DOD Peer Reviewed Medical Clinical Trial Award

The summary for the DOD Peer Reviewed Medical Clinical Trial Award grant is detailed below. This summary states who is eligible for the grant, how much grant money will be awarded, current and past deadlines, Catalog of Federal Domestic Assistance (CFDA) numbers, and a sampling of similar government grants. Verify the accuracy of the data FederalGrants.com provides by visiting the webpage noted in the Link to Full Announcement section or by contacting the appropriate person listed as the Grant Announcement Contact. If any section is incomplete, please visit the website for the Dept of the Army USAMRAA, which is the U.S. government agency offering this grant.
DOD Peer Reviewed Medical Clinical Trial Award: The PRMRP Clinical Trial Award mechanism is being offered for the first time in FY08. This award supports rapid implementation of clinical trials of interventions with the potential to have a significant impact on a disease or condition addressed in one of the FY08 PRMRP topic areas. All proposed clinical trials must be responsive to the health care needs of the Armed Forces and family members, the U.S. Veteran population, and the general public and may address prevention, detection, diagnosis, treatment, and/or quality of life. The clinical trial may be designed to evaluate a pharmacologic agent (drug or biologic), device, or behavioral intervention. Funding from this award mechanism cannot be used for preclinical research studies. Each proposal should contain only one clinical trial with a distinct study design. Investigational New Drug (IND) or Investigational Device Exemption (IDE) applications should be submitted or approved prior to proposal submission. The Government reserves the right to withdraw funding if IND/IDE approval is not received within 6 months of the award date. Principal Investigators (PIs) must clearly specify in the Clinical Protocol (main body of the proposal) which type of clinical trial is being proposed: Phase I, Phase I/II, Phase II, or Phase III. For descriptions of each type of clinical trial, please refer to www.fda.gov/cder/guidance/6384dft.htm and http://www.clinicaltrials.gov. The proposed clinical trial is expected to begin within 12 months of the award date. The following are important aspects of the Clinical Trial Award submission: . Demonstrate availability of, and access to, a suitable patient population that will support a meaningful outcome for the study . Describe clearly defined and appropriate endpoints for the proposed clinical trial . Clearly articulate the statistical analysis plan . Discuss the potential impact of the study results for patients with the specified disease/condition . Include a named study coordinator who will guide the clinical protocol through Institutional Review Board (IRB), Human Subjects Research Review Board (HSRRB), and other regulatory approval processes, coordinate activities from all sites participating in the trial, and coordinate participant accrual See the Program Announcement for the full Funding Opportunity Description.
Federal Grant Title: DOD Peer Reviewed Medical Clinical Trial Award
Federal Agency Name: Dept of the Army USAMRAA
Grant Categories: Science and Technology
Type of Opportunity: Discretionary
Funding Opportunity Number: W81XWH-08-PRMRP-CTA
Type of Funding: Cooperative Agreement Grant
CFDA Numbers: 12.420
CFDA Descriptions: Military Medical Research and Development
Current Application Deadline: No deadline provided
Original Application Deadline: Jul 02, 2008
Posted Date: Mar 26, 2008
Creation Date: Mar 26, 2008
Archive Date: Aug 01, 2008
Total Program Funding: $7,500,000
Maximum Federal Grant Award:
Minimum Federal Grant Award:
Expected Number of Awards: 2
Cost Sharing or Matching: No
Applicants Eligible for this Grant
Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled "Additional Information on Eligibility"
Grant Announcement Contact
PA HELP: 301-619-7079; [email protected]
eReceipt HELP: 301-682-5507; [email protected]
[email protected] CDMRP Helpdesk
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