Study identifier:D4191C00003
ClinicalTrials.gov identifier:NCT02087423
EudraCT identifier:2013-005427-16
CTIS identifier:2024-512379-10-00
A Phase II,Non-comparative,Open label, Multi-centre, International Study of MEDI4736, in Patients with Locally Advanced or Metastatic Non Small Cell Lung Cancer (Stage IIIB-IV) who have received at least 2 Prior Systemic Treatment Regimens Including 1 Platinum-based Chemotherapy Regimen
Non-small Cell Lung Cancer
Phase 2
No
MEDI4736
All
446
Interventional
18 Years - 130 Years
Allocation: Non-randomized
Endpoint Classification: Efficacy
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Verified 01 Aug 2024 by AstraZeneca
AstraZeneca
-
No locations available
Arms | Assigned Interventions |
---|---|
Experimental: MEDI4736 see below | Drug: MEDI4736 MEDI4736 (durvalumab) by intravenous infusion every two weeks. Treatment from Day 1 for a maximum of 12 months or study drug withdrawal if this occurs earlier. Patients who achieve CR, PR or SD through the end of the initial 12-month treatment period can restart treatment with MEDI4736 (durvalumab) when they eventually do progress. This retreatment period can continue for as long as the investigator considers to patient to be receiving clinical benefit. |