CG Oncology to Host Conference Call and Webcast on BOND-003 Data on Thursday, December 5, 2024
December 02 2024 - 8:00AM
CG Oncology, Inc. (NASDAQ: CGON), a late-stage clinical
biopharmaceutical company focused on developing and commercializing
a potential backbone bladder-sparing therapeutic for patients with
bladder cancer, today announced it will host a conference call and
live webcast at 7 am CST on December 5, 2024, to discuss results
from the Phase 3 BOND-003 trial of cretostimogene monotherapy in
high-risk BCG-unresponsive non-muscle invasive bladder cancer
(NMIBC). In addition to company executives, this call will feature
Mark Tyson, II, M.D., M.P.H., urologic oncologist at Mayo Clinic,
and lead investigator in the BOND-003 study. Dr. Tyson is
presenting the results as a late breaking abstract at the Society
of Urologic Oncology (SUO) 25th Annual Meeting in Dallas, TX at
11:45 am CST on December 5, 2024.
Individuals can access the webcast via the link
on the company's Investor Relations
website, https://ir.cgoncology.com. An archive will be
available following the completion of the call.
About Bladder CancerMore than
83,000 people are estimated to be diagnosed with bladder cancer in
2024. NMIBC is the most common form of bladder cancer, representing
approximately 75% of newly diagnosed cases. Bladder cancer is the
sixth most common form of cancer in the United States, and men
account for three quarters of newly diagnosed cases.
About Cretostimogene
GrenadenorepvecCretostimogene grenadenorepvec is an
investigational, intravesically delivered oncolytic immunotherapy
that has been studied in a clinical development program, which
includes more than 250 patients with Non-Muscle Invasive Bladder
Cancer (NMIBC). This program includes two Phase 3 clinical trials;
BOND-003 for high-risk BCG-unresponsive NMIBC and PIVOT-006 for
intermediate-risk NMIBC. CG Oncology also has a Phase 2 trial,
CORE-008, evaluating the safety and efficacy of cretostimogene in
high-risk NMIBC. Additionally, we have initiated an Expanded Access
Program for cretostimogene in North America for patients who are
unresponsive to BCG and meet certain program eligibility
requirements. Cretostimogene is an investigational candidate, and
its safety and efficacy have not been established by the FDA or any
other health authority.
About CG OncologyCG Oncology is
a late-stage clinical biopharmaceutical company focused on
developing and commercializing a potential backbone bladder-sparing
therapeutic for patients afflicted with bladder cancer. CG Oncology
sees a world where urologic cancer patients may benefit from our
innovative immunotherapies to live with dignity and have an
enhanced quality of life. To learn more, please visit:
www.cgoncology.com.
Forward Looking Statements CG
Oncology cautions you that statements contained in this press
release regarding matters that are not historical facts are
forward-looking statements. The forward-looking statements are
based on our current beliefs and expectations and include, but are
not limited to, the potential therapeutic benefits of
cretostimogene for high-risk and intermediate-risk NMIBC patients.
Actual results may differ from those set forth in this press
release due to the risks and uncertainties inherent in our
business, including, without limitation: additional patient data
related to cretostimogene that continues to become available may be
inconsistent with the data produced as of the data cutoff, and
further analysis of existing data and analysis of new data may lead
to conclusions different from those established as of the date
hereof; results from earlier clinical trials and preclinical
studies not necessarily being predictive of future results;
unexpected adverse side effects or inadequate efficacy of
cretostimogene that may limit its development, regulatory approval,
and/or commercialization; potential delays in the commencement,
enrollment and completion of clinical trials; and other risks
described in our filings with the Securities and Exchange
Commission (SEC), including under the heading “Risk Factors” in our
annual report on Form 10-K and other filings that we make with the
SEC from time to time (which are available at http://www.sec.gov).
You are cautioned not to place undue reliance on these
forward-looking statements, which speak only as of the date hereof,
and we undertake no obligation to update such statements to reflect
events that occur or circumstances that exist after the date
hereof. All forward-looking statements are qualified in their
entirety by this cautionary statement, which is made under the safe
harbor provisions of the Private Securities Litigation Reform Act
of 1995.
Contacts:
Media Sarah ConnorsVice President,
Communications and Patient Advocacy, CG Oncology(508)
654-2277sarah.connors@cgoncology.com
Investor RelationsChau ChengVice President, Investor Relations,
CG Oncology(949) 342-8939chau.cheng@cgoncology.com
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