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Intellia Therapeutics Announces Fourth Quarter and Full-Year 2018 Financial Results - Confirmed improved non-human primate liver editing and protein reduction of greater than 95 percent in transthyretin amyloidosis progr

Key Takeaway: Intellia Therapeutics Announces Fourth Quarter and Full-Year 2018 Financial Results CAMBRIDGE, Mass., Feb. 27, 2019 (GLOBE NEWSWIRE) Intellia Therapeutics, Inc. (NASDAQ:NTLA), a leading genome editing company focused on developing curative therapeutics using CRISPR/Cas9 techno

Full Press Release Details

Intellia Therapeutics Announces
Fourth Quarter and Full-Year 2018 Financial Results
CAMBRIDGE, Mass., Feb. 27, 2019 (GLOBE NEWSWIRE) Intellia Therapeutics, Inc. (NASDAQ:NTLA), a
leading genome editing company focused on developing curative therapeutics using CRISPR/Cas9 technology in both in vivo and ex vivo applications, today reported operational highlights and financial results for the fourth quarter and
year ended December 31, 2018. In addition, Intellia highlighted select corporate milestones for 2019 and upcoming events for the first quarter of 2019.
We are delivering on our full-spectrum strategy, and we expect to have two candidates in development in 2019. Our in vivo transthyretin
amyloidosis program is on track for IND filing in 2020, and by the end of this year we anticipate having our first engineered cell therapy development candidate targeting acute myeloid leukemia, said Intellia President and Chief Executive
Officer John Leonard, M.D. We have shown that a single lipid nanoparticle administration can produce very substantial transthyretin protein reduction in non-human primates, reaching levels that we
believe hold great therapeutic promise for patients. We also look forward to sharing additional data on our acute myeloid leukemia program this year. We believe our TCR-based, CRISPR-engineered cell therapy
will provide a much-needed option for patients.
Recent Operational Highlights
The Company has set forth the following for 2019 pipeline progression:
Company will participate in the following investor events:
Fourth Quarter and Full Year 2018 Financial Results
Intellia expects that its cash, cash equivalents and marketable securities as of December 31, 2018, as well as technology access and funding from Novartis
and Regeneron, will enable Intellia to fund its anticipated operating expenses and capital expenditure requirements into the first half of 2021. This expectation excludes any potential milestone payments or extension fees that could be earned and
distributed under the collaboration agreements with Novartis and Regeneron or any strategic use of capital not currently in the base-case planning assumptions.
About Intellia Therapeutics
Intellia Therapeutics is a leading genome editing company focused on developing curative therapeutics using the CRISPR/Cas9 system. Intellia believes the CRISPR/Cas9 technology has the potential to transform medicine
by permanently editing disease-associated genes in the human body with a single treatment course, and through improved cell therapies that can treat cancer and immunological diseases, or can replace patients diseased cells. The combination of
deep scientific, technical and clinical development experience, along with its leading intellectual property portfolio, puts Intellia in a unique position to unlock broad therapeutic applications of the CRISPR/Cas9 technology and create a new class
Forward-Looking Statements
This press release contains
forward-looking statements of Intellia Therapeutics, Inc. ( Intellia ) within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, express or
implied statements regarding Intellia s ability to advance and expand the CRISPR/Cas9 technology to develop into human therapeutic products, as well as our intellectual property portfolio; our ability to achieve stable or effective genome
editing; our ability to administer our CRISPR/Cas9 product candidates; the potential timing and advancement of our preclinical studies, including continuing non-human primate studies for our ATTR program and
other programs (such as alpha-1 antitrypsin deficiency (AATD) and AML), and clinical trials; the timing and potential achievement of milestones to advance our pipeline including nominating development
candidates and filing INDs; our ability to replicate or apply results achieved in our preclinical studies, including those in our ATTR, AATD and AML programs, in any future studies, including human clinical trials; the potential development of our
proprietary LNP/AAV hybrid delivery system to advance our complex genome editing capabilities; the potential development of other in vivo or ex vivo cell therapeutics of all types, and those targeting WT1 in AML in
particular, using CRISPR/Cas9 technology; our ability to conduct successful IND-enabling studies of a lead ATTR development candidate and subsequently submitting an IND application in 2020 that will be
accepted by the regulatory agencies; our intent to present additional ATTR data, additional insertion/repair data, and other preclinical data during 2019 or thereafter; our ability to advance a development candidate for a second indication by late
2019 or thereafter; our plans to commence manufacturing efforts in 2019; the intellectual property position and strategy of Intellia s licensors, or other parties from which it derives rights, as well as third-parties and competitors; actions
by government agencies; our growth as a company and the anticipated contribution of the members of our board of directors and our executives to our operations and progress; the impact of our collaborations on our development programs; the potential
timing of regulatory filings regarding our development programs; the potential commercialization opportunities, including value and market, for product candidates; our expectations regarding our uses of capital, expenses, future accumulated deficit
and other 2018 financial results; and our ability to fund operations into the first half of 2021.
Any forward-looking statements in this press release are based on management s current expectations and
beliefs of future events, and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties
include, but are not limited to: risks related to Intellia s ability to protect and maintain our intellectual property position; risks related to Intellia s relationship with third parties, including our licensors; risks related to the
ability of our licensors to protect and maintain their intellectual property position; uncertainties related to the initiation and conduct of studies and other development requirements for our product candidates; the risk that any one or more of
Intellia s product candidates will not be successfully developed and commercialized; the risk that the results of preclinical studies will not be predictive of future results in connection with future studies; and the risk that Intellia s
collaborations with Novartis or Regeneron or its other ex vivo collaborations will not continue or will not be successful. For a discussion of these and other risks and uncertainties, and other important factors, any of which
could cause Intellia s actual results to differ from those contained in the forward-looking statements, see the section entitled Risk Factors in Intellia s most recent annual report on Form
10-K as well as discussions of potential risks, uncertainties, and other important factors in Intellia s other filings with the Securities and Exchange Commission. All information in this press
release is as of the date of the release, and Intellia undertakes no duty to update this information unless required by law.
INTELLIA THERAPEUTICS, INC.
CONSOLIDATED STATEMENTS OF OPERATIONS (UNAUDITED)
(Amounts in thousands, except per share data)
Three Months Ended December 31, Twelve Months Ended December 31,
2018 2017 2018 2017
Collaboration revenue $ 7,880 $ 6,668 $ 30,434 $ 26,117
Operating expenses:
Research and development 19,918 21,170 89,115 67,647
General and administrative 8,708 10,213 32,189 28,025
Total operating expenses 28,626 31,383 121,304 95,672
Operating loss (20,746 ) (24,715 ) (90,870 ) (69,555 )
Interest income 1,680 752 5,527 2,012
Net loss $ (19,066 ) $ (23,963 ) $ (85,343 ) $ (67,543 )
Net loss per share, basic and diluted $ (0.43 ) $ (0.61 ) $ (1.98 ) $ (1.88 )
Weighted average shares outstanding, basic and diluted 44,215 39,155 43,069 36,006
INTELLIA THERAPEUTICS, INC.
CONSOLIDATED BALANCE SHEET DATA (UNAUDITED)
(Amounts in thousands)
December 31, 2018 December 31, 2017
Cash, cash equivalents and marketable securities $ 314,059 $ 340,678
Total assets 347,315 376,235
Total liabilities 69,395 75,638
Total stockholders equity 277,920 300,597
Last updated: Feb 27, 2019