CARGO Therapeutics Names Kapil Dhingra, M.B.B.S., to Board of Directors
15 Avril 2024 - 10:05PM
CARGO Therapeutics, Inc. (Nasdaq: CRGX), a clinical-stage
biotechnology company positioned to advance next generation,
potentially curative cell therapies for cancer patients, today
announced it has appointed Kapil Dhingra, M.B.B.S., to the
Company’s Board of Directors. Dr. Dhingra is a medical
oncologist and a physician-scientist bringing more than 25 years of
strategic clinical development experience in oncology, including
cell therapy, with a proven track record in drug development,
patient care and academic research.
Dr. Dhingra’s development experience spans several oncology
companies, both as a Board member or in senior leadership. He is
currently Chairman of the Board for LAVA Therapeutics, a member of
the Board of Supervisors for Servier and a member of the Board of
Directors of Black Diamond Therapeutics, Inc., Replimune, Inc., and
Median Technologies. He previously served on the Board of Autolus
Therapeutics plc from the company’s inception until the recent
Biologics License Application (BLA) filing of its CAR T-cell
therapy.
“We are pleased to welcome Dr. Dhingra to our Board,” said Gina
Chapman, President and Chief Executive Officer, CARGO Therapeutics.
“As a veteran clinical oncology leader with demonstrated experience
in cell therapy development and expertise in bringing new
therapeutics through the clinic to commercialization, his guidance
will prove especially valuable as we advance our lead candidate
firi-cel and a pipeline of next generation, potentially curative
CAR T-cell therapies.”
“CARGO has already made tremendous clinical progress with their
differentiated anti-CD22 approach and rapidly enrolling Phase 2
clinical trial in relapsed or refractory large B-cell lymphoma,”
said Kapil Dhingra, M.B.B.S., member of the Board of Directors,
CARGO Therapeutics. “I look forward to contributing to CARGO’s
continued success as we prioritize developing firi-cel and an
exciting pipeline with potential to expand to other B-cell
malignancies.”
In 2008, Dr. Dhingra founded and continues to be a managing
member of KAPital Consulting, LLC, a healthcare consulting firm
providing strategic advisory services to biotechnology companies.
Previously he served as Head of the Oncology Disease Biology
Leadership Team and Head of Oncology Clinical Development at The
Roche Group (Roche), during which he led numerous drug approvals.
Prior to joining Roche, he worked in the oncology clinical
development group at Eli Lilly and Company.
Dr. Dhingra has also served as a faculty member at The
University of Texas M.D. Anderson Cancer Center, Indiana University
School of Medicine and Memorial Sloan Kettering Cancer Center.
About CARGO Therapeutics
CARGO Therapeutics, Inc. is a clinical-stage biotechnology
company positioned to advance next generation, potentially curative
cell therapies for cancer patients. CARGO’s programs, platform
technologies, and manufacturing strategy are designed to directly
address the limitations of approved cell therapies, including
limited durability of effect, safety concerns and unreliable
supply. CARGO is currently evaluating its lead program,
firicabtagene autoleucel (firi-cel) (CRG-022), an autologous CD22
chimeric antigen receptor (CAR) T-cell therapy candidate, in a
potentially pivotal Phase 2 clinical study in patients with large
B-cell lymphoma (LBCL) whose disease relapsed or was refractory
(R/R) to CD19 CAR T-cell therapy. CARGO also plans to evaluate
firi-cel (CRG-022) in patients at earlier stages of disease,
including LBCL and other hematologic malignancies. Beyond its lead
program, CARGO is leveraging its proprietary cell engineering
platform technologies to develop a pipeline of programs that
incorporate multiple transgene therapeutic “cargo” designed to
enhance CAR T-cell persistence and trafficking to tumor lesions, as
well as to help safeguard against tumor resistance and T-cell
exhaustion. CARGO’s founders are pioneers and world-class experts
in CAR T-cell therapy, and its team has significant experience and
success developing, manufacturing, launching and commercializing
oncology and cell therapy products. For more information, please
visit the CARGO Therapeutics website at https://cargo-tx.com/.
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(Twitter): @CARGOTx
Cautionary Note Regarding Forward-Looking
StatementsThis press release contains forward-looking
statements within the meaning of Section 27A of the Securities Act
of 1933, as amended, and Section 21E of the Securities Exchange Act
of 1934, as amended. In some cases, you can identify
forward-looking statements by terminology such as “aim,”
“anticipate,” “assume,” “believe,” “contemplate,” “continue,”
“could,” “design,” “due,” “estimate,” “expect,” “goal,” “intend,”
“may,” “objective,” “plan,” “positioned,” “potential,” “predict,”
“seek,” “should,” “target,” “will,” “would” and other similar
expressions that are predictions of or indicate future events and
future trends, or the negative of these terms or other comparable
terminology. All statements other than statements of historical
facts contained in this press release are forward-looking
statements. These forward-looking statements include, but are not
limited to, statements about: advancement of CARGO’s clinical
programs; the potential benefits from treatment with CD19 CAR
T-cell therapies; timing of data reports, including the release of
interim data from the Company’s ongoing Phase 2 clinical trial of
CRG-022; the implementation of CARGO’s strategic plans for its
business and product candidates; and whether the Company’s cash and
cash equivalents will be able to fund operations through 2025.
Forward-looking statements are not guarantees of future performance
and are subject to risks and uncertainties that could cause actual
results and events to differ materially from those anticipated,
including, but not limited to, risks and uncertainties related to:
the company’s ability to obtain necessary capital to fund its
clinical programs; the early stages of clinical development of the
company’s product candidates; the company’s ability to obtain
regulatory approval of and successfully commercialize its product
candidates; any undesirable side effects or other properties of the
company’s product candidates; the company’s reliance on third-party
suppliers and manufacturers, including CROs; the outcomes of any
future collaboration agreements; and the company’s ability to
adequately maintain intellectual property rights for its product
candidates. These and other risks are described in greater detail
under the section titled Risk Factors” contained in the company’s
prospectus filed with the Securities and Exchange Commission (SEC)
on November 13, 2023 pursuant to Rule 424(b) under the Securities
Act and the company’s other filings with the SEC. Any
forward-looking statements that the company makes in this press
release are made pursuant to the Private Securities Litigation
Reform Act of 1995, as amended, and speak only as of the date of
this press release. Except as required by law, the company
undertakes no obligation to publicly update any forward-looking
statements, whether as a result of new information, future events
or otherwise.
Media Contact:Kimberly
MuscaraKimberly@redhousecomms.com
Investor Contact:Jessica
Serrajserra@cargo-tx.com
CARGO Therapeutics (NASDAQ:CRGX)
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