EXPIRED
MORRIS K. UDALL PARKINSON'S DISEASE RESEARCH CENTERS OF EXCELLENCE RELEASE DATE: October 7, 2002 (This PAR has been reissued, see PAR-06-058) (see NOT-NS-03-021 and NOT-NS-03-020) PA NUMBER: PAR-03-004 EXPIRATION DATE: 2 November 2005, unless reissued National Institute of Neurological Disorders and Stroke (NINDS) (http://www.ninds.nih.gov) National Institute of Environmental Health Sciences (NIEHS) (http://www.niehs.nih.gov) THIS PA CONTAINS THE FOLLOWING INFORMATION o Purpose of this PA o Research Objectives o Research Scope o Mechanism(s) of Support o Funds Available o Eligible Institutions o Individuals Eligible to Become Principal Investigators o Special Requirements o Where to Send Inquiries o Submitting an Application o Peer Review Process o Review Criteria o Award Criteria o Required Federal Citations: PURPOSE OF THIS PA In response to continuing research progress and opportunity, and in recognition of continuing Congressional interest to intensify and to expand basic and clinical research in Parkinson's disease, The National Institute of Neurological Disorders and Stroke (NINDS) and the National Institute of Environmental Health Sciences (NIEHS) invite qualified investigators to submit grant applications for the establishment of Morris K. Udall Parkinson's Disease Research Centers of Excellence. The purpose of this Program Announcement (PA) is to encourage additional research opportunities and discoveries that will lead to improved diagnosis and treatment of patients with Parkinson's Disease and related neurodegenerative disorders, based on a better understanding of the fundamental cause(s) of the disease. It is expected that these Centers will form a consortium of investigators that will foster an environment that will enhance research effectiveness in a multi-disciplinary setting, utilizing specialized methods relevant to the study of these disorders. There were two previous requests (http://grants.nih.gov/grants/guide/rfa-files/RFA-NS-98-001.html and http://grants.nih.gov/grants/guide/rfa-files/RFA-NS-99-004.html. RESEARCH OBJECTIVES The overall purpose of this initiative is to continue to support and develop outstanding Parkinson's disease research centers of excellence. Each center may contain either basic or clinical research or proportions of each that are appropriate for the research objectives. Emphasis is placed on multi-disciplinary and collaborative studies that can best be carried out in a Center setting. The organizational structure of the Center should be flexible to allow the expeditious translation of new scientific findings and new technological developments to clinical research. Studies might include, but are not limited to, the epidemiology, natural history, pathogenesis or treatment of PD and related disorders. To generate new ideas, develop young investigators, and enhance the national PD research infrastructure each center should have a research-training component identifying opportunities for either basic or clinical inter- institutional research collaborations. This component is to allow young investigators to work for a time at the center or allow center investigators to travel between Centers to learn new techniques. Centers are expected to be characterized by a broad but thematically coherent set of investigations bearing on the etiology, pathogenesis and treatment of PD. To the extent that they inform and/or expand research on Parkinson's disease, investigations on related neurodegenerative disorders may be included. It is anticipated that the ensemble of individual Centers will constitute a comprehensive and systematic pursuit of the needs and opportunities in PD research. Each single center will focus on a select subset of topics according to its individual strengths while continuing to expand the PD research enterprise through collaborations. To facilitate interaction and collaboration between the Centers a consortium will be established. RESEARCH SCOPE New research techniques have created extraordinary opportunities for further exploration into the etiology, pathogenesis, diagnosis and treatment of Parkinson's disease and related neurodegenerative disorders. Topics of investigation within a center might include, but are not limited to: o Clinical studies of Parkinson's disease, parkinsonism, and related disorders. o The natural history of PD and related disorders including prospective clinical assessment, neuropathological analysis, and banking of brain tissue from individuals with Parkinson's disease who agree to participate in an autopsy program. o Studies to address the non-motor aspects of Parkinson's disease. o Development of therapeutic technology related to Parkinson's disease. o Epidemiological and genetic studies to identify risk and susceptibility factors. o Studies on gene-environment interactions as risk factors for Parkinson's disease. o Translational research. o Cellular and molecular mechanisms of cell injury and death in Parkinson's disease and related neurodegenerative disorders. o Studies of the structure, function, composition, role, and possible interrelationship of proteins and inclusion bodies implicated in the pathogenesis of Parkinson's disease and related disorders. o Development of animal models and their use for investigation of pathophysiology and efficacy of therapeutic intervention. o Development