Seqirus

Closed portfolio with a later-stage archive tilt

According to ClinicalTrials.gov-derived indexes, Seqirus sits in the top decile of US sponsors by registered trial count (#626 of 15,742 sponsors by registered trial count).

25 total trials none currently recruiting 24 completed later-stage tilt top decile by trial count

Seqirus: 25 sponsored US clinical trials, none currently recruiting.

Seqirus sponsors 25 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 24 completed. 14 of these trials are in Phase 3-4 (later-stage) and 9 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Influenza, Human, with 4 trials.

Top-decile sponsor footprint

Seqirus ranks in the top decile of sponsors by registered trial count (#626 of 15,742 sponsors by registered trial count). Volume at this scale usually reflects a long institutional pipeline, read phase tilt and therapeutic areas below before treating it as current-year activity.

Trial completion reliability score

A 90/100

24 of 24 decided trials (Completed vs. Terminated on ClinicalTrials.gov) reached their planned completion (100.0%), vs. national p10 68.4% / p90 100% among 1,234 sponsors with at least 10 decided trials. Still-open trials (Recruiting, Active-not-recruiting, Not-yet-recruiting) are excluded since they have not reached an outcome yet.

Indexed trials (enrollment closed)

25 total, page 1 of 1

ACTIVE NOT RECRUITING Phase 3

A Clinical Study to Evaluate the Efficacy, Safety and Immunogenicity of an Adjuvanted Influenza Vaccine Compared to a Non-adjuvanted Influenza Vaccine in Adults ≥65 Years of Age

NCT06087640

COMPLETED Phase 3

The Celljuvant Study: A Phase 3 Immunogenicity and Safety Study of aQIVc Vaccine in Adults Aged 50 Years and Older

NCT06015282

COMPLETED Phase 1

Study to Evaluate Immunogenicity, Safety and Tolerability of Adjuvanted and Non-Adjuvanted H2N3 Influenza Vaccines in Adults

NCT05875961

COMPLETED Phase 2

Study to Evaluate Safety and Immunogenicity of Different Priming and Booster Regimens With Adjuvanted H5N8 and/or H5N6 Influenza Vaccine in Adults

NCT05874713

COMPLETED Phase 2

Safety and Immunogenicity of Different Formulations of an MF59-Adjuvanted Influenza Vaccine in Older Adults ≥50 Years of Age

NCT05501561

COMPLETED Phase 2

A Study to Evaluate Safety and Immunogenicity of One or Two Booster Vaccinations With H5N6 Influenza Vaccine in Adults Primed With H5N1 Influenza Vaccine or Unprimed

NCT05422326

COMPLETED Phase 3

A Clinical Study to Evaluate the Immunogenicity and Safety of an Adjuvanted Quadrivalent Influenza Vaccine Compared With a Licensed Quadrivalent Vaccine in Adults 50 to 64 Years of Age

NCT05044195

COMPLETED Phase 2

Safety and Immunogenicity of an MF59-Adjuvanted Influenza Vaccine in Older Adults

NCT04576702

COMPLETED Phase 3

Safety and Immunogenicity Study of QIVc in Healthy Pediatric Subjects

NCT04074928

COMPLETED Phase 3

Phase 3 Safety and Immunogenicity Study of aQIV in Elderly Adults

NCT03314662

COMPLETED

Afluria Pregnancy Registry

NCT03442582

COMPLETED

Flucelvax (TIVc or QIVc) Pregnancy Registry

NCT03438487

COMPLETED Phase 3

A Study to Evaluate the Immunogenicity and Safety of Seqirus Quadrivalent Influenza Vaccine (QIV) in a Pediatric Population 6 Months Through 59 Months of Age.

