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Spots Global Cancer Trial Database for Prime-boost Vaccine Study in Women With Low-grade Cervical HPV Lesions

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Trial Identification

Brief Title: Prime-boost Vaccine Study in Women With Low-grade Cervical HPV Lesions

Official Title: A Phase 1b/2, Randomised, Placebo-controlled, Dose-ranging Study to Evaluate Safety, Tolerability and Immunogenicity of a Chimpanzee Adenovirus (ChAdOx1)-Vectored Multigenotype High Risk Human Papillomavirus (hrHPV) Vaccine and Modified Vaccinia Ankara (MVA)-Vectored Multigenotype hrHPV Vaccine in Women With Low-grade HPV-related Cervical Lesions

Study ID: NCT04607850

Study Description

Brief Summary: A Phase 1b/2 multi-centre study evaluating the safety, efficacy and immunogenicity of prime-boost vaccines ChAdOx1-HPV and MVA-HPV in women with HPV related low grade cervical lesions.

Detailed Description: The study consists of an open label, non-randomised, dose escalation Lead in phase. 9 participants with high-risk HPV, in cohorts of 3 in 3 dose ascending groups, will be vaccinated after SMC safety data reviews. This is followed by a blinded, randomised Main phase with 96 participants with high-risk HPV, in parallel running dose cohorts (three different doses of ChAdOx1-HPV plus two different doses of MVA-HPV versus placebo plus placebo boost). At least 60 of these participants will take part in the immunogenicity sub-study. A blinded, randomised expansion phase investigating the effects of up to two different main phase doses against placebo will be further defined prior to commencing this phase of the study.

Keywords

Eligibility

Minimum Age: 25 Years

Eligible Ages: ADULT

Sex: FEMALE

Healthy Volunteers: No

Locations

UZA, Antwerp, , Belgium

Erasme Hospital, Brussels, , Belgium

UZ Brussel, Brussels, , Belgium

UZ Gent, Gent, , Belgium

UZ Leuven, Leuven, , Belgium

Parnu Hospital Womens and Childrens Clinic, Parnu, , Estonia

East-Tallinn Central Hospital, Tallinn, , Estonia

North Estonia Medical Centre Foundation Surgery Clinic, Tallinn, , Estonia

Tartu University Hospital Womens Clinic, Tartu, , Estonia

Aberdeen Royal Infirmary, Aberdeen, , United Kingdom

University Hospital Bristol NHS Trust, Bristol, , United Kingdom

Liverpool Women's NHS Foundation Trust, Liverpool, , United Kingdom

Royal Victoria Infirmary, Newcastle Upon Tyne, , United Kingdom

Nottingham University Hospital NHS Trust, Nottingham, , United Kingdom

The University of Oxford, Nuffield Department of Women's & Reproductive Health, Oxford, , United Kingdom

Royal Preston Hospital, Preston, , United Kingdom

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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