Mesothelioma Stratified Therapy (MiST) : A Multi-drug Phase II Trial in Malignant Mesothelioma

NCT03654833 · Status: UNKNOWN · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 186

Last updated 2023-03-14

No results posted yet for this study

Summary

MiST is a British Lung Foundation funded, University of Leicester Study, a multi-arm stratified therapy based clinical trial for patients with relapsed mesothelioma.

The goal of MiST is to enable acceleration of novel, effective personalised therapy as a basis for improving survival outcomes for patients with mesothelioma.

Conditions

  • Mesothelioma, Malignant

Interventions

DRUG

Rucaparib

PARP inhibitor

DRUG

Abemaciclib

CDK4/6 inhibitor

DRUG

pembrolizumab & bemcentinib

PD1 checkpoint inhibitor, AXL inhibitor

DRUG

Atezolizumab & Bevacizumab

PDL1 checkpoint inhibitor, VEGF inhibitor

DRUG

Dostarlimab and Niraparib

IG Antibody, PARP Inhibitor

Sponsors & Collaborators

  • British Lung Foundation

    collaborator OTHER
  • Clovis Oncology, Inc.

    collaborator INDUSTRY
  • Eli Lilly and Company

    collaborator INDUSTRY
  • Merck Sharp & Dohme LLC

    collaborator INDUSTRY
  • BerGenBio ASA

    collaborator INDUSTRY
  • Roche Pharma AG

    collaborator INDUSTRY
  • University Hospitals, Leicester

    collaborator OTHER
  • The Christie NHS Foundation Trust

    collaborator OTHER
  • GlaxoSmithKline

    collaborator INDUSTRY
  • University of Leicester

    lead OTHER

Principal Investigators

  • Dean Fennell, PhD, FRCP · University of Leicester

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-01-28
Primary Completion
2023-10-31
Completion
2023-10-31

Countries

  • United Kingdom

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03654833 on ClinicalTrials.gov