Study on Two Adjuvanted Dose Levels of Panblok H7+MF59 Compared for Immunogenicity and Safety With an Unadjuvanted Dose of Panblok H7 in Participants 18 Years of Age and Older
A Parallel-group, Phase I/II, Randomized, Modified Double-blind, 3-arm, Active Comparator, Multi-center, Prevention Study to Evaluate the Immunogenicity and Safety of Two Adjuvanted Dose Levels of Panblok H7+MF59 Influenza Vaccine Compared With an Unadjuvanted Dose of Panblok H7 in Participants 18 Years of Age and Older
Sponsor: Sanofi Pasteur, a Sanofi Company
This PHASE1/PHASE2 trial investigates Healthy Volunteers and Influenza and is currently completed. Sanofi Pasteur, a Sanofi Company leads this study, which shows 13 recorded versions since 2022 — indicating substantial longitudinal coverage. Longitudinal tracking of infectious disease trials helps identify durability of treatment effects.
Status Flow
Change History
13 versions recorded-
Oct 2025 — Present [monthly]
Completed PHASE1/PHASE2
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Sep 2025 — Oct 2025 [monthly]
Completed PHASE1/PHASE2
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Mar 2025 — Sep 2025 [monthly]
Completed PHASE1/PHASE2
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Sep 2024 — Mar 2025 [monthly]
Completed PHASE1/PHASE2
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Jul 2024 — Sep 2024 [monthly]
Completed PHASE1/PHASE2
Phase: PHASE1_PHASE2 → PHASE1/PHASE2
▶ Show 8 earlier versions
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Apr 2024 — Jul 2024 [monthly]
Completed PHASE1_PHASE2
Status: Active Not Recruiting → Completed · Phase: PHASE2 → PHASE1_PHASE2
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Nov 2023 — Apr 2024 [monthly]
Active Not Recruiting PHASE2
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Oct 2023 — Nov 2023 [monthly]
Active Not Recruiting PHASE2
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Sep 2023 — Oct 2023 [monthly]
Active Not Recruiting PHASE2
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May 2023 — Sep 2023 [monthly]
Active Not Recruiting PHASE2
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Apr 2023 — May 2023 [monthly]
Active Not Recruiting PHASE2
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Mar 2023 — Apr 2023 [monthly]
Active Not Recruiting PHASE2
Status: Recruiting → Active Not Recruiting
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Dec 2022 — Mar 2023 [monthly]
Recruiting PHASE2
First recorded
Nov 2022
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Sanofi Pasteur, a Sanofi Company
For direct contact, visit the study record on ClinicalTrials.gov .