An Evaluation of the Impact of PD-1 Pathway Blockade on Reproductive Safety of Therapeutic PD-1 Inhibitors von Poulet, Frederique M., Wolf, Jayanthi J., Herzyk, Danuta J., DeGeorge, Joseph J.

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Analysis of exposure margins in developmental toxicity studies for detection of human teratogens von Andrews, Paul A., Blanset, Diann, Costa, Priscila Lemos, Green, Martin, Green, Maia L., Jacobs, Abigail, Kadaba, Rajkumar, Lebron, Jose A., Mattson, Britta, McNerney, Mary Ellen, Minck, Daniel, Oliveira, Luana de Castro, Theunissen, Peter T., DeGeorge, Joseph J.

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A Brief History of Use of Animals in Biomedical Research and Perspective on Non-Animal Alternatives von Kinter, Lewis B, DeHaven, Ron, Johnson, David K, DeGeorge, Joseph J

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An Industry Perspective on the Utility of Short-Term Carcinogenicity Testing in Transgenic Mice in Pharmaceutical Development von Storer, Richard D., Sistare, Frank D., Vijayaraj Reddy, M., Degeorge, Joseph J.

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Exposure assessments in reproductive and developmental toxicity testing: An IQ-DruSafe industry survey on current practices and experiences in support of exposure-based high dose s... von Andrews, Paul A., McNerney, Mary Ellen, DeGeorge, Joseph J.

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Current nonclinical testing paradigms in support of safe clinical trials: An IQ Consortium DruSafe perspective von Butler, Lynne D., Guzzie-Peck, Peggy, Hartke, James, Bogdanffy, Matthew S., Will, Yvonne, Diaz, Dolores, Mortimer-Cassen, Elisabeth, Derzi, Mazin, Greene, Nigel, DeGeorge, Joseph J.

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Assessment of the clinical cardiac drug‐drug interaction associated with the combination of hepatitis C virus nucleotide inhibitors and amiodarone in guinea pigs and rhesus monkeys... von Regan, Christopher P., Morissette, Pierre, Regan, Hillary K., Travis, Jeffery J., Gerenser, Pamela, Wen, Jianzhong, Fitzgerald, Kevin, Gruver, Shaun, DeGeorge, Joseph J., Sannajust, Frederick J.

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Scientific Knowledge and Technology, Animal Experimentation, and Pharmaceutical Development von Kinter, Lewis B, DeGeorge, Joseph J

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An Analysis of Pharmaceutical Experience with Decades of Rat Carcinogenicity Testing: Support for a Proposal to Modify Current Regulatory Guidelines von Sistare, Frank D., Morton, Daniel, Alden, Carl, Christensen, Joel, Keller, Douglas, Jonghe, Sandra De, Storer, Richard D., Reddy, M. Vijayaraj, Kraynak, Andrew, Trela, Bruce, Bienvenu, Jean-Guy, Bjurström, Sivert, Bosmans, Vanessa, Brewster, David, Colman, Karyn, Dominick, Mark, Evans, John, Hailey, James R., Kinter, Lewis, Liu, Matt, Mahrt, Charles, Marien, Dirk, Myer, James, Perry, Richard, Potenta, Daniel, Roth, Arthur, Sherratt, Philip, Singer, Thomas, Slim, Rabih, Soper, Keith, Fransson-Steen, Ronny, Stoltz, James, Turner, Oliver, Turnquist, Susan, van Heerden, Marjolein, Woicke, Jochen, DeGeorge, Joseph J.

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Regulatory Forum Commentary Counterpoint: Dose Selection for Tg.rasH2 Mouse Carcinogenicity Studies von Darbes, Jarig, Sistare, Frank D., DeGeorge, Joseph J.

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Role of chronic toxicology studies in revealing new toxicities von Galijatovic-Idrizbegovic, Alema, Miller, Judith E., Cornell, Wendy D., Butler, James A., Wollenberg, Gordon K., Sistare, Frank D., DeGeorge, Joseph J.

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Carcinogenicity Testing and the Evaluation of Regulatory Requirements for Pharmaceuticals von Contrera, Joseph F, Jacobs, Abigail C, DeGeorge, Joseph J

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Characterization of an investigative safety pharmacology model to assess comprehensive cardiac function and structure in chronically instrumented conscious beagle dogs von Regan, Christopher P., Stump, Gary L., Detwiler, Theodore J., Chen, Li, Regan, Hillary K., Gilberto, David B., DeGeorge, Joseph J., Sannajust, Frederick J.

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Safety Assessment of Drug Metabolites: Implications of Regulatory Guidance and Potential Application of Genetically Engineered Mouse Models that Express Human P450s von Powley, Mark W, Frederick, Clay B, Sistare, Frank D, DeGeorge, Joseph J

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Applications of Toxicogenomics to Nonclinical Drug Development: Regulatory Science Considerations von Sistare, Frank D., DeGeorge, Joseph J.

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An Evaluation of Chronic 6- and 12-Month Rat Toxicology Studies as Predictors of 2-Year Tumor Outcome von Reddy, M. V., Sistare, F. D., Christensen, J. S., DeLuca, J. G., Wollenberg, G. K., DeGeorge, J. J.

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Predictive Value of Preclinical Toxicology Studies for Platinum Anticancer Drugs von CLARK, D. L, ANDREWS, P. A, SMITH, D. D, DEGEORGE, J. J, JUSTICE, R. L, BEITZ, J. G

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Considerations for Toxicology Studies of Respiratory Drug Products von Degeorge, Joseph J, Ahn, Chang Ho, Andrews, Paul A, Brower, Margaret E, Choi, Young S, Chun, Misoon Y, Du, Tao, Lee-Ham, Doo Young, McGuinn, W.David, Pei, Luqi, Sancilio, Lawrence F, Schmidt, Wendelyn, Sheevers, Hilary V, Sun, C.Joseph, Tripathi, Satish, Vogel, W.Mark, Whitehurst, Virgil, Williams, Shannon, Taylor, Alan S

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Food and Drug Administration Viewpoints on Toxicokinetics: The View from Review von Degeorge, Joseph J.

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An Industry Perspective on the Utility of Short-Term Carcinogen- icity Testing in Transgenic Mice in Pharmaceutical Development von STORER, Richard D, SISTARE, Frank D, VIJAYARAJ REDDY, M, DEGEORGE, Joseph J

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