GDUFA Research Outcomes
Quantitative Methods & Models
The Generic Drug User Fee Amendments (GDUFA) science and research program facilitates patient access to high-quality generic drugs by advancing research in areas where generic product development has been limited or prevented due to knowledge gaps about the kind of evidence needed to demonstrate that a generic product is the same as its brand name reference listed drug product. Leaders and experts across the generic industry collaborate to establish GDUFA research priorities for the most pressing scientific challenges they face with generic product development. Scientists and clinicians from industry, academia, and the U.S. Food and Drug Administration (FDA) strategically design research in these areas so that the outcomes help to build scientific bridges across the knowledge gaps, thereby facilitating pharmaceutical manufacturers to develop generic drugs that were previously challenging or unfeasible to develop.
A major GDUFA science and research priority is to facilitate the utility of model-integrated evidence (MIE) to support demonstrations of bioequivalence (BE). The advancement of research in this area focuses on developing tools and advancing approaches to integrate complementary in silico (modeling), in vivo, and in vitro evidence in ways that collectively mitigate the risk of failure modes for BE and support a framework for virtual BE studies. For example, while it may not be feasible to adequately characterize the long-term bioavailability of drugs from LAI products using in vivo or in vitro methods alone, it may be feasible to integrate limited in vivo and in vitro data with PBPK models that generate the remaining evidence needed to support a demonstration of BE. This area includes research on the use of MIE to evaluate failure modes for BE and to optimize the design of BE studies.
Outcomes including scientific publications, presentations, and posters arising from GDUFA-funded research in this priority area are available in this section.
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Considerations for Using Model Master Files
Babiskin, Andrew
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Regulatory Perspective on Modeling Strategies Across Multiple Submissions
Babiskin, Andrew; Yoon, Miyoung
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Regulatory Perspective: Challenges and Opportunities to Enhance Model Sharing upon Regulatory Use
Babiskin, Andrew
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Use of PBPK Model to Evaluate Impact of Ophthalmic Drug Products Critical Quality Attributes of BA/BE Assessment
Babiskin, Andrew
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Assessing Bioequivalence for Generic Extended Release Formulations
Babiskin, Andrew
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Physiologically-based Absorption Modeling and Simulation used in Assessing Bioequivalence for Ophthalmic Products
Babiskin, Andrew
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Modeling Dermal Drug Absorption from Complex Semisolid Formulations: Insights from Multi-Phase, Multi-Layer MechDermA Model
Zhao, Liang (should be Arora S)
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Novel Model-Integrated Designs for Bioequivalence Studies of LAI Products: A Complete Framework with the MonolixSuite
Ayral, Geraldine
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Integrating Topical Drug Product Quality Attributes Within Physiologically-based Pharmacokinetic Models
Zhao, Liang
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Simulating the Effect of Propylene Glycol on Acyclovir (Zovirax� Cream, 5%) Permeation Across the Skin Using a Physiologically Based Pharmacokinetic (PBPK) Model of In Vitro Flow-through Skin Permeation
Arora, S; Patel, N; Polak, S; Jamei, M; Tsakalozou, E; Ghosh, P; Alam, K; Liu, X; Namjoshi, S; Grice, J; Mohammed, Y; Roberts, M