Immunocore to report second quarter 2024 financial results and host call on August 8, 2024
01 Agosto 2024 - 6:00AM
Immunocore to report second quarter 2024
financial results and host call on August 8, 2024
(OXFORDSHIRE, England & CONSHOHOCKEN, Penn.
& ROCKVILLE, Md., US, 01 August 2024) Immunocore Holdings plc
(Nasdaq: IMCR) (“Immunocore” or the “Company”), a commercial-stage
biotechnology company pioneering and delivering transformative
immunomodulating medicines to radically improve outcomes for
patients with cancer, infectious diseases and autoimmune diseases,
today announced that it will report second quarter financial
results, before the US markets open on Thursday, August 8, 2024.
Following the announcement, the Company will host a live
teleconference and webcast at 8:00 a.m. EDT (1:00 p.m. BST) to
discuss their financial results and provide a business and
portfolio update.
Audio WebcastThe call will be
webcast live and can be accessed by visiting ‘Events’, under
‘Events and Presentations’, via the ‘Investors’ section of
Immunocore’s website at www.immunocore.com. Following the event, a
replay will also be made available for a limited time.
Conference Call
Details:Domestic (toll-free): 877-405-1239International
(toll): +1 201-389-0851
About Immunocore
Immunocore is a commercial-stage biotechnology
company pioneering the development of a novel class of TCR
bispecific immunotherapies called ImmTAX – Immune mobilizing
monoclonal TCRs Against X disease – designed to treat a broad range
of diseases, including cancer, autoimmune, and infectious disease.
Leveraging its proprietary, flexible, off-the-shelf ImmTAX
platform, Immunocore is developing a deep pipeline in multiple
therapeutic areas, including five clinical stage programs in
oncology and infectious disease, advanced pre-clinical programs in
autoimmune disease and multiple earlier pre-clinical programs. The
Company’s most advanced oncology TCR therapeutic, KIMMTRAK has been
approved for the treatment of HLA-A*02:01-positive adult patients
with unresectable or metastatic uveal melanoma in the United
States, European Union, Canada, Australia, and the United
Kingdom.
Forward Looking Statements
This press release contains “forward-looking
statements” within the meaning of the safe harbor provisions of the
Private Securities Litigation Reform Act of 1995. Words such as
“may,” “will,” “believe,” “expect,” “plan,” “anticipate,” and
similar expressions (as well as other words or expressions
referencing future events or circumstances) are intended to
identify forward-looking statements. All statements, other than
statements of historical facts, included in this press release are
forward-looking statements. These statements include, but are not
limited to, statements regarding the marketing and therapeutic
potential of KIMMTRAK for mUM; the expected clinical benefits of
KIMMTRAK and the Company’s other product candidates, including
extended overall survival benefit; expectations regarding
commercialization of KIMMTRAK in the United States, Germany and
France as well as in other EU member states; expectations regarding
receipt of regulatory approvals and completion of related
procedures; expectations regarding the success and performance of
obligations under Immunocore’s collaboration agreements with third
parties; expectations regarding Immunocore’s cash runway;
Immunocore’s sales and marketing plans, including with respect to
the United States, Germany and France; the potential for and timing
of commercial availability of KIMMTRAK in additional countries and
the ability to reach patients in a timely manner; the value
proposition of Immunocore’s product candidates, including KIMMTRAK
in mUM and its benefit as an orphan indication, including
expectations regarding the potential market opportunity;
physician’s feedback, endorsements, guidelines and interest in
prescribing KIMMTRAK as the standard of care for mUM; Immunocore’s
efforts to expand patients’ access to medicine; future development
plans of KIMMTRAK, including the timing or likelihood of expansion
into additional markets or geographies; expectations regarding the
design, progress, timing, scope and results of Immunocore’s
existing and planned clinical trials, including the randomized
Phase 2/3 clinical trial in previously treated advanced melanoma
and PRAME and MAGE-A4 clinical trials. Any forward-looking
statements are based on management’s current expectations and
beliefs of future events and are subject to a number of risks and
uncertainties that could cause actual events or results to differ
materially and adversely from those set forth in or implied by such
forward-looking statements, many of which are beyond the Company’s
control. These risks and uncertainties include, but are not limited
to, the impact of the ongoing and evolving COVID-19 pandemic on the
Company’s business, financial position, strategy and anticipated
milestones, including Immunocore’s ability to conduct ongoing and
planned clinical trials; Immunocore’s ability to obtain a clinical
supply of current or future product candidates or commercial supply
of KIMMTRAK or any future approved products, including as a result
of the COVID-19 pandemic, war in Ukraine or global geopolitical
tension; Immunocore’s ability to obtain and maintain regulatory
approval of its product candidates, including KIMMTRAK;
Immunocore’s ability and plans in continuing to establish and
expand a commercial infrastructure and to successfully launch,
market and sell KIMMTRAK and any future approved products;
Immunocore’s ability to successfully expand the approved
indications for KIMMTRAK or obtain marketing approval for KIMMTRAK
in additional geographies in the future; the delay of any current
or planned clinical trials, whether due to the COVID-19 pandemic,
patient enrollment delays or otherwise; Immunocore’s ability to
successfully demonstrate the safety and efficacy of its product
candidates and gain approval of its product candidates on a timely
basis, if at all; competition with respect to market opportunities;
unexpected safety or efficacy data observed during preclinical
studies or clinical trials; actions of regulatory agencies, which
may affect the initiation, timing and progress of clinical trials
or future regulatory approval; Immunocore’s need for and ability to
obtain additional funding, on favorable terms or at all, including
as a result of rising inflation, interest rates and general market
conditions, and the impacts thereon of the COVID-19 pandemic, war
in Ukraine and global geopolitical tension; Immunocore’s ability to
obtain, maintain and enforce intellectual property protection for
KIMMTRAK or any product candidates it is developing; and the
success of Immunocore’s current and future collaborations,
partnerships or licensing arrangements. These and other risks and
uncertainties are described in greater detail in the section titled
"Risk Factors" in Immunocore’s filings with the Securities and
Exchange Commission, including Immunocore’s most recent Annual
Report on Form 20-F for the year ended December 31, 2021 filed with
the Securities and Exchange Commission on March 3, 2022, as well as
discussions of potential risks, uncertainties, and other important
factors in the Company’s subsequent filings with the Securities and
Exchange Commission. All information in this press release is as of
the date of the release, and the Company undertakes no duty to
update this information, except as required by law.
Contact Information
Immunocore
Sébastien Desprez, Head of CommunicationsT: +44
(0) 7458030732E: sebastien.desprez@immunocore.comFollow on Twitter:
@Immunocore
Investor Relations
Clayton Robertson, Head of Investor RelationsT:
+1 (215) 384-4781E: ir@immunocore.com
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