Media
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Latest Press Release
U.S. FDA Accepts Biologics License Application for Ryzneuta™
- 28 May 2021
Evive Biotech’s GMP Facility Receives Manufacture License of Pharmaceutical Products
- 7 April 2021
Evive Biotech Submits Biologics License Application to US FDA for Ryzneuta™
- 31 March 2021
Evive Biotech and Dr. Xiao Qiang Yan Form Joint Venture to Further Develop Bi-specific Antibody Platform ITab
- 10 February 2021
Evive Biotech Announces First Patient Dosed in Phase 2 Study to Evaluate the Efficacy and Safety of F-652 in Patients with Moderate to Severe COVID-19
- 2 February 2021
Mucosal Immunology Article Details IL-22’s Critical Role in Maturation of Certain Epithelial Cells
- 15 January 2021
Evive Biotech Meets Primary and Secondary Endpoints in Global Phase III Clinical Trial for Their Novel Chemotherapy-induced Neutropenia Treatment
- 7 July 2020
Evive Successfully Concludes China Phase III Clinical Trial of F-627 for Chemotherapy-induced Neutropenia
- 6 January 2020
Evive Receives Orphan-Drug Designation from the U.S. FDA for F-652 for the Treatment of Acute Graft vs Host Disease
- 22 October 2019
