Success Metrics

Clinical Success Rate
89.5%

Based on 17 completed trials

Completion Rate
89%(17/19)
Active Trials
3(14%)
Results Posted
71%(12 trials)
Terminated
2(9%)

Phase Distribution

Ph phase_3
6
27%
Ph not_applicable
1
5%
Ph phase_2
8
36%
Ph phase_4
2
9%
Ph phase_1
5
23%

Phase Distribution

5

Early Stage

8

Mid Stage

8

Late Stage

Phase Distribution22 total trials
Phase 1Safety & dosage
5(22.7%)
Phase 2Efficacy & side effects
8(36.4%)
Phase 3Large-scale testing
6(27.3%)
Phase 4Post-market surveillance
2(9.1%)
N/ANon-phased studies
1(4.5%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

89.5%

17 of 19 finished

Non-Completion Rate

10.5%

2 ended early

Currently Active

3

trials recruiting

Total Trials

22

all time

Status Distribution
Active(3)
Completed(17)
Terminated(2)

Detailed Status

Completed17
Recruiting3
Terminated2

Development Timeline

Analytics

Development Status

Total Trials
22
Active
3
Success Rate
89.5%
Most Advanced
Phase 4

Trials by Phase

Phase 15 (22.7%)
Phase 28 (36.4%)
Phase 36 (27.3%)
Phase 42 (9.1%)
N/A1 (4.5%)

Trials by Status

recruiting314%
terminated29%
completed1777%

Recent Activity

Clinical Trials (22)

Showing 20 of 22 trialsScroll for more
NCT06800261Phase 1

Clinical Trial of PCV24 in Infants Aged 2-23 Months

Recruiting
NCT06617715Phase 3

Clinical Trial of 13-Valent Pneumococcal Conjugate Vaccine

Recruiting
NCT07300644Phase 2

Clinical Trial of PCV24 in Infants and Children Aged 2 Months to 5 Years

Recruiting
NCT06562790Phase 1

Study of Gamma PN3 in the Elderly

Completed
NCT01312389Phase 1

A Clinical Trial of Autologous Oxidized Tumor Cell Lysate Vaccine For Recurrent Ovarian, Fallopian Tube or Primary Peritoneal Cancer

Terminated
NCT00023504Phase 4

Antibody Production in Immune Disorders

Terminated
NCT01041573Phase 3

Safety and Immunogenicity of the Japanese Encephalitis Vaccine IC51 (IXIARO®) in a Pediatric Population

Completed
NCT00861744Phase 2

Immunogenicity of GSKs' MMR Vaccine (209762) vs. M-M-R® II, When Given With Routine Vaccines at 12-15 Months of Age

Completed
NCT01098474Phase 2

Safety and Immunogenicity Study of a Candidate Tuberculosis Vaccine in Healthy Infants

Completed
NCT01215175Phase 1

Safety and Tolerability Study for the Pneumococcal Conjugate Vaccine V114 Versus Prevnar™ (V114-001)

Completed
NCT00578175Phase 2

Immunogenicity and Safety of GlaxoSmithKline Biologicals' MMRV Vaccine vs. ProQuad® in Children 12-14 Months of Age

Completed
NCT01307449Not Applicable

Systems Biology of PNEUMOVAX®23 and PREVNAR 13®

Completed
NCT00129129Phase 2

Comparison of GSKBiologicals' Hib-MenCY-TT Vaccine vs Licensed Hib Conjugate or Meningococcal Vaccine

Completed
NCT00289783Phase 3

Safety and Immunogenicity Study of Hib-MenCY-TT Vaccine Compared to Licensed Hib Conjugate Vaccine

Completed
NCT00197002Phase 3

Immune Response & Safety of a Hepatitis A Vaccine Given Together With a Pneumococcal Vaccine in Healthy Children 15 m of Age

Completed
NCT00304382Phase 4

Humoral Determinants of Immunity to Pneumococcal Infection

Completed
NCT00323622Phase 2

Long-Term Follow-up of Children for a 2-Year Period to Confirm the Safety and Immunogenicity of GSK 257049 Vaccine

Completed
NCT00345683Phase 3

Safety of Hib-MenCY-TT Vaccine Versus Licensed Hib Conjugate Vaccine, Given at 12 to 15 Months of Age.

Completed
NCT00729001Phase 2

Study of Two Doses of GSK Biologicals' Live Attenuated HRV Vaccine (Two Different Formulations) in Healthy Infants.

Completed
NCT00594347Phase 3

Immunogenicity and Safety of a Booster Dose of Pneumo 23® in 12 to 18 Months-Old Children Primed With Prevnar

Completed

Drug Details

Intervention Type
BIOLOGICAL
Total Trials
22