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 that three abstracts highlighting
cretostimogene will be presented at the American Urological
Association (AUA) Annual Meeting, taking place at Henry B. González
Convention Center in San Antonio, TX from May 3-6, 2024. CG
Oncology is exhibiting at the AUA meeting at booth #100.
“We are excited to share encouraging 12-month Phase 3
monotherapy results from the BOND-003 study at AUA 2024,” said
Ambaw Bellete, President and Chief Operating Officer, CG Oncology.
“Our presence reinforces our commitment to improving outcomes for
patients diagnosed with bladder cancer across the disease
spectrum.”
Details of the oral presentations are as follows:
Pivotal Results from BOND-003: A Phase 3, Single-arm
Study of Intravesical Cretostimogene Grenadenorepvec for the
Treatment of High Risk, BCG-Unresponsive Non-Muscle Invasive
Bladder Cancer with Carcinoma in SituAbstract Number:
24-11358Session: Paradigm-shifting, Practice-changing Clinical
Trials in UrologyPresenter: Mark D. Tyson, M.D., Urologic
Oncologist at Mayo Clinic, Scottsdale, AZPresentation Date &
Time: May 3, 2024, 10:23-10:31am Central Daylight TimeLocation:
Henry B. González Convention Center, Stars at Night Ballroom
PIVOT-006: A Phase 3, Randomized Study
of Adjuvant Intravesical Cretostimogene Grenadenorepvec versus
Surveillance for the Treatment of Intermediate Risk Non-Muscle
Invasive Bladder Cancer Following Transurethral Resection of
Bladder TumorSession: Clinical Trials in Progress, Bladder
CancerPresenter: Robert Svatek, M.D., Urologic Oncologist at
University of Texas Health Science Center, San Antonio,
TXPresentation Date & Time: May 5, 2024, 10:24-11:32am Central
Daylight TimeLocation: Henry B. González Convention Center,
Learning Lab
BOND-003- Cohort P: A Multi-national, Single-arm Study
of Intravesical Cretostimogene Grenadenorepvec for the Treatment of
High Risk, Papillary Only, BCG-Unresponsive Non-Muscle Invasive
Bladder CancerSession: Clinical Trials in Progress,
Bladder CancerPresenter: Mark D. Tyson, M.D., Urologic Oncologist
at Mayo Clinic, Scottsdale, AZPresentation Date & Time: May 5,
2024, 10:56-11:04am Central Daylight TimeLocation: Henry B.
González Convention Center, Learning Lab
About Cretostimogene Grenadenorepvec
Cretostimogene is an investigational, intravesically delivered
oncolytic immunotherapy being evaluated in BOND-003, a Phase 3
clinical trial for the treatment of patients with high-risk
Non-Muscle Invasive Bladder Cancer (NMIBC) who are unresponsive to
Bacillus Calmette Guerin (BCG) therapy. Cretostimogene is also
being evaluated in a Phase 2 clinical trial (CORE-001) in
combination with pembrolizumab in the same indication and in a
Phase 3 monotherapy clinical trial (PIVOT-006) in intermediate-risk
NMIBC patients. In addition, cretostimogene is being evaluated in
an investigator-sponsored clinical trial in combination with
nivolumab for the treatment of muscle invasive bladder cancer.
About the BOND-003 Clinical Study
BOND-003 (NCT04452591) is a single-arm, open-label, Phase 3
clinical trial evaluating cretostimogene as monotherapy in patients
with high-risk NMIBC unresponsive to BCG therapy. The study has
enrolled 115 patients with BCG-unresponsive NMIBC across North
America and the Asia-Pacific region.
About the PIVOT-006 Clinical Study
PIVOT-006 (NCT06111235) is a randomized, open-label, Phase 3
clinical trial enrolling patients and evaluating adjuvant
cretostimogene in intermediate-risk NMIBC patients following
transurethral resection of the bladder tumor (TURBT). The primary
endpoint of PIVOT-006 is overall recurrence-free survival (RFS),
with secondary endpoints including RFS at 12 and 24 months and
progression-free survival.
About Bladder Cancer
More 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 CG Oncology
CG 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: interim results of a
clinical trial are not necessarily indicative of final results and
one or more of the clinical outcomes may materially change as
patient enrollment continues, following more comprehensive reviews
of the data, and as more patient data becomes available; potential
delays in the commencement, enrollment and completion of clinical
trials, including the BOND-003 and PIVOT-006 trials; our dependence
on third parties in connection with manufacturing, shipping and
clinical and preclinical testing; 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; and other risks
described in our filings with the SEC, including under the heading
“Risk Factors” in our annual report on Form 10-K and any subsequent
filings with the SEC. 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
Investor RelationsBing KungCG OncologyIR@cgoncology.com
MediaKimberly HaKKH Advisors(917)
291-5744kimberly.ha@kkhadvisors.com
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