Findings of Research Misconduct, 12264-12265 [2019-06206]

Download as PDF 12264 Federal Register / Vol. 84, No. 62 / Monday, April 1, 2019 / Notices accessing the Federal Advisory Committee Act (FACA) database that is maintained by the Committee Management Secretariat under the General Services Administration. The website for the FACA database is https:// www.facadatabase.gov/. Amy P. McNulty, Acting Director, Division of the Executive Secretariat. [FR Doc. 2019–06162 Filed 3–29–19; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Health Resources and Services Administration Charter Renewal for the Advisory Committee on Training in Primary Care Medicine and Dentistry Health Resources and Services Administration (HRSA), Department of Health and Human Services (HHS). ACTION: Notice. AGENCY: The Advisory Committee on Training in Primary Care Medicine and Dentistry (ACTPCMD or the Committee) has been rechartered. The effective date of the renewed charter is March 24, 2019. SUMMARY: FOR FURTHER INFORMATION CONTACT: Kennita R. Carter, MD, Designated Federal Official, at 301–945–3505 or email at BHWACTPCMD@hrsa.gov. A copy of the current committee membership, charter, and reports can be obtained by accessing the ACTPCMD’s website at https://www.hrsa.gov/ advisory-committees/primarycaredentist/. SUPPLEMENTARY INFORMATION: ACTPCMD provides advice and recommendations to the Secretary of HHS (Secretary) on policy, program development, and other matters of significance concerning the activities under section 747 of Title VII of the Public Health Service (PHS) Act, as it existed upon the enactment of Section 749 of the PHS Act in 1998. ACTPCMD prepares an annual report describing the activities of the Committee, including findings and recommendations made by the Committee concerning the activities under section 747, as well as training programs in oral health and dentistry. The annual report is submitted to the Secretary and Chair and ranking members of the Senate Committee on Health, Education, Labor and Pensions, and the House of Representatives Committee on Energy and Commerce. The Committee also develops, VerDate Sep<11>2014 17:22 Mar 29, 2019 Jkt 247001 publishes, and implements performance measures and guidelines for longitudinal evaluations of programs authorized under Title VII, Part C, of the PHS Act, and recommends appropriation levels for programs under this Part. Meetings are held not less than twice a year. The recharter for the ACTPCMD was approved on March 20, 2019, and the filing date is March 24, 2019. Recharter of the ACTPCMD gives authorization for the Committee to operate until March 24, 2021. A copy of the ACTPCMD charter is available on the ACTPCMD website at https://www.hrsa.gov/advisorycommittees/primarycare-dentist/ index.html. A copy of the charter can also be obtained by accessing the Federal Advisory Committee Act (FACA) database that is maintained by the Committee Management Secretariat under the General Services Administration. The website for the FACA database is https:// www.facadatabase.gov/. Amy P. McNulty, Acting Director, Division of the Executive Secretariat. [FR Doc. 2019–06161 Filed 3–29–19; 8:45 am] BILLING CODE 4165–15–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Office of Global Affairs: Stakeholder Listening Session in Preparation for the 72nd World Health Assembly Time and date: Monday, May 6, 2019, 10:00 a.m.–11:30 a.m. EST. Place: Hubert H. Humphrey Building, Auditorium, 200 Independence Ave. SW, Washington, District of Columbia 20201. Status: Open, but requiring RSVP to OGA.RSVP@hhs.gov by Friday, April 26, 2019. Purpose: The U.S. Department of Health and Human Services (HHS)— charged with leading the U.S. delegation to the 72nd World Health Assembly— will hold an informal Stakeholder Listening Session on Monday, May 6 from 10:00 a.m. to 11:30 a.m., in the Hubert H. Humphrey Building Auditorium, 200 Independence Ave. SW, Washington, DC 20201. The Stakeholder Listening Session will help the HHS Office of Global Affairs prepare the U.S. delegation for the World Health Assembly by taking full advantage of the knowledge, ideas, feedback, and suggestions from all individuals interested in and affected by agenda items to be discussed at the 72nd World Health Assembly. PO 00000 Frm 00075 Fmt 4703 Sfmt 4703 Time allotted to each attendee who wishes to comment, not to exceed three minutes, will be communicated at the beginning of session, and will depend on the number of comments anticipated. Written comments are welcome and encouraged, even if you are planning on attending in person. Please send your written comments to OGA.RSVP@ hhs.gov. Your input