and function of the neural circuitry involved in PD and related disorders, including those functions affected by the disease process or treatment. o Molecular and cell biology of the dopaminergic systems and other relevant neurotransmitters and neuromodulators and their function in the brain. o Exploration of trophic factors and their receptors that promote the survival of dopamine neurons in the adult brain. o Neuronal reconstruction using engineered cell lines that are relevant to Parkinson's disease. o Markers of PD onset, progression and response to therapy. MECHANISM OF SUPPORT The mechanism of support for the Morris K. Udall Parkinson's Disease Research Centers of Excellence is the Research Center Grant (P50). Responsibility for planning, direction, and execution of the proposed research centers will rest solely with the applicant. Because the nature and scope of the research proposed in response to this PA may vary, it is anticipated that the size of the award may also vary. It is expected that grants will not exceed one million dollars per year direct costs for five years. At this time, it is not known if this PA will be reissued. Any future unsolicited competing continuation applications based on this project will compete with all NIH investigator-initiated applications and be reviewed according to the customary peer review procedures. Investigators seeking to carry out pilot studies of therapies in preparation for a clinical trial should apply under the auspices of the NINDS Pilot clinical trial grant program announcement PAR-01-119. This announcement can be found at http://grants.nih.gov/grants/guide/pa-files/PAR-01-119.html). Since such applications must conform to the intent of both program announcements, including the additional review criteria of PAR-01-119, potential applicants are strongly encouraged to contact NINDS program staff for guidance. Close collaboration and integration between research center activities and clinical trials is encouraged. FUNDS AVAILABLE Applications based on this PA will compete with all NIH investigator- initiated applications and be reviewed according to the customary peer review procedures. Awards pursuant to this PA are contingent upon the availability of funds and the receipt of applications that address a sufficient number of the topics identified in the "RESEARCH SCOPE". ELIGIBLE INSTITUTIONS You may submit (an) application(s) if your institution has any of the following characteristics: o For-profit or non-profit organizations o Public or private institutions, such as universities, colleges, hospitals, and laboratories o Units of State and local governments o Eligible agencies of the Federal government o Domestic institutions or organizations o Faith-based or community based organizations INDIVIDUALS ELIGIBLE TO BECOME PRINCIPAL INVESTIGATORS Any individual with the skills, knowledge, and resources necessary to carry out the proposed research is invited to work with their institution to develop an application for support. Individuals from underrepresented racial and ethnic groups as well as individuals with disabilities are always encouraged to apply for NIH programs. SPECIAL REQUIREMENTS Consortium and Annual Meeting: Investigators who participate in this PA will collaborate with other investigators in the existing consortium. Synthesis of the individual Center's research projects into an integrated research effort to understand and treat Parkinson's disease will require multidisciplinary collaboration, communication of research results and ideas, and sharing of research resources. To facilitate such interactions, the NINDS will coordinate an annual meeting. The PI and other representatives from each Center will attend this meeting. As appropriate, this meeting will also be open to interested members of the research community and representatives of health research voluntary agencies. Collaborative Studies: The consortium structure is put in place to facilitate collaboration among participating investigators. As discussed in the "RESEARCH OBJECTIVES", a mission of the consortium is to foster interdisciplinary efforts among members. Examples of interdisciplinary efforts may consist of the sharing of ideas, results, reagents, resources, and the exchange of post-doctoral students, etc. The cost of attendance at the annual meeting and of participating in collaborative studies should be built into the proposed budget. WHERE TO SEND INQUIRIES We encourage inquiries concerning this PA and welcome the opportunity to answer questions from potential applicants. Inquiries may fall into three areas: scientific/research, peer review, and financial or grants management issues: Direct your questions about scientific/research issues to: Eugene J. Oliver, Ph.D. Program Director Neurodegeneration Cluster National Institute of Neurological Disorders and Stroke Neuroscience Center, RM 2203 6001 Executive Blvd MSC 9525 Bethesda, MD 20892-9525 Phone: 301-496-5680 FAX: 301-480-1080 Email: [email protected] Annette Kirshner, Ph.D. Program Administrator National Institute of Environmental Health Sciences Box 12233 MD EC-23 RTP, NC 27709 Phone: 919-541-0488 FAX: 919-541-5064 Email: [email protected] Cindy Lawler, Ph.D. Program Administrator National Institute of Environmental Health Sciences Box 12233 MD EC-23 RTP, NC 27709 Phone: 919-316-4671 