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08.08.2017 17:56:32

DGAP-Ad hoc: MOLOGEN AG

DGAP-Adhoc: MOLOGEN AG: Results of the extension phase of the exploratory phase Ib/IIa study in HIV

DGAP-Ad-hoc: MOLOGEN AG / Key word(s): Study results
MOLOGEN AG: Results of the extension phase of the exploratory phase Ib/IIa study in HIV

08-Aug-2017 / 17:56 CET/CEST
Disclosure of an inside information acc. to Article 17 MAR, transmitted by DGAP - a service of EQS Group AG.
The issuer is solely responsible for the content of this announcement.


Insider information pursuant to Section 17 MAR

MOLOGEN AG: Results of the extension phase of the exploratory phase Ib/IIa study in HIV

Berlin, 8 August 2017 - The biopharmaceutical company MOLOGEN AG (ISIN DE0006637200; Frankfurt Stock Exchange Prime Standard: MGN) presents key results of the extension phase of the exploratory phase Ib/IIa TEACH trial, a cooperation with the Aarhus University Hospital in Denmark. The study was designed to evaluate the Company's lead product, the immunotherapeutic agent lefitolimod, in HIV-positive patients on antiretroviral therapy (ART). The main study results are as follows:

- Sustained increases in activation of important immune cells (CD4 and CD8 T cells) were observed throughout the dosing period of 24 weeks.

- Lefitolimod triggered maturation of other important immune cells (B cells) towards antibody-producing cells.

- After interruption of ART, one of the nine patients who participated in that study part showed viral control for more than 20 weeks, whereas the interval until viral rebound is generally two weeks.

- The intervention had no detectable effects on the size of viral reservoir in peripheral blood in the total study population of 12 patients, which was defined as the primary endpoint of the extension phase of the study.

- 24 weeks of lefitolimod treatment was safe and well tolerated in HIV patients on ART, corroborating the favourable safety profile already seen in cancer patients.

In summary these data suggest - although lefitolimod alone on top of ART did not show the desired effect on the viral reservoir - lefitolimod could be an important combination partner for other interventions aiming at HIV cure, such as monoclonal antibodies or vaccines.
A more extensive evaluation of the TEACH data is currently ongoing including further immune and HIV reservoir parameters.

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.


08-Aug-2017 CET/CEST The DGAP Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases.
Archive at www.dgap.de


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, Tradegate Exchange

 
End of Announcement DGAP News Service

599813  08-Aug-2017 CET/CEST

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