Synlogic Reports Fourth Quarter and Full Year 2018 Financial Results and Provides Business Update
– Ended 2018 with approximately $123 million in cash and investments, which provides runway through 2020 –
– Clinical trial readouts expected in mid-2019 from two Synthetic Biotic™ medicines and first IND application expected from Synlogic’s immuno-oncology platform in second half of 2019 –
– Company will host a conference call and webcast at 8:00 am ET today –
CAMBRIDGE, Mass.--(BUSINESS WIRE)-- Synlogic, Inc. (Nasdaq: SYBX), a clinical stage company applying synthetic biology to probiotics to develop novel, living medicines, today reported its financial results for the fourth quarter and full year ended December 31, 2018.
“2019 is an exciting year for Synlogic as we continue to advance out platform and programs,” said Aoife Brennan, M.B., Ch.B. Synlogic’s president and chief executive officer. “Data expected mid-year from clinical trials of SYNB1020 and SYNB1618, in patients with hyperammonemia and phenylketonuria, respectively, will guide our plans for future development of our Synthetic Biotic medicines in these areas and additional rare metabolic diseases. We are also exploring new applications of our platform as we advance our first immuno-oncology program toward submission of an Investigational New Drug (IND) application and into clinical studies. Furthermore, with our increased capability to manufacture clinical trial material, we are now in a position to advance our programs through development as expeditiously as possible.”
2019 Priorities
Pipeline
- Presentation of top-line data from Phase 1b/2a study of SYNB1020 in patients with cirrhosis and elevated blood ammonia expected by mid-year. The double-blind, placebo-controlled study is designed to assess safety and tolerability, the ability of orally administered SYNB1020 to lower blood ammonia as well as its effect on several exploratory measures associated with hyperammonemia in this population. These data will provide valuable information for both platform development and the development path for Synlogic’s hyperammonemia program.
- Presentation of top-line data from study to evaluate SYNB1618 in patients with PKU expected by mid-year. The second part of this double-blind, placebo-controlled study is designed to assess safety and tolerability of orally administered SYNB1618 in a single dose (N=4) and multiple dose cohort (N=10) of patients with phenylketonuria (PKU). Additional endpoints of the study will explore the production of biomarkers of SYNB1618 activity that are expected to provide information as to the differences in pharmacodynamics of the Synthetic Biotic medicine in patients versus healthy volunteers.
- Advancement of SYNB1891 immuno-oncology program candidate to enable filing of an IND application in the second half of the year. SYNB1891 is an intra-tumorally administered Synthetic Biotic medicine engineered to produce cyclic di-AMP (CDA), an agonist of the STING pathway, that is designed to serve as a dual innate activator of the immune system as a potential treatment for solid tumors.
- Continued progress and refinement of manufacturing and process development. Synlogic is developing and manufacturing solid oral Synthetic Biotic formulations suitable for Phase 2 clinical trials and beyond.
- Advancement of new research programs to expand product pipeline.
- Presentation and publication of data at major scientific and medical meetings. Synlogic is committed to publishing and presenting data that demonstrate the breadth of Synlogic’s Synthetic Biotic platform.
- Advancement of collaboration. On March 6, 2019, Synlogic announced that its collaboration with AbbVie to develop a Synthetic Biotic medicine for the treatment of inflammatory bowel disease (IBD) had advanced into lead optimization triggering a milestone payment to Synlogic. The two companies will work together to develop and enable the selection of a suitable candidate for entry into IND-enabling studies.
Corporate
- Continued strengthening of Synlogic’s leadership. In February 2019, Synlogic announced the appointment of Patricia N. Hurter, Ph.D., Senior Vice President of Pharmaceutical and Preclinical Sciences at Vertex Pharmaceuticals, Inc., to its board of directors. Synlogic is also conducting a search to fill the position of Chief Medical Officer vacated by Dr. Brennan.
- Continued exploration of additional strategic opportunities. Synlogic expects to develop additional strategic collaborations to expand the reach of the Synthetic Biotic platform.
Fourth Quarter 2018 Financial Results
For the three months
ended December 31, 2018, Synlogic reported a consolidated net loss of
$11.9 million, or $0.47 per share, compared to a net loss of $11.7
million, or $0.74 per share, for the corresponding period in 2017.
