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UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 8-K
CURRENT REPORT
PURSUANT TO SECTION 13 OR 15(d)
OF THE SECURITIES EXCHANGE ACT OF 1934
Date of Report (Date of earliest event reported):
November 11, 2024
NOVAVAX, INC.
(Exact name of registrant as specified
in charter)
Delaware |
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0-26770 |
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22-2816046 |
(State or Other Jurisdiction
of Incorporation) |
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(Commission File Number) |
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(I.R.S. Employer
Identification No.) |
700 Quince Orchard Road
Gaithersburg, Maryland 20878
(Address of Principal Executive Offices,
including Zip Code)
(240) 268-2000
(Registrant’s telephone number,
including area code)
(Former name or former address, if changed since
last report.)
Check the appropriate box below if the Form 8-K
filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General
Instruction A.2. below):
¨ |
Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
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¨ |
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
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¨ |
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
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¨ |
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities registered pursuant to Section
12(b) of the Act:
Title of each class |
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Trading
Symbol(s) |
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Name of each exchange on which
registered |
Common Stock, Par Value $0.01 per share |
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NVAX |
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The Nasdaq Global Select Market |
Indicate by check mark whether the registrant
is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2
of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging
growth company ¨
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ¨
Item 7.01. Regulation FD
Disclosure.
On November 11, 2024, Novavax,
Inc. (“Novavax”) issued the press release furnished as Exhibit 99.1 to this Current Report on Form 8-K and incorporated herein
by reference.
The information in Item 7.01
is being furnished and shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934,
as amended, or otherwise subject to the liabilities of that Section and shall not be deemed incorporated by reference into any registration
statement or other document filed pursuant to the Securities Act of 1933, as amended, or the Securities Exchange Act of 1934, as amended,
except as shall be expressly set forth by specific reference in such filing. In addition, the contents of Novavax’s website are
not incorporated by reference into this Current Report on Form 8-K and you should not consider information provided on Novavax’s
website to be part of this Current Report on Form 8-K.
Item 8.01. Other Events.
On
October 16, 2024, Novavax disclosed that the U.S. Food and Drug Administration (“FDA”) had placed a clinical hold on
Novavax’s Investigational New Drug Application (“IND”) for its COVID-19-Influenza Combination and stand-alone
influenza vaccine candidates. On November 11, 2024, Novavax announced that the FDA has removed the previously disclosed clinical
hold on Novavax’s IND for its COVID-19-Influenza Combination and stand-alone influenza vaccine candidates.
Item
9.01. Financial Statements and Exhibits.
(d) Exhibits.
SIGNATURES
Pursuant to the requirements
of the Securities Exchange Act of 1934, the Registrant has duly caused this report to be signed on its behalf by the undersigned hereunto
duly authorized.
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Novavax, Inc. |
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Date: November 11, 2024 |
By: |
/s/ Mark J. Casey |
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Name: |
Mark J. Casey |
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Title: |
Executive Vice President, Chief Legal Officer and
Corporate Secretary |
Exhibit
99.1
Press Release |
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U.S.
FDA Removes Clinical Hold on Novavax’s COVID-19-Influenza Combination and Stand-alone Influenza Phase 3 Trial
GAITHERSBURG,
Md., November 11, 2024 – Novavax, Inc. (Nasdaq: NVAX), a global company advancing protein-based vaccines with its Matrix-M™
adjuvant, today announced that the U.S. Food and Drug Administration (FDA) has removed the clinical hold on Novavax’s Investigational
New Drug (IND) application for its COVID-19-Influenza Combination (CIC) and stand-alone influenza vaccine candidates. The FDA has cleared
the Company to begin enrolling the planned Phase 3 trial following the determination that Novavax satisfactorily addressed all clinical
hold issues. Novavax will be working with the clinical trial investigators and other partners to resume trial activities as quickly as
possible.
“We
thank the FDA for their partnership and thorough review of the additional information provided as part of our response package,”
said Robert Walker, MD, Chief Medical Officer, Novavax. “The information provided to the FDA confirmed the severe adverse event
was not related to our vaccine. We plan to start our Phase 3 trial as soon as possible."
The
clinical hold announced on October 16, 2024, resulted from a spontaneous report of a serious adverse event in a participant who received
investigational CIC vaccine in a Phase 2 trial that completed in 2023. The FDA had requested additional information on this event, initially
reported as motor neuropathy. The additional information included a change in the event term to amytrophic lateral sclerosis, a condition
that is not known to be immune-mediated or associated with vaccination, which in this event was assessed as not related to vaccination.
About
Novavax
Novavax,
Inc. (Nasdaq: NVAX) promotes improved health by discovering, developing and commercializing innovative vaccines to help protect against
serious infectious diseases. Novavax, a global company based in Gaithersburg, Md., U.S., offers a differentiated vaccine platform that
combines a recombinant protein approach, innovative nanoparticle technology and Novavax's patented Matrix-M adjuvant to enhance the immune
response. The Company's portfolio includes its COVID-19 vaccine and its pipeline includes its CIC and stand-alone influenza vaccine candidates.
In addition, Novavax's adjuvant is included in the University of Oxford and Serum Institute of India's R21/Matrix-M malaria vaccine.
Please visit novavax.com and LinkedIn for more information.
Forward-Looking
Statements
Statements
herein relating to the timing of the initiation of the Phase 3 trial for Novavax’s CIC and stand-alone influenza vaccine candidates
are forward-looking statements. Novavax cautions that these forward-looking statements are subject to numerous risks and uncertainties
that could cause actual results to differ materially from those expressed or implied by such statements. These risks and uncertainties
include, without limitation, challenges satisfying, alone or together with partners, various safety, efficacy and product characterization
requirements, including those related to process qualification and assay validation, necessary to satisfy applicable regulatory authorities;
resource constraints, including human capital and manufacturing capacity, on the ability of Novavax to pursue planned regulatory pathways;
challenges or delays in clinical trials, including the enrolment of trial participants; manufacturing, distribution or export delays
or challenges; Novavax's exclusive dependence on Serum Institute of India Pvt. Ltd. for co-formulation and filling and the impact of
any delays or disruptions in their operations on the delivery of customer orders; and those other risk factors identified in the "Risk
Factors" and "Management's Discussion and Analysis of Financial Condition and Results of Operations" sections of Novavax's
Annual Report on Form 10-K for the year ended December 31, 2023, and subsequent Quarterly Reports on Form 10-Q, as filed with the Securities
and Exchange Commission (SEC). We caution investors not to place considerable reliance on forward-looking statements contained in this
press release. You are encouraged to read our filings with the SEC, available at www.sec.gov and www.novavax.com, for a
discussion of these and other risks and uncertainties. The forward-looking statements in this press release speak only as of the date
of this document, and we undertake no obligation to update or revise any of the statements. Our business is subject to substantial risks
and uncertainties, including those referenced above. Investors, potential investors, and others should give careful consideration to
these risks and uncertainties.
Contacts:
Investors
Luis
Sanay, CFA
240-268-2022
ir@novavax.com
Media
Giovanna
Chandler
240-720-7804
media@novavax.com
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