will contribute to informing U.S. positions as we negotiate with our international colleagues at the World Health Assembly on these important health topics. The draft agenda for the 72nd World Health Assembly can be found at this website: https://apps.who.int/gb/ebwha/ pdf_files/WHA72/A72_1-en.pdf. The HHS Office of Global Affairs will organize the listening session by agenda item, and welcomes participation from all individuals, including individuals familiar with the following topics and groups: • Public health and advocacy activities; • State, local, and Tribal issues; • Private industry; • Minority health organizations; and • Academic and scientific organizations. RSVP: Due to security restrictions for entry into the HHS Hubert H. Humphrey Building, RSVPs are required for this event. Please send your full name and organization to OGA.RSVP@hhs.gov. Please RSVP no later than Friday, April 26, 2019. If you are not a U.S. citizen and do not have a U.S. government issued form of identification, please note this in the subject line of your RSVP, and our office will contact you to gain additional biographical information required for your clearance. Photo identification for all attendees is required for building access without exception. We look forward to hearing your comments related to the 72nd World Health Assembly agenda items. Dated: March 22, 2019. Glenn Garrett Grigsby, Director for Global Affairs. [FR Doc. 2019–06207 Filed 3–29–19; 8:45 am] BILLING CODE 4150–38–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Office of the Secretary Findings of Research Misconduct Office of the Secretary, HHS. Notice. AGENCY: ACTION: Findings of research misconduct have been made against SUMMARY: E:\FR\FM\01APN1.SGM 01APN1 Federal Register / Vol. 84, No. 62 / Monday, April 1, 2019 / Notices Edward J. Fox, Ph.D. (Respondent), Acting Assistant Professor in the Department of Pathology, University of Washington (UW). Dr. Fox engaged in research misconduct in research supported by National Cancer Institute (NCI), National Institutes of Health (NIH), grants R01 CA193649, R01 CA160674, P01 CA77852, and R01 CA102029. The administrative actions, including supervision for a period of one (1) year, were implemented beginning on March 18, 2019, and are detailed below. FOR FURTHER INFORMATION CONTACT: Wanda K. Jones, Dr. P.H., Interim Director, Office of Research Integrity, 1101 Wootton Parkway, Suite 750, Rockville, MD 20852, (240) 453–8200. SUPPLEMENTARY INFORMATION: Notice is hereby given that the Office of Research Integrity (ORI) has taken final action in the following case: Edward J. Fox, Ph.D., University of Washington: Based on Respondent’s admission, an inquiry conducted by UW, and additional analysis conducted by ORI in its oversight review, ORI found that Dr. Edward J. Fox, Acting Assistant Professor in the Department of Pathology, UW, engaged in research misconduct in research supported by NCI, NIH, grants R01 CA193649, R01 CA160674, P01 CA77852, and R01 CA102029. Respondent neither admits nor denies ORI’s finding of research misconduct related to grant application R01 CA193649–01A1. Respondent and ORI desire to close this matter without further expense of time and other resources and thus have entered into a Voluntary Settlement Agreement (Agreement). With respect to grant application R01 CA193649–01A1, Respondent acknowledges that his research records were poorly maintained and lacked the documentation necessary to support the reported preliminary results. ORI found that Respondent engaged in research misconduct by intentionally, knowingly, or recklessly: • Fabricating data and analyses in a manuscript submitted to Nature,1 which was subsequently voluntarily withdrawn. These fabricated data and analyses also appear in Figure 1 of grant progress report R01 CA193649–02.2 1 Fox, E.J., Schmitt, M.W., Reid-Bayliss, K.S., Geraghty, R., O’Donoghue, D.P., Mulcahy, H.E., Leahy, D.T., Sheahan, K., Beckman, R.A., & Loeb, L.A. ‘‘Extensive subclonal mutations in human colorectal cancers detected by duplex sequencing.’’ Accepted for publication in Nature (hereafter referred to as the ‘‘Nature manuscript’’). 