Success Metrics

Clinical Success Rate
95.5%

Based on 21 completed trials

Completion Rate
95%(21/22)
Active Trials
2(8%)
Results Posted
71%(15 trials)
Terminated
1(4%)

Phase Distribution

Ph phase_2
6
25%
Ph phase_1
1
4%
Ph phase_3
14
58%
Ph phase_4
2
8%

Phase Distribution

1

Early Stage

6

Mid Stage

16

Late Stage

Phase Distribution23 total trials
Phase 1Safety & dosage
1(4.3%)
Phase 2Efficacy & side effects
6(26.1%)
Phase 3Large-scale testing
14(60.9%)
Phase 4Post-market surveillance
2(8.7%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

95.5%

21 of 22 finished

Non-Completion Rate

4.5%

1 ended early

Currently Active

2

trials recruiting

Total Trials

24

all time

Status Distribution
Active(2)
Completed(21)
Terminated(1)

Detailed Status

Completed21
Terminated1
Active, not recruiting1
Recruiting1

Development Timeline

Analytics

Development Status

Total Trials
24
Active
2
Success Rate
95.5%
Most Advanced
Phase 4

Trials by Phase

Phase 11 (4.3%)
Phase 26 (26.1%)
Phase 314 (60.9%)
Phase 42 (8.7%)

Trials by Status

terminated14%
active_not_recruiting14%
recruiting14%
completed2188%

Recent Activity

Clinical Trials (24)

Showing 20 of 24 trialsScroll for more
NCT07286370Phase 2

A Study to Evaluate Safety, Reactogenicity, and Immune Response of GVGH iNTS-TCV Vaccine Against Invasive Nontyphoidal Salmonella Disease and Typhoid Fever in Infants

Recruiting
NCT05759520Phase 3

Phase III Clinical Trial of 13-valent Pneumococcal Conjugate Vaccine (Multivalent Conjugate) in Infants

Active Not Recruiting
NCT03565159Phase 4

Pneumococcal Vaccination to Accelerate Immune Recovery in Sepsis Survivors

Completed
NCT04031846Phase 3

Safety, Tolerability, and Immunogenicity of V114 in Healthy Infants (V114-025)

Completed
NCT02255227Phase 2

Anti-pneumococcal Vaccine Strategy in Patients Treated With Immunosuppressants or Biotherapies for CIBD

Terminated
NCT04016714Phase 3

Safety, Tolerability, and Immunogenicity of a 3-dose Regimen of V114 in Healthy Infants (PNEU-PED-EU-2/V114-026)

Completed
NCT03896477Phase 3

Study of 10-valent Pneumococcal Conjugate Vaccine (Pneumosil) Administered in a 2+1 Schedule to Healthy Infants

Completed
NCT01939158Phase 3

Immunogenicity and Safety Study of 1 and 2 Doses of GlaxoSmithKline (GSK) Biologicals' Meningococcal Vaccine MenACWY-TT (GSK134612) in Toddlers, Persistence up to 5 Years After Vaccination and Co-administration With Pfizer's Prevenar 13™Vaccine

Completed
NCT03207750Phase 3

This Study Will Evaluate the Immunogenicity, Reactogenicity and Safety of the Routine Infant Vaccines Pediarix®, Hiberix® and Prevenar 13® When Co-administered With GlaxoSmithKline (GSK) Biologicals' Liquid Human Rotavirus Vaccine (HRV) as Compared to GSK's Licensed Lyophilized Vaccine

Completed
NCT01942174Phase 3

VACcination In Methotrexate Treated Rheumatoid Arthritis Patients

Completed
NCT01453998Phase 2

Safety and Immunogenicity of a Booster Dose of New Formulations of GlaxoSmithKline Biologicals' DTPa-HBV-IPV/Hib Vaccine (GSK217744)

Completed
NCT02308540Phase 1

Safety and Immunogenicity of a 10 Valent Pneumococcal Conjugate Vaccine (SIILPCV10) in Healthy Adults, Toddlers, Infants

Completed
NCT01204658Phase 2

Safety & Immunogenicity of Pneumococcal Vaccine 2189242A Co-administered With DTPa-HBV-IPV/Hib in Healthy Infants

Completed
NCT01341639Phase 3

Safety, Tolerability, and Immunogenicity of V419 in Healthy Infants When Given at 2, 3, 4 and 12 Months (V419-007)

Completed
NCT01480258Phase 3

Safety, Tolerability, and Immunogenicity of V419 in Healthy Infants When Given at 2, 4, and 11 to 12 Months (V419-008)

Completed
NCT01839188Phase 3

Spanish Mixed HEXA/PENTA/HEXA Schedule (V419-010)

Completed
NCT01439360Phase 3

An Efficacy Study of GlaxoSmithKline (GSK) Biologicals' Candidate Influenza Vaccine GSK2321138A in Children

Completed
NCT01248884Phase 2

Safety and Immunogenicity of New Formulations of GlaxoSmithKline Biologicals' DTPa-HBV-IPV/Hib Vaccine (GSK217744)

Completed
NCT01090453Phase 2

Study of GlaxoSmithKline Biologicals' GSK2202083A Vaccine in Healthy Infants

Completed
NCT01839175Phase 3

Concomitant Administration of a New Hexavalent Vaccine With a Meningococcal Serogroup C Conjugate Vaccine in Healthy Infants During Primary Series Immunisation Followed by Booster Vaccination

Completed

Drug Details

Intervention Type
COMBINATION PRODUCT
Total Trials
24