FAX: 919-541-5064 Email: [email protected] Direct your questions about peer review issues to: Alan Willard, Ph.D. Chief, Scientific Review Branch National Institute of Neurological Disorders and Stroke Neuroscience Center, RM 3208 6001 Executive Blvd MSC 9529 Bethesda, MD 20892-9529 Phone: 301-496-9223 FAX: 301-402-0182 Email: [email protected] Direct your questions about financial or grants management matters to: King P. Bond Jr. Grants Management Officer National Institute of Neurological Disorders and Stroke Neuroscience Center, Suite 3254 6001 Executive Blvd MSC 9537 Bethesda, MD 20892-9537 Phone: 301-496-3813 FAX: 301-402-0219 Email: [email protected] Lerlita Garcia Grants Management Specialist National Institute of Environmental Health Sciences Box 12233 MD EC-22 RTP, NC 27709 Phone: 919-316-4638 FAX: 919-541-2860 Email: [email protected] SUBMITTING AN APPLICATION Applications must be prepared using the PHS 398 research grant application instructions and forms (rev. 5/2001). The PHS 398 is available at http://grants.nih.gov/grants/funding/phs398/phs398.html in an interactive format. For further assistance contact Grants Info, Telephone (301) 710-0267, Email: [email protected]. APPLICATION RECEIPT DATES: Applications submitted in response to this program announcement will be accepted at the standard application deadlines, which are available at http://grants.nih.gov/grants/dates.htm. Application deadlines are also indicated in the PHS 398 application kit. SPECIFIC INSTRUCTIONS FOR APPLICATIONS REQUESTING $500,000 OR MORE PER YEAR: Applications requesting $500,000 or more in direct costs for any year must include a cover letter identifying the NIH staff member within one of NIH institutes or centers who has agreed to accept assignment of the application. Applicants requesting more than $500,000 must carry out the following steps: 1) Contact the IC program staff at least 6 weeks before submitting the application, i.e., as you are developing plans for the study; 2) Obtain agreement from the IC staff that the IC will accept your application for consideration for award; and, 3) Identify, in a cover letter sent with the application, the staff member and IC who agreed to accept assignment of the application. This policy applies to all investigator-initiated new (type 1), competing continuation (type 2), competing supplement, or any amended or revised version of these grant application types. Additional information on this policy is available in the NIH Guide for Grants and Contracts, October 19, 2001 at http://grants.nih.gov/grants/guide/notice-files/NOT-OD-02-004.html. SENDING AN APPLICATION TO THE NIH: Submit a signed, typewritten original of the application, including the Checklist, and three signed, photocopies, in one package to: Center For Scientific Review National Institutes Of Health 6701 Rockledge Drive, Room 1040, MSC 7710 Bethesda, MD 20892-7710 Bethesda, MD 20817 (for express/courier service) At the time of submission, two additional copies of the application must be sent to: Eugene J. Oliver, Ph.D. Program Director Neurodegeneration Cluster National Institute of Neurological Disorders and Stroke Neuroscience Center, RM 2203 6001 Executive Blvd MSC 9525 Bethesda, MD 20892-9525 Phone: 301-496-5680 FAX: 301-480-1080 Email: [email protected] APPLICATION PROCESSING: Applications must be received by or mailed on or before the receipt dates described at http://grants.nih.gov/grants/funding/submissionschedule.htm. The CSR will not accept any application in response to this PA that is essentially the same as one currently pending initial review unless the applicant withdraws the pending application. The CSR will not accept any application that is essentially the same as one already reviewed. This does not preclude the submission of a substantial revision of an application already reviewed, but such application must include an Introduction addressing the previous critique. The NINDS Guidelines for the development of Program Project and Center Applications should be followed when preparing the application. They are available on the NINDS home page at: http://www.ninds.nih.gov/index.htm. The PA title and number must be typed on line 2 of the face page of the application form and the YES box must be marked. PEER REVIEW PROCESS Applications submitted for this PA will be assigned on the basis of established PHS referral guidelines. An appropriate scientific review group convened by NINDS in accordance with the standard NIH peer review procedures (HTTP://www.csr.nih.gov/refrev.htm) will evaluate applications for scientific and technical merit As part of the initial merit review, all applications will: o Receive a written critique o Undergo a selection process in which only those applications deemed to have the highest scientific merit, generally the top half of the applications under review, will be discussed and assigned a priority score. o Receive a second level review by the National Advisory Council of the relevant participating IC or Board. REVIEW CRITERIA The goals of NIH-supported research are to advance our understanding of biological systems, improve the control of disease, and enhance health. In the written comments, reviewers will be asked to discuss the following aspects of your application in order to judge the likelihood that the proposed research will have a