Protara Therapeutics to Present New Interim Data from Phase 2 ADVANCED-2 Trial of TARA-002 in Patients with NMIBC at the 25th Annual Meeting of the Society of Urologic Oncology
2024年11月16日 - 7:52AM
Protara Therapeutics, Inc. (Nasdaq: TARA), a clinical-stage
company developing transformative therapies for the treatment of
cancer and rare diseases, today announced that data from an
interim analysis of the ongoing Phase 2 open-label ADVANCED-2 trial
of TARA-002 in patients with non-muscle invasive bladder cancer
(NMIBC) will be featured during a poster session at the upcoming
25th Annual Meeting of the Society of Urologic Oncology (SUO)
taking place December 4, 2024 to December 6, 2024, in Dallas,
Texas. The presentation will include safety data featured in
the abstract published today on the SUO website, as well as updated
safety and new efficacy data from approximately 20 enrolled
patients, the majority of whom are six-month evaluable.
ADVANCED-2 (NCT05951179) is a Phase 2 open-label
trial assessing intravesical TARA-002 in NMIBC patients with
carcinoma in situ or CIS (± Ta/T1) who are Bacillus Calmette-Guérin
(BCG)-unresponsive (n≈100) and BCG-Naïve (n=27). The
BCG-Unresponsive cohort has been designed to be registrational in
alignment with the FDA’s 2024 BCG-Unresponsive Non-muscle Invasive
Bladder Cancer: Developing Drugs and Biological Products for
Treatment Draft Guidance for Industry. Trial subjects received an
induction with or without a reinduction course of six weekly
intravesical instillations of TARA-002, followed by a maintenance
course of three weekly installations every three months in the
BCG-Unresponsive cohort. Details of the poster
presentation are as follows:
Title: ADVANCED-2: Phase 2
Open-Label Study to Evaluate Safety and Anti-Tumor Activity of
Intravesical Instillation of TARA-002 in Adults with High-Grade
Non-Muscle Invasive Bladder Cancer Poster Number:
119Poster Category: NMIBCSession
Title: Bladder Cancer Session Date and
Time: Thursday, December 5, 2024, 1:15 p.m. – 2:15 p.m.
CT
About TARA-002
TARA-002 is an investigational cell therapy in
development for the treatment of NMIBC and of LMs, for which it has
been granted Rare Pediatric Disease Designation by the U.S. Food
and Drug Administration. TARA-002 was developed from the same
master cell bank of genetically distinct group A Streptococcus
pyogenes as OK-432, a broad immunopotentiator marketed as
Picibanil® in Japan by Chugai Pharmaceutical Co., Ltd and also
approved in Taiwan. Protara has successfully shown manufacturing
comparability between TARA-002 and OK-432.
When TARA-002 is administered, it is
hypothesized that innate and adaptive immune cells within the cyst
or tumor are activated and produce a pro-inflammatory response with
release of cytokines such as tumor necrosis factor (TNF)-alpha,
interferon (IFN)-gamma IL-6, IL-10, IL-12. TARA-002 also directly
kills tumor cells and triggers a host immune response by inducing
immunogenic cell death, which further enhances the antitumor immune
response.
About Non-Muscle Invasive Bladder Cancer
(NMIBC)
Bladder cancer is the 6th most common cancer in
the United States, with NMIBC representing approximately 80% of
bladder cancer diagnoses. Approximately 65,000 patients are
diagnosed with NMIBC in the United States each year. NMIBC is
cancer found in the tissue that lines the inner surface of the
bladder that has not spread into the bladder muscle.
About Protara Therapeutics,
Inc.
Protara is a clinical-stage biotechnology
company committed to advancing transformative therapies for people
with cancer and rare diseases. Protara’s portfolio includes its
lead candidate, TARA-002, an investigational cell-based therapy in
development for the treatment of non-muscle invasive bladder cancer
(NMIBC) and lymphatic malformations (LMs). The Company is
evaluating TARA-002 in an ongoing Phase 2 trial in NMIBC patients
with carcinoma in situ (CIS) who are unresponsive or naïve to
treatment with Bacillus Calmette-Guérin (BCG), as well as a Phase 2
trial in pediatric patients with LMs. Additionally, Protara is
developing IV Choline Chloride, an investigational phospholipid
substrate replacement for patients on parenteral nutrition who are
otherwise unable to meet their choline needs via oral or enteral
routes. For more information, visit www.protaratx.com.
Forward-Looking Statements
Statements contained in this press release regarding matters
that are not historical facts are "forward looking statements"
within the meaning of the Private Securities Litigation Reform Act
of 1995. Protara may, in some cases, use terms such as “predicts,”
“believes,” “potential,” “proposed,” “continue,” “designed,”
“estimates,” “anticipates,” “expects,” “plans,” “intends,” “may,”
“could,” “might,” “will,” “should” or other words or expressions
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forward-looking statements. Such forward-looking statements include
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beliefs, projections, outlook, analyses or current expectations
concerning, among other things: Protara’s business strategy,
including its development plans for its product candidates and
plans regarding the timing or outcome of existing or future
clinical trials; statements related to expectations regarding
interactions with the FDA; Protara’s financial position; statements
regarding the anticipated safety or efficacy of Protara’s product
candidates; and Protara’s outlook for the remainder of the year.
Because such statements are subject to risks and uncertainties,
actual results may differ materially from those expressed or
implied by such forward-looking statements. Factors that contribute
to the uncertain nature of the forward-looking statements include:
risks that Protara’s financial guidance may not be as expected, as
well as risks and uncertainties associated with: Protara’s
development programs, including the initiation and completion of
non-clinical studies and clinical trials and the timing of required
filings with the FDA and other regulatory agencies; general market
conditions; changes in the competitive landscape; changes in
Protara’s strategic and commercial plans; Protara’s ability to
obtain sufficient financing to fund its strategic plans and
commercialization efforts; having to use cash in ways or on timing
other than expected; the impact of market volatility on cash
reserves; failure to attract and retain management and key
personnel; the impact of general U.S. and foreign, economic,
industry, market, regulatory, political or public health
conditions; and the risks and uncertainties associated with
Protara’s business and financial condition in general, including
the risks and uncertainties described more fully under the caption
“Risk Factors” and elsewhere in Protara's filings and reports with
the United States Securities and Exchange Commission. All
forward-looking statements contained in this press release speak
only as of the date on which they were made and are based on
management's assumptions and estimates as of such date. Protara
undertakes no obligation to update any forward-looking statements,
whether as a result of the receipt of new information, the
occurrence of future events or otherwise, except as required by
law.
Company Contact:
Justine O'MalleyProtara
TherapeuticsJustine.OMalley@protaratx.com646-817-2836
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