Histogenics and FDA Conclude Discussions Regarding NeoCart® Phase 3 Clinical Trial Data and Regulatory Pathway
December 21 2018 - 4:05PM
Histogenics Corporation (Histogenics) (Nasdaq: HSGX), today
provided an update on the NeoCart regulatory pathway based on
discussions with the U.S. Food and Drug Administration (the
FDA). Based on the feedback received from the FDA, while the
NeoCart Phase 3 clinical trial resulted in certain compelling data,
the FDA indicated that an additional clinical trial would need to
be completed before it would accept a submission of a Biologics
License Application (BLA) for NeoCart. The FDA indicated
receptivity to novel clinical trial methodologies and regenerative
medicine advanced therapy designations in order to support
additional data for a future potential submission. However,
considering the time and funding required to conduct such a trial,
Histogenics expects to suspend the development of NeoCart and does
not plan to submit a BLA at this time.
In connection with this outcome, Histogenics
intends to implement a restructuring plan to reduce costs and has
engaged Canaccord Genuity LLC to evaluate the full range of
potential strategic alternatives to maximize value for
stakeholders, which includes, but is not limited to, acquisitions,
business combinations, joint ventures, public and private capital
raises, recapitalization, and sale transaction options, including a
sale of assets or intellectual property. Since these efforts
may not be successful and in light of its limited cash reserves
Histogenics is considering all possible alternatives, including
restructuring activities, a wind-down of operations, or seek
chapter 11 bankruptcy protection to complete or execute a
restructuring transaction or liquidation.
Histogenics has also determined not to proceed
at this time with its earlier plans to conduct a stockholder
meeting to increase its authorized shares and a reverse split, for
which it had filed a preliminary proxy statement with the
Securities Exchange Commission (the SEC) on October 18, 2018.
About Histogenics
Corporation
Histogenics (Nasdaq: HSGX) develops
restorative cell therapies that may offer rapid-onset pain relief
and restored function. Histogenics’ technology platform has
the potential to be used for a broad range of restorative cell
therapy indications. For more information on Histogenics and
NeoCart, please visit www.histogenics.com.
Forward-Looking Statements
Various statements in this release are
“forward-looking statements” under the securities laws. Words
such as, but not limited to, “anticipate,” “believe,” “can,”
“could,” “expect,” “estimate,” “design,” “goal,” “intend,” “may,”
“might,” “objective,” “plan,” “predict,” “project,” “target,”
“likely,” “should,” “will,” and “would,” or the negative of these
terms and similar expressions or words, identify forward-looking
statements. Forward-looking statements are based upon current
expectations that involve risks, changes in circumstances,
assumptions and uncertainties.
Important factors that could cause actual
results to differ materially from those reflected in Histogenics’
forward-looking statements include, among others: statements
regarding the future business operations of the Company; the
prospect for the successful sale of the Company or of any of the
Company’s assets; the possibility of a liquidating distribution to
Company stockholders; the ability of the Company to pay its
creditors and successfully complete an orderly wind down; and other
factors that are described in the “Risk Factors” and “Management’s
Discussion and Analysis of Financial Condition and Results of
Operations” sections of Histogenics’ Annual Report on Form 10-K for
the year ended December 31, 2017 and Quarterly Report on Form 10-Q
for the quarter ended September 30, 2018, which are on file with
the SEC and available on the SEC’s website at www.sec.gov. In
addition to the risks described above and in Histogenics’ Annual
Report on Form 10-K and Quarterly Reports on Form 10-Q, Current
Reports on Form 8-K and other filings with the SEC, other unknown
or unpredictable factors also could affect Histogenics’
results.
There can be no assurance that the actual
results or developments anticipated by Histogenics will be realized
or, even if substantially realized, that they will have the
expected consequences to, or effects on, Histogenics.
Therefore, no assurance can be given that the outcomes stated in
such forward-looking statements and estimates will be achieved.
All written and verbal forward-looking
statements attributable to Histogenics or any person acting on its
behalf are expressly qualified in their entirety by the cautionary
statements contained or referred to herein. Histogenics
cautions investors not to rely too heavily on the forward-looking
statements Histogenics makes or that are made on its behalf.
The information in this release is provided only as of the date of
this release, and Histogenics undertakes no obligation, and
specifically declines any obligation, to update or revise publicly
any forward-looking statements, whether as a result of new
information, future events or otherwise.
Contacts:
Investor Relations:
Tel: +1 (781) 547-7909
InvestorRelations@histogenics.com
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