98-33282. American College for Advancement in Medicine; Analysis to Aid Public Comment  

  • [Federal Register Volume 63, Number 241 (Wednesday, December 16, 1998)]
    [Notices]
    [Pages 69291-69292]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 98-33282]
    
    
    -----------------------------------------------------------------------
    
    FEDERAL TRADE COMMISSION
    
    [File No. 9623147]
    
    
    American College for Advancement in Medicine; Analysis to Aid 
    Public Comment
    
    AGENCY: Federal Trade Commission.
    
    ACTION: Proposed Consent Agreement.
    
    -----------------------------------------------------------------------
    
    SUMMARY: The consent agreement in this matter settles alleged 
    violations of federal law prohibiting unfair or deceptive acts or 
    practices or unfair methods of competition. The attached Analysis to 
    Aid Public Comment describes both the allegations in the draft 
    complaint that accompanies the consent agreement and the terms of the 
    consent order--embodied in the consent agreement--that would settle 
    these allegations.
    
    DATES: Comments must be received on or before February 16, 1999.
    
    ADDRESSES: Comments should be directed to: FTC/Office of the Secretary, 
    Room 159, 600 Pa. Ave., NW., Washington, DC 20580.
    
    FOR FURTHER INFORMATION CONTACT:
    Dean Graybill, FTC/H-200, Washington, D.C. 20580. (202) 326-3284 or 
    Richard Cleland, FTC/H-200, Washington, D.C. 20580. (202) 326-3088.
    
    SUPPLEMENTARY INFORMATION: Pursuant to Section 6(f) of the Federal 
    Trade Commission Act, 38 Stat. 721, 15 U.S.C. 46 and Section 2.34 of 
    the Commission's Rules of Practice (16 CFR 2.34), notice is hereby 
    given that the above-captioned consent agreement containing a consent 
    order to cease and desist, having been filed with and accepted, subject 
    to final approval, by the Commission, has been placed on the public 
    record for a period of sixty (60) days. The following Analysis to Aid 
    Public Comment describes the terms of the consent agreement, and the 
    allegations in the complaint. An electronic copy of the full text of 
    the consent agreement package can be obtained from the FTC Home Page 
    (for December 8, 1998), on the World Wide Web, at ``http://www.ftc.gov/
    os/actions97.htm.'' A paper copy can be obtained from the FTC Public 
    Reference Room, Room H-130, 600 Pennsylvania Avenue, NW., Washington, 
    D.C. 20580, either in person or by calling (202) 326-3627. Public 
    comment is invited. Such comments or views will be considered by the 
    Commission and will be available for inspection and copying at its 
    principal office in accordance with Section 4.9(b)(6)(ii) of the 
    Commission's Rules of Practice (16 CFR 4.9(b)(6)(ii).
    
    Analysis of Proposed Consent Order To Aid Public Comment
    
        The Federal Trade Commission has accepted an agreement to a 
    proposed consent order from the American College for Advancement in 
    Medicine (``ACAM'' or the ``proposed respondent''). ACAM is an 
    incorporated non-profit professional association comprised principally 
    of physicians. The Commission has alleged that ACAM promotes EDTA 
    chelation therapy to the public as an effective treatment for 
    atherosclerosis, i.e., blocked arteries. Chelation therapy consists of 
    the intravenous injection into the body of a chemical substance 
    (ethylene diamine tetraacetic acid, (``EDTA'')), which, after bonding 
    with metals and minerals in the bloodstream, is expelled through the 
    body's excretory functions. ACAM promotes this service to consumers 
    through print materials and a Web site.
        The proposed consent order has been placed on the public record for 
    sixty (60) days for reception of comments by interested persons. 
    Comments received during this period will become part of the public 
    record. After sixty (60) days, the Commission will again review the 
    agreement and will decide whether it should withdraw from the agreement 
    or make final the agreement's proposed order.
        The Commission has alleged that proposed respondent has made false 
    and unsubstantiated claims in its
    
    [[Page 69292]]
    
    advertising materials that are likely to mislead consumers concerning 
    (1) the effectiveness of EDTA chelation therapy to treat 
    atherosclerosis; and (2) the existence of scientific proof of the 
    effectiveness of EDTA chelation therapy.
        The proposed consent order addresses the alleged misrepresentations 
    cited in the accompanying complaint by prohibiting proposed respondent 
    from representing in any future advertising for chelation therapy that 
    EDTA chelation therapy is effective to treat atherosclerosis unless the 
    representation is supported by competent and reliable scientific 
    evidence (Part I.A). In addition, the proposed order requires that 
    proposed respondent have competent and reliable scientific evidence to 
    support any claims about the effectiveness or comparative effectiveness 
    of chelation therapy for any disease of the human circulatory system 
    (Part I.B).
        The proposed consent order also prohibits proposed respondent from 
    misrepresenting in any future advertising for chelation therapy, the 
    existence, contents, validity, results, conclusions or interpretations 
    of any test, study, or research (Part II). Part III of the order allows 
    proposed respondent to make representations permitted in labeling by 
    the U.S. Food and Drug Administration.
        The proposed consent order also requires that ACAM send a letter to 
    its membership notifying them of the existence of the FTC order and 
    advising them that any member who makes unsubstantiated advertising 
    claims for chelation therapy could be subject to an enforcement action 
    (Part IV). Other provisions in the consent order are customary record 
    keeping, reporting and notification requirements as well as a 
    ``sunsetting'' clause prescribing that the order automatically expires 
    20 years from either the date that the order becomes effective or the 
    date of the last enforcement action.
        The complaint and consent agreement in this matter address issues 
    raised by certain statements that respondent made in its promotional 
    brochures and other materials that were distributed to the public. The 
    Commission's action should not be construed to regulate how doctors use 
    or prescribe drugs in the course of treating their patients or other 
    choice of therapy issues.
        The purpose of this analysis is to facilitate public comment on the 
    proposed order, and is not intended to constitute an official 
    interpretation of the agreement and proposed order or to modify in any 
    way their terms.
    
        By direction of the Commission.
    Donald S. Clark,
    Secretary.
    [FR Doc. 98-33282 Filed 12-15-98; 8:45 am]
    BILLING CODE 6750-01-M
    
    
    

Document Information

Published:
12/16/1998
Department:
Federal Trade Commission
Entry Type:
Notice
Action:
Proposed Consent Agreement.
Document Number:
98-33282
Dates:
Comments must be received on or before February 16, 1999.
Pages:
69291-69292 (2 pages)
Docket Numbers:
File No. 9623147
PDF File:
98-33282.pdf