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Enlivex Announces Allowance of New Chinese Patent Covering Allocetra Immunotherapy

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Enlivex Therapeutics Ltd. has received a notice of allowance for a new patent in China concerning its immunotherapy product candidate, ALLOCETRA. This patent is expected to provide enhanced intellectual property protection, covering methods, uses, and pharmaceutical compositions. The patent is anticipated to be issued in Q4 2020. ALLOCETRA aims to address unmet medical needs related to organ dysfunction and acute multiple organ failure due to conditions such as Sepsis and COVID-19, in addition to treating solid tumors through immunotherapy mechanisms.

Positive
  • New patent allowance for ALLOCETRA expected to enhance intellectual property protection.
  • ALLOCETRA targets critical medical conditions with unmet needs, potentially increasing demand.
Negative
  • Patent approval is not guaranteed and may face hurdles before final issuance.
  • Relying on regulatory approvals poses risks that could affect commercialization timelines.

Nes-Ziona, Israel, Sept. 16, 2020 (GLOBE NEWSWIRE) -- Enlivex Therapeutics Ltd., a clinical-stage immunotherapy company, today announced that the China National Intellectual Property Administration (CNIPA)  issued a notice of allowance for a new patent application covering ALLOCETRATM, the company’s immunotherapy product candidate.  Upon issuance, the new patent will provide added intellectual property protection, including methods, uses and pharmaceutical compositions. The company expects that this new patent will be issued in China during the fourth quarter of 2020.

ALLOCETRATM has been designed to provide a novel immunotherapy mechanism of action that targets life-threatening clinical indications that are defined as “unmet medical needs”, including organ dysfunction and acute multiple organ failure associated with Sepsis and COVID-19,  as well as treating solid tumors by modulating such tumors’ microenvironment.

ABOUT ENLIVEX

Enlivex is a clinical stage immunotherapy company, developing an allogeneic drug pipeline for immune system rebalancing. Immune system rebalancing is critical for the treatment of life-threatening immune and inflammatory conditions which involve hyper-expression of cytokines (Cytokine Release Syndrome) and for which there are no approved treatments (unmet medical needs), as well as solid tumors immune-checkpoint rebalancing.  For more information, visit http://www.enlivex.com.

Safe Harbor Statement:  This press release contains forward-looking statements, which may be identified by words such as “expects,” “plans,” “projects,” “will,” “may,” “anticipates,” “believes,” “should,” “would”, “could,” “intends,” “estimates,” “suggests,” “has the potential to” and other words of similar meaning, including statements regarding expected cash balances, market opportunities for the results of current clinical studies and preclinical experiments, the effectiveness of, and market opportunities for, ALLOCETRATM programs. All such forward-looking statements are made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995.  Investors are cautioned that forward-looking statements involve risks and uncertainties that may affect Enlivex’s business and prospects, including the risks that Enlivex may not succeed in generating any revenues or developing any commercial products; that the products in development may fail, may not achieve the expected results or effectiveness and/or may not generate data that would support the approval or marketing of these products for the indications being studied or for other indications; that ongoing studies may not continue to show substantial or any activity; and other risks and uncertainties that may cause results to differ materially from those set forth in the forward-looking statements. The results of clinical trials in humans may produce results that differ significantly from the results of clinical and other trials in animals. The results of early-stage trials may differ significantly from the results of more developed, later-stage trials. The development of any products using the ALLOCETRATM product line could also be affected by a number of other factors, including unexpected safety, efficacy or manufacturing issues, additional time requirements for data analyses and decision making, the impact of pharmaceutical industry regulation, the impact of competitive products and pricing and the impact of patents and other proprietary rights held by competitors and other third parties.  In addition to the risk factors described above, investors should consider the economic, competitive, governmental, technological and other factors discussed in Enlivex’s filings with the Securities and Exchange Commission, including in the Company’s most recent Annual Report on Form 20-F filed with the Securities and Exchange Commission.  The forward-looking statements contained in this press release speak only as of the date the statements were made, and we do not undertake any obligation to update forward-looking statements, except as required under applicable law.

ENLIVEX CONTACT                                                                            
Shachar Shlosberger, CFO                                                                    
Enlivex Therapeutics, Ltd.                                                                      
shachar@enlivexpharm.com

INVESTOR RELATIONS CONTACT
Eric Ribner
LifeSci Advisors
eric@lifesciadvisors.com



FAQ

What is the significance of the new patent for ENLV's ALLOCETRA?

The new patent will provide enhanced intellectual property protection for ALLOCETRA, covering its methods, uses, and compositions.

When is the new patent for ALLOCETRA expected to be issued?

The patent is anticipated to be issued in the fourth quarter of 2020.

What conditions does ALLOCETRA aim to treat?

ALLOCETRA is designed to treat life-threatening conditions such as organ dysfunction and acute multiple organ failure related to Sepsis and COVID-19.

What are the potential risks associated with the new patent for ENLV?

There is a risk that the patent approval may face challenges, and reliance on regulatory approvals can affect commercialization timelines.

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