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The AAPS Journal|May 1, 2008
Evaluation of methods for estimating time to steady state with examples from phase 1 studiesLata Maganti, Deborah L Panebianco, Andrea L MaesThe AAPS Journal|May 1, 2008
Role of biotransformation studies in minimizing metabolism-related liabilities in drug discoveryYue-Zhong Shu, Benjamin M Johnson, Tian J YangThe AAPS Journal|May 1, 2008
Use of the Biopharmaceutical Classification System in early drug developmentM Sherry KuThe AAPS Journal|April 26, 2008
Topical ocular delivery of NSAIDsMunish Ahuja, Avinash S Dhake, Surendra K Sharma, et al.The AAPS Journal|May 27, 2008
Application of the biopharmaceutical classification system in clinical drug development--an industrial viewJack Cook, William Addicks, Yunhui Henry WuThe AAPS Journal|May 27, 2008
In vitro studies are sometimes better than conventional human pharmacokinetic in vivo studies in assessing bioequivalence of immediate-release solid oral dosage formsJames E PolliThe AAPS Journal|January 22, 2025
Operating Characteristics of the Simulated Healthy Participant Approach in Impaired Clearance StudiesSana Gupta, Vivek Purohit, Yuchen Wang, et al.The AAPS Journal|January 23, 2025
Evaluating the Immunogenicity Risk of Protein Therapeutics by Augmenting T Cell Epitope Prediction with Clinical FactorsZicheng Hu, Patrick Wu, Steven J SwansonThe AAPS Journal|February 4, 2025
Pharmaceutical Sciences: Insights and Observations from Academic Chairs and Vice ChairsKristy M Ainslie, Albert A Bowers, Robert H Chichewicz, et al.Pageof 239