SPECIAL NOTE REGARDING
FORWARD-LOOKING STATEMENTS
This prospectus and the
documents incorporated by reference in this prospectus include
forward-looking statements within the meaning of Section 27A
of the Securities Act of 1933, as amended, or the Securities Act,
and Section 21E of the Exchange Act that relate to future
events or to our future operations or financial performance. Any
forward-looking statement involves known and unknown risks,
uncertainties and other factors that may cause our actual results,
levels of activity, performance or achievements to differ
materially from any future results, levels of activity, performance
or achievements expressed or implied by such forward-looking
statement. Forward-looking statements include statements, other
than statements of historical fact, about, among other
things:
•
the progress, number, scope,
cost, duration or results of our development activities,
nonclinical studies and clinical trials of odevixibat (formerly
known as A4250), elobixibat, A3384 or any of our other product
candidates or programs, such as the target indication(s) for
development or approval, the size, design, population, conduct,
cost, objective or endpoints of any clinical trial, or the timing
for initiation or completion of or availability of results from any
clinical trial (including our Phase 2 trial of elobixibat in
patients with NAFLD and NASH; PEDFIC 1, our Phase 3 clinical
trial of odevixibat in patients with PFIC; BOLD, our pivotal
clinical trial of odevixibat in patients with biliary atresia or
our planned pivotal trial of odevixibat in Alagille syndrome, or
ALGS) for submission or approval of any regulatory filing, access
to the Expanded Access Program (EAP) for odevixibat, or meetings
with regulatory authorities;
•
the potential benefits that may
be derived from any of our product candidates;
•
the timing of and our ability
to obtain and maintain regulatory approval of our existing product
candidates, any product candidates that we may develop, and any
related restrictions, limitations, or warnings in the label of any
approved product candidates;
•
any payment that EA Pharma Co.,
Ltd., or EA Pharma, may make to us or any other action or decision
that EA Pharma may make concerning elobixibat or our business
relationship;
•
the potential impacts of the
COVID-19 pandemic on our business;
•
our future operations,
financial position, revenues, costs, expenses, uses of cash,
capital requirements, our need for additional financing or the
period for which our existing cash resources will be sufficient to
meet our operating requirements; or
•
our strategies, prospects,
plans, expectations, forecasts or objectives.
Words such as, but not limited
to, “believe,” “expect,” “anticipate,” “estimate,” “forecast,”
“intend,” “may,” “plan,” “potential,” “predict,” “project,”
“targets,” “likely,” “will,” “would,” “could,” “should,”
“continue,” “scheduled” and similar expressions or phrases, or the
negative of those expressions or phrases, are intended to identify
forward-looking statements, although not all forward-looking
statements contain these identifying words. Although we believe
that we have a reasonable basis for each forward-looking statement
contained or incorporated by reference in this prospectus, we
caution you that these statements are based on our estimates and
projections of the future that are subject to known and unknown
risks and uncertainties and other important factors that may cause
our actual results, level of activity, performance, experience or
achievements to differ materially from those expressed or implied
by any forward-looking statement. Actual results, level of
activity, performance, experience or achievements may differ
materially from those expressed or implied by any forward-looking
statement as a result of various important factors, including our
critical accounting policies and risks and uncertainties relating,
among other things, to:
•
the design, size, duration and
endpoints for, and results from, PEDFIC 1, our Phase 3
clinical trial of odevixibat in patients with PFIC or our related
extension study, or any other trials that will be required to
obtain marketing approval for odevixibat to treat patients with
PFIC, biliary atresia or any other pediatric cholestatic liver
disease, for elobixibat to treat NASH, or for A3384 as a potential
treatment for gastrointestinal diseases or disorders;
•
whether favorable findings from
clinical trials of odevixibat to date, including findings in
indications other than PFIC, will be predictive of results from
future clinical trials, including the trials