Viral Load Reduction Meets Primary Endpoint of Phase 2a Study
WATERTOWN, Mass., Aug. 22 /PRNewswire-FirstCall/ -- Panacos
Pharmaceuticals, Inc. (Nasdaq: PANC) ("Panacos" or "the Company"), a
biotechnology company dedicated to developing the next generation of antiviral
therapeutic products, today announced the successful completion of a Phase 2a
clinical study of its lead HIV drug candidate, PA-457, and provided
preliminary analysis of the results. The study met its primary endpoint by
demonstrating a statistically significant reduction in the level of HIV in the
blood, known as viral load, compared to placebo. The median reduction in
viral load in the trial was greater than 1 log10, or a 90% decrease, at the
highest dose. PA-457 is the first in a new class of HIV drugs called
Maturation Inhibitors, with broad activity against HIV, including strains
resistant to currently approved drugs, the most common cause of HIV treatment
failure.
In this randomized double-blind Phase 2a study, performed at leading
academic centers in the US, PA-457 at one of four doses (25, 50, 100 or 200mg;
6 patients per group) or placebo (8 patients), was administered orally once
daily for 10 days to HIV-infected subjects not on other antiretroviral
therapy. The primary endpoint was viral load reduction on Day 11. Other
endpoints included safety, tolerability and pharmacokinetics of the drug.
At the 100 and 200 mg doses, PA-457 treatment for 10 days resulted in
statistically significant reductions in viral load compared to placebo, with
individual decreases of up to 1.7 log10. At the 200mg dose level, the median
viral load change at Day 11 was -1.03 log10. Median Day 11 values at the
other dose levels were: Placebo: +0.03 log10; 25mg: +0.05 log10; 50mg: -0.17
log10; 100mg: -0.48 log10. In patients with baseline viral loads under
100,000 copies/ml the median Day 11 reduction was -1.52 log10 at the 200mg
dose level (three of six patients) and -0.56 log10 at the 100mg dose level
(five of six patients).
Genetic analysis of HIV in patients pre- and post- treatment, available
now for 21 out of 33 patients in the study, showed no evidence of the
development of resistance to PA-457, the same result as seen previously in a
single dose study with PA-457. All doses were observed to be generally safe
and well tolerated with no Grade 3 or 4 laboratory abnormalities. All adverse
experiences were mild or moderate and no dose-limiting toxicity was
identified. One moderate adverse event was classified as possibly related to
drug and was categorized as serious based on the subject's hospitalization for
diagnostic tests. It involved a patient with a 5-year history of poorly
controlled hypertension who exhibited transient findings of a possible lacunar
cerebrovascular accident, a known complication of hypertension.
Graham P. Allaway Ph.D., Chief Operating Officer of Panacos, said: "This
study indicates that PA-457 has potent anti-HIV activity, providing further
clinical proof of principle for this new class of antiretroviral drugs. The
overall viral load reduction at the 200mg dose of over 1 log10 strongly
supports further development of PA-457. The 1.5 log10 viral load reduction
seen in patients at the 200mg dose with less than 100,000 viral copies/ml may
potentially reflect the potency of the drug when used in combination therapy
in normal clinical practice." Panacos is submitting the results of this study
as a late breaker abstract to the 45th Interscience Conference on
Antimicrobial Agents and Chemotherapy (ICAAC), to be held in New Orleans, LA
September 21-24, 2005. If accepted, a detailed description of the study will
be provided at that conference.
"We are extremely pleased with the results of this important Phase 2a
study," commented Samuel K. Ackerman, MD, Chairman and CEO of Panacos. "We
believe that PA-457 is a potential breakthrough drug which could play a role
throughout the HIV treatment spectrum, including both naive and treatment-
experienced patients, based on once-a-day oral dosing, potent activity
observed against drug resistant virus and a promising safety profile. We now
plan to move forward aggressively to initiate a Phase 2b study of the drug in
the first half of 2006."
About PA-457
PA-457 is a small molecule, oral HIV drug candidate. It works by a
mechanism different from that of approved drugs or other drugs in development,
by blocking a key step in the processing of a viral core protein called
capsid. This novel mechanism of action, called maturation inhibition, was
discovered by Panacos scientists and their collaborators. Preclinical studies
have shown that PA-457 retains full activity against drug-resistant virus, is
effective in an animal model of HIV infection and should be suitable for use
in combination therapy with other drugs. A previous clinical study indicated
that a single oral dose of PA-457 has antiviral activity in HIV-infected
patients, including individuals infected with drug resistant strains.
Clinical results to date will need to be confirmed and extended in longer term
trials with larger patient numbers prior to approval.
The US Food and Drug Administration (FDA) has granted Fast Track
designation to PA-457. Fast Track is a process designed to expedite
development and approval of new drugs that may have the potential to improve
treatment for serious or life-threatening diseases. Developers of Fast
Tracked products have greater access to FDA resources as well as eligibility
for rolling NDA submissions. In addition, Fast Track designation may enable
priority FDA review and accelerated approval.
About Panacos Pharmaceuticals
Panacos, formerly known as V. I. Technologies, Inc. or VITEX, is
developing the next generation of anti-infective products through discovery
and development of small molecule oral drugs for the treatment of HIV and
other major human viral diseases. Panacos' proprietary discovery technologies
and lead therapeutic candidate PA-457 focus on novel targets in the virus life
cycle, including virus fusion and virus maturation. For more information on
Panacos, please visit our web site at: http://www.panacos.com.
Except for the historical information contained herein, the matters
discussed are forward-looking statements made pursuant to the safe harbor
provisions of the Private Securities Litigation Reform Act of 1995. These
statements involve risks and uncertainties, such as the progress of clinical
development of PA-457, including the Company's plan to initiate a Phase 2b
study in the first half of 2006, and the timing of results of clinical trials,
the execution of the Company's financing plans, the potential role of PA-457
in treatment of HIV patients, the timely availability of new products, market
acceptance of the Company's products, the impacts of competitive products and
pricing, government regulation of the Company's products, the Company's
ability to complete product development collaborations and other strategic
transactions and other risks and uncertainties set forth in the Company's
filings with the Securities and Exchange Commission. These risks and
uncertainties could cause actual results to differ materially from any
forward-looking statements made herein.
CONTACT:
Peyton Marshall
Executive Vice President & CFO
617-926-1551
pmarshall@panacos.com
SOURCE Panacos Pharmaceuticals, Inc.
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Related links:
http://www.panacos.com
CONTACT:
Peyton Marshall, Executive Vice President &
CFO of Panacos Pharmaceuticals, +1-617-926-1551,
pmarshall@panacos.com
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