Research and development expenses were $8.9 million for the three months ended December 31, 2018 compared to $7.7 million for the corresponding period in 2017. The increase was primarily due to an increase in compensation-related expenses associated with increased headcount and increases in expenses related to the lease of a larger facility at 301 Binney Street in Cambridge, Massachusetts, which Synlogic occupied in January 2018.
General and administrative expenses for the three months ended December 31, 2018 were $4.0 million compared to $4.3 million for the corresponding period in 2017. The decrease was primarily due to decreases in professional fees such as audit, legal and tax services, partially offset by increases in compensation-related expenses associated with increased headcount and increases in expenses related to the lease of Synlogic’s facility at 301 Binney Street.
Revenue was $0.1 million for the three months ended December 31, 2018 and December 31, 2017. Revenue is associated with the payments received for services performed under the Synlogic’s collaboration with AbbVie to develop a Synthetic Biotic medicine for the treatment of IBD.
As of December 31, 2018, Synlogic had cash, cash equivalents, and short-term investments of $122.7 million.
Full Year 2018 Financial Results
For the year ended December
31, 2018, consolidated net loss was $48.4 million, or $2.03 per share,
compared to a consolidated net loss of $40.4 million, or $6.00 per
share, for the year ended December 31, 2017. Revenues were $2.5 million
for the year ended December 31, 2018, compared to $2.4 million for the
same period in 2017. Total operating expenses were $53.8 million for the
year ended December 31, 2018, compared to $43.3 million for the same
period in 2017. The increase in operating expenses was primarily due to
compensation-related expenses associated with increased headcount,
increased expenses related to the lease of Synlogic’s facility at 301
Binney Street and increased external costs associated with development
of Synlogic’s Synthetic Biotic programs, including process and
formulation development, pre-clinical and clinical studies.
Conference Call & Webcast Information
Synlogic will host
a conference call and live webcast today at 8:00 a.m. ET today, Tuesday,
March 12, 2019. To access the live webcast, please visit the “Event
Calendar” page within the Investors
and Media section of the Synlogic website. Alternatively, investors
may listen to the call by dialing +1 (844) 815-2882 from locations in
the United States or +1 (213) 660-0926 from outside the United States.
The conference ID number is 2181868. For those unable to participate in
the conference call or webcast, a replay will be available for 30 days
on the Investors and Media section of the Synlogic website.
About Synlogic
Synlogic is pioneering the development of a
novel class of living medicines, Synthetic Biotic medicines, based on
its proprietary drug development platform. Synlogic leverages the tools
and principles of synthetic biology to genetically engineer beneficial
microbes to perform or deliver critical functions missing or damaged due
to disease. Synthetic Biotic medicines are designed to act locally and
have a systemic effect to address disease in patients. Synlogic’s two
lead programs, SYNB1020 and SYNB1618, are orally administered and target
hyperammonemia as a result of liver damage or genetic disease, and
phenylketonuria, respectively. Synlogic is also developing SYNB1891 as
an intratumorally-administered Synthetic Biotic medicine for the
treatment of cancer. In addition, the company is leveraging the broad
potential of its platform to create additional Synthetic Biotic
medicines for the treatment of liver disease, as well as inflammatory
and immune disorders including Synlogic’s collaboration with AbbVie to
develop Synthetic Biotic-based treatments for inflammatory bowel disease
(IBD). For more information, please visit www.synlogictx.com.
