HPV-Related Cervical Carcinoma
28
7
11
13
Key Insights
Highlights
Success Rate
93% trial completion (above average)
Clinical Risk Assessment
Based on trial outcomes
Moderate Risk
Score: 50/100
3.6%
1 terminated out of 28 trials
92.9%
+6.4% vs benchmark
4%
1 trials in Phase 3/4
15%
2 of 13 completed with results
Key Signals
Data Visualizations
Phase Distribution
Trial Status
Trial Success Rate
Benchmark: 86.5%
Based on 13 completed trials
Clinical Trials (28)
Detecting HPV DNA in Anal and Cervical Cancers
E7 TCR-T Cell Immunotherapy for Human Papillomavirus (HPV) Associated Cancers
Phase Ib/II of TG4001 and Avelumab in HPV16 Positive R/M Cancers
A Study to Evaluate Lenti-HPV-07 Immunotherapy Against HPV+ Cervical or Oropharyngeal Cancer
Dynamic ctDNA Assessment in Cervical and Anal Canal Tumors: Optimizing Follow-up and Clinical Outcomes
A Basket Study of Customized Autologous TCR-T Cell Therapies in Patients With Locally Advanced (Unresectable) or Metastatic Solid Tumors
Cervical Cancer Screening Based on First-void Urine Self-sampling to Reach un(Der)-Screened Women: ScreenUrSelf Trial
Comparison of 5-ALA Photodynamic Therapy and CO2 Laser for Treating Persistent Low-Grade Cervical Lesions With High-Risk HPV Infection
HPV in Sentinel Lymph Nodes of Cervical Cancer Patients
Phase 1 Dose-escalation Study of FluBHPVE6E7 in HPV16-infected Women
HPV Immunological Markers of Cervical Persistent Infection and Oncogenesis
Efficacy and Safety of VB10.16 Alone or in Combination With Atezolizumab in Patients With Advanced Cervical Cancer.
Developing a Combined Molecular Screening and Triage Test for Cervical Cancer in Self-samples
Self-collected Vaginal and Urine Samples in HIV-positive Women
Self-Testing Options in the Era of Primary HPV Screening for Cervical Cancer Trial
Dry Run of the ScreenUrSelf Trial
STI Knowledge and HPV Vaccine Acceptance in Bamako, Mali in 2012
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.
CASUS: Validation for Detection of Precursor Lesions
Immunogenicity AND Safety Study of the 11 Valent Recombinant Human Papillomavirus Vaccine (Hansenulapolymorpha)