Full Press Release Details
Enlivex Doses First Patient in Placebo-Controlled Phase IIb Clinical
Trial Evaluating Allocetra in Severe and Critical COVID-19 Patients with ARDS
the randomized, multi-center trial are expected in Q2-2022
Nes-Ziona, Israel, September 22, 2021 (GLOBE NEWSWIRE) -
Enlivex Therapeutics Ltd. (Nasdaq: ENLV, the "Company"), a clinical-stage macrophage reprogramming immunotherapy company
targeting diseased macrophages in patients with sepsis, COVID-19 and solid tumors, today announced the initiation of dosing in its multi-center,
placebo-controlled, randomized, blinded, Phase IIb clinical trial evaluating AllocetraTM in severe and critical COVID-19 patients
with acute respiratory distress syndrome (ARDS).
The Phase IIb trial is expected to recruit up to 152 severe or
critical COVID-19 patients (76 AllocetraTM plus standard-of-care, 76 placebo plus standard-of-care) in clinical centers
in Israel and certain European countries, and is designed to assess the safety and efficacy of AllocetraTM when administered
in addition to standard-of-care treatment. The co-primary endpoints of the trial are ventilation-free survival and recovery for each of
its two patient sub-populations (severe and critical). In addition, the trial will assess several secondary endpoints, including evaluation
of long-COVID-19 symptoms. Top-line data from the trial are expected in the second quarter of 2022.
"We believe that recent variant-driven surges in COVID-19
cases around the world have emphasized the need for novel treatments that can address the most serious forms of the disease," said
Dr. Oren Hershkovitz, Chief Executive Officer of Enlivex. "They also reinforce our belief that even with vaccines available, COVID-19
will migrate from a pandemic to an endemic, with multiple variants continuing to circulate throughout the population. Through Allocetra's
continued development, we hope to provide physicians with an effective treatment option that can improve survival and decrease the length
of hospitalization for patients in severe or critical condition. The initiation of dosing in our Phase IIb trial represents an important
step towards this goal. The study was already approved by several Ethics Committees from leading Israeli hospitals, and we are committed
to accelerate the patient's recruitment by opening many sites both in Israel and specific EU countries as fast as possible".
Prof. Dror Mevorach, Chief Scientific Officer of Enlivex, added,
"We believe AllocetraTM has a broadly applicable mechanism of action for reprogramming macrophages and that was
demonstrated through the promising results in prior clinical trials in severe and critical COVID-19 patients. We aim to build on these
data through the progression of this placebo-controlled Phase IIb study and look forward to its continued advancement."
Enlivex previously reported positive top-line results from Phase Ib
and Phase II investigator-initiated clinical trials of AllocetraTM in COVID-19 patients in severe and critical condition.
Aggregate data from the two trials demonstrated that AllocetraTM was safe and well tolerated. Moreover, at the end of
these trials' 28-day follow-up periods, a 0% (0/21) mortality rate was observed and 90.5% (19/21) of patients recovered from their
respective severe/critical condition and were discharged from the hospital after an average of 5.6 days following AllocetraTM administration.
AllocetraTM is being developed as a universal, off-the-shelf
cell therapy designed to reprogram macrophages into their homeostatic state. Diseases such as solid cancers, sepsis, COVID-19 and
many others reprogram macrophages out of their homeostatic state. These non-homeostatic macrophages contribute significantly to the severity
of the respective diseases. By restoring macrophage homeostasis, AllocetraTM has the potential to provide a novel immunotherapeutic
mechanism of action for life-threatening clinical indications that are defined as "unmet medical needs", as a stand-alone
therapy or in combination with leading therapeutic agents.
Enlivex is a clinical stage macrophage reprogramming
immunotherapy company developing AllocetraTM, a universal, off-the-shelf cell therapy designed to reprogram macrophages
into their homeostatic state. Resetting non-homeostatic macrophages into their homeostatic state is critical for immune system rebalancing
and resolution of life-threatening conditions. 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, the expected timing of clinical trials' results for, and market opportunities
for, ALLOCETRATM programs, as well as potential changes in the severity level of the COVID-19 pandemic (including due
to new variants of the virus) and the effect of such changes on pace of patient recruitment into clinical trials, manufacturing delays,
and changes in market opportunities. 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 be delayed and/or 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.
Shachar Shlosberger, CFO
Enlivex Therapeutics, Ltd.
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