Point Therapeutics Announces New Data Evaluating Its Lead Compound, Talabostat, in Four Distinct Cancers
31 May 2006 - 9:53PM
Business Wire
Point Therapeutics, Inc. (NASDAQ: POTP) announced today that new
data evaluating talabostat's anti-tumor activity in Phase 2 studies
in advanced chronic lymphocytic leukemia (CLL), metastatic
melanoma, metastatic colorectal cancer and in a preclinical
osteosarcoma model will be presented in four separate presentations
at the 42nd American Society of Clinical Oncology (ASCO) Annual
Meeting in Atlanta, Georgia. These studies support Point
Therapeutics' clinical program, which includes two Phase 3 trials
in metastatic non-small cell lung cancer and Phase 2 trials in
advanced CLL, metastatic melanoma and metastatic pancreatic cancer.
"We believe that these presentations underscore talabostat's
potential use in a wide range of cancers," said Don Kiepert,
President and CEO of Point Therapeutics. "We are pleased that Point
has two posters accepted for presentation--one on our Phase 2 study
of talabostat and rituximab in advanced CLL and another on our
Phase 2 study of talabostat and cisplatin in Stage IV metastatic
melanoma patients. There will also be investigator presentations of
a pharmacodynamic study of talabostat in metastatic colorectal
cancer patients and a preclinical study of talabostat's
anti-metastatic properties in an osteosarcoma model." Talabostat is
an oral, targeted therapy, which is currently in clinical
development for potential use in oncology. Talabostat is a known
dipeptidyl peptidase (DPP) inhibitor. DPPs are enzymes that appear
to regulate several different physiological processes including
those involved in tumor growth and host responses to cancer, type 2
diabetes, and immune responses to vaccines. The Company believes
that talabostat employs a novel dual mechanism of action by (1)
targeting a DPP called fibroblast activation protein (FAP) that is
uniquely expressed in the tumor stroma, or connective tissue of the
tumor, while (2) concurrently stimulating the immune system,
enabling the body to promote its natural ability to attack tumors.
Details of talabostat data that will be presented at ASCO are:
Saturday, June 3rd: 8:00 a.m. - 12:00 p.m. -- Phase II
pharmacodynamic study of the fibroblast activation protein
inhibitor Val-boro-Pro in patients with metastatic colorectal
cancer (Abstract #3594) - Building B, Level 1, Hall B5, Poster #P10
- Fox Chase Cancer Center, lead author: Dr. Jonathan Cheng -- Phase
II study of talabostat and rituximab in
fludarabine/rituximab-resistant or refractory patients with CLL
(Abstract # 6598) - Building B, Level 1, Hall B5, Poster #EE6
-Indiana Oncology and Hematology Consultants, lead author: Dr.
Khuda Khan Sunday, June 4: 8:15 a.m -- Reduction of murine
osteosarcoma lung metastases using the dipeptidyl peptidase
inhibitor, talabostat (Abstract #9009) - Building B, Level 2, Room
B211 - National Cancer Institute, lead author: Dr. Su Young Kim
Monday, June 5: 1:00 p.m. - 5:00 p.m. -- Phase 2 trial of
talabostat and cisplatin in patients with stage IV melanoma
(Abstract #8040) - Building B, Level 1, Hall B5, Poster #A11 - Mary
Crowley Medical Research Center, lead author: Dr. Casey Cunningham
About Point Therapeutics, Inc.: Point is a Boston-based
biopharmaceutical company developing a portfolio of dipeptidyl
peptidase (DPP) inhibitors for use in cancer, type 2 diabetes and
as vaccine adjuvants. Point is currently studying its lead product
candidate, talabostat, in two Phase 3 trials in non-small cell lung
cancer. Point is also studying talabostat in several Phase 2
trials, including as a single-agent in metastatic melanoma, in
combination with cisplatin in metastatic melanoma, in combination
with rituximab in advanced chronic lymphocytic leukemia, and in
combination with gemcitabine in metastatic pancreatic cancer. In
addition, Point's portfolio includes two other DPP inhibitors in
preclinical development--PT-630 for type 2 diabetes and PT-510 as a
vaccine adjuvant. Certain statements contained herein are not
strictly historical and are "forward looking" statements as defined
in the Private Securities Litigation Reform Act of 1995. This
information includes statements with respect to the company's
clinical development programs and the timing of initiation and
completion of its clinical trials. Forward-looking statements are
statements that are not historical facts, and can be identified by,
among other things, the use of forward-looking language, such as
"believes," "feels," "expects," "may," "will," "should," "seeks,"
"plans," "schedules to," "projects," "anticipates" or "intends" or
the negative of those terms, or other variations of those terms of
comparable language, or by discussions of strategy or intentions. A
number of important factors could cause actual results to differ
materially from those projected or suggested in the forward looking
statement, including the risk factors described in Point's
quarterly report on Form 10-K for the quarter ended March 31, 2006
and from time to time in Point's periodic and other reports filed
with the Securities and Exchange Commission.
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