Study of FAK (Defactinib) and PD-1 (Pembrolizumab) Inhibition in Advanced Solid Malignancies (FAK-PD1)

NCT02758587 · Status: UNKNOWN · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 59

Last updated 2018-03-19

No results posted yet for this study

Summary

This study will explore whether defactinib (a FAK inhibitor) can be safely and tolerably combined with pembrolizumab (a PD-1 inhibitor) and will look for early indications of improved anticancer immunotherapy. It will focus on three key cancers, all in clear need of improved therapies - NSCLC, pancreatic cancer and mesothelioma.

Conditions

  • Carcinoma, Non-small-cell Lung
  • Mesothelioma
  • Pancreatic Neoplasms

Interventions

DRUG

Defactinib

cross reference with arm/group descriptions

DRUG

Pembrolizumab

cross reference with arm/group descriptions

Sponsors & Collaborators

  • University of Glasgow

    collaborator OTHER
  • Cancer Research UK

    collaborator OTHER
  • Merck Sharp & Dohme LLC

    collaborator INDUSTRY
  • Verastem, Inc.

    collaborator INDUSTRY
  • University of Edinburgh

    collaborator OTHER
  • University of Southampton

    collaborator OTHER
  • University of Leicester

    collaborator OTHER
  • Queen's University, Belfast

    collaborator OTHER
  • NHS Greater Glasgow and Clyde

    lead OTHER

Principal Investigators

  • Stefan Symeonides · Edinburgh Cancer Research Centre, University of Edinburgh, Western General Hospital, Edinburgh EH4 2XR

  • Jeff Evans · Beatson West of Scotland Cancer Centre, 1053 Great Western Road, Glasgow G12 0YN

  • Christian Ottensmeier · Cancer Research UK Centre, Southampton University Hospitals and University of Southampton, Southampton SO16 6YD

  • Dean Fennell · Department of Cancer Studies, University of Leicester, Leicester Royal Infirmary, Leicester LE2 7LX

  • Vicky Coyle · Belfast Health and Social Care Trust, Cancer Centre, Lisburn Road, Belfast BT9 7BL

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-07-04
Primary Completion
2019-05-31
Completion
2021-12-31

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 NCT02758587 on ClinicalTrials.gov