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The AAPS Journal|September 4, 2025
Pharmacokinetics of Racemic Eflornithine in Human Plasma and Cerebrospinal Fluid: Clinical Perspectives for L-eflornithine Against Human African TrypanosomiasisMikael Boberg, Kesara Na-Bangchang, Michael Ashton, et al.
The AAPS Journal|September 4, 2025
Cellular Immunogenicity Assessments in CAR-T Cell Therapies: Current Insights and Future DirectionsMadhan Masilamani, Nanda Balasubramanian, Johanna Mora, et al.
The AAPS Journal|August 7, 2016
Strategies to Determine Assay Format for the Assessment of Neutralizing Antibody Responses to BiotherapeuticsBonnie Wu, Shan Chung, Xu-Rong Jiang, et al.
The AAPS Journal|August 4, 2016
Development of a Flow-Through USP-4 Apparatus Drug Release Assay to Evaluate Doxorubicin LiposomesWenmin Yuan, Rui Kuai, Zhipeng Dai, et al.
The AAPS Journal|May 17, 2020
Why Do the Majority of Submissions for Bridging from a Prefilled Syringe to an Autoinjector Include Bioequivalence Studies in Order to Demonstrate Comparability?William J Lambert
The AAPS Journal|May 12, 2020
Modeling Temperature-Dependent Dermal Absorption and Clearance for Transdermal and Topical Drug ApplicationsTerri D LaCount, Qian Zhang, Jinsong Hao, et al.
The AAPS Journal|July 25, 2015
A Neutralizing Antibody Assay Based on a Reporter of Antibody-Dependent Cell-Mediated CytotoxicityYuling Wu, Jia J Li, Hyun Jun Kim, et al.
The AAPS Journal|July 2, 2015
Assessment of In Vivo Clinical Product Performance of a Weak Basic Drug by Integration of In Vitro Dissolution Tests and Physiologically Based Absorption ModelingXuan Ding, Ivelina Gueorguieva, James A Wesley, et al.
The AAPS Journal|June 27, 2015
Evaluation of Approaches to Deal with Low-Frequency Nuisance Covariates in Population Pharmacokinetic AnalysesChakradhar V Lagishetty, Stephen B Duffull
The AAPS Journal|May 24, 2015
Regulatory Considerations for Approval of Generic Inhalation Drug Products in the US, EU, Brazil, China, and IndiaSau L Lee, Bhawana Saluja, Alfredo García-Arieta, et al.
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