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NCT04191226

Genetic Mutation in Recurrent Cervical Cancer

Status unknown Last updated 20 December 2019
What this trial tests

trial testing Multi-gene panel testing in Recurrent Cervical Cancer in 300 participants. Status unknown.

Timeline
19 December 2019
Primary endpoint
1 January 2022
1 January 2023

Quick facts

Lead sponsorLei Li
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment300
Start date19 December 2019
Primary completion1 January 2022
Estimated completion1 January 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Lei Li — full company profile →

Who can join

18 and older, female only, with Recurrent Cervical Cancer or Nucleotide Variant. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Little is known about the characteristics of genetic mutation in recurrent cervical cancer. This study is to explore the targeted genetic mutations via a multi-gene panel, which consists of more than 500 hundred genes. The mutation characteristics are to be revealed in single nucleotide variants, copy number variations, insertion-deletion variations, and genomic structural variations. The total mutation burden (TMB) will be calculated. The status of microsatellite instability, expression of PD-1 and PD-L1 antibodies are also tested. These findings will be studies in association with the patients' prognosis and sensitivity to platinum-based chemotherapy and immunotherapy.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Recurrent Cervical Cancer

Currently open trials in the same condition.

Other Lei Li trials

Trials by the same sponsor.

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Data sources for this page

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