95-28053. Notice of Hearings and Request for Comments on Issues Relating to Patent Protection for Nucleic Acid Sequences  

  • [Federal Register Volume 60, Number 219 (Tuesday, November 14, 1995)]
    [Notices]
    [Pages 57223-57224]
    From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
    [FR Doc No: 95-28053]
    
    
    
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    DEPARTMENT OF COMMERCE
    Patent and Trademark Office
    
    
    Notice of Hearings and Request for Comments on Issues Relating to 
    Patent Protection for Nucleic Acid Sequences
    
    AGENCY: Patent and Trademark Office, Commerce.
    
    ACTION: Notice of hearings and request for comments.
    
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    SUMMARY: The Patent and Trademark Office (PTO) will hold public 
    hearings, and it requests comments, on issues relating to patent 
    protection for nucleic acid sequences. Interested members of the public 
    are invited to testify at public hearings and to present written 
    comments on any of the topics outlined in the supplementary information 
    section of this notice.
    
    DATES: Public hearings will be held on Wednesday, November 29, 1995, 
    from 9:00 a.m. until 1:00 p.m., and Thursday, December 7, 1995, from 
    9:00 a.m. until 1:00 p.m.
        Those wishing to present oral testimony at any of the hearings must 
    request an opportunity to do so no later than Monday, November 27, 
    1995, for the November 29 hearing, or Tuesday, December 5, 1995, for 
    the December 7 hearing.
        Speakers may provide a written copy of their testimony for 
    inclusion in the record of the proceedings no later than Monday, 
    December 18, 1995.
        Written comments will be accepted by the PTO until December 18, 
    1995.
        Written comments and transcripts of the hearings will be available 
    for public inspection on or about Monday, January 22, 1996.
    
    ADDRESSES: The November 29 hearing will be held from 9:00 a.m. until 
    1:00 p.m. at the University of California, San Diego, The Mandeville 
    Auditorium/Recital Hall, Muir Campus, La Jolla, California.
        The December 7 public hearing will be held from 9:00 a.m. until 
    1:00 p.m. in Suite 912, Commissioner's Conference Room, Crystal Park 
    Building No. 2, 2121 Crystal Drive, Arlington, Virginia.
        Requests to testify should be sent to Esther Kepplinger by 
    telephone at (703) 306-2714, by facsimile transmission at (703) 308-
    6879, or by mail marked to her attention addressed to the Assistant 
    Commissioner for Patents, Box DAC, Washington, D.C. 20231. No request 
    for oral testimony will be accepted through electronic mail.
        Written comments should be addressed to the Assistant Commissioner 
    for Patents, Box DAC, Washington, D.C. 20231, marked to the attention 
    of Esther Kepplinger. Comments may also be submitted by facsimile 
    transmission at (703) 308-6879, with a confirmation copy mailed to the 
    above address, or by electronic mail over the Internet to 
    sequence@suspto.gov.''
        Written comments and transcripts of the hearings will be maintained 
    for public inspection in Suite 520 of Crystal Park One, 2011 Crystal 
    Drive, Arlington, Virginia. Transcripts and comments provided in 
    machine readable format will also be available through anonymous file 
    transfer protocol (ftp) via the internet (address: 
    sequence@suspto.gov).
    
    FOR FURTHER INFORMATION CONTACT: Esther Kepplinger by telephone at 
    (703) 306-2714, by facsimile transmission to (703) 308-6879, by 
    electronic mail at ekepplin@uspto.gov, or by mail marked to her 
    attention addressed to the Assistant Commissioner for Patents, Box DAC, 
    Washington, D.C. 20231.
    
    SUPPLEMENTARY INFORMATION:
    
    I. Background
    
        With the growth of the biotechnology industry have come significant 
    changes in the process of research, development and commercialization 
    of biotechnology inventions. For at least a decade, patent applications 
    claiming nucleic acid sequences, such as genes composed of 
    deoxyribonucleic acid (``DNA''), have been examined and granted patent 
    rights by the PTO. These sequences typically encode known proteins or 
    proteins for which applicant discovered a function. Scientific and 
    technological advances have permitted researchers to identify large 
    numbers of gene fragments rapidly. Armed with databases containing the 
    sequences of known genes, they can identify a novel sequence. The ease 
    of sequencing large numbers of random nucleic acid fragments has 
    resulted in the filing of a growing number of patent applications each 
    claiming thousands of nucleic acid sequences. This is a serious problem 
    for the PTO. While the PTO has recently acquired sophisticated and 
    costly hardware and software necessary to search applications 
    containing such sequences, their examination will significantly burden 
    the existing system and may necessitate the acquisition of many 
    additional, expensive, massively parallel processor computers to 
    complete examination in a reasonable time.
        PTO estimates that the computer search time for one hundred 
    sequences is about fifteen hours and the examiner time for evaluating 
    the sequence search results is about sixty-five hours. The estimated 
    cost for computer search time for one hundred sequences is $1500. 
    Although the number of cases involving large numbers of sequences 
    presently before the PTO is small, it is estimated that the cost to 
    search and examine these cases will be $8 million. These estimates 
    represent searches by a massively parallel processor computer of 
    commercially available databases.
        Applications that claim excessively long sequences present similar 
    challenges, since the claimed sequence must be broken up into numerous 
    smaller sequences in order to be searched.
        An additional issue has been raised relating to what is known as 
    the Human Genome Initiative (HGI).
        The HGI is a project to obtain the entire DNA sequence in the human 
    genome. Many of the benefits expected from the HGI are due to the 
    characterization of expressed nucleic acid sequences in the human 
    genome and their protein products.
        Some individuals believe that expressed nucleic acid sequences in 
    the human genome should not be patentable because of the possibility 
    that a patent to a gene fragment could preclude future use of the gene 
    or its protein product. This, it is argued, could inhibit future 
    research efforts to isolate the entire gene or to develop medically 
    beneficial protein compounds. Others believe that 
    
