| Q.
A study meeting the UCLA definition of a clinical trial will be conducted
as a cooperative group trial under NIH funding. Can the clinical trial
facilities and administrative cost rate of 26% TDC be used?
A. No.
Studies supported in whole or in part with federal funding must
apply the applicable Federal research facilities and administrative
cost rate (currently 54.5% MTDC on campus or 26% MTDC off campus).
Q.
A study will be funded by an industry Sponsor via a subcontract
to UCLA, with prime funding provided by the Federal government.
Since the funds will be received directly from the industry Sponsor,
can the clinical trial facilities and administrative cost rate of
26% be applied?
A. No.
Because Federal flow-through funds are involved, the applicable
Federal research facilities and administrative cost rate should
be applied.
Q.
A study fully funded by a for-profit entity will involve testing
of an investigational drug or device in animals. Which facilities
and administrative cost rate applies?
A. The
clinical trial indirect rate only applies to clinical testing in
human subjects. Pre-clinical laboratory and animal studies are specifically
excluded. Therefore, the applicable Federally-negotiated research
facilities and administrative cost rate would apply.
Q.
A pharmaceutical company has requested that the University run specialized
tests on samples obtained in a clinical trial. Would the clinical
trial facilities and administrative cost rate apply?
A. No.
The clinical trial rate applies only to studies involving the direct
clinical testing of investigational products in human subjects.
If the University's sole involvement is to run tests, the applicable
Other Sponsored Activities rate would apply (currently 32% MTDC
on campus and 26% MTDC off campus).
Q.
An investigator has agreed to analyze data collected in an industry-sponsored
clinical trial conducted at both UCLA and other sites. Which facilities
and administrative cost rate applies?
A. The
applicable Federally-negotiated research rate would apply.
Q.
The University has been asked by a for-profit sponsor to recruit
and enroll human subjects in order to collect data that will be
submitted to a patient registry. Is this considered a clinical trial,
and would the clinical trial facilities and administrative cost
rate apply?
A. Data
collection studies for registry purposes, even if human subjects
are involved, are not considered clinical trials. Therefore, the
clinical trial facilities and administrative cost rate would not
apply, and the applicable Other Sponsored Activities facilities
and administrative cost rate should be used.
Last
updated on 09/15/2006
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