substantial impact on the pursuit of these goals: o Significance o Approach o Innovation o Investigator o Environment The scientific review group will address and consider each of these criteria in assigning your application's overall score, weighting them as appropriate for each application. Your application does not need to be strong in all categories to be judged likely to have major scientific impact and thus deserve a high priority score. For example, you may propose to carry out important work that by its nature is not innovative, but is essential to move a field forward. (1) SIGNIFICANCE: Does your study address an important problem? If the aims of your application are achieved, how do they advance scientific knowledge? What will be the effect of these studies on the concepts or methods that drive this field? (2) APPROACH: Are the conceptual framework, design, methods, and analyses adequately developed, well integrated, and appropriate to the aims of the project? Do you acknowledge potential problem areas and consider alternative tactics? (3) INNOVATION: Does your project employ novel concepts, approaches or methods? Are the aims original and innovative? Does your project challenge existing paradigms or develop new methodologies or technologies? (4) INVESTIGATOR: Are you appropriately trained and well suited to carry out this work? Is the work proposed appropriate to your experience level as the principal investigator and to that of other researchers (if any)? (5) ENVIRONMENT: Does the scientific environment in which your work will be done contribute to the probability of success? Do the proposed experiments take advantage of unique features of the scientific environment or employ useful collaborative arrangements? Is there evidence of institutional support? ADDITIONAL REVIEW CRITERIA: In addition to the above criteria, your application will also be reviewed with respect to the following: o INTEGRATION AND COLLABORATION: The adequacy of the proposed Center to integrate across research projects and collaborate across laboratories including basic and clinical approaches (for applications that propose basic and clinical research). Activities in each project should inform and advance the others and the proposed collaborative activities should provide synergy to the proposed Center. o PROTECTIONS: The adequacy of the proposed protection for humans, animals, or the environment, to the extent they may be adversely affected by the project proposed in the application. o INCLUSION: The adequacy of plans to include subjects from both genders, all racial and ethnic groups (and subgroups), and children as appropriate for the scientific goals of the research. Plans for the recruitment and retention of subjects will also be evaluated. (See Inclusion Criteria included in the section on Federal Citations, below) o DATA SHARING: The adequacy of the proposed plan to share data, resources, and tools. o BUDGET: The reasonableness of the proposed budget and the requested period of support in relation to the proposed research. AWARD CRITERIA Applications submitted in response to a PA will compete for available funds with all other recommended applications. The following will be considered in making funding decisions: o Scientific merit of the proposed project as determined by peer review o Availability of funds o Relevance to program priorities REQUIRED FEDERAL CITATIONS MONITORING PLAN AND DATA SAFETY AND MONITORING BOARD: Research components involving Phase I and II clinical trials must include provisions for assessment of patient eligibility and status, rigorous data management, quality assurance, and auditing procedures. In addition, it is NIH policy that all clinical trials require data and safety monitoring, with the method and degree of monitoring being commensurate with the risks (NIH Policy for Data Safety and Monitoring, NIH Guide for Grants and Contracts, June 12, 1998: http://grants.nih.gov/grants/guide/notice-files/not98-084.html). INCLUSION OF WOMEN AND MINORITIES IN CLINICAL RESEARCH: It is the policy of the NIH that women and members of minority groups and their sub-populations must be included in all NIH-supported clinical research projects unless a clear and compelling justification is provided indicating that inclusion is inappropriate with respect to the health of the subjects or the purpose of the research. This policy results from the NIH Revitalization Act of 1993 (Section 492B of Public Law 103-43). All investigators proposing clinical research should read the AMENDMENT "NIH Guidelines for Inclusion of Women and Minorities as Subjects in Clinical Research - Amended, October, 2001," published in the NIH Guide for Grants and Contracts on October 9, 2001 (http://grants.nih.gov/grants/guide/notice-files/NOT-OD-02-001.html); a complete copy of the updated Guidelines are available at http://grants.nih.gov/grants/funding/women_min/guidelines_amended_10_2001.htm. The amended policy incorporates: the use of an NIH definition of clinical research; updated racial and ethnic categories in compliance with the new OMB standards; clarification of language governing NIH-defined Phase III clinical trials consistent with the new PHS Form 398; and updated roles and responsibilities of NIH staff and the extramural community. The policy continues to require for all NIH- defined Phase