paul.nowak wrote: Matt, thanks for the comments. I made an error on the version of Plone. It's 2.5 Plone running on Zope 2.9x.
In regards to the additional products, we have a skin installed and we have a product that we had custom developed for us that connects to a PostgreSQL database. We've looked at slow PostgreSQL queries causing problems and have not been able to find an issue. We've also tested for the case where the PostgreSQL server is down and have not been able to create an issue. We therefor...
SEATTLE, WA -- (MARKET WIRE) -- 02/12/07 -- Targeted Genetics Corporation (NASDAQ: TGEN)
provides an update today on its ongoing Phase I/II trial of tgAAC94 in
patients with inflammatory arthritis. tgAAC94 is an investigational
therapeutic designed to inhibit the activity of tumor necrosis factor-alpha
(TNF-alpha), a key mediator of inflammation. The data reported today
support the safety and tolerability of a single and repeat intra-articular
injections of tgAAC94 to affected joints at doses up to 1x10(13) DNase
Resistant Particles per milli-liter (DRP/mL) of joint fluid in subjects
with and without systemic TNF-alpha antagonists. The data also continue to
suggest that treatment with tgAAC94 may lead to improvements in signs and
symptoms of arthritis in injected joints.
Interim analysis of the first three cohorts (n=61) indicate reduction of
tenderness and swelling of the injected joint after tgAAC94 administration.
The subjects, approximately half of whom were on systemic TNF-alpha
antagonists, received an injection of blinded study drug into the knee,
ankle, wrist, MCP or elbow. Thirty-nine subjects have received a second
injection of open-label tgAAC94. Enrollment is ongoing and the effect of
treatment and its duration continues to be evaluated.
As previously presented at the American College of Rheumatology Annual
Scientific meeting in November 2006, among the first 41 subjects randomized
to the two lower doses of tgAAC94 or placebo, 7 of 10 subjects (70%) who
received placebo qualified for open label tgAAC94 prior to 30 weeks, in
contrast to 16 of 31 subjects (52%) who received tgAAC94. The median time
to second injection was 120, 129 and 145 days for subjects who received
placebo, tgAAC94 1x10(11) DRP/mL and tgAAC94 1x10(12) DRP/mL, respectively.
"The data evaluated thus far are encouraging and we are very pleased that
positive treatment response trends continue," said H. Stewart Parker,
President and CEO of Targeted Genetics. "We are currently on track to
complete enrollment of all 120 subjects in the study in the next few
months, and plan to present additional interim data at multiple scientific
venues during 2007."
About Targeted Genetics
Targeted Genetics Corporation is a biotechnology company committed to the
development of innovative targeted molecular therapies for the prevention
and treatment of acquired and inherited diseases with significant unmet
medical need. Targeted Genetics' proprietary Adeno-Associated Virus (AAV)
technology platform allows it to deliver genes encoding proteins to
increase gene function, as well as RNAi to decrease or silence gene
function. Targeted Genetics' product development efforts target
inflammatory arthritis, AIDS prophylaxis, congestive heart failure and
Huntington's disease. To learn more about Targeted Genetics, visit Targeted
Genetics' website at www.targetedgenetics.com.
Safe Harbor Statement under the Private Securities Litigation Reform Act of
1995:
This release contains forward-looking statements regarding the data to be
collected in this trial, the establishment or determination of efficacy
endpoints from the data collected in the trial, the timely and complete
accrual of patients in the trial and our ability to commercialize tgAAC94
and other statements about our plans, objectives, intentions and
expectations. These statements, involve current expectations, forecasts of
future events and other statements that are not historical facts.
Inaccurate assumptions and known and unknown risks and uncertainties can
affect the accuracy of forward-looking statements. Factors that could
affect our actual results include, but are not limited to, our ability to
obtain, maintain and protect our intellectual property, our ability to
raise capital when needed, our ability to recruit and enroll suitable trial
participants, the timing, nature and results of research and clinical
trials, potential development of alternative technologies or more effective
processes by competitors, and, our ability to obtain and maintain
regulatory or institutional approvals, as well as other risk factors
described in Item 1A. Risk Factors in our report on Form 10-K for the year
ended December 31, 2005 and updated in Item 1A. Risk Factors in our Form
10-Q for the quarter ended September 30, 2006. You should not rely unduly
on these forward-looking statements, which apply only as of the date of
this release. We undertake no duty to publicly announce or report revisions
to these statements as new information becomes available that may change
our expectations.
Investor and Media Contact:
Stacie D. Byars
Director, Communications
Targeted Genetics Corporation
(206) 521-7392