OXURION to Present at the Lytham Partners Fall 2021 Investor Conference
05 Octobre 2021 - 08:00AM
Leuven, BELGIUM, Boston, MA, US – 5 October,
2021 – 08.00 AM CET – Oxurion NV (Euronext Brussels: OXUR), a
biopharmaceutical company developing next generation standard of
care ophthalmic therapies, with a clinical stage portfolio in
vascular retinal disorders, today announces its management will
present at the Lytham Partners Fall 2021 Investor Conference.
- Lytham Partners Fall 2021 Investor Conference, October
5-7, 2021. Pre-recorded CEO Presentation available starting on
October 5 at 10:15 AM ET.
For more information, please visit Oxurion’s
events
page:www.oxurion.com/news-events#view-conferences_events-page
END
For further information please
contact:
Oxurion NV Tom Graney Chief Executive Officer Tel: +32 16 75 13 10
tom.graney@oxurion.com Michael Dillen Chief Corporate
Development Tel: +32 479 783583 Michael.dillen@oxurion.com
|
EU MEDiSTRAVA ConsultingDavid Dible/ Sylvie Berrebi/Frazer HallTel:
+44 20 7638 9571oxurion@medistrava.com USWestwicke, an ICR
CompanyChristopher BrinzeyTel: +1 617 835
9304chris.brinzey@westwicke.com |
About Oxurion
Oxurion (Euronext Brussels: OXUR) is a biopharmaceutical company
developing next generation standard of care ophthalmic therapies,
which are designed to better preserve vision in patients with
retinal vascular disorders including diabetic macular edema (DME),
the leading cause of vision loss in diabetic patients worldwide as
well as other conditions, including wet age-related macular
degeneration (AMD) and retinal vein occlusion (RVO).
Oxurion is aiming to build a leading global franchise in the
treatment of retinal vascular disorders based on the successful
development of its two novel therapeutics:
- THR-687 is a highly selective pan-RGD integrin antagonist that
is initially being developed as a potential first line therapy for
DME patients. Positive topline results in a Phase 1 clinical study
assessing THR-687 as a treatment for DME were announced in 2020.
Oxurion is currently conducting a Phase 2 clinical trial
(“INTEGRAL”) evaluating THR-687 in patients with DME. THR-687 also
has the potential to deliver improved treatment outcomes for
patients with wet AMD and RVO.
- THR-149 is a potent plasma kallikrein inhibitor being developed
as a potential new standard of care for the 40-50% of DME patients
showing suboptimal response to anti-VEGF therapy. THR-149 has shown
positive topline Phase 1 results for the treatment of DME. The
company is currently conducting a Phase 2 clinical trial
(“KALAHARI”) evaluating multiple injections of THR-149 in DME
patients previously showing a suboptimal response to anti-VEGF
therapy. Following positive data from Part A of this Phase 2 study
(dose selection), the Company has initiated Part B of the
study.
Oxurion is headquartered in Leuven, Belgium, and
is listed on the Euronext Brussels exchange under the symbol OXUR.
More information is available at www.oxurion.com.
Important information about forward-looking
statements
Certain statements in this press release may be
considered “forward-looking”. Such forward-looking statements are
based on current expectations, and, accordingly, entail and are
influenced by various risks and uncertainties. The Company
therefore cannot provide any assurance that such forward-looking
statements will materialize and does not assume an obligation to
update or revise any forward-looking statement, whether as a result
of new information, future events, or any other reason. Additional
information concerning risks and uncertainties affecting the
business and other factors that could cause actual results to
differ materially from any forward-looking statement is contained
in the Company’s Annual Report. This press release does not
constitute an offer or invitation for the sale or purchase of
securities or assets of Oxurion in any jurisdiction. No
securities of Oxurion may be offered or sold within the United
States without registration under the U.S. Securities Act of 1933,
as amended, or in compliance with an exemption therefrom, and in
accordance with any applicable U.S. state securities laws.
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