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Ventaleon GmbH

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DGAP-News News vom 07.06.2017

Ventaleon presents Phase II results with inhaled LASAG in severe influenza at ISAM Congress 2017

DGAP-News: Ventaleon GmbH / Key word(s): Study/Study results

07.06.2017 / 10:00
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Press Release

Ventaleon presents Phase II results with inhaled LASAG in severe influenza at ISAM Congress 2017

  • Study evaluated efficacy and safety of inhaled LASAG for treatment of severe influenza in hospitalized patients compared to standard of care treatment alone
  • Significant reduction in time to alleviation of symptoms and of clinical signs
  • No significant safety differences between LASAG and placebo

Gemuenden, Germany, 07 June, 2017 - Ventaleon GmbH, a biotechnology company focusing on the development of inhaled treatments against viral infections, today presented data from its Phase II trial with inhaled LASAG (D,L-lysine acetylsalicylate‧glycine) in severe influenza at the 21st Congress of the International Society for Aerosols in Medicine (ISAM) being held in Santa Fe, NM, USA. LASAG, a compound with a novel antiviral mode of action, has been shown to inhibit the signaling factor NF-KB that is essential for the replication of influenza viruses. This is believed to be the first time that a host-cell signalling inhibitor with an off-virus effect demonstrated efficacy as an antiviral drug.

Prof. Dr. Oliver Planz, Head of the group "Translational Immunology of Infection" in the Department of Immunology of University of Tuebingen, Germany., and co-author of the study, said: "Therapeutic intervention strategies against severe, hospitalized influenza are limited. The data presented at ISAM support that inhaled LASAG in addition to standard of care has the potential to significantly reduce time to alleviation of symptoms in hospitalized patients with severe influenza. I look forward to this treatment being evaluated in larger clinical studies."

"We are excited with the results presented for inhaled LASAG in patients with severe influenza, as they clearly support advancing this program in development," said Dr. Ulrich Dauer, CEO of Ventaleon. "We just initiated a Phase Ib challenge study to show the causal effect of LASAG inhalation on the influenza virus, which is an important step in preparing for pivotal trials."

The randomized, double-blind, placebo-controlled Phase II clinical trial evaluated aerosolized LASAG compared to placebo for the treatment of severe influenza (as shown by composite symptom scores (CSS) >=14). In addition to standard of care treatment, inhaled LASAG or placebo were administered three times daily in adult hospitalized patients with acute serious influenza. A total of 41 patients (LASAG: n=24; placebo: n=17) completed the study per protocol.

The primary endpoint of the study was time to alleviation of clinical influenza symptoms. The LASAG group showed significantly reduced time to alleviation of symptoms compared to placebo (38.3 hrs vs. 56.2 hrs; Satterthwaite t-test p=0.0365). The secondary endpoint of alleviation of clinical signs (including body temperature and oxygen saturation) was also significantly improved in the LASAG group compared to placebo (24.9 hrs vs. 44.1 hrs; one-sided t-test p=0.00246).

LASAG was generally well tolerated with no significant safety differences between the LASAG and placebo groups. Based on the data of this Phase II study together with results from the ongoing Phase Ib challenge trial expected towards year end, Ventaleon will define its pivotal development strategy for this first in class product candidate for severe hospitalized influenza and explore the potential to extend the inhaled LASAG therapy to a broader patient base suffering from viral infections.

For further information, please contact:

Ventaleon GmbH
Dr. Ulrich Dauer, CEO
Tel.: +49-6453-58530-40

Media Inquiries
MC Services AG
Katja Arnold, Dr. Brigitte Keller
Tel: +49 89 21022 0

About Ventaleon GmbH:

Ventaleon GmbH is a biotechnology company focused on the development of inhaled treatments against viral infections. The Company's lead therapy candidate is an inhaled form of LASAG (D,L-lysine acetylsalicylate * glycine), which it is developing to treat severe influenza. A proof-of-concept study in influenza patients with moderate to severe symptoms demonstrated more rapid symptom decline when administered inhaled LASAG compared to standard of care. The Company is currently preparing to enter a pivotal clinical trial with inhaled LASAG. Ventaleon was founded as a spin-off from Activaero and is supported by a group of leading international investors, including Coöperatief LSP U.A,, BioMedInvest II LP, Abalis Finance AG, Vesalius Biocapital I S.A., Venture Incubator AG, CatheyWorldInvestment Ltd. and BayBg.

07.06.2017 Dissemination of a Corporate News, transmitted by DGAP - a service of EQS Group AG.
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