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Clinical Trials/NCT03727880
NCT03727880
Completed
Phase 2

A Randomized Phase II Study of Pembrolizumab With or Without Defactinib, a Focal Adhesion Kinase Inhibitor Following Chemotherapy as a Neoadjuvant and Adjuvant Treatment for Resectable Pancreatic Ductal Adenocarcinoma (PDAC)

Lei Zheng3 sites in 1 country28 target enrollmentJune 4, 2019

Overview

Phase
Phase 2
Intervention
Pembrolizumab
Conditions
Resectable Pancreatic Ductal Adenocarcinoma (PDAC)
Sponsor
Lei Zheng
Enrollment
28
Locations
3
Primary Endpoint
Pathologic Complete Response (pCR) Rate
Status
Completed
Last Updated
2 months ago

Overview

Brief Summary

This study will test the effectiveness (anti-tumor activity), safety, and ability to increase the body's immune system to fight pancreatic cancer by combining standard chemotherapy before and after surgery, with study drug PD-1 antibody, pembrolizumab, with and without study drug, focal adhesion kinase inhibitor (FAK), defactinib, in people with "high risk" resectable (surgically removable) pancreatic cancer. The purpose of this study is to evaluate if reprograming the tumor microenvironment by targeting FAK following chemotherapy can potentiate anti-programmed death-1 (PD-1) antibody.

Registry
clinicaltrials.gov
Start Date
June 4, 2019
End Date
January 15, 2025
Last Updated
2 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Lei Zheng
Responsible Party
Sponsor Investigator
Principal Investigator

Lei Zheng

Executive Director of University of Texas Health Science Center at San Antonio Cancer Center

The University of Texas Health Science Center at San Antonio

Eligibility Criteria

Inclusion Criteria

  • Age ≥18 years.
  • Has pancreatic ductal adenocarcinoma
  • Has resectable disease at the time of diagnosis
  • Has not received any systemic therapy for pancreatic ductal adenocarcinoma
  • Has stage ≤ IIb disease at time of diagnosis and enrollment
  • Elevated tumor marker, CA (carbohydrate antigen) 19-9 \>200
  • ECOG performance status 0 or 1
  • Patient must have adequate organ function defined by the study-specified laboratory tests.
  • Must use acceptable form of birth control while on study.
  • Ability to understand and willingness to sign a written informed consent document.

Exclusion Criteria

  • Patients who have received any prior chemotherapy, radiotherapy or investigational agents for pancreatic cancer.
  • Patients who have received prior treatment with anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CTLA-4, or with an agent directed to another stimulatory or co-inhibitory T-cell receptor (e.g., CTLA-4, OX 40, CD137).
  • Has received prior therapy with FAK inhibitor.
  • Woman who are pregnant or breastfeeding.
  • Have received a live vaccine or live-attenuated vaccine within 30 days prior to study drug.
  • Is currently or has participated in another investigational study within 4 weeks prior to receiving study drug.
  • History or current use of immunosuppressive medications within 7 days prior to study medications.
  • Has a known additional malignancy that is progressing or has required active treatment within the past 2 years or that is expected to require active treatment within two years.
  • Has active autoimmune disease that has required systemic treatment in the past 2 years.
  • Has a history of (non-infectious) pneumonitis/interstitial lung disease or current pneumonitis.

Arms & Interventions

Arm A - Pembrolizumab and Defactinib

Intervention: Pembrolizumab

Arm A - Pembrolizumab and Defactinib

Intervention: Defactinib

Arm B - Pembrolizumab

Intervention: Pembrolizumab

Outcomes

Primary Outcomes

Pathologic Complete Response (pCR) Rate

Time Frame: 4 years

Percent of subjects with a pathologic complete response (pCR) per the tumor regression grade scores established by the College of American Pathologist: Grade 0= complete response (no viable cancer cells), Grade 1= near complete response (single cells or rare small groups of cancer cells), Grade 2= partial response (residual tumor with evidence of regression), or Grade 3= no response (extensive residual tumor with no evidence of regression).

Secondary Outcomes

  • Overall Survival (OS)(4 years)
  • Disease Free Survival (DFS)(4 years)
  • Number of Participants Experiencing Study Drug-related Toxicities(4 years)

Study Sites (3)

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