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1.
Toxicol Pathol ; 32 Suppl 2: 17-8, 2004.
Article in English | MEDLINE | ID: mdl-15503660

ABSTRACT

In the Federal Register of January 10, 2000 (65 FR 1399), FDA published a draft guidance entitled "Photosafety Testing." The notice gave interested persons an opportunity to submit comments. As a result of the comments, certain sections of the guidance were reworded to improve clarity. A final guidance was published in May 2003. The final guidance further emphasizes that a flexible approach can be used to address adverse photoeffects and that specific assays are not required. Moreover, it encourages the development of methods that can efficiently be used to evaluate human safety. The guidance describes a consistent, science-based approach for testing of topically and systemically administered drug products.


Subject(s)
Guidelines as Topic , Industry , Photosensitizing Agents/adverse effects , Safety/standards , 3T3 Cells , Animals , Drug Evaluation , Mice , Toxicity Tests, Acute , United States , United States Food and Drug Administration
2.
Am J Ther ; 11(3): 213-7, 2004.
Article in English | MEDLINE | ID: mdl-15133537

ABSTRACT

Toxicological studies constitute an essential part of the effort in developing a botanical supplement into a drug product. The US Food and Drug Administration recently published a draft guidance and established a special botanical review team to assist academic and industry sponsors to manage this and other regulatory considerations related to this unique group of drug products. In this article, the current state of regulatory viewpoints on issues related to requirements and recommendations of various types of nonclinical toxicity studies in support of advanced phases clinical trials and filing a New Drug Application of a botanical are discussed. Topics include nonclinical pharmacology/toxicology view of previous human experience and initial clinical trial, regulatory perspectives on acute toxicity studies, chronic toxicity studies, mutagenicity studies, reproductive toxicity studies, and carcinogenicity studies on botanicals. Certain regulatory review-related issues are also presented. It is anticipated that through a proactive 2-way communication between the Agency and the sponsor, toxicological development of botanical drug product can be significantly facilitated.


Subject(s)
Drugs, Investigational/adverse effects , Plant Preparations/adverse effects , Toxicology , United States Food and Drug Administration , Animals , Carcinogenicity Tests , Clinical Trials as Topic , Humans , Mutagenicity Tests , United States
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