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John Bell, chair of CIRM SAB
Academy of Medical Sciences photo |
The $3 billion California stem cell agency is preparing to take a
close look at recommendations from key advisors that it should focus
more sharply on a handful projects in order to transform research
rapidly into commercial therapies.
The governing board's
Science Subcommittee on Nov. 22 will examine the proposals by its new
Scientific Advisory Board(SAB), created last
summer as the result of a $700,000
Institute of Medicine study.
Among other things, the advisory board said
CIRM directors
should zero in on six to eight projects that would lead to early stage
clinical trials.
The recommendations come as the agency, known as CIRM, is wrestling with its own
mortality. Cash for new awards will run out in 2017. The directors
next month will hear a consultant's report on a plan for financing
the agency's future. It is expected to involve some sort of
public-private funding, which will only be forthcoming if the agency
demonstrates research results that resonate with possible funding
sources.
At last month's governing board meeting, CIRM director
Sherry
Lansing, a former Hollywood film studio chief, former chair of the UC
regents and a prodigious fundraiser, sounded an urgent note.
She said that the agency is “trying desperately to get a win.”
She raised the possibility of putting out a “do-you-need-help”
RFA which would target applicants that have well-developed projects
that could be moved ahead rapidly with some cash.
The Oct. 9 board meeting was the first time that Lansing and the other
28 CIRM directors had seen the recommendations, which were
prepared outside of public view. They were only received by the
agency staff two days before the board meeting.
The agency has yet to post on the Internet the full SAB document.
However, the
California Stem Cell Report asked for a copy, and the
complete text can be found at end of this item.
The report said,
“(F)or stem cell research to continue to advance at its current
pace in California, future potential investors and supporters of stem
cell research must perceive a tangible benefit to human health, and
this can only happen through a clear success at the stage of clinical
proof of concept. It is important that this occurs during the
currently projected lifespan of CIRM, so that deserving projects and
resources are positioned in the strongest way possible to attract
future investments after expiration of the current CIRM funds.”
The agency's scientific advisors, only one of whom is from California, said the agency has a “strong chance of
success” in securing additional funding if it moves “at speed.”
The panel, chaired by Sir
John Bell of
Oxford University in the
United Kingdom, said it was “optimistic” that “a clinical
proof of concept can be achieved in one or more settings with CIRM
projects within the next three years.”
The report contained some comments that indicate that the advisors
are not fully aware of all the circumstances surrounding CIRM. The
panel prepared its report after being briefed by CIRM staff and four academic recipients who had
received CIRM awards. No representatives from industry were heard. The advisors' report said,
“The SAB had a very positive view of the interactions between
CIRM and the commercial sector.”
Many in the biotech community, however, have been less than
pleased with CIRM, to point of holding
a private dinner to air their grievances with then CIRM Chairman
Robert Klein, filing multiple
appeals of grant reviewer decisions and
testifying before the Institute of Medicine. Only a tiny percentage of the $1.9 billion
in CIRM awards has gone to business.
The agency, however, is working diligently to improve its industry
relations, which are critical to turning research into something that
can actually be used in the marketplace.
The advisors, handpicked by departing CIRM President
Alan Trounson, praised
CIRM's achievements so far as “considerable” and
“transformative.” But it noted that the agency lagged behind
other funding bodies in terms of “attention and attribution.”
The panel said,
“CIRM has been catalytic in generating many of the scientific
advances in this field, but its brand recognition internationally and even nationally is limited and this should be corrected.”
The agency has suffered in the past from PR missteps but has
been moving with some success in the past year to gain more favorable
attention. However, it remains a relatively young organization. It
receives almost no coverage in the mainstream media and very little
more in the scientific media. Breaking through the media clutter is
difficult, especially given that CIRM has not been part of major stem cell developments that naturally generate front page
attention.
The SAB recommendations have been largely endorsed by the agency's
staff. Following the Nov. 22 meeting on the proposals, they will go to the full governing board at its December meeting for action. The
public can attend the meeting Nov. 22 in San Francisco and a
teleconference location in Duarte at the
City of Hope. Advance
comments can be filed with CIRM via email at info@cirm.ca.gov.