Published:
Progen Resumes Phase 1 Development of Anti-Cancer Agent, PG-11047
Progen Resumes Phase 1 Development of Anti-Cancer Agent, PG-11047
BRISBANE, Australia, May 14 /PRNewswire-FirstCall/ -- Progen
Pharmaceuticals Limited (ASX:PGL; Nasdaq: PGLA) today announced that the
Company has resumed patient enrolment in the phase 1 dose-escalation study of
its recently acquired polyamine analogue, PG-11047 (formerly CGC-11047) for
patients with advanced cancer.
Progen has commenced development of PG-11047 - the lead clinical compound
in the Company's polyamine program - following its acquisition of Cellgate,
Inc earlier this year. The first patient to be recruited into the trial
re-initiation has been enrolled at the University of Chicago.
The trial is exploring the potential of PG-11047 as a single anti-cancer
agent and is designed to assess the agent's maximum tolerated dose. Under
CellGate, the trial had recruited 31 patients and had shown little evidence of
toxicity, while using significantly higher doses than most previous studies of
polyamine compounds.
Justus Homburg, Progen's CEO, said, "Since the acquisition of CellGate, we
have been assessing our portfolio of clinical and pre-clinical compounds in
order to determine which to drive forward. Our re-initiation of PG-11047 in
phase 1 clinical development is the first step in driving potential value from
our expanded portfolio of first-in-class oncology therapies."
Data from the trial will be used in parallel with a separate PG-11047
study assessing the agent in combination with other marketed anti-cancer drugs
as the basis for determining potential phase 2 development. Progen expects the
study to produce data within the next 12 months.
About Progen: Progen Pharmaceuticals is a globally focused biotechnology
company committed to the discovery, development and commercialization of small
molecule pharmaceuticals primarily for the treatment of cancer. Progen has
operations inAustralia and the US.
About PG-11047: PG-11047 is a polyamine analogue which modifies the
production of natural polyamines. Polyamines are a class of chemical which are
involved in regulation of cell growth. They are overproduced in many cancers,
and PG-11047 is believed to restore polyamine reduction to natural levels.
Despite being the focus of scientific interest for many years, this mechanism
is unique, and if successful, PG-11047 could become a first-in-class oncology
product. To date, PG-11047 has been shown to have anti-tumor activity in
animal models, combined with a good safety profile.
Progen Information:
Justus Homburg, CEO
Progen Pharmaceuticals Limited
T: +61 7 3842 3333
E: justush@progen-pharma.com
Media and Investor Relations:
Cindy Ingram, Investor Relations Manager
Progen Pharmaceuticals Limited
T: +61 7 3842 3333
E: cindyi@progen-pharma.com
This press release contains forward-looking statements that are based on
current management expectations. These statements may differ materially from
actual future events or results due to certain risks and uncertainties,
including without limitation, risks associated with drug development and
manufacture, risks inherent in the extensive regulatory approval process
mandated by the United States Food and Drug Administration and the Australian
Therapeutic Goods Administration, delays in obtaining the necessary approvals
for clinical testing, patient recruitment, delays in the conduct of clinical
trials, market acceptance of PI-88, PI-166 and other drugs, future capital
needs, general economic conditions, and other risks and uncertainties detailed
from time to time in the Company's filings with the Australian Securities
Exchange and the United States Securities and Exchange Commission. Moreover,
there can be no assurance that others will not independently develop similar
products or processes or design around patents owned or licensed by the
Company, or that patents owned or licensed by the Company will provide
meaningful protection or competitive advantages.
SOURCE Progen Pharmaceuticals Limited
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Tags: Biotechnology, Pharmaceuticals, Healthcare, Health,
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