VLA1553 full dose + VLA1553 half dose + Control

Phase 2Completed
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Interest: 29/100
29
Hype Score

Development Stage

Pre-clinical
Phase 1
3
Phase 2
4
Phase 3
5
Approved
Indication / Disease

Chikungunya Virus Infection

Conditions

Chikungunya Virus Infection

Trial Timeline

Dec 18, 2023 → Jul 2, 2025

About VLA1553 full dose + VLA1553 half dose + Control

VLA1553 full dose + VLA1553 half dose + Control is a phase 2 stage product being developed by Valneva SE for Chikungunya Virus Infection. The current trial status is completed. This product is registered under clinical trial identifier NCT06106581. Target conditions include Chikungunya Virus Infection.

What happened to similar drugs?

0 of 11 similar drugs in Chikungunya Virus Infection were approved

Approved (0) Terminated (2) Active (9)
🔄CHIKV VLP/adjuvant + PlaceboBavarian NordicPhase 3
🔄CHIKV VLP/adjuvant + PlaceboBavarian NordicPhase 3
🔄CHIKV VLP vaccine + PlaceboBavarian NordicPhase 3
🔄CHIKV VLP vaccine + PlaceboBavarian NordicPhase 3
VLA1553Valneva SEPhase 3
🔄Biological Vaccine VLA1553Valneva SEPhase 3

Hype Score Breakdown

Clinical
12
Activity
8
Company
9
Novelty
0
Community
0

Clinical Trials (1)

NCT IDPhaseStatus
NCT06106581Phase 2Completed

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44
CHIKV VLP vaccine + PlaceboBavarian NordicPhase 3
44
Live-attenuated CHIKV vaccine VLA1553Valneva SEPre-clinical
27
VLA1553Valneva SEPhase 3
26
Live-attenuated CHIKV vaccine VLA1553Valneva SEPre-clinical
24
Biological Vaccine VLA1553Valneva SEPhase 3
34
Active + PlaceboValneva SEPhase 3
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Live-attenuated CHIKV vaccine VLA1553 + Vaccine(s) approved for use during pregnancy by the MoHValneva SEPre-clinical
27
VLA1553Valneva SEPhase 3
38
VLA1553 + ControlValneva SEPhase 3
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VLA1553 + PlaceboValneva SEPhase 3
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VLA1553Valneva SEPhase 1
23