Notice Number: NOT-OD-08-006Key Dates
Release Date: October 16, 2007Issued by
Department of Health and Human ServicesNotice is hereby given that the Office of Research Integrity
(ORI) and the Acting Assistant Secretary for Health have taken
final action in the following case:Jon Sudb[oslash], D.D.S., Norwegian Radium Hospital: Based on the
findings of an investigation conducted by the Investigation
Commission appointed by Norwegian Radium Hospital (NRH) and the
University of Oslo, the respondent's own admission, and additional
analysis and information obtained by the Office of Research
Integrity (ORI) during its oversight review, the U.S. Public Health
Service (PHS) found that Jon Sudb[oslash], D.D.S., former doctoral
student and faculty member, University of Oslo, and former
physician in the Department of Medical Oncology and Radiotherapy,
NRH, engaged in scientific misconduct by reporting fabricated
and/or falsified research in grant application 1 P01 CA106451-01
submitted to the National Cancer Institute (NCI), National
Institutes of Health (NIH), and its first-year progress
report.
Specifically, PHS found that Dr. Sudb[oslash] engaged in scientific
misconduct by falsifying and fabricating research that served as
the rationale for Project 1, ``Oral Cancer Prevention with
Molecular Targeting Therapy,' with Dr. Jon Sudb[oslash], as project
leader, in the grant application, and by falsifying a progress
report for the awarded grant. In particular, in Figure 1 of the
Background and Significance section of the grant application, Dr.
Sudb[oslash] reported fabricated/falsified results for the effects
of lesion ploidy upon survival in patients with oral pre-malignant
lesions. In the Preliminary Data section of the grant application,
Dr. Sudb[oslash] reported several events intended to demonstrate
his experience in the research field that the Investigation
Commission stated ``appear as pure fiction.' Also, in the first
yearly progress report for the funded grant, Dr. Sudb[oslash]
falsified the number of patients that had been screened for
admission to the study.
In addition to three publications for which Dr. Sudb[oslash]
admitted falsifying and/or fabricating data, the Investigation
Commission found at least twelve other publications that warranted
retraction because they could not be considered valid. The research
reported in these publications was not supported by PHS funds.
However, the publications address the same general research area as
that addressed in the grant application and demonstrate a pervasive
pattern of falsification/fabrication in research reporting on the
part of Dr. Sudb[oslash]. The falsified/fabricated data presented
in the grant application purport to demonstrate the feasibility of
preventing cancer in a high risk population with nontoxic oral
agents.
Dr. Sudb[oslash] has entered into a Voluntary Exclusion Agreement
(Agreement) in which he has voluntarily agreed, beginning on August
31, 2007: (1) To exclude himself permanently from any contracting
or subcontracting with any agency of the United States Government
and from eligibility or involvement in nonprocurement programs of
the United States Government as delineated in the OMB Guidelines to
Agencies on Governmentwide Debarment and Suspension at 2 CFR Part
376, et seq.; Dr. Sudb[oslash] agrees that he will not petition HHS
to reverse or reduce the scope of the permanent voluntary exclusion
or other administrative actions that are the subject of this
Agreement; and (2) To exclude himself permanently 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 or contractor to PHS.Specifically, PHS found that Dr. Sudb[oslash] engaged in scientific
misconduct by falsifying and fabricating research that served as
the rationale for Project 1, ``Oral Cancer Prevention with
Molecular Targeting Therapy,' with Dr. Jon Sudb[oslash], as project
leader, in the grant application, and by falsifying a progress
report for the awarded grant. In particular, in Figure 1 of the
Background and Significance section of the grant application, Dr.
Sudb[oslash] reported fabricated/falsified results for the effects
of lesion ploidy upon survival in patients with oral pre-malignant
lesions. In the Preliminary Data section of the grant application,
Dr. Sudb[oslash] reported several events intended to demonstrate
his experience in the research field that the Investigation
Commission stated ``appear as pure fiction.' Also, in the first
yearly progress report for the funded grant, Dr. Sudb[oslash]
falsified the number of patients that had been screened for
admission to the study.
In addition to three publications for which Dr. Sudb[oslash]
admitted falsifying and/or fabricating data, the Investigation
Commission found at least twelve other publications that warranted
retraction because they could not be considered valid. The research
reported in these publications was not supported by PHS funds.
However, the publications address the same general research area as
that addressed in the grant application and demonstrate a pervasive
pattern of falsification/fabrication in research reporting on the
part of Dr. Sudb[oslash]. The falsified/fabricated data presented
in the grant application purport to demonstrate the feasibility of
preventing cancer in a high risk population with nontoxic oral
agents.
Dr. Sudb[oslash] has entered into a Voluntary Exclusion Agreement
(Agreement) in which he has voluntarily agreed, beginning on August
31, 2007: (1) To exclude himself permanently from any contracting
or subcontracting with any agency of the United States Government
and from eligibility or involvement in nonprocurement programs of
the United States Government as delineated in the OMB Guidelines to
Agencies on Governmentwide Debarment and Suspension at 2 CFR Part
376, et seq.; Dr. Sudb[oslash] agrees that he will not petition HHS
to reverse or reduce the scope of the permanent voluntary exclusion
or other administrative actions that are the subject of this
Agreement; and (2) To exclude himself permanently 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 or contractor to PHS.In addition to three publications for which Dr. Sudb[oslash]
admitted falsifying and/or fabricating data, the Investigation
Commission found at least twelve other publications that warranted
retraction because they could not be considered valid. The research
reported in these publications was not supported by PHS funds.
However, the publications address the same general research area as
that addressed in the grant application and demonstrate a pervasive
pattern of falsification/fabrication in research reporting on the
part of Dr. Sudb[oslash]. The falsified/fabricated data presented
in the grant application purport to demonstrate the feasibility of
preventing cancer in a high risk population with nontoxic oral
agents.
Dr. Sudb[oslash] has entered into a Voluntary Exclusion Agreement
(Agreement) in which he has voluntarily agreed, beginning on August
31, 2007: (1) To exclude himself permanently from any contracting
or subcontracting with any agency of the United States Government
and from eligibility or involvement in nonprocurement programs of
the United States Government as delineated in the OMB Guidelines to
Agencies on Governmentwide Debarment and Suspension at 2 CFR Part
376, et seq.; Dr. Sudb[oslash] agrees that he will not petition HHS
to reverse or reduce the scope of the permanent voluntary exclusion
or other administrative actions that are the subject of this
Agreement; and (2) To exclude himself permanently 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 or contractor to PHS.Dr. Sudb[oslash] has entered into a Voluntary Exclusion Agreement
(Agreement) in which he has voluntarily agreed, beginning on August
31, 2007: (1) To exclude himself permanently from any contracting
or subcontracting with any agency of the United States Government
and from eligibility or involvement in nonprocurement programs of
the United States Government as delineated in the OMB Guidelines to
Agencies on Governmentwide Debarment and Suspension at 2 CFR Part
376, et seq.; Dr. Sudb[oslash] agrees that he will not petition HHS
to reverse or reduce the scope of the permanent voluntary exclusion
or other administrative actions that are the subject of this
Agreement; and (2) To exclude himself permanently 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 or contractor to PHS.InquiriesFor further information contact:
Director
Division of Investigative Oversight
Office of Research Integrity
1101 Wootton Parkway
Suite 750
Rockville, MD 20852
(240) 453-8800