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Completed Phase 4 Interventional Results available

Durvalumab Long-Term Safety and Efficacy Study

ClinicalTrials.gov ID: NCT04078152

Public ClinicalTrials.gov record NCT04078152. 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 Nov 7, 2026, 5:26 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-Label, Multi-Center, Global Study to Evaluate Long Term Safety and Efficacy in Patients Who Are Receiving or Who Previously Received Durvalumab in Other Protocols (WAVE)

Brief summary

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

The aims of the study are to monitor the long-term safety of durvalumab, to provide continued treatment or retreatment with durvalumab to eligible patients, and to collect overall survival (OS) information.

Study identification

NCT ID
NCT04078152
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
AstraZeneca
Industry
Enrollment
163 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 130 Years
Sex
All
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
Sep 5, 2019 (Actual)
Primary completion
Oct 31, 2022 (Actual)
Completion
Oct 31, 2024 (Actual)
Last update posted
Dec 20, 2024

2019 – 2024

United States locations

U.S. sites
12
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
Research Site Fullerton California 92835 —
Research Site Washington D.C. District of Columbia 20007 —
Research Site Augusta Georgia 30912 —
Research Site Baltimore Maryland 21201 —
Research Site Minneapolis Minnesota 55407 —
Research Site St Louis Missouri 63110 —
Research Site Mineola New York 11501 —
Research Site Chapel Hill North Carolina 27514 —
Research Site Huntersville North Carolina 28078 —
Research Site Greenville South Carolina 29605 —
Research Site Nashville Tennessee 37203 —
Research Site Dallas Texas 75251 —

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 104 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04078152, 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 Dec 20, 2024 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04078152 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →