Aura Biosciences to Present Phase 2 Safety Data Evaluating Suprachoroidal Administration of Belzupacap Sarotalocan (AU-011) in Patients with Choroidal Melanoma at the ESMO 2022 Congress
September 07 2022 - 6:00AM
Business Wire
Aura Biosciences Inc. (NASDAQ: AURA), a clinical-stage
biotechnology company developing a novel class of virus-like drug
conjugate (VDC) therapies for multiple oncology indications, today
announced that Phase 2 data evaluating the safety of suprachoroidal
administration using its first VDC product candidate, belzupacap
sarotalocan (AU-011), for the first-line treatment of patients with
early-stage choroidal melanoma (indeterminate lesions and small
choroidal melanoma (IL/CM)) will be presented at the ESMO 2022
Congress, being held September 9-13, 2022, in Paris, France.
Details for ESMO 2022 poster presentation:
Title: A Phase 2 Trial of AU-011, an Investigational,
Virus-Like Drug Conjugate (VDC) for the Treatment of Primary
Indeterminate Lesions and Small Choroidal Melanoma (IL/CM) using
Suprachoroidal Administration Presenter: Hakan Demirci,
University of Michigan Session: Melanoma and Other Skin
Tumors Presentation #: 842P Date/Time: Saturday,
September 10, 2022, at 2:15 p.m. CEST
The presentation will be available on the “Scientific
Presentations” section of “VDC Platform” page of the Aura
Biosciences website on Saturday, September 10, 2022.
About Aura Biosciences
Aura Biosciences, Inc. is a clinical-stage biotechnology company
developing virus-like drug conjugates (VDCs), a novel class of
therapies, for the treatment of multiple oncology indications.
Aura’s lead VDC candidate, belzupacap sarotalocan (AU-011),
consists of a virus-like particle conjugated with an anti-cancer
agent. Belzupacap sarotalocan selectively targets and destroys
cancer cells and activates the immune system with the potential to
create long-lasting anti-tumor immunity. Belzupacap sarotalocan is
currently in development for ocular cancers, with an ongoing Phase
2 dose escalation clinical trial evaluating first-line treatment of
choroidal melanoma, a vision- and life-threatening form of eye
cancer where standard of care with radiotherapy leaves patients
with severe comorbidities, including major vision loss. Aura plans
to develop belzupacap sarotalocan across its ocular oncology
franchise including for the treatment of patients with choroidal
metastases. In addition, leveraging Aura’s technology platform,
Aura is developing belzupacap sarotalocan more broadly across
multiple cancers, starting with a planned Phase 1 clinical trial in
patients with non-muscle invasive bladder cancer. Aura is
headquartered in Cambridge, MA.
For more information, visit aurabiosciences.com, or follow us on
Twitter and LinkedIn.
Forward Looking Statement
This press release contains forward-looking statements within
the meaning of the Private Securities Litigation Reform Act of
1995, as amended, and other federal securities laws. Any statements
that are not statements of historical fact may be deemed to be
forward looking statements. Words such as “may,” “will,” “could”,
“should,” “expects,” “intends,” “plans,” “anticipates,” “believes,”
“estimates,” “predicts,” “projects,” “seeks,” “endeavor,”
“potential,” “continue” or the negative of such words or other
similar expressions that can be used to identify forward-looking
statements. These forward looking statements include express or
implied statements regarding Aura’s future expectations, plans and
prospects, including, without limitation, statements regarding the
expected timing of updates on the Company’s data from its Phase 2
clinical trials of belzupacap sarotalocan (AU-011).
The forward-looking statements in this press release are neither
promises nor guarantees, and investors should not place undue
reliance on these forward-looking statements because they involve
known and unknown risks, uncertainties, and other factors, many of
which are beyond Aura’s control and which could cause actual
results to differ materially from those expressed or implied by
these forward-looking statements, including, without limitation,
uncertainties inherent in clinical trials and in the availability
and timing of data from ongoing clinical trials; the expected
timing for submissions for regulatory approval or review by
governmental authorities; the risk that the results of Aura’s
clinical trials may not be predictive of future results in
connection with future clinical trials; whether Aura will receive
regulatory approvals to conduct trials or to market products;
whether Aura’s cash resources will be sufficient to fund its
foreseeable and unforeseeable operating expenses and capital
expenditure requirements; risks, assumptions and uncertainties
regarding the impact of the continuing COVID-19 pandemic on Aura’s
business, operations, strategy, goals and anticipated timelines;
Aura’s ongoing and planned pre-clinical activities; and Aura’s
ability to initiate, enroll, conduct or complete ongoing and
planned clinical trials. These risks, uncertainties, and other
factors include those risks and uncertainties described under the
heading “Risk Factors” in Aura’s Quarterly Report on Form 10-Q for
the quarter ended June 30, 2022 filed with the U.S. Securities and
Exchange Commission (SEC) and in subsequent filings made by Aura
with the SEC, which are available on the SEC’s website at
www.sec.gov. Except as required by law, Aura disclaims any
intention or responsibility for updating or revising any
forward-looking statements contained in this press release in the
event of new information, future developments or otherwise. These
forward-looking statements are based on Aura’s current expectations
and speak only as of the date hereof and no representations or
warranties (express or implied) are made about the accuracy of any
such forward-looking statements.
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version on businesswire.com: https://www.businesswire.com/news/home/20220907005542/en/
Investor and Media Contact: Matthew DeYoung Argot
Partners 212-600-1902 | aura@argotpartners.com
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