Zafgen Presented Full Results of Phase 2 Clinical Trial for ZGN-1061 at the American Diabetes Association's 79th Scientific S...
10 Junio 2019 - 6:00AM
Zafgen, Inc. (Nasdaq:ZFGN), a clinical-stage biopharmaceutical
company leveraging its proprietary knowledge of MetAP2 systems
biology to develop novel therapies for patients affected by a range
of metabolic diseases, today announced that the Company presented
the full results of its Phase 2 clinical trial for ZGN-1061 in an
oral presentation at the American Diabetes Association's 79th
Scientific Sessions. Zafgen also presented a poster on data
demonstrating that treatment with ZGN-1061 improved measures of
glycemic control, including insulin sensitivity and beta-cell
function.
Zafgen previously announced positive results from its Phase 2
clinical trial conducted outside the U.S., including data for the
second cohort that included doses up to 1.8 mg, in January 2019.
The clinical trial met all of its primary objectives at the 1.8 mg
dose, which included glycemic control, or change in A1C, and safety
and tolerability. The 12-week data demonstrated that treatment with
the 1.8 mg dose of ZGN-1061 produced substantially more improvement
in A1C versus placebo than the 0.9 mg dose versus placebo.
Progressive and notable reduction in body weight also occurred in
patients treated with the 1.8 mg dose. The data showed a favorable
safety and tolerability profile for ZGN-1061, with no
treatment-related serious adverse events and no cardiovascular (CV)
safety signals observed in the trial.
The Phase 2 clinical trial also examined the effects of ZGN-1061
on other markers of glycemic control. In data presented during the
poster session, patients who participated in a mixed-meal tolerance
test demonstrated significant improvements in postprandial glucose
excursion with ZGN-1061 (p<0.001 for both the 0.9 and 1.8 mg
doses) and a trend for improvement in insulin levels from baseline
to Week 12. ZGN-1061 also demonstrated improvement in beta-cell
function and insulin sensitivity in an exploratory combined
analysis of 0.9+1.8 mg ZGN-1061 (p=0.02 and p=0.07) using a
modeling approach. These data suggest improved glycemic control
with ZGN-1061 may be driven by changes in insulin sensitivity and
beta-cell function in this population of patients with advanced
diabetes.
The poster will be available on the Company’s website.
About ZafgenZafgen (Nasdaq:ZFGN) is a
clinical-stage biopharmaceutical company leveraging its proprietary
MetAP2 biology platform to develop novel therapies for patients
affected by complex metabolic diseases. Zafgen has pioneered the
study of MetAP2 inhibitors in both common and rare metabolic
disorders. Learn more at www.zafgen.com.
Safe Harbor Statement Various statements
in this release concerning Zafgen's future expectations,
plans and prospects, including without
limitation, Zafgen's expectations regarding the
development and use of ZGN-1061 as a treatment for metabolic
diseases, nonclinical or clinical options to resolve the clinical
hold concerning ZGN-1061, and Zafgen's expectations with
respect to the timing and success of its nonclinical studies and
clinical trials of ZGN-1061 and its other product candidates, and
Zafgen’s expectations regarding the length of its cash runway, may
constitute forward-looking statements for the purposes of the safe
harbor provisions of The Private Securities Litigation Reform Act
of 1995 and other federal securities laws. Forward-looking
statements can be identified by terminology such as "anticipate,"
"believe," "could," "could increase the likelihood," "estimate,"
"expect," "intend," "is planned," "may," "should," "will," "will
enable," "would be expected," "look forward," "may provide,"
"would" or similar terms, variations of such terms or the negative
of those terms. Actual results may differ materially from those
indicated by these forward-looking statements as a result of
various important factors, including, without
limitation, Zafgen's ability to successfully demonstrate
the efficacy and safety of ZGN-1061, ZGN-1258, ZGN-1345 and its
other product candidates and to differentiate them from first
generation MetAP2 inhibitors, such as beloranib, the nonclinical
and clinical results for ZGN-1061, ZGN-1258, ZGN-1345 and its other
product candidates, which may not support further development and
marketing approval, actions of regulatory agencies, which may
affect the initiation, timing and progress of nonclinical studies
and clinical trials of its product candidates, Zafgen's
ability to successfully engage with the FDA concerning
the clinical hold on a clinical trial of ZGN-1061 and to design and
conduct a nonclinical study or clinical trial demonstrating
sufficient data to exclude cardiovascular risk to an acceptable
degree and demonstrating the risk is reasonable to type 2 diabetes
or other indications, Zafgen’s ability to overcome the full
clinical hold placed on ZGN-1061 by the FDA and obtain
regulatory approval, Zafgen’s ability to continue to evaluate
ZGN-1258 and to advance the program in nonclinical and clinical
development, Zafgen's ability to obtain, maintain and
protect its intellectual property, Zafgen's ability to
enforce its patents against infringers and defend its patent
portfolio against challenges from third parties, competition from
others developing products for similar uses, Zafgen’s ability to
manage operating expenses, Zafgen's ability to obtain
additional funding to support its business activities and establish
and maintain strategic business alliances and new business
initiatives when needed, Zafgen’s ability to attract and
retain personnel, Zafgen’s dependence on third parties for
development, manufacture, marketing, sales and distribution of
product candidates, and unexpected expenditures, as well as those
risks more fully discussed in the section entitled "Risk Factors"
in Zafgen's most recent Annual Report on Form 10-K filed
with the Securities and Exchange Commission, as well as
discussions of potential risks, uncertainties, and other important
factors in Zafgen's subsequent filings with
the Securities and Exchange Commission, including without
limitation Zafgen’s Quarterly Reports on Form 10-Q. In addition,
any forward-looking statements represent Zafgen's views
only as of today and should not be relied upon as representing its
views as of any subsequent date. Zafgen explicitly disclaims
any obligation to update any forward-looking statements, whether as
a result of new information, future events or otherwise.
Media/Investor Relations Contacts:Zafgen, Inc.
Patricia Allen Chief Financial Officer 617-648-9792
MediaKrystle GibbsTen Bridge Communications
krystle@tenbridgecommunications.com 508-479-6358
InvestorsJohn
WoolfordWestwickejohn.woolford@westwicke.com443-213-0506
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