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Clinical Trial Summary

This is a randomized, multi-center, double-blind, placebo-controlled, global, Phase III study to determine the efficacy and safety of durvalumab + Chemoradiotherapy versus Chemoradiotherapy alone as treatment in Women With Locally Advanced Cervical Cancer


Clinical Trial Description

Women will be randomized in a 1:1 ratio to receive treatment with concurrent durvalumab + standard of care (SoC) or Placebo + Soc, followed by durvalumab/placebo maintenance for 24 months. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03830866
Study type Interventional
Source AstraZeneca
Contact
Status Completed
Phase Phase 3
Start date February 15, 2019
Completion date July 3, 2023

See also
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