CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 24 enrolled
Drug / intervention
MEDI4736 +2 moredrug
Likely dose
MEDI4736 50 mgfrom 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/NCT02592551
NCT02592551Phase 2Completed

Window Of Opportunity Phase II Study Of MEDI4736 Or MEDI4736 + Tremelimumab In Surgically Resectable Malignant Pleural Mesothelioma

Baylor College of Medicine·interventional·Posted Oct 30, 2015·Updated Sep 29, 2022

In Brief

A Phase 2 clinical trial evaluating MEDI4736, Tremelimumab, and 1 other intervention for Mesothelioma. Completed, enrolled 24 participants across 1 site.

Detailed Summary

The objective of this study is to determine whether MEDI4736 or combination therapy with MEDI4736 + tremelimumab are associated with favorable alterations of the intratumoral immunologic environment in subjects undergoing resectional surgery for Malignant Pleural Mesothelioma MPM.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsMesothelioma
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20162017201820192020202120222023202420252026
First PostedOct 30, 2015
Enrollment StartMay 11, 2016
Primary CompletionAug 6, 2019
Study CompletionSep 1, 2022
TodayJul 2, 2026
Enrollment to primary: 3.2 yearsPosted 10.7 years ago

Interventions

MEDI4736drug

MEDI4736 is formulated at 50 mg/mL in 26 mM histidine/histidine-HCl, 275 mM trehalose dihydrate, 0.02% (w/v) polysorbate 80, pH 6.0.

Tremelimumabdrug

Tremelimumab Drug Product is formulated at a nominal concentration of 20 mg/mL in 20 mM histidine/histidine hydrochloride, 222 mM trehalose dihydrate, 0.02% (weight/volume \[w/v\]) polysorbate 80, 0.27 mM disodium edetate dihydrate (EDTA), pH 5.5.

no other nameother

Neither MEDI4736 nor Tremelimumab will be used.