Considerations for Toxicology Studies of Respiratory Drug Products

Author:

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

Publisher

Elsevier BV

Subject

Toxicology,General Medicine

Reference16 articles.

1. Reactive Airways Disfunction Syndrome (RADS). Persistant asthma syndrome after high level irritant exposures;Brooks;Chest,1985

2. Monro and Mehta proposal for use of single dose toxicology studies to support single dose studies of new drugs in humans;Choudary;Clin. Pharmacol. Ther.,1996

3. Potential roles for preclinical pharmacology in Phase I clinical trials;Collins;Cancer Treat. Rep.,1986

4. Pharmacologically guided Phase I clinical trials based upon preclinical drug development;Collins;J. Natl. Cancer Inst.,1990

5. A retrospective comparison of the results of 6 and 12 month non-rodent toxicity studies;Contrera;Adverse Drug React. Toxicol. Rev.,1993

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