CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 76 enrolled
Drug / intervention
PDR001 +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03365791
NCT03365791Phase 2Completed

Modular Phase 2 Study to Link Combination Immune-therapy to Patients With Advanced Solid and Hematologic Malignancies. Module 9: PDR001 Plus LAG525 for Patients With Advanced Solid and Hematologic Malignancies.

Novartis Pharmaceuticals·interventional·Posted Dec 7, 2017·Updated May 27, 2022

In Brief

A Phase 2 clinical trial evaluating PDR001 and LAG525 for Small Cell Lung Cancer and 7 related conditions. Completed, enrolled 76 participants across 20 sites.

Detailed Summary

The purpose of this signal seeking study is to determine whether treatment with PDR001 and LAG525 demonstrates sufficient efficacy in advanced malignancies to warrant further study.

Study Details

Timeline

Phase 2CompletedFinished
201820192020202120222023202420252026
First PostedDec 7, 2017
Enrollment StartJan 24, 2018
Primary CompletionFeb 21, 2019
Study CompletionSep 17, 2020
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 8.6 years ago

Interventions

PDR001biological

PDR001 is a high-affinity, ligand-blocking, humanized anti-programmed death-1 (PD-1) IgG4 antibody that blocks the binding of Programmed death-ligand 1 (PD-L1) and programmed death-ligand 2 (PD-L2) to PD-1.

LAG525biological

LAG525 is a high-affinity, ligand-blocking, humanized anti-LAG-3 IgG4 antibody which blocks the binding of the known LAG-3 ligand MHC class II to LAG-3.