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approves Cellect's grant application

Key Takeaway: the agreement signed with South Korean Cell2in approves Cellect's grant application Korea-Israel Industrial R&D Foundation (KORIL-RDF) approves grant for the collaboration between Cellect and Cell2in, providing financing for the joint project Shai Yarkoni, Cellect CEO commen

Full Press Release Details

the agreement signed with
South Korean Cell2in
approves Cellect's grant application
Korea-Israel Industrial R&D Foundation (KORIL-RDF) approves grant for the collaboration between Cellect and Cell2in, providing
financing for the joint project
Shai Yarkoni, Cellect CEO commented:
grant approval by KORIL-RDF acknowledges the commercial and scientific potential that may arise from our collaboration with Cell2in.
The grant opens the door for larger collaboration and commercial opportunities."
Aviv, Israel - Dec 17, 2018 - Cellect Biotechnology Ltd. (Nasdaq: APOP), a developer of a novel stem cell production
technology, announced that KORIL-RDF, has approved Cellect's grant application, submitted with Cell2in, a Korean cell therapy
company with whom a collaboration agreement was signed recently.
agreement will potentially enhance and accelerate the development of Cellect's ApoGraft Technology Platform. In addition,
the combination of the two technologies may result in a synergic effect on stem cell expansion, and open new potential applications.
to the agreement, Cellect will use Cell2in proprietary FreSHtracer technology for the functional identification of stem cells.
Both companies will collaborate on a proof-of-concept of combining technologies in order to significantly improve stem cells selection
process. Upon potentially successful results, both companies plan to broaden their collaboration to provide a combined solution
that will benefit multiple stem cell therapy products covering a wide range of diseases.
Cellect is aiming to show more efficient quantification, as compared to current industry standards of mesenchymal stem cells (MSCs)
and hematopoietic stem cells (HSCs), and validation through quantification that Fas Ligand (FasL), Cellect's main active
ingredient, accelerates MSC expansion relative to processes currently used in approved products as well as products in clinical
Cellect advances its clinical program towards the commercialization of its products, it becomes more important to continuously
seek ways to use Cellect's technology with other products in order to maintain its leadership position for enabling cell
therapy. The grant is to be finalized pending proposed budget review and signatures.
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 Cell2in. 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, http://www.sec.gov, and in the Company's
periodic filings with the SEC.
Leibovitz, Chief Financial Officer
Last updated: Dec 17, 2018