Opportunity ID: 92014

General Information

Document Type: Grants Notice
Funding Opportunity Number: W81XWH-11-PCRP-CTA
Funding Opportunity Title: DoD FY11 Prostate Cancer Research Program Clinical Trial Award
Opportunity Category: Discretionary
Opportunity Category Explanation: –
Funding Instrument Type: Cooperative Agreement
Grant
Category of Funding Activity: Science and Technology and other Research and Development
Category Explanation: –
Expected Number of Awards: 3
Assistance Listings: 12.420 — Military Medical Research and Development
Cost Sharing or Matching Requirement: No
Version: Synopsis 1
Posted Date: May 05, 2011
Last Updated Date: –
Original Closing Date for Applications: Sep 01, 2011
Current Closing Date for Applications: Sep 01, 2011
Archive Date: Oct 01, 2011
Estimated Total Program Funding: $1,800,000
Award Ceiling: $0
Award Floor: $0

Eligibility

Eligible Applicants: Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled “Additional Information on Eligibility”
Additional Information on Eligibility: –

Additional Information

Agency Name: Dept. of the Army — USAMRAA
Description: The PCRP Clinical Trial Award mechanism was first offered in FY01. Since then, 97 Clinical
Trial Award applications have been received, and 18 have been recommended for funding.
The PCRP Clinical Trial Award supports rapid execution of clinical trials (Phase 0/I, Phase I,
Phase I/II, or Phase II for drugs, Class II or III for devices) to test novel approaches with the potential to have a major impact on the treatment or management of prostate cancer. Funding from this award mechanism must support a clinical trial and cannot be used for preclinical
research studies. A clinical trial is defined as a prospective accrual of patients where an
intervention (i.e., drug, device, biologic, surgical procedure, rehabilitative modality, behavioral intervention, or other) is tested on a human subject for a measurable outcome with respect to exploratory information, safety, effectiveness, and/or efficacy. This outcome represents a direct effect on the subject of that intervention or interaction. Exploratory clinical trials (Phase 0) may be submitted for the PCRP Clinical Trial Award, but they must be accompanied by a Phase I clinical trial (Phase 0/I). Principal Investigators (PIs) must clearly specify in their applications which type of clinical trial, including phase or class designation (if applicable), is being
proposed. PIs are encouraged to accompany their trials with correlative studies that address one
or more of the PCRP focus areas (see Program Description above). PIs conducting correlative
studies must describe in detail the study aims, procedures or methods, and plans for data
management and analysis, including an appropriately powered statistical plan. For more
information on clinical trials and phase/class of study, a Human Subject Resource Document is
provided at https://cdmrp.org/Program_Announcements_and_Forms/.
Studies in a broad range of areas related to prostate cancer clinical management and care will be accepted under this PCRP Clinical Trial Award, including but not limited to:
� Evaluations of novel drugs, biologics, or devices
� Survivorship
� Diet
� Quality of life
� Psychosocial interventions
� Behavioral studies
All applications for the Clinical Trial Award are highly recommended to address one of the
FY11 PCRP overarching challenges. The PCRP seeks to fund projects from the wide spectrum
of basic to clinical research; however, if the proposed project does not address one of the
overarching challenges, the application should provide a description to justify how the project
will nevertheless address a critical need in the field of prostate cancer research and/or patient
care.
The following are important aspects of submission for the PCRP Clinical Trial Award:
� The application should include a thorough discussion of the potential for the proposed
intervention and study results to lead to a major impact on the treatment or management
of prostate cancer.
� New for FY11: The application must include documentation of an existing Investigational New Drug (IND) or Investigational Device Exemption (IDE), if applicable.
� The intervention to be tested should be based on sound scientific rationale that is
established through logical reasoning, critical review, and analysis of the literature.
� The inclusion of preliminary data that are relevant to the proposed research is required;
any unpublished preliminary data should originate from the laboratory of the PI or
collaborators named on this application.
� The application should demonstrate availability of and access to a suitable human subject population that will support a meaningful outcome for the study. The PI should discuss how accrual goals will be achieved, and how standards of care may impact the study
population.
� The application should demonstrate documented availability of and access to the
drug/compound, device, and/or materials needed.
� The proposed clinical trial should include clearly defined and appropriate endpoints.
� The application should include a detailed statistical analysis plan, including a power
analysis reflecting sample size projections that will clearly answer the objectives of the
study.
� The proposed clinical trial is expected to begin no later than 12 months after the award
date.
� New for FY11: PIs must discuss how the clinical trial will be funded to its planned
completion with either: support with funds from the PCRP, support from the applicant
institution, and/or support from another agency or entity. Documentation of necessary
funding from other sources, if applicable, is required, and will be requested at a later
date for Clinical Trial Award applications recommended for funding.
� New for FY11: The application should include a Transition Plan that describes a clear
path to further develop the intervention after the end of the award period of
performance.
Use of Human Subjects and Human Anatomical Substances: All Department of Defense
(DOD)-funded research involving new and ongoing research with human subjects and human
anatomical substances must be reviewed by the local Institutional Review Board (IRB) of record.
However, IRB approval at the time of submission is NOT required. In addition, these studies
must also be reviewed and approved by the US Army Medical Research and Materiel Command
(USAMRMC) Office of Research Protections (ORP), Human Research Protection Office (HRPO). The HRPO is mandated to comply with specific laws and directives governing all research involving human subjects that is supported by the DOD. These laws and directives are rigorous and detailed, and will require information in addition to that supplied to the IRB of
record. Allow a minimum of 4 months for regulatory review and approval processes. Refer to the General Application Instructions, Appendix 5, for more information.
Link to Additional Information: –
Grantor Contact Information: If you have difficulty accessing the full announcement electronically, please contact:

301-682-5507
Email:help@cdmrp.org

Version History

Version Modification Description Updated Date

Folder 92014 Full Announcement-1 -> pcrp_fy11_cta_pa_gg.pdf

Folder 92014 Full Announcement-1 -> pcrp_fy11_cta_ind_ide_documentation form_gg.pdf

Packages

Agency Contact Information: 301-682-5507
Email: help@cdmrp.org
Who Can Apply: Organization Applicants

Assistance Listing Number Competition ID Competition Title Opportunity Package ID Opening Date Closing Date Actions
12.420 PKG00052133 May 05, 2011 Sep 01, 2011 View

Package 1

Mandatory forms

92014 RR_SF424_1_2-1.2.pdf

92014 PerformanceSite_1_4-1.4.pdf

92014 RR_Budget-1.1.pdf

92014 RR_KeyPersonExpanded_1_2-1.2.pdf

Optional forms

92014 RR_SubawardBudget30-1.2.pdf

2025-07-13T04:07:23-05:00

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