[Federal Register Volume 77, Number 72 (Friday, April 13, 2012)]
[Notices]
[Pages 22320-22321]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2012-8903]
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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.
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SUMMARY: Notice is hereby given that the Office of Research Integrity
(ORI) has taken final action in the following case:
Peter J. Francis, M.D., Ph.D., Oregon Health Sciences University:
Based on the report of an investigation conducted by Oregon Health
Sciences University (OHSU) and additional analysis conducted by ORI in
its oversight review, ORI found that Dr. Peter J. Francis, Associate
Professor, Casey Eye Institute, OHSU, engaged in research misconduct in
research reported in two grant applications, R01 EY021214-01 and
resubmitted as R01 EY021214-01A1, that he submitted to the National Eye
Institute (NEI), National Institutes of Health (NIH).
Specifically, ORI finds that the Respondent fabricated results of a
pilot experiment in which he claimed to have injected retinal pigment
epithelial (RPE) cells obtained from Rhesus monkey embryonic stem cells
(ECS) into a strain of rats (RCS) that develops retinal degeneration.
Respondent claimed that after the injection of ECS-derived RPE
cells 21 days postnatal, the rats were tested at day 60 postnatal for
optomotor acuity, and that the retinal histology of eyes receiving ECS-
derived RPE cells, compared to mock-injected controls, showed enhanced
photoreceptor preservation and no adverse effects. Respondent admitted
that this experiment had not been conducted either by the time the
original grant application had been submitted or by the time the later
R01 EY021214-01A1 application was submitted.
Dr. Francis has entered into a Voluntary Settlement Agreement
(Agreement) and has voluntarily agreed for a period of two (2) years,
beginning on March 29, 2012:
(1) To have his research supervised; Respondent agrees to ensure
that prior to the submission of an application for U.S. Public Health
Service (PHS) support for a research project on which the Respondent's
participation is proposed and prior to Respondent's participation in
any capacity on PHS-supported research, the institution employing him
must submit a plan for supervision of Respondent's duties to ORI for
approval; the plan for supervision must be designed to ensure the
scientific integrity of Respondent's research contribution; Respondent
agrees that he shall not participate in any PHS-supported research
after sixty
[[Page 22321]]
(60) days from the effective date of this Agreement until such a
supervision plan is submitted to and approved by ORI; Respondent agrees
to maintain responsibility for compliance with the agreed upon
supervision plan;
(2) that this supervisory plan provided by any institution
employing him shall provide assurance that each application for PHS
funds, or report, manuscript, or abstract involving PHS supported
research in which Respondent was involved was based on actual
experiments or was otherwise legitimately derived, that the data,
procedures, and methodology were accurately reported in the
application, report, manuscript, or abstract, and that the text in such
submissions was his own or properly cited the source of copied language
and ideas; and
(3) 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 FURTHER INFORMATION CONTACT: Director, Division of Investigative
Oversight, Office of Research Integrity, 1101 Wootton Parkway, Suite
750, Rockville, MD 20852, (240) 453-8800.
John Dahlberg,
Director, Division of Investigative Oversight, Office of Research
Integrity.
[FR Doc. 2012-8903 Filed 4-12-12; 8:45 am]
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