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Second-line Study of PEGPH20 and Pembro for HA High Metastatic PDAC

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT03634332
Recruitment Status : Recruiting
First Posted : August 16, 2018
Last Update Posted : May 7, 2019
Sponsor:
Collaborators:
Merck Sharp & Dohme Corp.
Halozyme Therapeutics
University of Washington
Information provided by (Responsible Party):
Pancreatic Cancer Research Team

Brief Summary:

This study is the study of the combination of PEGPH20 and Pembrolizumab (MK-3475) for patients with previously treated Hyaluronan High (HA-high) metastatic pancreatic ductal adenocarcinoma. This study is an interventional, unblinded, open label study. Approximately 35 subjects will be enrolled. The trial will require approximately a total of 18 months, including 12 months for enrollment, with an additional 6 months for patient follow-up, data collection and study closure.

Each subject will participate in the trial from the time the subject signs the Informed Consent Form (ICF) through the final contact. After a screening phase of up to 21 days, eligible subjects will receive PEGPH20 beginning with Cycle 1 Day 1, on Days 1, 8 15 of every 3 week-cycles and pembrolizumab beginning on Cycle 1 Day 1 (2-4 hrs after PEGPH20), every 3-week-cycles.

Treatment with PEGPH20 and pembrolizumab will continue until progressive disease (PD), unacceptable adverse events (AEs), intercurrent illness that prevents further administration of treatment, investigator's decision to withdraw the subject, subject withdraws consent, pregnancy of the subject, noncompliance with trial treatment or procedure requirements, subject receives 35 treatments (approximately 24 months) of pembrolizumab, or administrative reasons requiring cessation of treatment. Subjects who discontinue for reasons other than PD will have post-treatment follow-up for disease status until PD, initiating a non-study cancer treatment, withdrawing consent, or becoming lost to follow-up. All subjects will be followed by telephone for overall survival (OS) until death, withdrawal of consent, or the end of the study.

After the end of treatment, each subject will be followed for 30 days for AE monitoring. Serious adverse events (SAE) and events of clinical interest (ECI) will be collected for 90 days after the end of treatment or for 30 days after the end of treatment if the subject initiates new anticancer therapy, whichever is earlier.


Condition or disease Intervention/treatment Phase
Pancreatic Ductal Adenocarcinoma Pancreatic Cancer Pancreatic Neoplasms Drug: PEGPH20 Biological: Pembrolizumab Phase 2

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 35 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Intervention Model Description: Single Treatment Arm for Second-Line treatment of Specific sub-set (HA high) of advanced pancreatic cancer patients
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Phase II Study of PEGPH20 and Pembrolizumab (MK-3475) for Patients With Previously Treated Hyaluronan High (HA-High) Metastatic Pancreatic Ductal Adenocarcinoma
Actual Study Start Date : May 1, 2019
Estimated Primary Completion Date : October 2020
Estimated Study Completion Date : January 2021

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: PEGPH20 plus Pembrolizumab
All patients will receive treatment with PEGPH20 3 micrograms/kg IV weekly x 3, and pembrolizumab 200 mg IV every 3 weeks, in 3-week cycles.
Drug: PEGPH20
PEGPH20 is a PEGylated, neutral-pH-active human hyaluronidase PH20 produced by recombinant DNA technology

Biological: Pembrolizumab
Pembrolizumab is a potent and highly selective humanized monoclonal antibody (mAb) of the IgG4/kappa isotype designed to directly block the interaction between PD-1 and its ligands, PD-L1 and PD-L2
Other Names:
  • Keytruda
  • MK-3475




Primary Outcome Measures :
  1. Progression Free Survival [ Time Frame: PFS will be assessed from Date of registration through study closure, up to 24 months. PFS is calculated as the number of days from date of registration to date of disease progression or symptomatic deterioration, or death due to any cause. ]
    Evaluate the progression-free survival (PFS) for patients treated with pembrolizumab and PEGPH20


Secondary Outcome Measures :
  1. Number of participants with treatment-related adverse events as assessed by CTCAE v5.0 [ Time Frame: Safety and Tolerability using CTCAE v5.0 will be assessed from Day 1 of study treatment through 30-days past the last study treatment per patient, through study closure, up to 24 months. ]
    Evaluate the safety and tolerability of this treatment combination as assessed by CTCAE v5.0.

