SYMON-I Study of Symphony IL-6 Suggests Prediction of Mortality in Sepsis Patients
26 Junho 2024 - 9:00AM
Bluejay Diagnostics, Inc. (NASDAQ: BJDX), today announced results
from the primary analysis of SYMON-I, a multicenter pilot clinical
study investigating the role of interleukin-6 (IL-6) in patients
diagnosed with sepsis and septic shock. This prospective study
assessed the utility of IL-6 upon initial presentation to the
intensive care unit (ICU).
The primary analysis of the SYMON-I study (registered clinical
trial number NCT06181604) highlighted that IL-6 levels within 24
hours of sepsis or septic shock diagnosis and admission to the ICU
may predict patient mortality out to 28 days. These findings will
be validated in the SYMON-II pivotal study.
Furthermore, a secondary outcome of the SYMON-I study showed
that IL-6 levels within 24 hours of sepsis or septic shock
diagnosis and admission to the ICU is a predictor of patient
mortality during their hospitalization. Other secondary outcomes
showed that lactate and Sequential Organ Failure Assessment (SOFA),
standard clinical tests used for sepsis and septic shock patients,
were not predictors of patient mortality out to 28 days.
Mark Feinberg, M.D., the Chief Medical Advisor to Bluejay
Diagnostics and an Associate Professor of Medicine at Harvard
Medical School, Boston, commented, “These results are a testament
to the dedication of our team and the collaboration across centers.
Understanding the role of IL-6 as a prognostic biomarker for
mortality and other important critical care endpoints, may
ultimately inform how IL-6 can be incorporated into the management
of patients with sepsis or septic shock, potentially saving
thousands of lives annually.”
Future Directions: Bluejay Diagnostics is
planning to initiate the SYMON-II pivotal clinical study in Q3
2024. If the results are positive, the Company intends to use
SYMON-II as support in a 510(k) application to the FDA in 2025 for
the following intended use: Symphony IL-6 is intended for use to
determine the IL-6 concentration as an aid in assessing the
cumulative 28-day risk of all-cause mortality in conjunction with
other laboratory findings and clinical assessments for patients
diagnosed with sepsis or septic shock in the ICU. The Company
intends to present the SYMON-I and SYMON-II results at future
national scientific meetings and publish in peer-reviewed
publications. The Company’s ability to engage in and complete these
activities will be contingent upon it raising additional capital to
continue funding its operations and remain a going concern.
Neil Dey, Chief Executive Officer at Bluejay Diagnostics,
commented, “The SYMON clinical study program marks an important
step forward in the fight against sepsis, offering potential new
avenues for identifying patients at high risk of sepsis-associated
mortality and opportunities for improving patient survival rates.
Further studies are expected to build on these findings and refine
the understanding of IL-6 as a key biomarker in managing sepsis
effectively.”
About the Symphony System:
The Symphony Test platform is designed to determine patient
acuity for triage and monitoring based on the measurement of a
specific biomarker. The Symphony IL-6 Test to determine patient
acuity for sepsis triage and monitoring (“Symphony IL-6 Test”) is
currently Bluejay’s lead product candidate.
About the SYMON Clinical Study Program:
The SYMON Clinical Study Program include SYMON-I and SYMON-II.
SYMON-I is a pilot study to determine IL-6 levels associated with
various endpoints, including, but not limited to 28-day all-cause
mortality and in-hospital mortality. The SYMON-II study is the
pivotal study to validate the outcomes of the SYMON-I study, which
the Company plans to use to support a 510(k) application to the
FDA.
About Bluejay Diagnostics: Bluejay Diagnostics,
Inc. is committed to advancing healthcare by developing accessible,
affordable, rapid and direct biomarker testing, in whole blood,
near patient. Bluejay’s first product candidate, an IL-6 test for
sepsis triage, is designed to provide accurate, reliable results in
approximately 20 minutes from ‘Sample-To-Result’ to help medical
professionals make earlier and better triage/treatment decisions.
Based in Acton, Massachusetts, Bluejay aims to improve clinical
outcomes through timely and precise diagnostic tests.
Symphony is a registered trademark of Bluejay
Diagnostics, Inc.
Forward Looking Statements:
This press release contains statements that the Company believes
are “forward-looking statements” within the meaning of the Private
Litigation Reform Act. These statements include, but are not
limited to, statements relating to the expected nature and timing
of the Company’s planned FDA submission and related plans for
clinical study completion, whether the Company’s cash position will
be sufficient to fund operations needed to achieve regulatory
approval and initial commercialization of the Symphony IL-6 Test,
whether such regulatory approval will actually occur, and the
continuation of the Company as a going concern. Forward-looking
statements are usually identified by the use of words such as
“anticipates,” “believes,” “estimates,” “expects,” “intends,”
“may,” “plans,” “projects,” “seeks,” “should,” “suggest”, “will,”
and variations of such words or similar expressions or their
negatives (as well as other words and expressions referencing
future events, conditions, or circumstances). The Company has based
these forward-looking statements on its current expectations and
projections about future events, nevertheless, actual results or
events could differ materially from the plans, intentions and
expectations disclosed in, or implied by, the forward-looking
statements the Company makes. These statements are only predictions
and involve known and unknown risks, uncertainties, and other
factors, including those discussed in the Company’s filings with
the Securities and Exchange Commission, including as set forth in
the “Risk Factors” section of the Company’s Annual Report on Form
10-K for the fiscal year ended December 31, 2023, as updated by the
Company’s Quarterly Report on Form 10-Q for the fiscal quarter
ended March 31, 2024. You should not place undue reliance on these
statements, as they are subject to risks and uncertainties, and
actual results and performance in future periods may be materially
different from any future results or performance suggested by the
forward-looking statements in this release. This press release
speaks as of the date indicated above. The Company undertakes no
obligation to update any forward-looking statements, whether as a
result of new information, future events, or otherwise. The Company
expressly disclaims any obligation to update or revise any
forward-looking statements found herein to reflect any changes in
the Company’s expectations of results or any change in events.
Investor Contact:Neil DeyBluejay Diagnostics,
Inc.neil.dey@bluejaydx.com978-631-0310
Website: www.bluejaydx.com
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