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GUIDANCE DOCUMENT

Developing Products for Weight Management Revision 1 February 2007

Download the Draft Guidance Document Read the Federal Register Notice
Draft

Not for implementation. Contains non-binding recommendations.

Docket Number:
FDA-2007-D-0435
Issued by:
Guidance Issuing Office
Center for Drug Evaluation and Research

This guidance provides recommendations to industry regarding the development of drugs and therapeutic biologics (hereafter products) regulated within the Center for Drug Evaluation and Research (CDER) in the Food and Drug Administration (FDA) for the indication of weight management. This guidance applies to products intended to be used for medical weight loss, which can be defined as a long-term reduction in fat mass with a goal of reduced morbidity and mortality through quantifiable improvements in biomarkers such as blood pressure, lipids, and HbA1c. This guidance revises the draft Guidance for the Clinical Evaluation of Weight-Control Drugs that issued in September 1996. When finalized, this guidance will replace the September 1996 draft guidance.

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You can submit online or written comments on any guidance at any time (see 21 CFR 10.115(g)(5))

If unable to submit comments online, please mail written comments to:

Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852

All written comments should be identified with this document's docket number: FDA-2007-D-0435.

 
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