DGAP-News: MOLOGEN AG: MOLOGEN AG: Extension of TEACH study based on supportive first study results

DGAP-News: MOLOGEN AG / Key word(s): Study/Conference
MOLOGEN AG: MOLOGEN AG: Extension of TEACH study based on supportive first
study results

14.03.2016 / 08:30
The issuer is solely responsible for the content of this announcement.

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PRESS RELEASE N 4/ 2016 of 03/14/2016

MOLOGEN AG: Extension of TEACH study based on supportive first study
results

Berlin, 14 March 2016 – The biotech company MOLOGEN AG (ISIN DE0006637200;
Frankfurt Stock Exchange Prime Standard: MGN) announced today that the
TEACH study with its immunomodulatory lefitolimod (MGN1703) in HIV patients
will be extended as a result of the broad immune system activation induced
by the drug. This was shown by the increased activation of various immune
markers. In conclusion and consistent with the underlying hypothesis,
lefitolimod (MGN1703) dosing led to the activation of plasmacytoid
dendritic cells (pDC), natural killer cells (NK) and T cells in HIV
patients during the antiretroviral therapy (ART). Thus, lefitolimod
(MGN1703) could serve as a robust immune stimulator or “kill” agent in
“kick and kill” HIV eradication trials. Initially patients received one
month of treatment and now the protocol has been amended to give a longer
treatment of six months with lefitolimod (MGN1703) in some more patients.
Recruitment of these patients is expected in the next few weeks and final
study results will now be available in the first half of 2017.

“We are excitedly following the developments of lefitolimod in HIV. The
strong enhancement of antiviral immune responses observed after a short
course of treatment gives us the rationale to extend the study, also at the
light of the very good safety profile of the drug,” said Ole Schmeltz
Søgaard, MD, PhD, Associate Professor at the Aarhus University Hospital,
Dept. of Infectious Diseases, Aarhus, Denmark.

“We have always believed that the immunomodulator lefitolimod could also
play a role in infective diseases. We look forward to the results in HIV
patients treated for a longer period of time with great interest,” said Dr.
Alfredo Zurlo, Chief Medical Officer of MOLOGEN AG.

The aim of the TEACH study is to see if the immunotherapy with MGN1703 can
activate the innate and adaptive immune system in HIV patients, to enhance
killing of the HIV infected cells.

Initial results of the first patients treated in the trial will be
presented at the Keystone HIV Symposia (Keystone Symposia on molecular and
cellular biology conference) from 20 – 24 March 2016 in Olympic Valley,
USA.

Abstract & Poster details:
Abstract title: “Toll-like receptor 9 enhancement of antiviral immunity in
chronic HIV-1 infection (TEACH)”

Poster:
Presentation: 24 March 2016, Poster session 4
Poster #: 4025
Poster Title: “Toll-like receptor 9 enhancement of antiviral immunity in
chronic HIV-1 infection (TEACH)”

For more information on the Keystone conference please visit:
http://www.keystonesymposia.org/

Furthermore, a publication is now available in the prestigious Journal of
Virology:
http://jvi.asm.org/search?fulltext=doi%3A10.1128%2FJVI.00222-16&submit=yes
&x=0&y=0

About TEACH
TEACH (Toll-like receptor 9 enhancement of antiviral immunity in chronic
HIV infection) is a non-randomized interventional phase I/IIa trial of
lefitolimod (MGN1703) in HIV-infected patients. In the first phase of the
study, 15 participants received four weeks of lefitolimod (MGN1703) therapy
(60 mg s.c. twice weekly). The extension phase will include 10-11 more
patients who will be treated for six months with lefitolimod. During the
treatment period, each participant will be closely monitored for the safety
and therapeutic effects of the drug. Aarhus University Hospital, Aarhus,
Denmark is conducting the trial in two hospital centers in Denmark and
already received funding from the American Foundation for AIDS research
(amfAR). MOLOGEN is providing the immunomodulator lefitolimod (MGN1703).

