Key Insights

Highlights

Success Rate

93% trial completion (above average)

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 50/100

Termination Rate

3.6%

1 terminated out of 28 trials

Success Rate

92.9%

+6.4% vs benchmark

Late-Stage Pipeline

4%

1 trials in Phase 3/4

Results Transparency

15%

2 of 13 completed with results

Key Signals

2 with results93% success

Data Visualizations

Phase Distribution

20Total
Not Applicable (10)
P 1 (5)
P 2 (4)
P 4 (1)

Trial Status

Completed13
Recruiting7
Active Not Recruiting4
Unknown2
Withdrawn1
Terminated1

Trial Success Rate

92.9%

Benchmark: 86.5%

Based on 13 completed trials

Clinical Trials (28)

Showing 20 of 20 trials
NCT04857528Recruiting

Detecting HPV DNA in Anal and Cervical Cancers

NCT05686226Phase 2Recruiting

E7 TCR-T Cell Immunotherapy for Human Papillomavirus (HPV) Associated Cancers

NCT03260023Phase 1Active Not Recruiting

Phase Ib/II of TG4001 and Avelumab in HPV16 Positive R/M Cancers

NCT06319963Phase 1RecruitingPrimary

A Study to Evaluate Lenti-HPV-07 Immunotherapy Against HPV+ Cervical or Oropharyngeal Cancer

NCT06640283Phase 2Recruiting

Dynamic ctDNA Assessment in Cervical and Anal Canal Tumors: Optimizing Follow-up and Clinical Outcomes

NCT05973487Phase 1Active Not Recruiting

A Basket Study of Customized Autologous TCR-T Cell Therapies in Patients With Locally Advanced (Unresectable) or Metastatic Solid Tumors

NCT05996783Not ApplicableActive Not Recruiting

Cervical Cancer Screening Based on First-void Urine Self-sampling to Reach un(Der)-Screened Women: ScreenUrSelf Trial

NCT06052033Not ApplicableRecruitingPrimary

Comparison of 5-ALA Photodynamic Therapy and CO2 Laser for Treating Persistent Low-Grade Cervical Lesions With High-Risk HPV Infection

NCT03749707Not ApplicableCompleted

HPV in Sentinel Lymph Nodes of Cervical Cancer Patients

NCT05829629Phase 1Recruiting

Phase 1 Dose-escalation Study of FluBHPVE6E7 in HPV16-infected Women

NCT06339684Active Not RecruitingPrimary

HPV Immunological Markers of Cervical Persistent Infection and Oncogenesis

NCT06099418Phase 2WithdrawnPrimary

Efficacy and Safety of VB10.16 Alone or in Combination With Atezolizumab in Patients With Advanced Cervical Cancer.

NCT06598176Not ApplicableRecruiting

Developing a Combined Molecular Screening and Triage Test for Cervical Cancer in Self-samples

NCT05783167Completed

Self-collected Vaginal and Urine Samples in HIV-positive Women

NCT04679675Not ApplicableCompleted

Self-Testing Options in the Era of Primary HPV Screening for Cervical Cancer Trial

NCT05996796Not ApplicableCompleted

Dry Run of the ScreenUrSelf Trial

NCT05767138Completed

STI Knowledge and HPV Vaccine Acceptance in Bamako, Mali in 2012

NCT05061940Terminated

This SCR-103 Protocol Will Permit Sites to Proactively Assess TAA, HLA and HPV-16 Status in Patients With Selected Solid Tumors to Determine Suitability for Repertoire Immune Medicines Treatment Protocols.

NCT04530201Not ApplicableCompleted

CASUS: Validation for Detection of Precursor Lesions

NCT04436133Phase 2Completed

Immunogenicity AND Safety Study of the 11 Valent Recombinant Human Papillomavirus Vaccine (Hansenulapolymorpha)

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