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    the benefits of the patent system should not be withheld from this area 
    of technology, because research and development would be drastically 
    curtailed due to the inability to protect capital investments or to 
    reap financial rewards from those investments. Appropriate policies 
    must be established to address these challenges.
    
    II. Issues for Public Comment
    
        Interested members of the public are invited to testify or to 
    present written comments related to the above topics, including the 
    following issues:
        1. Is there a more cost-effective way to examine applications 
    containing large numbers of sequences or excessively long sequences, in 
    view of the PTO's limited human and computer resources?
        2. How should the significantly higher cost associated with 
    searching applications claiming large numbers of sequences or 
    excessively long sequences be underwritten? For example:
        (a) By fees from all applications?
        (b) By fees from the biotechnology industry applications only?
        (c) By fees from those specific applications involving large 
    numbers of sequences or extraordinarily long sequences?
        3. Will the patenting of a complete genome of an organism inhibit 
    rather than promote advancement of the biotechnology arts? If so, why?
        4. Will the patenting of human genome fragments inhibit rather than 
    promote advancement of the biotechnology arts? If so, why?
    
    III. Guidelines for Oral Testimony
    
        Individuals wishing to testify at the hearings must adhere to the 
    following guidelines:
        1. Requests to testify must include the speaker's name, 
    affiliation, title, phone number, fax number, mailing address, and 
    Internet mail address (if available).
        2. Speakers will be provided between seven and fifteen minutes to 
    present their remarks. The exact amount of time allocated per speaker 
    will be determined after the final number of parties testifying has 
    been determined. All efforts will be made to accommodate requests for 
    additional time for testimony presented before the day of the hearing.
        3. Requests to testify may be accepted on the date of the hearing 
    if sufficient time is available on the schedule. No one will be 
    permitted to testify without prior approval.
        A schedule providing approximate times for testimony will be 
    provided to all speakers the morning of the day of the hearing.
        Speakers are advised that the schedule for testimony may be subject 
    to change during the course of the hearings.
    
    IV. Guidelines for Written Comments
    
        Written comments should include the following information:
        1. Name and affiliation of the individual responding.
        2. If applicable, an indication of whether comments offered 
    represent views of the respondent's organization or are the 
    respondent's personal views.
        3. If applicable, information on the respondent's organization, 
    including the type of organization (e.g., business, trade group, 
    university, non-profit organization) and general areas of interest.
        Information that is provided pursuant to this notice will be made 
    part of the public record. In view of this, parties should not provide 
    information they do not wish publicly disclosed. Parties who would like 
    to rely on confidential information to illustrate a point being made 
    are requested to summarize or otherwise provide the information in a 
    way that will permit its public disclosure.
        Parties offering testimony or written comments should provide their 
    comments in machine readable format, if possible. Such submissions 
    should be provided by electronic mail messages over the Internet, or on 
    a 3.5'' floppy disk formatted for use in either a Macintosh or MS-DOS 
    based computer. Machine readable submissions should be provided as 
    unformatted text (e.g., ACSII or plain text), or formatted text in one 
    of the following file formats: Microsoft Word (Macintosh, DOS or 
    Windows versions) or WordPerfect (Macintosh, DOS or Windows versions).
    
    V. Guidelines for Comments via Internet
    
        Comments received via the Internet should include the same 
    information requested in the guidelines set out for written comments.
    
    VI. Other Information
    
        Questions regarding the facilities and lodging in the La Jolla, 
    California, area should be directed to the University of California, 
    San Diego, Special Events, by phone at (619) 534-6386, or by fax to 
    (619) 534-0905. Parking permits are required for on-campus parking and 
    may be purchased in advance through the Parking Office or on November 
    29 at Information booths at the university. Questions regarding parking 
    should be directed to the Special Events Parking Office at (619) 534-
    9682, or by fax to (619) 534-9685.
    
        Dated: November 8, 1995.
    Bruce A. Lehman,
    Assistant Secretary of Commerce and Commissioner of Patents and 
    Trademarks.
    [FR Doc. 95-28053 Filed 11-13-95; 8:45 am]
    BILLING CODE 3510-16-M
    
    

Document Information

Published:
11/14/1995
Department:
Patent and Trademark Office
Entry Type:
Notice
Action:
Notice of hearings and request for comments.
Document Number:
95-28053
Dates:
Public hearings will be held on Wednesday, November 29, 1995, from 9:00 a.m. until 1:00 p.m., and Thursday, December 7, 1995, from 9:00 a.m. until 1:00 p.m.
Pages:
57223-57224 (2 pages)
PDF File:
95-28053.pdf