Symposium Summary

Author:

Tepper Jeffrey S.1,Kuehl Philip J.2,Cracknell Stuart3,Nikula Kristen J.4,Pei Luqi5,Blanchard James D.6

Affiliation:

1. Tepper Nonclinical Consulting, San Carlos, CA, USA

2. Lovelace Respiratory Research Institute, Albuquerque, NM, USA

3. Group Director, Aerosol Technology, Huntingdon Life Sciences, Somerset, NJ, USA

4. Executive Vice President and CSO, Seventh Wave Laboratories, LLC, Maryland Heights, MO, USA

5. US Food and Drug Administration, Silver Spring, MD, USA

6. Preclinical Development, Aradigm Corp, Hayward, CA, USA

Abstract

Developing inhaled drugs requires knowledge of lung anatomy, cell biology, respiratory physiology, particle physics, and some plumbing. Although dose makes the poison, in the context of an inhaled drug, the “dose” is not easily defined. This lack of clarity around dose poses issues and challenges in the design of inhalation toxicology programs. To better understand dose, the influence of ventilation is discussed as are the perturbations in pulmonary function observed with inhalation exposure that can affect dose. Methods for determining inhaled drug deposition to arrive at an estimate of lung dose are examined. Equally important to understanding dose are the techniques used to deliver aerosols to animals. With a better understanding of dose and inhalation exposure, species-specific histopathologic lesions, both common background and toxicologically significant lesions, are reviewed. Finally, insight into how regulators synthesize and evaluate these complex findings to assess clinical safety risks is presented.

Publisher

SAGE Publications

Subject

Toxicology

Reference26 articles.

1. Association of Inhalation Toxicologists (AIT) Working Party Recommendation for Standard Delivered Dose Calculation and Expression in Non-Clinical Aerosol Inhalation Toxicology Studies with Pharmaceuticals

2. Challenges in inhaled product development and opportunities for open innovation

3. Toxicologic Testing of Inhaled Pharmaceutical Aerosols

4. Methods, Measurements, and Interpretation of Animal Lung Function in Health and Disease

5. ICH-S7A. Guidance for industry S7A safety pharmacology studies for human pharmaceuticals. Center for Drug Evaluation and Research (U.S.); Center for Biologics Evaluation and Research (U.S.) Conf Author(s): International Conference on Harmonisation. U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and Research; Center for Biologics Evaluation and Research, Rockville, MD. 2001.

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