The National Institute of Child Health and Human Development (NICHD) is seeking research statements from parties interested in entering into a Cooperative Research and Development Agreement (CRADA). The purpose of the CRADA is to develop new strategies for the identification of MATER (Maternal Effect Gene) specific to the remodeling of chromosomal architecture, and the transcription and translation that support healthy mammalian oocytes and early embryonic development. The project is part of the ongoing activities of the Developmental Endocrinology Branch (DEB), Division of Intramural Research, NICHD. The term of the CRADA will be up to five (5) years.
Interested parties should notify this office in writing of their intent to file a formal proposal no later than April 11, 2001. Formal proposals must be submitted to this office no later than May 11, 2001.
Research Statements should be submitted to Kate Sinclair Dunn, Technology Development Specialist, Technology Development and Commercialization Branch, National Cancer Institute, National Institutes of Health, Executive Plaza South, Room 450, 6120 Executive Blvd., MSC 7182, Bethesda, MD 20892-7182, Phone: 301-496-0477, Fax: 301-402-2117, e-mail firstname.lastname@example.org. Scientific questions should be addressed to Lawrence M. Nelson, M.D., Head, Gynecological Endocrinology Unit Developmental Endocrinology Branch, NICHD, NIH, Building 10, Room 10N262, Bethesda, MD 20892-1862; Phone (direct): 301-402-6608, Office: 301-496-4686; Fax: 301-402-0574, e-mail: Lawrence_Nelson@nih.gov. Inquiries directed to obtaining patent license(s) related to participation in the CRADA opportunity should be addressed to Dennis Penn, Pharm.D., MPH, Senior Technology Licensing Specialist, Office of Technology Transfer, National Institutes of Health, 6011 Executive Blvd., Suite 325, Rockville, MD 20852-3804, Phone: 301-496-7735, Fax: 301-402-0220, e-mail: email@example.com.End Preamble Start Supplemental Information
A CRADA is the anticipated joint agreement to be entered into by NICHD and a collaborator pursuant to the Federal Technology Transfer Act of 1986 (15 U.S.C. 3710 a), as amended. A CRADA is an agreement designed to enable certain collaborations between Government laboratories and non-Government laboratories. It is not a grant, and is not a contract for the procurement of goods/services. The NICHD is prohibited from transferring funds to a CRADA Collaborator. Under a CRADA, the NICHD can offer the selected collaborator access to facilities, staff, materials, and expertise. The collaborator may contribute facilities, staff, materials, expertise, and funding to the collaboration. A CRADA collaborator may elect an option to an exclusive or non-exclusive license to Government intellectual property rights arising under the CRADA, and may qualify as a co-inventor of new technology developed under the CRADA. As between two or more sufficient, overlapping research proposals (where the overlap cannot be cured), the NICHD, as specified in 15 U.S.C. 3710a(c)(4), will give special consideration to small businesses, and will give preference to business units located in the U.S. that agree to manufacture CRADA products in the U.S.
The CRADA will employ a MATER null mouse line to examine the role of MATER in effecting the embryonic program switch from the maternal genome to the zygotic genome. The project's goal is to define MATER's role in embryonic transcription, transition from control by the maternal to the zygotic genome, signal transduction, cell cycle control, and to identify proteins that interact with MATER. A strategy should be developed to extract RNA from oocytes and early stage mouse embryos to create cDNA libraries to identify the genes that are critical to oocyte function and early embryonic development. Furthermore, a strategy will be implemented for development of a chip technology for oocyte and embryonic gene activation. Preimplantation mouse embryos may also be used for protein analysis and profiling. Specific gene loci or gene sequences that are identified will be analyzed and may be employed in the molecular manipulation of animal oocytes or early embryos.
The described methods are the subject of a U.S. provisional patent application filed October 18, 2000 by the Public Health Service on behalf of the Federal Government. Furthermore, the initial report and characterization of the invention is described in: Tong et al., Mamm. Genome 11:281-287, 2000. Commercialization of new CRADA technology may require obtaining an appropriate PHS license.
The collaborator in this endeavor is expected to commit scientific personnel commensurate with the level of research activities defined by the CRADA Research Plan. It is anticipated that PHS laboratories and/or those of the collaborator will be utilized, as appropriate, for the research activities as defined by the Research Plan. NICHD anticipates, in addition, that the Collaborator, as appropriate, will provide funding for the project.
The NICHD anticipates that its role may include, but not be limited to, the following:
(1) Plan research studies, interpret research results, and, as appropriate, jointly publish the conclusions with the collaborator;
(2) Provide collaborator with access to existing NICHD research data (both already collected and yet to be collected);
(3) Provide staff, expertise, and materials for the development and testing of promising products;
(4) Provide work space and equipment for testing of any prototype compositions developed.
The NICHD anticipates that the role of the successful collaborator will include the following:
(1) Provide significant intellectual, scientific, and technical expertise in the development and manufacture of relevant products;
(2) Plan research studies, interpret research results, and, as appropriate, jointly publish the conclusions; and
(3) Provide NICHD a supply of necessary materials, access to necessary proprietary technology and/or data, and as necessary for the project, staff and funding in support of the research goals.
Other contributions may be necessary for particular proposals.
Proposals submitted for consideration should address, as best as possible and to the extent relevant to the proposal, each of the following: Start Printed Page 14398
A. Scientific advisors and staff with a demonstrated record of research success related to remodeling of chromosomal architecture, transcription, and translation, and
(i) Technical expertise of the Collaborator's Principal Investigator and laboratory group in the technology described above,
(2) Reliability as a Research Partner
A. Willingness to commit best effort and to provide adequate and sustained resources and/or funding, as appropriate, to support the CRADA studies, and
B. Development of this technology, as outlined in the CRADA Collaborator's proposal, and
C. Ability to develop and produce products in a timely manner, as applicable (for example, as demonstrated by a history of meeting benchmarks in licenses), and
D. Commitment to supporting the advancement of scientific research, as evidenced by a willingness to jointly publish research results in a prompt manner, and
E. Willingness to be bound by DHHS and PHS policies regarding:
(i) the public distribution of unmodified genetic sequences and research tools,
(ii) the care and handling of animals, and
(iii) testing in human subjects.
(3) Physical Resources
A. An established headquarters, with office space and basic office equipment, and
B. Access to the organization during business hours by telephone, facsimile, courier, U.S. Post, e-mail, the World-Wide-Web, and, as appropriate, other evolving information technologies, and
C. Sufficient financial and material resources to support, at a minimum, the anticipated activities of the CRADA to meet the needs of NICHD under the proposal.
The collaborator is encouraged to propose, in the written research statement, related applications and technologies other than those specifically described herein.Start Signature
Dated: February 26, 2001.
[FR Doc. 01-6038 Filed 3-9-01; 8:45 am]
BILLING CODE 4140-01-P