NCT02914275

COMPLETED Phase 3

A Study to Evaluate Safety, Immunogenicity, and Lot-to-Lot Consistency of H5N1 Subunit Influenza Virus Vaccine in Healthy Adult Subjects ≥18 Years of Age

NCT02839330

COMPLETED Phase 3

A Study to Evaluate the Immunogenicity and Safety of Seqirus Quadrivalent Influenza Vaccine (QIV) in a Pediatric Population 5 Through 17 Years of Age

NCT02545543

COMPLETED Phase 3

Clinical Study to Evaluate Safety, Immunogenicity of Investigational Flu Vaccine Compared to an Approved Flu Vaccine (QIV) in Children Previously Vaccinated in Trial V118_05

NCT02255409

COMPLETED Phase 4

A Study to Evaluate the Safety and Tolerability of Trivalent Influenza Virus Vaccine in Children Aged 5 Years to < 9 Years

NCT02212106

COMPLETED Phase 3

A Study to Evaluate the Immunogenicity and Safety of bioCSL Quadrivalent Influenza Vaccine (QIV) in Adults Aged 18 Years and Above.

NCT02214225

COMPLETED Phase 1

Safety and Immunogenicity of a Four Influenza Vaccines in Children Ages 6 Months Old to Less Than 48 Months Old

NCT02035696

COMPLETED Phase 3

Clinical Study to Evaluate the Safety, Immunogenicity and Efficacy of Investigational Flu Vaccine Compared to Approved Flu Vaccine in Children.

NCT01964989

COMPLETED Phase 3

A Study to Determine the Immunogenicity and Safety Profile of CSL Limited's Influenza Virus Vaccine Compared to a US Licensed Comparator Influenza Virus Vaccine in a Pediatric Population

NCT00959049

COMPLETED Phase 2

A Clinical Trial of CSL's 2009 H1N1 Influenza Vaccine (CSL425) in Healthy Adults in the USA

NCT00958126

COMPLETED Phase 2

A Clinical Trial of CSL's 2009 H1N1 Influenza Vaccine (CSL425) in a Healthy Pediatric Population in the USA

NCT00958243

COMPLETED Phase 1

Dose Ranging Study to Evaluate Immunogenicity and Safety of Adjuvanted or Non-adjuvanted Cell Culture-derived H5N1 Influenza Vaccine in Young Adults (18-40 Years Old)

NCT00812019

COMPLETED Phase 4

A Study to Determine the Immunogenicity and Safety Profile of CSL Limited's Influenza Virus Vaccine Compared to a US Licensed Comparator Influenza Virus Vaccine

NCT00735475

Phase Distribution

PhaseTrial count
Phase 1 3
Phase 2 6
Phase 3 12
Phase 4 2

Therapeutic Areas

How the Seqirus archive is shaped

25 indexed studies, none listed as recruiting (0% open); 24 completed (96%).

Phase mix: 14 late (III/IV) vs 9 early (I/II) (later-stage heavy).

Top condition: Influenza, Human (4 trials), 0 others listed.

How to read a closed sponsor archive

When recruiting_count is zero, the indexed set is completed or otherwise not open. Phase tilt still describes where archived studies sat on the investigational pathway. Re-check ClinicalTrials.gov before acting.

Seqirus: archived-pipeline peers nationwide

Peers matched on 25 indexed studies with no current recruiting: volume and archive shape, not condition overlap.

Seqirus sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot). 2×2 strategic matrix plotting 9 entities by Total trials (X) and Recruiting share (Y), with a crosshair dividing the plot into four quadrants. Higher volume & more openFocused & more openHigher volume, mostly closedSmaller & mostly closed 051015202530 0%5%10%15% Total trials Recruiting share SeqirusArcus BiosciencesArcutis BiotherapeuticsArdelyxDrexel University College of Medicine10xBio22nd Century Group23andMe3-C Institute for Social Development
Seqirus sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot).

Seqirus sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together.

Sponsors near 25 archived trials

Sponsors with similar archive density (± trial count)

What to do with this Seqirus page

25 registered trials is a research-attention snapshot, not an endorsement of Seqirus or any single study.

  • None of Seqirus's trials are currently recruiting in this registry; that can change as new trials post, or check the broader research index. Browse research indexes
  • Influenza, Human is the condition Seqirus studies most, compare against other sponsors active in the same condition before evaluating a specific study. See Influenza, Human trials
  • Bring the specific trial ID (NCT number) to your own doctor before enrolling, this page is a directory, not medical guidance. Read the trial-finding guide

Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.

Seqirus pipeline card: 25 registered trials from official public datasets.Report a data error.