Biotech company Alvotech S.A. (NASDAQ:ALVO) announced on Wednesday that it has initiated a confirmatory patient study for AVT16, a biosimilar candidate to Entyvio (vedolizumab).
The study aims to demonstrate comparative efficacy, safety and immunogenicity of AVT16 and Entyvio in patients with moderate to severe active ulcerative colitis.
Entyvio is indicated for the treatment of ulcerative colitis and Crohn's disease. With global sales of approximately USD5.4bn in the past 12 months, Entyvio is a significant market opportunity for biosimilars.
The AVT16-GL-C01 multicentre study will compare AVT16 to Entyvio in a double-blind parallel design. Participants will be followed to assess disease activity using a standardised score.
Alvotech's biosimilars portfolio targets various therapeutic areas, including autoimmune diseases, eye disorders, bone disease, respiratory disease and cancer. With two approved biosimilars and three additional candidates in development, Alvotech is expanding its presence in the biosimilars market.
Nutshell Therapeutics' NTS071 p53 allosteric reactivator cleared for US clinical trial
Innovent's limertinib receives Chinese regulatory approval for first-line treatment of lung cancer
bioMérieux launches PCR wastewater test to support early detection of infectious disease outbreaks
Clario partners with AWS on advancing clinical data analysis with generative AI
Zynext Ventures invests in Feldan Therapeutics
Sanofi advances respiratory pipeline with positive amlitelimab data and expanded clinical programmes
Sichuan Kelun-Biotech reveals sacituzumab tirumotecan (sac-TMT) clinical studies results
Amgen's IMDELLTRA shows superior overall survival in small cell lung cancer trial
SciTech Development secures second FDA clearance for ST-001 in early-stage cancer trials
Mabwell's B7-H3-targeting ADC clinical trial application receives Chinese regulatory approval
Dupixent receives approval in Japan as first biologic for COPD treatment
Vast Therapeutics' ALX1 drug candidate granted QIDP designation by US FDA