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Completed Phase 3 Interventional Results available

Study of Durvalumab With Chemoradiotherapy for Women With Locally Advanced Cervical Cancer (CALLA)

ClinicalTrials.gov ID: NCT03830866

Public ClinicalTrials.gov record NCT03830866. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 9:03 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III, Randomized, Multi-Center, Double-Blind, Global Study to Determine the Efficacy and Safety of Durvalumab in Combination With and Following Chemoradiotherapy Compared to Chemoradiotherapy Alone for Treatment in Women With Locally Advanced Cervical Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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

Study identification

NCT ID
NCT03830866
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
770 participants

Conditions and interventions

Interventions

Biological · Drug · Radiation

Eligibility (public fields only)

Age range
18 Years to 130 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 15, 2019 (Actual)
Primary completion
Jan 20, 2022 (Actual)
Completion
Jul 3, 2023 (Actual)
Last update posted
Jul 26, 2024

2019 – 2023

United States locations

U.S. sites
16
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
Research Site Phoenix Arizona 85016 —
Research Site La Jolla California 92093 —
Research Site Orange California 92868 —
Research Site Fort Myers Florida 33905 —
Research Site Miami Florida 33136 —
Research Site Augusta Georgia 30912 —
Research Site Ann Arbor Michigan 48109 —
Research Site Lake Success New York 11042 —
Research Site The Bronx New York 10461 —
Research Site Cleveland Ohio 44111 —
Research Site Cleveland Ohio 44124 —
Research Site Cleveland Ohio 44195 —
Research Site Nashville Tennessee 37203 —
Research Site Dallas Texas 75235 —
Research Site Dallas Texas 75390 —
Research Site Spring Texas 77380 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 101 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03830866, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 26, 2024 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03830866 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →