Current Report Filing (8-k)
October 24 2016 - 12:01PM
Edgar (US Regulatory)
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):
October 24, 2016
ADVAXIS,
INC.
(Exact
Name of Registrant as Specified in Charter)
Delaware
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000-28489
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02-0563870
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(State
or Other Jurisdiction
of Incorporation)
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(Commission
File Number)
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(IRS
Employer
Identification No.)
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305
College Road East
Princeton,
New Jersey, 08540
(Address
of Principal Executive Offices)
(609)
452-9813
(Registrant’s
telephone number, including area code)
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:
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[ ]
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Written
communications pursuant to Rule 425 under the Securities Act.
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[ ]
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Soliciting
material pursuant to Rule 14a-12 under the Exchange Act.
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Pre-commencement
communications pursuant to Rule 14d-2b under the Exchange Act.
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Pre-commencement
communications pursuant to Rule 13e-4(c) under the Exchange Act.
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Item
7.01 Regulation FD Disclosure.
A
copy of the press release of Advaxis, Inc. (the “Company”) dated October 24, 2016 relating to the announcement discussed
in Item 8.01 below is attached hereto as Exhibit 99.1.
The
information furnished pursuant to this Item 7.01, including Exhibit 99.1, shall not be deemed “filed” for purposes
of Section 18 of the Securities Exchange Act of 1934 (the “Exchange Act”) or otherwise subject to the liabilities
under that Section and shall not be deemed to be incorporated by reference into any filing of the Company under the Securities
Act of 1933 or the Exchange Act, except as shall be expressly set forth by specific reference in such filing.
Item
8.01 Other Events.
On
October 24, 2016, the Company announced results from the early closure of Study GOG-0265, a two-stage, Phase 2 study conducted
by the Gynecologic Oncology Group (now part of NRG Oncology) and supported by the Cancer Therapy Evaluation Program of the National
Cancer Institute, in patients with persistent or recurrent metastatic (squamous or non-squamous cell) carcinoma of the cervix
(“PRmCC”).
Based
on protocol defined prognostic factors of patients who enrolled in the study (n=50), a 12-month survival rate of 25 percent would
have been expected. Comparing this expected 25 percent 12-month overall survival rate to the 38 percent 12-month overall survival
rate actually observed across the total study population, treatment with axalimogene filolisbac resulted in a 52 percent increase
in the expected 12-month overall survival rate. Safety observations were predominately Grade 1, 2 and 3 infusion-related adverse
events, such as chills, fever, nausea and hypotension.
Due
to these findings, the Company believes that axalimogene filolisbac demonstrated a meaningful improvement in the 12-month overall
survival rate in this patient population. Therefore, the Company voluntarily closed the study early.
Based
on these data, the Company plans to pursue registrational opportunities in Europe in 2017.
Item
9.01. Financial Statements and Exhibits.
(d)
Exhibits.
The
following exhibit is furnished as a part of this report
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99.1
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Press
Release dated October 24, 2016.
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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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ADVAXIS,
INC.
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(Registrant)
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By:
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/s/
Daniel J. O’Connor
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Daniel
J. O’Connor
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President
and Chief Executive Officer
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Date:
October 24, 2016
INDEX
TO EXHIBITS
Exhibit
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Number
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Description
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99.1
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Press
Release dated October 24, 2016.
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