evaluated the number of applications received and the number allowed to proceed. We a
Publikováno v:
Hepatology (Baltimore, Md.). 67(2)
On July 18, 2017, the U.S. Food and Drug Administration (FDA) approved sofosbuvir/velpatasvir/voxilaprevir (SOF/VEL/VOX) (Vosevi) fixed-dose combination (FDC), an interferon-free, complete regimen for adult patients with chronic hepatitis C virus (HC
Autor:
Susan Zhou, Karen Qi, Min Min, Kimberly A Struble, Jeffrey Murray, Kirk M. Chan-Tack, Guoxing Greg Soon, Rafia Bhore, Thomas Hammerstrom, Debra Birnkrant
Publikováno v:
AIDS Patient Care and STDs. 26:444-453
Women are often underrepresented in randomized clinical trials (RCT) of HIV-1 drugs. As a result, determining whether women have different virologic outcomes compared to men is not always possible because the gender-related analyses usually lack stat
Publikováno v:
Postgraduate Medicine. 121:107-113
Cryptococcosis continues to have a high mortality rate in human immunodeficiency virus (HIV)-positive patients despite advances made in antifungal treatment, intracranial pressure management, and antiretroviral therapy. This retrospective chart revie
Autor:
Jennifer L. DiGiacinto, Kimberly A Struble, Kirk M Chan-Tack, Kellie S. Reynolds, Sarah M. Robertson
Publikováno v:
The Journal of Clinical Pharmacology. 48:518-523
One of the numerous regulatory functions of the Food and Drug Administration (FDA) is the evaluation of drug-drug interactions and the determination of appropriate dose adjustments, if necessary, to ensure the safe and effective use of medications. T