A Multicenter Observational PMS Study Assessing Durvalumab Safety in Indian Adults With Resectable NSCLC

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAstraZeneca

About this trial

This will be a single-arm, multicenter, prospective, observational, real-world study and the data source is the patients' medical record at each site. A total of 78 patients will be enrolled in the study.

Eligibility criteria

Qualifiers

Patients with newly diagnosed previously untreated resectable NSCLC (tumors ≥ 4 cm and/or node positive) and no known EGFR mutations or ALK rearrangements prescribed with durvalumab as per local prescriber information.

Provision of signed, written and dated informed consent

Disqualifiers

Presence of unresectable or metastatic disease.

Prior treatment with durvalumab for any other indications

Requires concurrent treatment for cancers other than resectable NSCLC

Concurrently participating in any other clinical trial

Trial design

Treatments tested in this trial

  • IMFINZI

Treatment groups

No treatment groups listed

Locations

This trial has no locations

Sponsors and collaborators