Short title

This Act may be cited as the

Ovarian Cancer Biomarker Research Act of 2007

Grants for establishment and operation of research centers for the study of ovarian cancer biomarkers

Subpart 1 of part C of the Public Health Service Act is amended by adding at the end the following new section:

417E.

Grants for establishment and operation of research centers for the study of ovarian cancer biomarkers

(a)

In general

The Director of the Institute, in consultation with the directors of other relevant institutes and centers of the National Institutes of Health and the Department of Defense Ovarian Cancer Research Program, shall enter into cooperative agreements with, or make grants to, public or nonprofit entities to establish and operate centers to conduct research on biomarkers for use in risk stratification for, and the early detection and screening of, ovarian cancer, including fallopian tube cancer or primary peritoneal cancer. Each center shall be known as an Ovarian Cancer Biomarker Center of Excellence. (b)

Research funded

Federal payments made under a cooperative agreement or grant under subsection (a) may be used for research on any of the following: (1)The development and characterization of new biomarkers, and the refinement of existing biomarkers, for ovarian cancer. (2)The clinical and laboratory validation of such biomarkers, including technical development, standardization of assay methods, sample preparation, reagents, reproducibility, portability, and other refinements. (3)The development and implementation of clinical and epidemiological research on the utilization of biomarkers for the early detection and screening of ovarian cancer. (4)The development and implementation of repositories for new tissue, urine, serum, and other biological specimens (such as ascites and pleural fluids). (c)

First agreement or grant

Not later than 1 year after the date of the enactment of this section, the Director of the Institute shall enter into the first cooperative agreement or make the first grant under this section. (d)

Availability of banked specimens

The Director of the Institute shall make available for research conducted under this section banked serum and tissue specimens from clinical research regarding ovarian cancer that was funded by the Department of Health and Human Services. (e)

Report

Not later than the end of fiscal year 2009, and annually thereafter, the Director of the Institute shall submit a report to the Congress on the cooperative agreements entered into and the grants made under this section. (f)

Authorization of appropriations

For the purpose of carrying out this section, there are authorized to be appropriated $25,000,000 for each of the fiscal years 2009 through 2012, and such sums as may be necessary for each of the fiscal years 2013 through 2019. Such authorization of appropriations is in addition to any other authorization of appropriations that is available for such purpose.

Ovarian Cancer Biomarker Clinical Trial Committee

Subpart 1 of part C of the Public Health Service Act, as amended by section 2, is further amended by adding at the end the following new section:

417F.

Ovarian Cancer Biomarker Clinical Trial Committee

(a)

Ovarian Cancer Biomarker Research Committee established

The Director of the Institute shall establish an Ovarian Cancer Biomarker Clinical Trial Committee (in this section referred to as the Committee) to assist the Director to design and implement one or more national clinical trials, in accordance with this section, to determine the utility of using biomarkers validated pursuant to the research conducted under section 417E for risk stratification for, and early detection and screening of, ovarian cancer. (b)

Membership

(1)

Number

The Committee shall consist of 11 voting members and such number of nonvoting members as the Director of the Institute determines appropriate. (2)

Appointment

The members of the Committee shall be appointed by the Director of the Institute, in consultation with appropriate national medical societies, research societies, and patient advocate organizations, as follows: (A)

Voting members

The voting members of the Committee shall be appointed by the Director of the Institute as follows: (i)Two patient advocates. (ii)Two national experts in statistical analysis, clinical trial design, and patient recruitment. (iii)Two representatives from the Gynecologic Oncology Group. (iv)One representative from the Department of Defense Ovarian Cancer Research Program. (v)Four ovarian cancer researchers. (B)

Nonvoting members

The nonvoting members of the Committee shall include such individuals as the Director of the Institute determines to be appropriate. (3)

Pay

Members of the Committee shall serve without pay and those members who are full time officers or employees of the United States shall receive no additional pay by reason of their service on the Committee, except that members of the Committee shall receive travel expenses, including per diem in lieu of subsistence, in accordance with applicable provisions under chapter I of chapter 57 of title 5, United States Code. (c)

Chairperson

The voting members of the Committee appointed under subsection (b)(2) shall select a chairperson from among such members. (d)

Meetings

The Committee shall meet at the call of the chairperson or upon the request of the Director of the Institute, but at least four times each year. (e)

Clinical trial specifications

In designing and implementing the clinical trials under this section, the Director of the Institute shall provide for the following: (1)

Participation in trial

To the greatest extent possible, all academic centers, community cancer centers, and individual physician investigators (as defined in subsection (f)) shall have the opportunity to participate in the trials under this section and to enroll women at risk for ovarian cancer in the trials. (2)

Costs for enrollments

Subject to the availability of appropriations, all the costs to the centers and offices described in paragraph (1) for enrolling women in the trials under this section shall be reimbursed by the Institute. (3)

National data center

A national data center shall be established in and supported by the Institute to conduct statistical analyses of the data derived from the trials under this section and to store such analyses and data. (4)

Guidelines for medical community

Data and statistical analyses of the clinical trials under this section shall be used to establish clinical guidelines to provide the medical community with information regarding the use of biomarkers validated pursuant to the research conducted under section 417E for risk stratification for, and early detection and screening of, ovarian cancer. (f)

Individual physician investigator defined

For purposes of subsection (e)(1), the term individual physician investigator means a physician— (1)who is a faculty member at an academic institution or who is in a private medical practice; and (2)who provides health care services to women at risk for ovarian cancer. (g)

Report

Not later than the end of fiscal year 2009, and annually thereafter, the Director of the Institute shall submit a report to the Congress on the activities conducted under this section. (h)

Authorization of appropriations

For the purpose of carrying out this section, there are authorized to be appropriated $5,000,000 for each of the fiscal years 2009 through 2012, and such sums as may be necessary for each of the fiscal years 2013 through 2019. Such authorization of appropriations is in addition to any other authorization of appropriations that is available for such purpose.