Phase I Safety and Immunogenicity of FP-02.2 in Chronic Hepatitis B
A Phase I, Randomized, Double-blind, Placebo-controlled, Multi-centre, Ascending-dose Trial to Evaluate the Safety, Tolerability and Immunogenicity of Vaccine FP-02.2 in HBeAg-negative Hepatitis B Patients as an add-on Treatment to Entecavir or Tenofovir.
Sponsor: Altimmune, Inc.
This PHASE1 trial investigates Hepatitis B and is currently completed. Altimmune, Inc. leads this study, which shows 12 recorded versions since 2015 — indicating substantial longitudinal coverage. Longitudinal tracking of infectious disease trials helps identify durability of treatment effects.
Status Flow
Change History
12 versions recorded-
Sep 2025 — Present [monthly]
Completed PHASE1
-
Jun 2025 — Sep 2025 [monthly]
Completed PHASE1
-
Sep 2024 — Jun 2025 [monthly]
Completed PHASE1
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE1
-
Jan 2021 — Jul 2024 [monthly]
Completed PHASE1
▶ Show 7 earlier versions
-
Feb 2019 — Jan 2021 [monthly]
Completed PHASE1
Status: Active Not Recruiting → Completed
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Jun 2018 — Feb 2019 [monthly]
Active Not Recruiting PHASE1
-
Apr 2018 — Jun 2018 [monthly]
Active Not Recruiting PHASE1
-
Dec 2017 — Apr 2018 [monthly]
Active Not Recruiting PHASE1
Status: Recruiting → Active Not Recruiting
-
Aug 2017 — Dec 2017 [monthly]
Recruiting PHASE1
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Jun 2017 — Aug 2017 [monthly]
Recruiting PHASE1
-
Jan 2017 — Jun 2017 [monthly]
Recruiting PHASE1
First recorded
Jul 2015
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Altimmune, Inc.
For direct contact, visit the study record on ClinicalTrials.gov .