Forward-Looking Statements
This press release contains
“forward-looking statements” that involve substantial risks and
uncertainties for purposes of the safe harbor provided by the Private
Securities Litigation Reform Act of 1995. All statements, other than
statements of historical facts, included in this press release regarding
strategy, future operations, future financial position, future revenue,
projected expenses, prospects, plans and objectives of management are
forward-looking statements. In addition, when or if used in this press
release, the words “may,” “could,” “should,” “anticipate,” “believe,”
“estimate,” “expect,” “intend,” “plan,” “predict” and similar
expressions and their variants, as they relate to Synlogic may identify
forward-looking statements. Examples of forward-looking statements,
include, but are not limited to, statements regarding the potential of
Synlogic’s platform to develop therapeutics to address a wide range of
diseases, including: cancer, rare metabolic diseases, liver disease, and
inflammatory and immune disorders; the future clinical development of
Synthetic Biotic medicines; the approach Synlogic is taking to discover
and develop novel therapeutics using synthetic biology; the potential of
Synlogic’s technology to treat cancer, hyperammonemia, and
phenylketonuria; and Synlogic’s ability to develop and manufacture
Synthetic Biotic formulations. Actual results could differ materially
from those contained in any forward-looking statement as a result of
various factors, including: the uncertainties inherent in the
preclinical and clinical development process; the ability of Synlogic to
protect its intellectual property rights; and legislative, regulatory,
political and economic developments, as well as those risks identified
under the heading “Risk Factors” in Synlogic’s filings with the SEC. The
forward-looking statements contained in this press release reflect
Synlogic’s current views with respect to future events. Synlogic
anticipates that subsequent events and developments will cause its views
to change. However, while Synlogic may elect to update these
forward-looking statements in the future, Synlogic specifically
disclaims any obligation to do so. These forward-looking statements
should not be relied upon as representing Synlogic’s view as of any date
subsequent to the date hereof.
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Condensed Consolidated Statements of Operations |
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| (unaudited) | ||||||||||||||||||||
| (in thousands except share and per share data) | For the three months ended | For the year ended | ||||||||||||||||||
| December 31, 2018 | December 31, 2017 | December 31, 2018 | December 31, 2017 | |||||||||||||||||
| � | ||||||||||||||||||||
| Revenue | $ | 111 | $ | 111 | $ | 2,520 | $ | 2,444 | ||||||||||||
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| Operating expenses | ||||||||||||||||||||
| Research and development | 8,867 | 7,736 | 38,034 | 30,341 | ||||||||||||||||
| General and administrative | � | 3,952 | � | � | 4,293 | � | � | 15,716 | � | � | 12,927 | � | ||||||||
| Total operating expenses | � | 12,819 | � | � | 12,029 | � | � | 53,750 | � | � | 43,268 | � | ||||||||
| Loss from operation | (12,708 | ) | (11,918 | ) | (51,230 | ) | (40,824 | ) | ||||||||||||
| Other income(expense), net | � | 777 | � | � | 221 | � | � | 2,795 | � | � | 447 | � | ||||||||
| Net loss | $ | (11,931 | ) | $ | (11,697 | ) | $ | (48,435 | ) | $ | (40,377 | ) | ||||||||
| � | ||||||||||||||||||||
| Net loss per share attributable to common shareholders - basic and diluted | $ | (0.47 | ) | $ | (0.74 | ) | $ | (2.03 | ) | $ | (6.00 | ) | ||||||||
| Weighted-average common shares used in computing net loss per share attributable to common shareholders - basic and diluted | � | 25,269,396 | � | � | 15,871,223 | � | � | 23,882,685 | � | � | 6,724,641 | � | ||||||||
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Condensed Consolidated Balance Sheets Data |
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| (unaudited) | |||||||||
| (in thousands) | |||||||||
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December 31, 2018 |
December 31, 2017 |
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| Assets | |||||||||
| Cash, cash equivalents and short-term investments | $ | 122,729 | $ | 87,025 | |||||
| Fixed assets | 14,841 | 9,783 | |||||||
| Other assets | � | 2,770 | � | 2,891 | |||||
| Total assets | $ | 140,340 | $ | 99,699 | |||||
| � | |||||||||
| Liabilities and Stockholders' Equity | |||||||||
| Current liabilities | $ | 8,341 | $ | 9,027 | |||||
| Long-term liabilities | � | 7,901 | � | 5,634 | |||||
| Total liabilities | � | 16,242 | � | 14,661 | |||||
| Total stockholders' equity | � | 124,098 | � | 85,038 | |||||
| Total liabilities and stockholders' equity | $ | 140,340 | $ | 99,699 | |||||
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View source version on businesswire.com: https://www.businesswire.com/news/home/20190312005228/en/
MEDIA CONTACT:
Synlogic
Courtney Heath
Phone:
617-872-2462
Email: [email protected]
INVESTOR CONTACT:
Synlogic
Elizabeth Wolffe,
Ph.D.
Phone: 617-207-5509
Email: [email protected]
Source: Synlogic, Inc.