Bavarian Nordic
Bavarian Nordic sponsors 41 registered US clinical trials on ClinicalTrials.gov, 2 of them currently recruiting, and 36 completed. 14 of these trials are in Phase 3-4 (later-stage) and 26 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Chikungunya Virus Infection, with 2 trials.
Trial Pipeline
41 total, page 1 of 1
Comparability Trial of the MVA-BN Vaccine Manufactured in Different Production Cells
NCT07199569
A Safety and Immunogenicity Study of CHIKV VLP Vaccine in Children.
NCT07003984
A Phase 2 Trial in Healthy Adult Participants of the Recombinant MVA-BN-WEV Vaccine
NCT06899802
Long-term Follow-up Study to Evaluate Safety and Immunogenicity of PXVX0317 Single or Booster Vaccination
NCT06007183
ABNCoV2 Vaccine in Adult Subjects Previously Vaccinated for SARS-CoV-2
NCT05329220
Safety and Immunogenicity of CHIKV VLP Vaccine PXVX0317 in Adults ≥65 Years
NCT05349617
MVA-BN-RSV Vaccine Trial
NCT05238025
A Study to Assess the Safety and Immunogenicity of PXVX0317 Chikungunya Virus Virus-Like Particle Vaccine
NCT05065983
A Phase 3 Trial of the VLP-Based Chikungunya Vaccine PXVX0317 (CHIKV VLP Vaccine)
NCT05072080
TAEK-VAC-HerBy Vaccine for Brachyury and HER2 Expressing Cancer
NCT04246671
A Phase 1 Open Label Trial of Intravenous Administration of MVA-BN-Brachyury Vaccine in Patients With Advanced Cancer
NCT04134312
Phase 2 Open-label Study of Alum-adjuvanted Chikungunya Virus-like Particle Vaccine (PXVX0317)
NCT03992872
Vaccination Trial of a Recombinant MVA-BN-WEV Vaccine in Healthy Adult Subjects
NCT04131595
Freeze-Dried MVA-BN® Lot Consistency Smallpox Trial
NCT03699124
BN Brachyury and Radiation in Chordoma
NCT03595228
CV301 Combined With PD-1/L1 Blockade in Patients With Locally Advanced or Metastatic Urothelial Bladder Cancer
NCT03628716
Trial of a Chikungunya Vaccine, PXVX0317 CHIKV-VLP, in Healthy Adults
NCT03483961
Safety and Tolerability Trial (MVA-BN-Brachyury/FPV-Brachyury)
NCT03349983
VAXCHORA Pediatric Study to Assess Safety and Immunogenicity
NCT03220737
A Trial of CV301 in Combination With Anti-PD-1 Therapy in Subjects With Non-Small Cell Lung Cancer
NCT02840994
RSV-MVA-BN Vaccine Phase II Trial in ≥ 55 Year Old Adults
NCT02873286
Phase 4 Study To Assess The Safety Of Vivotif At Different Release Titers Among Travelers
NCT02391909
Trial to Evaluate the Safety, Tolerability and Immunogenicity of the Recombinant MVA BN® RSV Vaccine
NCT02419391
A Study of Live Oral Cholera Vaccine, PXVX200 in Healthy Older Adults
NCT02100631
A Phase 3 Lot to Lot Consistency Study of Live Oral Cholera Vaccine, PXVX0200 in Healthy Adults
NCT02094586
Randomized, Open-label Phase II Trial to Assess the Safety and Immunogenicity of MVA-BN Smallpox Vaccine in Immunocompromised Subjects With HIV Infection
NCT02038881
Safety and Efficacy Challenge Study of Live Oral Cholera Vaccine Candidate,PXVX0200, to Prevent Cholera
NCT01895855
A Phase II Trial to Compare a Liquid-frozen and a Freeze-dried Formulation of IMVAMUNE (MVA-BN®) Smallpox Vaccine in Vaccinia-naïve Healthy Subjects
NCT01668537
A Trial to Evaluate Immunogenicity and Safety of Three Consecutive Production Lots of IMVAMUNE® (MVA-BN®) Smallpox Vaccine in Healthy, Vaccinia-naïve Subjects
NCT01144637
Safety and Immunogenicity of the Live Oral Cholera Vaccine Candidate PXVX0200
NCT01585181
A Randomized, Double-blind, Phase 3 Efficacy Trial of PROSTVAC-V/F +/- GM-CSF in Men With Asymptomatic or Minimally Symptomatic Metastatic Castrate-Resistant Prostate Cancer
NCT01322490
A Safety and Immunology Study of a Modified Vaccinia Vaccine for HER-2(+) Breast Cancer After Adjuvant Therapy
NCT01152398
Special Access Program IMVAMUNE®
NCT03472014
A Study to Evaluate Safety and Immunogenicity of One and Two Doses of IMVAMUNE® Smallpox Vaccine in 56-80 Year Old Vaccinia-experienced Subjects
NCT00857493
Phase I Safety Study of a Recombinant MVA HIV Multiantigen Vaccine in HIV-infected Subjects
NCT00623259
A Safety Trial of MVA-BN®-PRO in Men With Androgen-Insensitive Prostate Cancer
NCT00629057
A Safety and Immunology Study of a Modified Vaccinia Vaccine for HER-2(+) Metastatic Breast Cancer
NCT00485277
A Phase II Study on Immunogenicity and Safety of MVA-BN® (IMVAMUNE™) Smallpox Vaccine in Subjects With Atopic Dermatitis
NCT00316602
Safety and Immunogenicity of IMVAMUNE® (MVA-BN®) Smallpox Vaccine in HIV Infected Patients
NCT00316589
Safety, Tolerability and Immune Response of IMVAMUNE (MVA-BN)Smallpox Vaccine in HIV Infected Patients
NCT00189904
PROSTVAC®-VF/TRICOM™ Vaccine for the Treatment of Metastatic Prostate Cancer After Failing Hormone Therapy
NCT00078585
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 12 |
| Phase 2 | 14 |
| Phase 3 | 12 |
| Phase 4 | 2 |
Therapeutic Areas
What the Pipeline for Bavarian Nordic Shows
According to the ClinicalTrials.gov registry, Bavarian Nordic is linked to 41 US clinical trials across every stage of research activity. Of those, 2 studies are currently recruiting, about 5% of the sponsor's indexed portfolio, and 36 are already marked complete, representing roughly 88% of the total.
The phase mix for Bavarian Nordic reports 14 late-stage studies (Phase 3 and Phase 4 combined) and 26 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Bavarian Nordic is Chikungunya Virus Infection with 2 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.