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Ocular Assessments in Patients Treated With Tivdak® in Recurrent or Metastatic Cervical Cancer


Active: Yes
Cancer Type: Cervical Cancer NCT ID: NCT06952660
Trial Phases: Phase IV Protocol IDs: C5721005 (primary)
NCI-2025-05282
Eligibility: 18 Years and older, Male and Female Study Type: Other
Study Sponsor: Pfizer Inc
NCI Full Details: http://clinicaltrials.gov/show/NCT06952660

Summary

TIVDAK is used for the treatment of cervical cancer that has come back after
chemotherapy. Chemotherapy is a treatment that uses medicines to stop the growth of
cancer cells. This is done either by killing the cells or by stopping them from growing.
The purpose of this study is to learn about possible side effects of TIVDAK, specially to
any side effect that is related to the eye. A side effect is anything a medicine does to
your body that is not part of how the medicine treats disease.

- This study is seeking for participants who: Are willing to take all the required eye
tests

- Have not received TIVDAK before

- Do not have any active eye issues.

Participants will receive TIVDAK once every 3 weeks as an infusion that will be injected
into the vein. Participants will visit an eye care provider at 3 stages:

- before starting the treatment,

- before each of the first 9 infusions

- then monthly for 3 months after they stop taking TIVDAK. Treatment with TIVDAK will
continue until it is not working anymore against the participant's cancer.

Treatment Sites in Georgia

Winship Cancer Institute of Emory University
1365 Clifton Road NE
Building C
Atlanta, GA 30322
winshipcancer.emory.edu

**Clinical trials are research studies that involve people. These studies test new ways to prevent, detect, diagnose, or treat diseases. People who take part in cancer clinical trials have an opportunity to contribute to scientists’ knowledge about cancer and to help in the development of improved cancer treatments. They also receive state-of-the-art care from cancer experts... Click here to learn more about clinical trials.