CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 137 enrolled
Drug / intervention
Recombinant PRAME protein combined with the AS15 Adjuvant System GSK2302032A +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/NCT01853878
NCT01853878Phase 2Completed

GSK2302032A Antigen-Specific Cancer Immunotherapeutic as Adjuvant Therapy in Patients With Non-Small Cell Lung Cancer

GlaxoSmithKline·interventional·Posted May 15, 2013·Updated Aug 28, 2019

In Brief

A Phase 2 clinical trial evaluating Recombinant PRAME protein combined with the AS15 Adjuvant System GSK2302032A and Placebo for Lung Cancer, Non-Small Cell. Completed, enrolled 137 participants across 39 sites in 9 countries.

Detailed Summary

The purpose of this study was to test a potential new kind of anti-cancer treatment, called PRAME immunotherapy in resected patients with lung cancer. Based on scientific and medical relevance, the clinical study was ended on 24 August 2016. The participants were no longer enrolled in the study, the follow ups on subjects were stopped and the collection and analysis of samples for further research purposes was stopped. After the stop to recruitment, the study was unblinded, as per the amended protocol, the study treatment was continued and completed with the subjects of the active treatment group who were willing to continue. Subjects in the placebo group were withdrawn. There was no longer an active follow-up of patients after discontinuation or completion of the treatment. The study ended 30 days after the last dose was administered. As a result, primary and secondary objectives were not assessed as planned. All clinical and safety data collected in the study were analysed descriptively. For each biological sample already collected in the scope of this study and not tested yet, testing was not performed by default, except if a scientific rationale remained relevant despite the premature termination of the study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesEstonia, France, Germany, Japan, Poland, Russia, South Korea, United Kingdom, United States
Collaborators--

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedMay 15, 2013
Enrollment StartJun 12, 2013
Primary CompletionAug 24, 2016
TodayJul 2, 2026
Enrollment to primary: 3.2 yearsPosted 13.1 years ago

Interventions

Recombinant PRAME protein combined with the AS15 Adjuvant System GSK2302032Abiological

Intramuscular administration

Placebobiological

Intramuscular administration