2 The subsequent grant progress report noted these data might not be reliable and indicated that the experiments were being re-run. VerDate Sep<11>2014 17:22 Mar 29, 2019 Jkt 247001 Respondent stated during the inquiry that two abstracts that appear in Cancer Research 3 are based on the fabricated data and analyses. • fabricating or falsifying data and analyses in the preliminary results section of grant application R01 CA193649–01A1, section C.1.a(iv). Specifically, ORI found that in the Nature manuscript and, where noted below, in grant progress report R01 CA193649–02 submitted to NCI, NIH, Respondent intentionally, knowingly, or recklessly: • Fabricated data for Figures 1c and 1d to show that the frequency of unique subclonal mutations in normal cells increases as people age, while the frequency of subclonal mutations in cancerous cells does not. • fabricated Figure 2b to show a pattern of subclonal mutations for the fabricated data from Figures 1c and 1d and fabricated the statistical analysis results to show statistically significant differences between tumor and normal mucosa; this figure also appears as Figure 1 in R01 CA193649–02. • fabricated data for Figure 3b to show predominantly neutral subclonal evolution. • fabricated the Extended Data Figures 1–5 and Extended Data Tables 3–5 by using the fabricated data from Figure 3b. • presented methods and data-based explanations that are fabricated because they were based on the fabricated data. ORI also specifically found that in grant application R01 CA193649–01A1, Respondent intentionally, knowingly, or recklessly: • Fabricated or falsified data for Figures 7, 8, and 9 to show how duplex sequencing methodology can document the distribution of subclonal mutations that are present in colorectal cancer.C • presented data-based explanations that are fabricated or falsified because some of them were based on the fabricated or falsified data. Dr. Fox entered into an Agreement and voluntarily agreed: (1) To have his research supervised for a period of one (1) year beginning on 3 Fox, E.J.P., Schmitt, M.W., Reid-Bayliss, K.S., Beckman, R.A., & Loeb, L.A. ‘‘Extensive subclonal mutations in human colorectal cancers detected by duplex sequencing.’’ [Abstract]. In: Proceedings of the 107th Annual Meeting of the American Association for Cancer Research, 2016 Apr 16–20, New Orleans, LA. Philadelphia (PA): AACR; Cancer Res. 76(14 Suppl):Abstract nr LB–338, 2016. Fox, E.J.P., Schmitt, M.W., Reid-Bayliss, K.S., Beckman, R.A., & Loeb, L.A. ‘‘Extensive subclonal mutations in human colorectal cancers detected by Duplex Sequencing.’’ [Abstract]. In: Proceedings of the AACR Special Conference on Colorectal Cancer: From Initiation to Outcomes, 2016 Sep 17–20, Tampa, FL. Philadelphia (PA): AACR; Cancer Res. 77(3 Suppl):Abstract nr A08, 2017. PO 00000 Frm 00076 Fmt 4703 Sfmt 4703 12265 March 18, 2019; Respondent agreed that prior to submission of an application for U.S. Public Health Service (PHS) support for a research project on which Respondent’s participation is proposed and prior to Respondent’s participation in any capacity on PHS-supported research, Respondent shall ensure that a plan for supervision of Respondent’s duties is submitted to ORI for approval; the supervision plan must be designed to ensure the scientific integrity of Respondent’s research contribution; Respondent agreed that he shall not participate in any PHS-supported research until such a supervision plan is submitted to and approved by ORI; Respondent agreed to maintain responsibility for compliance with the agreed upon supervision plan; (2) that for a period of one (1) year beginning on March 18, 2019, any institution employing him shall submit, in conjunction with each application for PHS funds, or report, manuscript, or abstract involving PHS-supported research in which Respondent is involved, a certification to ORI that the data provided by Respondent are based on actual experiments or are otherwise legitimately derived and that the data, procedures, and methodology are accurately reported in the application, report, manuscript, or abstract; (3) that if no supervisory plan is provided to ORI, Respondent will provide certification to ORI at the conclusion of the supervision period that he has not engaged in, applied for, or had his name included on any application, proposal, or other request for PHS funds without prior notification to ORI; (4) to exclude himself from serving in any advisory capacity to PHS including, but not limited to, service on any PHS advisory committee, board, and/or peer review committee, or as a consultant for a period of one (1) year beginning on March 18, 2019; and (5) as a condition of the Agreement, Respondent will recommend to the American Association for Cancer Research that the following two Cancer Research abstracts should be retracted: • Cancer Res. 76(14 Suppl.):Abstract nr LB–338, 2016 • Cancer Res. 77(3 Suppl.):Abstract nr A08, 2017 Respondent will copy ORI and UW on this correspondence. Wanda K. Jones, Interim Director, Office of Research Integrity. [FR Doc. 2019–06206 Filed 3–29–19; 8:45 am] BILLING CODE 4150–31–P E:\FR\FM\01APN1.SGM 01APN1