III clinical trials that: a) all applications or proposals and/or protocols must provide a description of plans to conduct analyses, as appropriate, to address differences by sex/gender and/or racial/ethnic groups, including subgroups if applicable; and b) investigators must report annual accrual and progress in conducting analyses, as appropriate, by sex/gender and/or racial/ethnic group differences. INCLUSION OF CHILDREN AS PARTICIPANTS IN RESEARCH INVOLVING HUMAN SUBJECTS: The NIH maintains a policy that children (i.e., individuals under the age of 21) must be included in all human subjects research, conducted or supported by the NIH, unless there are scientific and ethical reasons not to include them. This policy applies to all initial (Type 1) applications submitted for receipt dates after October 1, 1998. All investigators proposing research involving human subjects should read the "NIH Policy and Guidelines" on the inclusion of children as participants in research involving human subjects that is available at http://grants.nih.gov/grants/funding/children/children.htm. REQUIRED EDUCATION ON THE PROTECTION OF HUMAN SUBJECT PARTICIPANTS: NIH policy requires education on the protection of human subject participants for all investigators submitting NIH proposals for research involving human subjects. You will find this policy announcement in the NIH Guide for Grants and Contracts Announcement, dated June 5, 2000, at http://grants.nih.gov/grants/guide/notice-files/NOT-OD-00-039.html. HUMAN EMBRYONIC STEM CELLS (hESC): Criteria for federal funding of research on hESCs can be found at http://grants.nih.gov/grants/stem_cells.htm and at http://grants.nih.gov/grants/guide/notice-files/NOT-OD-02-005.html. Only research using hESC lines that are registered in the NIH Human Embryonic Stem Cell Registry will be eligible for Federal funding (see http://escr.nih.gov). It is the responsibility of the applicant to provide the official NIH identifier(s)for the hESC line(s)to be used in the proposed research. Applications that do not provide this information will be returned without review. PUBLIC ACCESS TO RESEARCH DATA THROUGH THE FREEDOM OF INFORMATION ACT: The Office of Management and Budget (OMB) Circular A-110 has been revised to provide public access to research data through the Freedom of Information Act (FOIA) under some circumstances. Data that are (1) first produced in a project that is supported in whole or in part with Federal funds and (2) cited publicly and officially by a Federal agency in support of an action that has the force and effect of law (i.e., a regulation) may be accessed through FOIA. It is important for applicants to understand the basic scope of this amendment. NIH has provided guidance at http://grants.nih.gov/grants/policy/a110/a110_guidance_dec1999.htm. Applicants may wish to place data collected under this PA in a public archive, which can provide protections for the data and manage the distribution for an indefinite period of time. If so, the application should include a description of the archiving plan in the study design and include information about this in the budget justification section of the application. In addition, applicants should think about how to structure informed consent statements and other human subjects procedures given the potential for wider use of data collected under this award. URLs IN NIH GRANT APPLICATIONS OR APPENDICES: All applications and proposals for NIH funding must be self-contained within specified page limitations. Unless otherwise specified in an NIH solicitation, Internet addresses (URLs) should not be used to provide information necessary to the review because reviewers are under no obligation to view the Internet sites. Furthermore, we caution reviewers that their anonymity may be compromised when they directly access an Internet site. HEALTHY PEOPLE 2010: The Public Health Service (PHS) is committed to achieving the health promotion and disease prevention objectives of "Healthy People 2010," a PHS-led national activity for setting priority areas. This PA is related to one or more of the priority areas. Potential applicants may obtain a copy of "Healthy People 2010" at http://www.health.gov/healthypeople. AUTHORITY AND REGULATIONS: This program is described in the Catalog of Federal Domestic Assistance No. 93.853 and 93.113, and is not subject to the intergovernmental review requirements of Executive Order 12372 or Health Systems Agency review. Awards are made under authorization of Sections 301 and 405 of the Public Health Service Act as amended (42 USC 241 and 284)and administered under NIH grants policies described at http://grants.nih.gov/grants/policy/policy.htm and under Federal Regulations 42 CFR 52 and 45 CFR Parts 74 and 92. The PHS strongly encourages all grant recipients to provide a smoke- free workplace and discourage the use of all tobacco products. In addition, Public Law 103-227, the Pro-Children Act of 1994, prohibits smoking in certain facilities (or in some cases, any portion of a facility) in which regular or routine education, library, day care, health care, or early childhood development services are provided to children. This is consistent with the PHS mission to protect and advance the physical and mental health of the American people.
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