HPV (Human papillomavirus) Vaccine

  • STATUS
    Recruiting
  • days left to enroll
    3
  • sponsor
    GSK
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Updated on 16 January 2023
See if I qualify
Online studies
Accepts healthy volunteers

Summary

Join us in investigating a study vaccine against HPV, which can lead to cervical and other cancers.

Description

The EVE Study is researching if an investigational vaccine is safe and whether it helps the body produce antibodies against the different variants of HPV. Clinical research studies need to include all kinds of people as certain conditions and medications or vaccines may affect people differently based on their age, sex, gender, and race or ethnicity. This study will compare the investigational vaccine with an already approved vaccine. There are over 100 known variants of HPV. Most lead to mild infections. Although, some types can cause cervical and other cancers in both women and men, the EVE Study will only enroll women. It is important for this study to focus on women because it has been estimated that in some countries over 99% of cervical cancers can be prevented.

Patients should be within a 30 mile radius of the facility

Details
Condition Human Papilloma Virus (HPV), Vaccines, *Healthy Volunteers, *Healthy Patient Studies, Women's Health
Clinical Study IdentifierTX310303
SponsorGSK
Last Modified on16 January 2023

Eligibility

 Yes No Not Sure

Inclusion Criteria

Female
Between 16 and 26 years of age
Have not previously been vaccinated against HPV
Clear my responses
Read more

How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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