Skip to content
  • About us
    • Our DNA
    • Board members
    • Our leadership
    • Partners
  • Pipeline
    • VTX-801 – Wilson’s disease
    • > VTX-801 in Wilson disease – GATEWAY – Phase 1/2 Clinical Trial
    • VTX-802 & VTX-803 – PFIC
    • VTX-804 – Citrullinemia Type 1
    • VTX–806 – Cerebrotendinous Xanthomatosis
  • Investors
  • News
  • Events
  • Patients & Families
    • Patient’s Stories
    • Patient advocacy
    • Patient & Families ressources
    • Compassionate Use and Expanded Access
  • Work at Vivet
Menu
  • About us
    • Our DNA
    • Board members
    • Our leadership
    • Partners
  • Pipeline
    • VTX-801 – Wilson’s disease
    • > VTX-801 in Wilson disease – GATEWAY – Phase 1/2 Clinical Trial
    • VTX-802 & VTX-803 – PFIC
    • VTX-804 – Citrullinemia Type 1
    • VTX–806 – Cerebrotendinous Xanthomatosis
  • Investors
  • News
  • Events
  • Patients & Families
    • Patient’s Stories
    • Patient advocacy
    • Patient & Families ressources
    • Compassionate Use and Expanded Access
  • Work at Vivet

Author: admin_viv3t

Vivet Therapeutics Announces 4 Presentations During the 2022 American Society Of Gene And Cell Therapy Annual Meeting

Vivet Therapeutics, a clinical-stage biotech company dedicated to developing gene therapy

Vivet presenting during 2022 ARM Meeting on the Med in Barcelona

Vivet Therapeutics BD Director, Thomas Daniel-Robin

VIVET ATTENDING 2021 WORLD ORPHAN DRUG CONGRESS EUROPE IN BARCELONA

Vivet Therapeutics CEO, Jean-Philippe Combal, will be participating to a panel during 2021 World Orphan Drug Congress Europe in Barcelona (Nov 15-18).

Vivet Therapeutics awarded with the Prix Galien MedStartup in New York

Vivet Therapeutics is very pleased and proud to have won the Prix Galien MedStartup Award for “Best Collaboration For the Developing Or Underserved Populations Worldwide”.

VIVET THERAPEUTICS ANNOUNCES 2 ORAL PRESENTATIONS AND 4 ABSTRACTS AT 2021 ESGCT ANNUAL MEETING

VIVET THERAPEUTICS ANNOUNCES 2 ORAL PRESENTATIONS AND 4 ABSTRACTS AT 2021 ESGCT ANNUAL MEETING

Vivet CDO, Anne Douar, presenting during SFTCG webinar on Gene Therapy for Wilson Disease

Vivet CDO, Anne Douar, will be presenting

GATEWAY clinical trial for Wilson Disease has now its website

Wilson Disease is a rare, progressive genetic disorder that causes excess copper to be stored in the body.

VTX‐801 Receives U.S. FDA Fast Track Designation for the Treatment of Wilson Disease

VTX-801 Receives U.S. FDA Fast Track Designation for the Treatment of Wilson Disease

Gene Therapy aims to be a one-time treatment that may stop or slow the progression of Wilson disease

Learn how  gene therapy aims to target the cause of  Wilson disease by delivering a working ATP7B gene into cells. ClinicalTrials are now open for this investigational therapy.

Congratulations to all Women in Gene Therapy and to Dr. Gloria González-Aseguinolaza our CSO @Vivet Therapeutics!

Congratulations to all Women in Gene Therapy and to Dr. Gloria González-Aseguinolaza our CSO @Vivet Therapeutics!

Next →
Twitter Linkedin
About us
  • Our DNA
  • Board members
  • Our leadership
  • Partners
  • Our DNA
  • Board members
  • Our leadership
  • Partners
Pipeline
  • VTX-801 – Wilson’s disease
  • > VTX-801 in Wilson disease – GATEWAY
  • VTX-802 & VTX-803 – PFIC
  • VTX-804 – Citrullinemia Type 1
  • VTX – 806 – Cerebrotendinous Xanthomatosis
  • VTX-801 – Wilson’s disease
  • > VTX-801 in Wilson disease – GATEWAY
  • VTX-802 & VTX-803 – PFIC
  • VTX-804 – Citrullinemia Type 1
  • VTX – 806 – Cerebrotendinous Xanthomatosis
Patients & Families
  • Patient stories
  • Patient advocacy
  • Patient & Families ressources
  • Compassionate Use and Expanded Access
  • Patient stories
  • Patient advocacy
  • Patient & Families ressources
  • Compassionate Use and Expanded Access
  • News
  • Events
  • Investors
  • Work at Vivet
  • Contact
  • News
  • Events
  • Investors
  • Work at Vivet
  • Contact

Vivet Therapeutics Cookie Policy