Vincerx Pharma, Inc. (Nasdaq: VINC), a biopharmaceutical company
aspiring to address the unmet medical needs of patients with cancer
through paradigm-shifting therapeutics, and Oqory, Inc., a private
biopharmaceutical company dedicated to developing next-generation
antibody drug conjugates (ADCs) for the treatment of cancer, today
highlighted Phase 1a/1b data for Oqory’s anti-TROP2 ADC, OQY-3258,
for patients with solid tumors. The companies also provided
insights into their proposed strategic merger, which aims to
advance OQY-3258 into global Phase 3 trials and build a
differentiated ADC pipeline by leveraging their combined expertise.
OQY-3258, also known as ESG401, is an anti-TROP2 ADC currently
under evaluation in three clinical trials:
- A Phase 1a/1b clinical trial for
patients with solid tumors (NCT04892342).
- A Phase 3 study in patients with
locally advanced or metastatic HR+/HER2- breast cancer
(NCT06383767).
- A Phase 3 study as a first-line
treatment in patients with unresectable recurrent or metastatic
triple-negative breast cancer (NCT06732323), which garnered
Breakthrough Designation from China’s National Medical Products
Administration (NMPA) on November 6, 2024.
As of August 2024, the Phase 1a/1b study had enrolled
approximately 150 patients, with promising preliminary results in
multiple breast cancer subtypes. Recent data highlights, including
those presented at the 2024 European Society for Medical Oncology
(ESMO), include:
- Evaluable patients with
previously untreated TNBC (n=25)
- As presented at ESMO, the confirmed
overall response rate (ORR) was 76% and disease control rate (DCR)
was 100%. Median duration of response (DOR) and progression-free
survival (PFS) had not yet been reached.
- A recent data cut from January 2025,
with ten additional patients (n=35) evaluable for efficacy, showed
an improved confirmed ORR of 80%, with median DOR and PFS still not
reached.
- Evaluable patients with late-stage TNBC (n=37)
- As presented at ESMO, the confirmed
ORR was 27% and DCR was 62%, with 6-month DOR and PFS rates of 39%
and 25%, respectively.
- Evaluable patients with HR+/HER2- breast cancer
(n=58)
- As presented at ESMO, the confirmed
ORR was 39%, DCR was 78%, and 6-month DOR and PFS rates of 70% and
55%, respectively, with a median (range) PFS of 7.4 (3.7-9.2)
months.
Also presented at ESMO, OQY-3258 demonstrated meaningful
activity in patients with brain metastases, reporting an
intracranial ORR of 41% (n=17), which included three complete and
four partial transcranial responses. Additionally, in patients with
brain metastases, PFS (95% confidence interval) was 4.6 (2.0-9.8)
months with OQY-3258 compared with 2.8 (1.5-3.9) months for
historical data with Trodelvy. OQY-3258 has demonstrated a
favorable safety profile, with the most common Grade ≥3 adverse
events being manageable hematologic toxicities, such as neutropenia
and leukopenia, that did not lead to treatment discontinuation.
Notably, no Grade ≥3 rash or interstitial lung disease/pneumonitis
was observed, and there was only one case each of Grade 3 diarrhea
and stomatitis. This differentiated safety profile sets OQY-3258
apart from other TROP2 ADCs.
“The compelling clinical activity demonstrated in our Phase
1a/1b trial highlights the potential of OQY-3258 to address
significant unmet needs in TROP2-expressing tumors,” said Michael
King, CEO of Oqory, Inc. “With its optimized serum-stable linker
design, OQY-3258 has shown a markedly lower incidence of severe
off-target toxicity compared with other marketed TROP2 therapies,
positioning it as a differentiated late-stage ADC for metastatic
breast cancer and other TROP2-expressing cancers. Our proposed
merger with Vincerx represents a pivotal step toward advancing this
asset into global Phase 3 trials and driving innovation in
next-generation ADCs.”
Raquel Izumi, Ph.D., Acting CEO of Vincerx, added, “The proposed
merger with Oqory reflects our commitment to develop transformative
therapies for patients with cancer. The promising efficacy and
favorable safety profile demonstrated by OQY-3258 highlights its
potential as a best-in-class anti-TROP2 ADC. By bringing together
Vincerx’s development expertise and Oqory’s ADC technologies, we
aim to accelerate the development of OQY-3258, while building a
pipeline of next-generation ADCs that address significant unmet
patient needs.”
About Proposed MergerVincerx and Oqory are
parties to a binding term sheet, as amended, pursuant to which
Oqory would merge into Vincerx, with Oqory equity holders expected
to own approximately 95% of the combined entity and Vincerx equity
holders expected to hold approximately 5%. The proposed merger
provides for a minimum fully diluted equity value of $13.66 million
for existing Vincerx stockholders at closing and, as a condition to
the closing of the merger, completion of a concurrent private
offering of Vincerx equity securities of at least $20 million.
Additionally, Oqory-designated investors will provide interim
financing to Vincerx of $1.5 million in two tranches, approximately
$1,000,000 of which was provided on December 27, 2024, and
approximately $500,000 of which is to be provided on or prior to
January 31, 2025. The entry into a definitive merger agreement is
contingent on a number of conditions, including satisfactory
completion of due diligence by Vincerx and Oqory, interim financing
for Vincerx in the amount of at least $500,000 on or prior to
January 31, 2025, commitments by investors for the concurrent
financing, and negotiation of the terms of a definitive merger
agreement. Once a definitive merger agreement is executed, the
closing of any merger will be subject to customary closing
conditions, including regulatory approvals, stockholder approval
from both parties, completion of the minimum $20 million financing,
and the continued listing of Vincerx's common stock on Nasdaq.
The description of the binding term sheet and proposed merger
contained herein is only a summary and is qualified in its entirety
by reference to the binding term sheet, as amended, a copy of which
has been filed by Vincerx with the Securities and Exchange
Commission.
About OQY-3258 (also known as ESG401)OQY-3258
is Oqory’s anti-TROP2 ADC with an optimized enzyme-dependent linker
technology and an SN-38 payload with established efficacy and
manageable side effect profile. As of August 2024, OQY-3258 has
completed Phase 1a/1b development in about 150 patients with solid
tumors, including metastatic HR+/HER2- and triple-negative breast
cancer. OQY-3258 has shown efficacy in these patients, including
reduction of brain metastasis and responses in heavily pretreated
patients. To date, OQY-3258 has exhibited a differentiated safety
profile versus other marketed TROP2 ADCs. Notably, no Grade ≥3
interstitial lung disease/pneumonitis or rash have been observed.
Gastrointestinal effects have been mild and mainly Grade 1/2.
Neutropenia and leukopenia have been the major adverse events,
which were manageable and did not result in discontinuation of
study drug. OQY-3258 is being evaluated in a Phase 3 study as
first-line treatment in patients with unresectable recurrent or
metastatic triple-negative breast cancer (NCT06732323) and in a
Phase 3 study in patients with unresectable locally advanced or
metastatic HR+/HER2- breast cancer (NCT06383767); both currently
conducted by Shanghai Escugen Biotechnology Co., Ltd., Oqory’s
development partner.
About Oqory, Inc.Oqory, Inc. is an innovator in
the field of ADCs with expertise in advancing targeted cancer
therapies. The Company’s pipeline includes multiple ADC programs,
with two currently in clinical development and several
next-generation ADCs in preclinical stages. These programs are
designed to address critical unmet needs in indications such as
breast cancer, non-small cell lung cancer, small cell lung cancer,
multiple myeloma, and other metastatic solid tumors. Powered by a
proprietary ADC platform, Oqory is focused on delivering therapies
that improve outcomes for patients with cancer.
Oqory is based in San Diego, California.
About Vincerx Pharma, Inc.Vincerx Pharma, Inc.
is a clinical-stage biopharmaceutical company committed to
developing differentiated and novel therapies to address the unmet
medical needs of patients with cancer. Vincerx’s pipeline consists
of a next-generation ADC, VIP943, currently in Phase 1; a small
molecule drug conjugate, VIP236, which has completed its Phase 1
study; a CDK9 inhibitor, enitociclib, which has completed a Phase 1
monotherapy study; a preclinical ADC, VIP924; and VersAptx™, a
versatile, next-generation bioconjugation platform.
Vincerx is based in San Mateo, California, and has a research
subsidiary in Monheim, Germany.
Forward-Looking Statements
This press release contains forward-looking statements within
the meaning of U.S. federal securities laws. Forward-looking
statements, which are based on certain assumptions and describe
future plans, strategies, expectations and events, can generally be
identified by the use of forward-looking terms such as “believe,”
“expect,” “may,” “will,” “should,” “would,” “could,” “suggest,”
“seek,” “intend,” “plan,” “goal,” “potential,” “on-target,” “on
track,” “project,” “estimate,” “anticipate,” or other comparable
terms. All statements other than statements of historical facts
included in this press release are forward-looking statements.
Forward-looking statements include, but are not limited to, the
entry into a definitive merger agreement; the anticipated terms and
conditions of the merger, including the $20 million equity
investment, and the amount and timing of the interim financing; the
expected ownership structure and value to Vincerx stockholders upon
closing of the merger; the anticipated effects and benefits of a
merger transaction; and Oqory’s pipeline, product candidates and
attributes, and clinical development, timing, and results.
Forward-looking statements are neither historical facts nor
assurances of future performance or events. Instead, they are based
only on current beliefs, expectations, and assumptions regarding
future business developments, future plans and strategies,
projections, anticipated events and trends, the economy, and other
future conditions. Forward-looking statements are subject to
inherent uncertainties, risks, and changes in circumstances that
are difficult to predict, many of which are outside the control of
Oqory and Vincerx.
Actual results, conditions, and events may differ materially
from those indicated in the forward-looking statements. Therefore,
you should not rely on any of these forward-looking statements.
Important factors that could cause actual results, conditions, and
events to differ materially from those indicated in the
forward-looking statements include, but are not limited to: the
satisfactory completion of the parties’ respective due diligence;
the completion of the interim financing; the parties’ capital
requirements, availability, and sufficiency of capital, and cash
runway; the results of Vincerx's due diligence review of Oqory,
which has not been completed as of the date hereof; the ability of
the parties to successfully negotiate and enter into a definitive
merger agreement and the actual terms thereof; the parties’ ability
to satisfy the conditions precedent to the merger to be contained
in a definitive merger agreement, including completion of the
concurrent offering of Vincerx equity securities of at least $20
million and stockholder approval from both parties; the closing of
the merger; the risk that any definitive merger agreement is
terminated after it is entered into but before consummation of any
proposed merger; market acceptance of the combined company; risks
associated with clinical development of the parties’ product
candidates; general economic, financial, legal, political, and
business conditions; and other risks and uncertainties including
those set forth in Vincerx’s Quarterly Report on Form 10-Q for the
quarter ended September 30, 2024 and subsequent reports filed with
the Securities and Exchange Commission (the “SEC”). Forward-looking
statements speak only as of the date hereof, and the parties
disclaim any obligation to update any forward-looking
statements.
Vincerx® and VersAptx™ are trademarks of Vincerx. Oqory and the
Oqory logo are trademarks of Oqory.
Additional InformationIn connection with the
proposed merger transaction, Vincerx will file relevant materials
with the SEC, including a proxy statement on Schedule 14A. A
definitive proxy statement will be sent to holders of Vincerx’s
common stock when it becomes available. Investors and
securityholders and other interested parties are urged to carefully
read the proxy statement (including any amendments or supplements
thereto) and any other documents filed with the SEC when they
become available, because they will contain important information
about Vincerx, Oqory, and the proposed merger. Investors and
securityholders may obtain free copies of these documents and other
documents filed with the SEC by Vincerx (when they become
available) through the website maintained by the SEC at
http://www.sec.gov, or by directing a request to: Vincerx Pharma,
Inc., 1825 S. Grant Street, San Mateo, CA 94402. Copies of the
documents filed by Vincerx are also available free of charge in the
“Investors—SEC Filings & Financials—SEC Filings” section of
Vincerx’s website at:
https://investors.vincerx.com/financial-information/sec-filings.
Participants in the SolicitationVincerx, Oqory,
and their respective directors and officers are or may be
considered “participants” (as defined in Section 14(a) of the
Securities Exchange Act of 1934) in the solicitation of proxies
from the holders of Vincerx’s common stock with respect to the
proposed transactions described herein. Information about Vincerx’s
directors and executive officers, including compensation, is set
forth in the sections entitled “Election of Directors—Directors and
Nominees” and “Executive Officers” of Vincerx’s definitive proxy
statement for its 2024 Annual Meeting of Stockholders, filed with
the SEC on April 10, 2024, the section entitled “Compensation of
Directors and Executive Officers” of Vincerx’s definitive proxy
statement for its special meeting of stockholders, filed with the
SEC on December 10, 2024 (the “2025 Special Meeting Proxy
Statement”), as well as the Vincerx’s Current Report on Form 8-K
filed on December 27, 2024.
Information about the ownership of Vincerx’s common stock by
Vincerx’s executive officers and directors is set forth in the
section entitled “Security Ownership of Certain Beneficial Owners
and Management” in the 2025 Special Meeting Proxy Statement, as
well as the Form 3 filed on January 6, 2025 for Kevin Haas. Updated
information regarding the identity of potential participants, and
their direct or indirect interests (by security holdings or
otherwise), will be reflected in Forms 3, 4, or 5 to be filed with
the SEC, as well as the section entitled “Security Ownership of
Certain Beneficial Owners and Management” of Vincerx’s definitive
proxy statement on Schedule 14A and other materials to be filed
with the SEC regarding the proposed transactions. All of these
documents are or will be available free of charge at the SEC’s
website at www.sec.gov and in the “Investors—SEC Filings &
Financials—SEC Filings” section of Vincerx’s website at
https://investors.vincerx.com/financial-information/sec-filings.
Stockholders, potential investors, and other readers should read
the definitive proxy statement carefully when it becomes available
before making any voting or investment decisions. These documents
can be obtained free of charge from the sources indicated
above.
No Offer or SolicitationThis communication
shall not constitute an offer to sell or the solicitation of an
offer to buy any securities, nor shall there be any sale of
securities, in any jurisdiction in which such offer, solicitation,
or sale would be unlawful prior to registration or qualification
under the securities laws of any such jurisdiction.
Contacts:
Gabriela JairalaVincerx Pharma,
Inc.gabriela.jairala@vincerx.com
Michael KingOqory, Inc.MKing@oqory.com
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