Agencies

[Federal Register Volume 84, Number 62 (Monday, April 1, 2019)]
[Notices]
[Pages 12264-12265]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-06206]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Office of the Secretary


Findings of Research Misconduct

AGENCY: Office of the Secretary, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: Findings of research misconduct have been made against

[[Page 12265]]

Edward J. Fox, Ph.D. (Respondent), Acting Assistant Professor in the 
Department of Pathology, University of Washington (UW). Dr. Fox engaged 
in research misconduct in research supported by National Cancer 
Institute (NCI), National Institutes of Health (NIH), grants R01 
CA193649, R01 CA160674, P01 CA77852, and R01 CA102029. The 
administrative actions, including supervision for a period of one (1) 
year, were implemented beginning on March 18, 2019, and are detailed 
below.

FOR FURTHER INFORMATION CONTACT: Wanda K. Jones, Dr. P.H., Interim 
Director, Office of Research Integrity, 1101 Wootton Parkway, Suite 
750, Rockville, MD 20852, (240) 453-8200.

SUPPLEMENTARY INFORMATION: Notice is hereby given that the Office of 
Research Integrity (ORI) has taken final action in the following case:
    Edward J. Fox, Ph.D., University of Washington: Based on 
Respondent's admission, an inquiry conducted by UW, and additional 
analysis conducted by ORI in its oversight review, ORI found that Dr. 
Edward J. Fox, Acting Assistant Professor in the Department of 
Pathology, UW, engaged in research misconduct in research supported by 
NCI, NIH, grants R01 CA193649, R01 CA160674, P01 CA77852, and R01 
CA102029.
    Respondent neither admits nor denies ORI's finding of research 
misconduct related to grant application R01 CA193649-01A1. Respondent 
and ORI desire to close this matter without further expense of time and 
other resources and thus have entered into a Voluntary Settlement 
Agreement (Agreement). With respect to grant application R01 CA193649-
01A1, Respondent acknowledges that his research records were poorly 
maintained and lacked the documentation necessary to support the 
reported preliminary results.
    ORI found that Respondent engaged in research misconduct by 
intentionally, knowingly, or recklessly:
     Fabricating data and analyses in a manuscript submitted to 
Nature,\1\ which was subsequently voluntarily withdrawn. These 
fabricated data and analyses also appear in Figure 1 of grant progress 
report R01 CA193649-02.\2\ Respondent stated during the inquiry that 
two abstracts that appear in Cancer Research \3\ are based on the 
fabricated data and analyses.
---------------------------------------------------------------------------

    \1\ Fox, E.J., Schmitt, M.W., Reid-Bayliss, K.S., Geraghty, R., 
O'Donoghue, D.P., Mulcahy, H.E., Leahy, D.T., Sheahan, K., Beckman, 
R.A., & Loeb, L.A. ``Extensive subclonal mutations in human 
colorectal cancers detected by duplex sequencing.'' Accepted for 
publication in Nature (hereafter referred to as the ``Nature 
manuscript'').
    \2\ The subsequent grant progress report noted these data might 
not be reliable and indicated that the experiments were being re-
run.
    \3\ Fox, E.J.P., Schmitt, M.W., Reid-Bayliss, K.S., Beckman, 
R.A., & Loeb, L.A. ``Extensive subclonal mutations in human 
colorectal cancers detected by duplex sequencing.'' [Abstract]. In: 
Proceedings of the 107th Annual Meeting of the American Association 
for Cancer Research, 2016 Apr 16-20, New Orleans, LA. Philadelphia 
(PA): AACR; Cancer Res. 76(14 Suppl):Abstract nr LB-338, 2016.
    Fox, E.J.P., Schmitt, M.W., Reid-Bayliss, K.S., Beckman, R.A., & 
Loeb, L.A. ``Extensive subclonal mutations in human colorectal 
cancers detected by Duplex Sequencing.'' [Abstract]. In: Proceedings 
of the AACR Special Conference on Colorectal Cancer: From Initiation 
to Outcomes, 2016 Sep 17-20, Tampa, FL. Philadelphia (PA): AACR; 
Cancer Res. 77(3 Suppl):Abstract nr A08, 2017.
---------------------------------------------------------------------------

