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PD-1 Antibody and Radiotherapy for Recurrent Cervical Cancer

L

Lei Li

Status

Unknown

Conditions

Objective Remission Rate
Immune Checkpoint Inhibitors
Anti-programmed Death-1 Antibody
Persistent Advanced Cervical Carcinoma
Overall Survival
Radiotherapy
Recurrent Cervical Carcinoma
Progression-free Survival
Metastatic Cervical Carcinoma
Severe Adverse Events

Treatments

Combination Product: Radiotherapy for targeted lesions and PD-1 antibody

Study type

Observational

Funder types

Other

Identifiers

NCT05310305
IMURADIO1

Details and patient eligibility

About

This study is to investigate retrospectively the effects of combination of immune checkpoint inhibitors anti-programmed death-1 antibody (PD-1 antibody) and radiotherapy for recurrent, metastatic and persistent advanced cervical carcinomas. Patients may or may not accept PD-1 antibody as maintenance therapy. Patients are followed up and the survival outcomes are evaluated. The primary endpoint are objective remission rate. The secondary endpoints are progression-free survival, overall survival and severe adverse events.

Enrollment

20 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged 18 years or older
  • Confirmed of recurrent, metastatic, and persistent advanced cervical cancer
  • Confirmed of subtypes of cervical squamous carcinoma, adenocarcinoma and adenosquamous carcinoma
  • Accepting radiotherapy with concurrent anti PD-1 therapy
  • With detailed follow-up outcomes

Exclusion criteria

  • Not meeting all of the inclusion criteria

Trial contacts and locations

1

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Central trial contact

Lei Li, M.D.

Data sourced from clinicaltrials.gov

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