TheraRadar
Clinical-Stage Companies / Valneva Austria

Valneva Austria

Pre-Approval PRO BETA
28
Total Trials
15
Phase 3
8
Phase 2
1
Recruiting
318
Score

Pipeline by Phase

Phase 3
15
Phase 2
8
Phase 1
8

Therapeutic Focus

Chikungunya Virus Infection Japanese Encephalitis SARS-CoV-2 Virus Infection Zika Virus Infection SARS-CoV-2 Infection

Clinical Trials (28)

NCT07133178 Phase 3 WITHDRAWN

A Trial to Evaluate the Safety and Immunogenicity of VLA1553 in Healthy Children

Started: 2/6/2026

NCT04838444 Phase 3 ACTIVE NOT RECRUITING

Antibody Persistence And Long Term Safety Of A Chikungunya Virus Vaccine (VLA1553)

Started: 4/2/2021

NCT06028841 Phase 3 WITHDRAWN

A Clinical Phase 3 Trial of VLA1553 in Adult Participants with Human Immunodeficiency Virus (HIV)

Started: 4/10/2024

NCT04786444 Phase 3 COMPLETED

Study to Demonstrate Consistency of Three Lots of a Live-attenuated Chikungunya Virus Vaccine Candidate in Healthy Adults

Started: 2/22/2021

NCT04956224 Phase 3 COMPLETED

Safety and Immunogenicity of VLA2001 Adults Aged ≥56 Years

Started: 8/9/2021

NCT04546724 Phase 3 COMPLETED

Pivotal Study to Evaluate Safety and Immunogenicity of a Live-Attenuated Chikungunya Virus Vaccine Candidate in Adults

Started: 9/17/2020

NCT04864561 Phase 3 COMPLETED

COV-COMPARE Immunogenicity of Vaccine VLA2001 Compared to AZD1222

Started: 4/26/2021

NCT01041573 Phase 3 COMPLETED

Safety and Immunogenicity of the Japanese Encephalitis Vaccine IC51 (IXIARO®) in a Pediatric Population

Started: 3/1/2010

NCT01047839 Phase 3 COMPLETED

Immunogenicity and Safety of the Japanese Encephalitis Vaccine IC51 (IXIARO®, JESPECT®) in a Pediatric Population in Non-endemic Countries

Started: 1/1/2010

NCT01246479 Phase 3 COMPLETED

Long Term Immunity and Safety Following Vaccination With the JEV IC51 (IXIARO®, JESPECT®) in Pediatric Population In Non Endemic Countries. Uncontrolled, Ph3 FU-Study

Started: 10/1/2010

NCT00776230 Phase 3 COMPLETED

Immunogenicity of a Commercial Batch of JEV IC51 up to 24 Months Post Filling

Started: 9/1/2008

NCT01296360 Phase 3 COMPLETED

Open-label, Randomized Study in a Pediatric Population in a JEV (Japanese Encephalitis Virus)-Endemic Country

Started: 12/1/2010

NCT06106581 Phase 2 COMPLETED

A Phase 2 Clinical Trial of VLA1553 in Healthy Children Aged 1 to 11 Years

Started: 12/18/2023

NCT05364242 Phase 2 COMPLETED

VLA2001 Booster in Adult Participants After Priming With mRNA COVID-19 Vaccine and/or Natural SARS-CoV-2 Infection

Started: 5/9/2022

NCT05298644 Phase 2 WITHDRAWN

COVID-19 Paediatric VLA2001-321 Study

Started: 10/1/2022

NCT03576183 Phase 2 COMPLETED

Study Confirming A Human Challenge Model and Investigating The Safety Of VLA1701

Started: 6/4/2018

NCT02316470 Phase 2 COMPLETED

Dose-Confirmation, Immunogenicity and Safety Study of the Clostridium Difficile Vaccine Candidate VLA84 in Healthy Adults Aged 50 Years and Older. Phase II Study

Started: 12/1/2014

NCT01563263 Phase 2 COMPLETED

Confirmatory Phase II/III Study Assessing Efficacy, Immunogenicity and Safety of IC43

Started: 3/1/2012

NCT00876252 Phase 2 COMPLETED

Study Assessing Immunogenicity and Safety of IC43 In Intensive Care Patients

Started: 12/1/2008

NCT06334393 Phase 1 COMPLETED

Phase 1 Trial to Assess the Safety and Immunogenicity of an Inactivated, Adjuvanted Whole Zika Virus Vaccine Candidate (VLA1601) in Healthy Adults

Started: 3/25/2024

NCT04671017 Phase 1 COMPLETED

Dose Finding Study to Evaluate The Safety, Tolerability and Immunogenicity of an Inactiviated, Adjuvanted SARS-CoV-2 Virus Vaccine Candidate Against Covid-19 in Healthy Subjects

Started: 12/16/2020

NCT03382964 Phase 1 COMPLETED

Study to Assess the Safety and Immunogenicity of a Chikungunya Virus Vaccine Candidate (VLA1553) in Healthy Volunteers

Started: 3/5/2018

NCT03425149 Phase 1 COMPLETED

Randomized, Placebo-controlled, Observer-blinded Phase 1 Safety and Immunogenicity Study of Inactivated Zika Virus Vaccine Candidate in Healthy Adults

Started: 2/24/2018

NCT01296386 Phase 1 COMPLETED

An Open-label Study Assessing Safety, Immunogenicity and Dose Response of IC84

Started: 12/1/2010

NCT01559831 Phase 1 WITHDRAWN

Immune Response in IXIARO Batch JEV09L37 Recipients Before and After Revaccination

Started: 6/1/2012

NCT00873431 Phase 1 COMPLETED

Open-Label Study Assessing The Safety, Immunogenicity and Dose Response of IC47

Started: 3/1/2009

NCT00778388 Phase 1 COMPLETED

Study Assessing Safety and Immunogenicity of IC43 Vaccination Against Pseudomonas Aeruginosa in Healthy Volunteers

Started: 9/1/2008

NCT01158599 Phase 4 COMPLETED

This is a Study to Assess the Safety and Immunogenicity of Ixiaro® (IC51) in an Elderly Population

Started: 6/1/2010

Drug Candidates

VLA1601 CpG 1018® 3M-052-AF VLA1553 Control VLA1553 full dose VLA1553 half dose Biological Vaccine VLA1553 VLA2001 Placebo
Activity Status: Active
Last Trial Started: 2/6/2026
Last Trial Ended: 2/27/2026
Trials (12 months): 1
Completed Trials: 23
Data sourced from ClinicalTrials.gov. This company has no FDA-approved drugs.