Ghantous H - Search Results

1

Regulatory toxicology perspectives on the development of botanical drug products in the United States.

Wu KM, Farrelly J, Birnkrant D, Chen S, Dou J, Atrakchi A, Bigger A, Chen C, Chen Z, Freed L, Ghantous H, Goheer A, Hausner E, Osterberg R, Rhee H, Zhang K. Wu KM, et al. Among authors: ghantous h. Am J Ther. 2004 May-Jun;11(3):213-7. doi: 10.1097/00045391-200405000-00010. Am J Ther. 2004. PMID: 15133537 Review.

2

Current regulatory toxicology perspectives on the development of herbal medicines to prescription drug products in the United States.

Wu KM, Ghantous H, Birnkrant DB. Wu KM, et al. Among authors: ghantous h. Food Chem Toxicol. 2008 Aug;46(8):2606-10. doi: 10.1016/j.fct.2008.05.029. Epub 2008 Jun 4. Food Chem Toxicol. 2008. PMID: 18614266 Review.

3

Current regulatory perspectives on genotoxicity testing for botanical drug product development in the U.S.A.

Wu KM, Dou J, Ghantous H, Chen S, Bigger A, Birnkrant D. Wu KM, et al. Among authors: ghantous h. Regul Toxicol Pharmacol. 2010 Feb;56(1):1-3. doi: 10.1016/j.yrtph.2009.09.012. Epub 2009 Sep 24. Regul Toxicol Pharmacol. 2010. PMID: 19782117

4

Timing of carcinogenicity studies and predictability of genotoxicity for tumorigenicity in anti-HIV drug development.

Wu KM, Powley MW, Ghantous H. Wu KM, et al. Among authors: ghantous h. Int J Toxicol. 2012 Jun;31(3):211-21. doi: 10.1177/1091581812439585. Epub 2012 May 1. Int J Toxicol. 2012. PMID: 22550047

5

Assessing a drug for an eradicated human disease: US Food and Drug Administration review of tecovirimat for the treatment of smallpox.

Chan-Tack KM, Harrington PR, Choi SY, Myers L, O'Rear J, Seo S, McMillan D, Ghantous H, Birnkrant D, Sherwat AI. Chan-Tack KM, et al. Among authors: ghantous h. Lancet Infect Dis. 2019 Jun;19(6):e221-e224. doi: 10.1016/S1473-3099(18)30788-6. Epub 2019 Mar 7. Lancet Infect Dis. 2019. PMID: 30853252 Review.

6

Benefit-risk assessment for brincidofovir for the treatment of smallpox: U.S. Food and Drug Administration's Evaluation.

Chan-Tack K, Harrington P, Bensman T, Choi SY, Donaldson E, O'Rear J, McMillan D, Myers L, Seaton M, Ghantous H, Cao Y, Valappil T, Birnkrant D, Struble K. Chan-Tack K, et al. Among authors: ghantous h. Antiviral Res. 2021 Nov;195:105182. doi: 10.1016/j.antiviral.2021.105182. Epub 2021 Sep 25. Antiviral Res. 2021. PMID: 34582915 Review.

7

Drug Development 101: A Primer.

Buckley LA, Bebenek I, Cornwell PD, Hodowanec A, Jensen EC, Murphy C, Ghantous HN. Buckley LA, et al. Among authors: ghantous hn. Int J Toxicol. 2020 Sep/Oct;39(5):379-396. doi: 10.1177/1091581820939083. Epub 2020 Aug 7. Int J Toxicol. 2020. PMID: 32762387

8

Predictivity/Translatability of Toxicities Observed in Nonclinical Toxicology Studies to Clinical Safety Outcomes in Drug Development: Case Examples.

Stagg NJ, Ghantous HN, Roth R, Hastings KL. Stagg NJ, et al. Among authors: ghantous hn. Int J Toxicol. 2020 Mar/Apr;39(2):141-150. doi: 10.1177/1091581819894281. Epub 2019 Dec 26. Int J Toxicol. 2020. PMID: 31875744

9

Practical Considerations in Determining Adversity and the No-Observed-Adverse-Effect-Level (NOAEL) in Nonclinical Safety Studies: Challenges, Perspectives and Case Studies.

Kale VP, Bebenek I, Ghantous H, Kapeghian J, Singh BP, Thomas LJ. Kale VP, et al. Among authors: ghantous h. Int J Toxicol. 2022 Mar-Apr;41(2):143-162. doi: 10.1177/10915818211073047. Epub 2022 Mar 1. Int J Toxicol. 2022. PMID: 35230174

10

Workshop proceedings: challenges and opportunities in evaluating protein allergenicity across biotechnology industries.

Stagg NJ, Ghantous HN, Ladics GS, House RV, Gendel SM, Hastings KL. Stagg NJ, et al. Among authors: ghantous hn. Int J Toxicol. 2013 Jan-Feb;32(1):4-10. doi: 10.1177/1091581812471864. Epub 2013 Jan 16. Int J Toxicol. 2013. PMID: 23324160

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