     fabricating or falsifying data and analyses in the 
preliminary results section of grant application R01 CA193649-01A1, 
section C.1.a(iv).
    Specifically, ORI found that in the Nature manuscript and, where 
noted below, in grant progress report R01 CA193649-02 submitted to NCI, 
NIH, Respondent intentionally, knowingly, or recklessly:
     Fabricated data for Figures 1c and 1d to show that the 
frequency of unique subclonal mutations in normal cells increases as 
people age, while the frequency of subclonal mutations in cancerous 
cells does not.
     fabricated Figure 2b to show a pattern of subclonal 
mutations for the fabricated data from Figures 1c and 1d and fabricated 
the statistical analysis results to show statistically significant 
differences between tumor and normal mucosa; this figure also appears 
as Figure 1 in R01 CA193649-02.
     fabricated data for Figure 3b to show predominantly 
neutral subclonal evolution.
     fabricated the Extended Data Figures 1-5 and Extended Data 
Tables 3-5 by using the fabricated data from Figure 3b.
     presented methods and data-based explanations that are 
fabricated because they were based on the fabricated data.
    ORI also specifically found that in grant application R01 CA193649-
01A1, Respondent intentionally, knowingly, or recklessly:
     Fabricated or falsified data for Figures 7, 8, and 9 to 
show how duplex sequencing methodology can document the distribution of 
subclonal mutations that are present in colorectal cancer.C
     presented data-based explanations that are fabricated or 
falsified because some of them were based on the fabricated or 
falsified data.
    Dr. Fox entered into an Agreement and voluntarily agreed:
    (1) To have his research supervised for a period of one (1) year 
beginning on March 18, 2019; Respondent agreed that prior to submission 
of an application for U.S. Public Health Service (PHS) support for a 
research project on which Respondent's participation is proposed and 
prior to Respondent's participation in any capacity on PHS-supported 
research, Respondent shall ensure that a plan for supervision of 
Respondent's duties is submitted to ORI for approval; the supervision 
plan must be designed to ensure the scientific integrity of 
Respondent's research contribution; Respondent agreed that he shall not 
participate in any PHS-supported research until such a supervision plan 
is submitted to and approved by ORI; Respondent agreed to maintain 
responsibility for compliance with the agreed upon supervision plan;
    (2) that for a period of one (1) year beginning on March 18, 2019, 
any institution employing him shall submit, in conjunction with each 
application for PHS funds, or report, manuscript, or abstract involving 
PHS-supported research in which Respondent is involved, a certification 
to ORI that the data provided by Respondent are based on actual 
experiments or are otherwise legitimately derived and that the data, 
procedures, and methodology are accurately reported in the application, 
report, manuscript, or abstract;
    (3) that if no supervisory plan is provided to ORI, Respondent will 
provide certification to ORI at the conclusion of the supervision 
period that he has not engaged in, applied for, or had his name 
included on any application, proposal, or other request for PHS funds 
without prior notification to ORI;
    (4) to exclude himself from serving in any advisory capacity to PHS 
including, but not limited to, service on any PHS advisory committee, 
board, and/or peer review committee, or as a consultant for a period of 
one (1) year beginning on March 18, 2019; and
    (5) as a condition of the Agreement, Respondent will recommend to 
the American Association for Cancer Research that the following two 
Cancer Research abstracts should be retracted:
     Cancer Res. 76(14 Suppl.):Abstract nr LB-338, 2016
     Cancer Res. 77(3 Suppl.):Abstract nr A08, 2017
    Respondent will copy ORI and UW on this correspondence.

Wanda K. Jones,
Interim Director, Office of Research Integrity.
[FR Doc. 2019-06206 Filed 3-29-19; 8:45 am]
 BILLING CODE 4150-31-P
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