Investigating the Combination of VB10.16 and Atezolizumab in Patients With HPV 16-positive Cervical Cancer
NCT04405349 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 52
Last updated 2023-12-15
Summary
This phase IIa study is designed to evaluate the safety and efficacy of multiple dosing with VB10.16 immunotherapy in combination with atezolizumab in patients with advanced or recurrent non-resectable HPV16-positive cervical cancer, who failed or are not eligible for current standard of care.
Conditions
- Cervical Cancer
- Cervix Cancer
Interventions
- BIOLOGICAL
-
VB10.16
Vaccination
- BIOLOGICAL
-
Intravenously infusion
Sponsors & Collaborators
-
Roche Pharma AG
collaborator INDUSTRY -
Vaccibody AS
collaborator INDUSTRY -
Nykode Therapeutics ASA
lead INDUSTRY
Principal Investigators
-
Siri Torhaug, MD · Nykode Therapeutics ASA
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-07-01
- Primary Completion
- 2023-11-24
- Completion
- 2023-11-24
Countries
- Belgium
- Bulgaria
- Czechia
- Germany
- Norway
- Poland
Study Locations
More Related Trials
-
Prevention of Human Papillomavirus (HPV) in 20 to 45 Year Old Chinese Women (V501-041)
NCT00834106 ·Status: COMPLETED ·Phase: PHASE3
-
Human Papillomavirus Vaccine Safety & Immunogenicity Trial in Healthy Young Adult Women With HPV Vaccine (GSK1674330A)
NCT00478621 ·Status: COMPLETED ·Phase: PHASE1
-
Efficacy and Immunogenicity Study of Recombinant Human Papillomavirus Bivalent(Type 16/18 )Vaccine
NCT01735006 ·Status: COMPLETED ·Phase: PHASE3
-
A Vaccine (PDS0101) Alone or in Combination With Pembrolizumab for the Treatment of Locally Advanced Human Papillomavirus-Associated Oropharynx Cancer
NCT05232851 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1/PHASE2
-
Broad Spectrum HPV Vaccine Tolerability, Immunogenicity, and Efficacy Study (V502-003)
NCT00365443 ·Status: WITHDRAWN ·Phase: PHASE2
-
Clinical Trial of Recombinant Human Papillomavirus Virus 16/18 Bivalent Vaccine
NCT01263327 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of V503, a 9-valent Human Papillomavirus (9vHPV) Vaccine in Females 12-26 Years of Age Who Have Previously Received GARDASIL™ (V503-006)
NCT01047345 ·Status: COMPLETED ·Phase: PHASE3
-
Vaccine To Prevent Cervical Intraepithelial Neoplasia or Cervical Cancer in Younger Healthy Participants
NCT00128661 ·Status: COMPLETED ·Phase: PHASE3
-
A Study to Evaluate the Immunogenicity, Safety and Tolerability of Quadrivalent Human Papillomavirus Vaccine (V501) in Chinese Girls Aged 9-19 Years and Young Women Aged 20-26 Years (V501-213)
NCT03493542 ·Status: COMPLETED ·Phase: PHASE3
-
Immune Persistence After the Whole Vaccination Shcedule With Recombination Quadrivalent HPV Vaccine
NCT05371353 ·Status: RECRUITING
-
Immunogenicity and Tolerability of V503 Versus GARDASIL (V503-009)
NCT01304498 ·Status: COMPLETED ·Phase: PHASE3
-
Clinical Trial Evaluating Secondary HPV Vaccination After Treatment of High-grade Cervical Lesions
NCT06658405 ·Status: RECRUITING ·Phase: PHASE2
-
Broad Spectrum HPV (Human Papillomavirus) Vaccine Study in 16-to 26-Year-Old Women (V503-001)
NCT00543543 ·Status: COMPLETED ·Phase: PHASE3
-
An Immuno-bridging Study of a Nonavalent HPV Vaccine (E.Coli) in Healthy Population Aged 9-17 vs Aged 18-26 Years Old
NCT05056402 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
Evaluation of Safety and Immunogenicity of Co-administering Human Papillomavirus (HPV) Vaccine With Other Vaccines in Healthy Female Subjects
NCT00426361 ·Status: COMPLETED ·Phase: PHASE3
-
SGN-00101 Vaccine in Treating Human Papillomavirus in Patients Who Have Abnormal Cervical Cells
NCT00091130 ·Status: COMPLETED ·Phase: PHASE2
-
Vvax001 Cancer Vaccine in Premalignant Cervical Lesions - Phase II
NCT06015854 ·Status: UNKNOWN ·Phase: PHASE2
-
Assessing Administration of pBI-11 Via Electroporation for the Treatment of Patients With HPV16/18+
NCT06210854 ·Status: NOT_YET_RECRUITING ·Phase: PHASE2
-
Study to Evaluate the Efficacy of the Human Papillomavirus Vaccine in Healthy Adult Women of 26 Years of Age and Older
NCT00294047 ·Status: COMPLETED ·Phase: PHASE3
-
Efficacy, Immunogenicity and Safety Study of Recombinant Human Papillomavirus Vaccine(6,11,16,18,31,33,45,52,58 Type)(E.Coli)
NCT04537156 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
A Study to Evaluate the Immunogenicity and Safety of GSK Biologicals' HPV Vaccine in Healthy Women Aged 18-35 Years
NCT00306241 ·Status: COMPLETED ·Phase: PHASE3
-
Safety Study of Recombinant Human Papillomavirus Vaccine(6,11,16,18,31,33,45,52,58 Type)(E.Coli)
NCT03813940 ·Status: COMPLETED ·Phase: PHASE1
-
Long-term Follow-up of Bivalent Human Papillomavirus (HPV) Vaccine Study in Women
NCT06776055 ·Status: ACTIVE_NOT_RECRUITING
-
A Study to Compare Immune Response of V503 to Gardasil in 16- to 26-year-old Men (V503-020)
NCT02114385 ·Status: COMPLETED ·Phase: PHASE3
-
Testing RG1-VLP Vaccine to Prevent HPV-related Cancers
NCT05985681 ·Status: RECRUITING ·Phase: PHASE1