The primary endpoint of the study is the change in proportions of activated
natural killer cells in the patients. Secondary study endpoints include,
among others, a collection of safety, virological, immunological and
pharmacodynamic data.

HIV infects the immune system and destroys or affects the proper function
of immune cells. Without antiretroviral treatment this eventually leads to
immune deficiency and the immune system can no longer fight off a wide
range of infections and diseases. HIV remains a serious worldwide health
issue. According to estimates by WHO and UNAIDS (United Nations Programme
on AIDS) 37 million people worldwide were living with HIV at the end of
2014. Some 2 million people became newly infected in that same year, and
1.2 million died as a result of HIV-related causes globally.

MOLOGEN AG
With new and unique technologies and active substances, the biotech company
MOLOGEN is one of the pioneers in the field of immunotherapy. Alongside a
focus on immuno-oncology, MOLOGEN also develops immunotherapies for the
treatment of infectious diseases.

The cancer immunotherapy lefitolimod (MGN1703) is the company’s lead
product and best-in-class TLR9 agonist. Treatment with lefitolimod
(MGN1703) triggers a broad and strong activation of the immune system. Due
to this mechanism of action, lefitolimod (MGN1703) has the potential to be
applied to various indications. Lefitolimod (MGN1703) is currently being
developed for first-line maintenance treatment of colorectal cancer
(pivotal study) and small cell lung cancer (randomized controlled trial).
Furthermore, it is also being investigated in a phase I study in HIV and a
phase I combination study with the checkpoint inhibitor Yervoy(R)
(ipilimumab) is expected to start within the first half 2016.

MOLOGEN’s pipeline focus is on new innovative immunotherapies to treat
diseases for which there is a high medical need.

www.mologen.com

Memberships in associations:
Biotechnologieverbund Berlin-Brandenburg (bbb) e.V. | BIO Deutschland e.V.
| DECHEMA – Society for chemical technology and biotechnology e.V. |
German industrial association of biotechnology (DIB) | Association for
the Promotion of Science and Humanities in Germany | Association of
German biotechnology companies (VBU) | Association of researching
manufacturers of pharmaceuticals e.V. (VFA) | Association of the chemical
industry e.V. (VCI)

MIDGE(R), dSLIM(R), EnanDIM(R) and MOLOGEN(R) are registered trademarks of
MOLOGEN AG.
Contact
Claudia Nickolaus
Head of Investor Relations & Corporate Communications
Tel: +49 – 30 – 84 17 88 – 38
Fax: +49 – 30 – 84 17 88 – 50
investor@mologen.com

Note about risk for future predictions
Certain information in this report contains forward-looking statements or
the corresponding statements with negation or versions deviating from this
or comparable terminology. These are described as forward-looking
statements. In addition, all of the information given here that refers to
planned or future results of business areas, key financial figures,
developments of the financial situation or other financial figures or
statistical data, is to be understood as such forward-looking statements.
The company points out to investors that they should not rely on these
forward-looking statements as predictions about actual future events. The
company is not obligated and refuses to accept any liability for the
forward-looking statements and has no obligation to update such statements
in order to accurately reflect the current situation.

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14.03.2016 Dissemination of a Corporate News, transmitted by DGAP – a
service of EQS Group AG.
The issuer is solely responsible for the content of this announcement.

The DGAP Distribution Services include Regulatory Announcements,
Financial/Corporate News and Press Releases.
Media archive at www.dgap-medientreff.de and www.dgap.de

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Language: English
Company: MOLOGEN AG
Fabeckstraße 30
14195 Berlin
Germany
Phone: 030 / 841788-0
Fax: 030 / 841788-50
E-mail: presse@mologen.com
Internet: www.mologen.com
ISIN: DE0006637200
WKN: 663720
Listed: Regulated Market in Frankfurt (Prime Standard); Regulated
Unofficial Market in Berlin, Dusseldorf, Hamburg, Munich,
Stuttgart

End of News DGAP News Service
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444677 14.03.2016

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