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signs Collaboration Agreement

Key Takeaway: signs Collaboration Agreement will combine their proprietary technologies with the goal of enhancement of growth and functionality of stem cells Aviv, Israel - July 5, 2018 - Cellect Biotechnology Ltd. (Nasdaq: APOP), a developer of a novel stem cell production technology, an

Full Press Release Details

signs Collaboration Agreement
will combine their proprietary technologies with the goal of
enhancement of growth and functionality of stem cells
Aviv, Israel - July 5, 2018 - Cellect Biotechnology Ltd. (Nasdaq: APOP), a developer of a novel stem cell production
technology, announced that it has signed a collaboration and material transfer agreement with the denovoMATRIX group of the Technische
Universit t Dresden (TU Dresden).
Dresden and its Center for Regenerative Therapies Dresden (CRTD), is one of the leading centers for stem cell research in Germany.
two entities believe that the combination of both proprietary technologies may result in significant enhancement of the overall
stem cell selection and expansion processes.
to the agreement, the team of denovoMATRIX employed by TU Dresden will conduct examinations into the tentative synergy between
Cellect's ApoGraft and the denovoMAtrix technology for the purpose of evaluating collaborative development of products
for regenerative medicine. To that end, a denovoMATRIX scientist will conduct a line of experiments in Cellect's R&D
the event of successful completion of the evaluation stage, both sides agreed to negotiate in good faith a potential mutual development
agreement, for the development of a stem cell related product. Cellect will have the sole discretion on determining the level
of success of the evaluation stage.
Cellect Biotechnology Ltd.
Biotechnology (NASDAQ: APOP) has developed a breakthrough technology for the selection of stem cells from any given tissue that
aims to improve a variety of stem cell-based therapies.
Company's technology is expected to provide research, hospitals and pharma companies with the tools to rapidly isolate stem
cells in quantity and quality allowing stem cell-based treatments and procedures in a wide variety of applications in regenerative
medicine. The Company's current clinical trial is aimed at bone marrow transplantations in cancer treatment.
press release contains forward-looking statements about the Company's expectations, beliefs and intentions. Forward-looking
statements can be identified by the use of forward-looking words such as "believe", "expect", "intend",
"plan", "may", "should", "could", "might", "seek", "target",
"will", "project", "forecast", "continue" or "anticipate" or their
negatives or variations of these words or other comparable words or by the fact that these statements do not relate strictly to
historical matters. For example, forward-looking statements are used in this press release when we discuss the Company's
belief regarding the results of any future collaboration with denovoMATRIX. These forward-looking statements and their implications
are based on the current expectations of the management of the Company only and are subject to a number of factors and uncertainties
that could cause actual results to differ materially from those described in the forward-looking statements. In addition, historical
results or conclusions from scientific research and clinical studies do not guarantee that future results would suggest similar
conclusions or that historical results referred to herein would be interpreted similarly in light of additional research or otherwise.
The following factors, among others, could cause actual results to differ materially from those described in the forward-looking
statements: the Company's history of losses and needs for additional capital to fund its operations and its inability to
obtain additional capital on acceptable terms, or at all; the Company's ability to continue as a going concern; uncertainties
of cash flows and inability to meet working capital needs; the Company's ability to obtain regulatory approvals; the Company's
ability to obtain favorable pre-clinical and clinical trial results; the Company's technology may not be validated and its
methods may not be accepted by the scientific community; difficulties enrolling patients in the Company's clinical trials;
the ability to timely source adequate supply of FasL; risks resulting from unforeseen side effects; the Company's ability
to establish and maintain strategic partnerships and other corporate collaborations; the scope of protection the Company is able
to establish and maintain for intellectual property rights and its ability to operate its business without infringing the intellectual
property rights of others; competitive companies, technologies and the Company's industry; unforeseen scientific difficulties
may develop with the Company's technology; and the Company's ability to retain or attract key employees whose knowledge
is essential to the development of its products.. Any forward-looking statement in this press release speaks only as of the date
of this press release. The Company undertakes no obligation to publicly update or review any forward-looking statement, whether
as a result of new information, future developments or otherwise, except as may be required by any applicable securities laws.
More detailed information about the risks and uncertainties affecting the Company is contained under the heading "Risk Factors"
in the Company's Annual Report on Form 20-F for the fiscal year ended December 31, 2017 filed with the U.S. Securities and Exchange
Commission ("SEC"), which is available on the SEC's website, www.sec.gov, and in the Company's periodic
filings with the SEC.
Leibovitz, Chief Financial Officer
Last updated: Jul 5, 2018