08.08.2017 17:56:32
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DGAP-Ad hoc: MOLOGEN AG
DGAP-Ad-hoc: MOLOGEN AG / Key word(s): Study results Insider information pursuant to Section 17 MAR - 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. Contact Note about risk for future predictions
08-Aug-2017 CET/CEST The DGAP Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases. |
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 |
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599813 08-Aug-2017 CET/CEST
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