Vaderis - a biotechnology company focussing on treatment of rare and Orphan Diseases caused by Vascular MalformationsVaderisVaderisVaderis

a biotechnology company focussing on treatment of rare and Orphan Diseases caused by Vascular Malformations

  • Home
  • Medical Need
  • Our Team
    • Leadership Team
      • Azmi Nabulsi
      • Tom Harris
      • Pierre Saint-Mezard
      • Maria Buckley
      • Hedvika Lazar
      • Damien Picard
    • Scientific Advisory Board
      • Dr. Hanny Al-Samkari, MD
      • Trevor Baglin
      • Prof. Joyce Bischoff
      • Dr. Elisabetta Buscarini
      • Prof. Guillaume Canaud
      • Prof. Murali Chakinala
      • Prof. Marie Faugnan, MD
      • Prof. James Gossage, MD
      • Frank Lebrin, PhD
      • Dr. J.J. (Hans-Jurgen) Mager, MD, PhD
    • Board
      • Giovanni Mariggi (Chair)
      • Nick Williams
      • Rahul Ballal
      • Luc Dochez
      • Trevor Baglin
      • Damien Picard
  • News
  • Contact Vaderis

Category Archives: Vaderis News

Vaderis   →  Vaderis News
02
Dec
Press Release October 02 2024
Date 02/12/2025
Categories Vaderis News

Vaderis Therapeutics Announces The New England Journal of Medicine Publishes Engasertib Proof-of-Concept and Long-Term Extension Results

PRESS RELEASE Vaderis Therapeutics Announces The New England Journal of Medicine Publishes Engasertib Proof-of-Concept and Lo...
Read More
Author Vaderis Therapeutics AG
17
Nov
Press Release October 02 2024
Date 17/11/2024
Categories Vaderis News

Vaderis Receives FDA Fast Track Designation for VAD044 for the Treatment of Hereditary Hemorrhagic Telangiectasia

Fast Track is an FDA process designed to facilitate the development and expedite the review of drugs to treat serious conditions and fill an unmet medical need. The FDA states the purpose of Fast Track to get important new drugs to the patient earlier.
Read More
Author Vaderis Therapeutics AG
05
Nov
Date 05/11/2024
Categories Vaderis News

Vaderis Announces Acceptance of Abstract on VAD044 Proof-of-Concept Clinical Trial

Abstract title - A Randomized, Placebo-Controlled, Multicenter Proof-of-Concept (POC) Study to Assess the Safety and Efficacy of the Novel Allosteric AKT Inhibitor, VAD044, in Adults with Hereditary Hemorrhagic Telangiectasia (HHT)
Read More
Author Vaderis Therapeutics AG
27
Aug
Press Release October 02 2024
Date 27/08/2024
Categories Vaderis News

Vaderis Announces Positive Clinical Proof-of-Concept Trial in HHT

Trial delivers positive results in first ever industry-led clinical trial in Hereditary Haemorrhagic Telangiectasia (HHT)
Read More
Author Vaderis Therapeutics AG
21
Aug
Date 21/08/2022
Categories Vaderis News

Vaderis Therapeutics AG announces Clinical Proof-of-Concept Trial in HHT

Vaderis is a biotechnology company focusing on treatment of rare and Orphan Diseases caused by Vascular Malformations
Read More
Author Vaderis Therapeutics AG

Switzerland
WSJ-350 3.05
Lichtstrasse 35
4056 Basel
info@vaderis.com

US
250 Parkway Drive
Suite 360
Lincolnshire, IL 60069
info@vaderis.com

HOME
MEDICAL NEED
LEADERSHIP TEAM
SCIENTIFIC ADVISORY BOARD
INVESTMENTS & PARTNERSHIPS
PIPELINE
NEWS
CONTACT VADERIS


Privacy


© Vaderis 2025