  2. Overall Response Rate [ Time Frame: ORR is assessed from Day 1 of treatment to study closure, up to 24 months. ORR is calculated by adding the Complete Responses (CR) with the Partial Responses (PR), based on RECIST v1.1, recorded at each disease evaluation for each patient. ]
    Evaluate the Overall Response Rate (ORR, CR + PR) based on RECIST v1.1

  3. Disease Control Rate [ Time Frame: DCR is assessed from Day 1 of treatment to study closure, up to 24 months. DCR is calculated by adding the Complete Responses, Partial Responses and Stable Disease, based on RECIST v1.1, recorded at each disease evaluation for each patient. ]
    Evaluate Disease Control Rate (DCR, CR +PR+SD)

  4. Duration of Response [ Time Frame: DOR is assessed from Day 1 of treatment to study closure, up to 24 months. DOR is calculated for patients who achieve a CR or PR, as the number of days from the date of response to the date of progression, or death, due to any cause. ]
    Evaluate the Duration of Response (DOR)

  5. Overall Survival [ Time Frame: Overall Survival is assessed from date of registration to study closure, up to 24 months. Overall Survival is calculated as the number of days from date of registration to date of death due to any cause. ]
    Evaluate the Overall Survival


Other Outcome Measures:
  1. Evaluate Plasma Hyaluronan (HA) levels [ Time Frame: Plasma Hyaluronan (HA) levels are measured in blood samples taken at Day 1 of every treatment cycle (1 cycle = 3 weeks), during each patient's study treatment, with data from these samples assessed until study closure, up to 24 months. ]
    Evaluate pre-and post-treatments plasma hyaluronan (HA) levels in blood samples, and correlate with ORR, PFS, and OS

  2. Evaluate immunological biomarkers using flow cytometry in tumor tissue samples [ Time Frame: Immunological biomarkers using flow cytometry are measured in tumor tissue samples taken at 3 timepoints during each patient's study treatment, with data from these samples assessed until study closure, up to 24 months. ]
    Evaluate pre-and post-treatment immunological biomarkers (the percentage and absolute count (cells/mm3) of T-cell subsets) using flow cytometry, in tumor tissue samples and correlate with ORR, PFS, and OS

  3. Evaluate immunological biomarkers--T-cell receptor (TCR) sequencing in tumor tissue samples [ Time Frame: Immunological biomarkers of T-cell receptor (TCR) sequencing are measured in tumor tissue samples taken at 3 timepoints during each patient's study treatment, with data from these samples assessed until study closure, up to 24 months. ]
    Evaluate pre-and post-treatment immunological biomarkers of T-cell receptor (TCR) sequencing in tumor tissue samples, and correlate with ORR, PFS, and OS

  4. Evaluate immunological biomarkers--focused gene profiling of the immune transcriptome [ Time Frame: Immunological biomarkers--focused gene profiling of the immune transcriptome--are measured in tumor tissue samples taken at 3 timepoints during each patient's study treatment, with data assessed until study closure, up to 24 months. ]
    Evaluate pre-and post-treatment immunological biomarkers--focused gene profiling of the immune transriptome--in tumor tissue samples, and correlate with ORR, PFS, and OS

  5. Evaluate immunological biomarkers--Immunohistochemistry (IHC) for T-cells, B-cells, and macrophages subsets [ Time Frame: Immunological biomarkers--IHC of T-cells, B-cells and macrophages subsets are measured in tumor tissue samples taken at 3 timepoints during each patient's study treatment, with data assessed until study closure, up to 24 months. ]
    Evaluate pre-and post-treatment immunological biomarkers--IHC of T-cells, B-cells, and macrophages subsets-- in tumor tissue samples, and correlate with ORR, PFS, and OS

  6. Evaluate Blood Translational Biomarker--Circulating cytokines/chemokines in plasma [ Time Frame: The Translational Biomarkers-- circulating cytokines/chemokines in plasma-- are measured in blood samples taken at 3 timepoints during each patient's study treatment, with data from these samples assessed until study closure, up to 24 months. ]
    Evaluate pre-and post-treatment Translational biomarkers of circulating cytokines/chemokines in plasma blood samples and correlate with ORR, PFS, and OS

  7. Evaluate Blood Translational Biomarkers--flow cytometry [ Time Frame: The Translational Biomarkers using flow cytometry are measured in blood samples taken at 3 timepoints during each patient's study treatment, with data assessed until study closure, up to 24 months. ]
    Evaluate pre-and post-treatment Translational biomarkers in blood samples (the percentage and absolute count (cells/mm3) of T-cell subsets) using flow cytometry, and correlate with ORR, PFS, and OS

  8. Evaluate Blood Translational Biomarkers--T cell receptor (TCR) sequencing [ Time Frame: The Translational Biomarker-- T-cell receptor (TCR) sequencing-- are measured in blood samples taken at 3 timepoints during each patient's study treatment, with data from these samples assessed until study closure, up to 24 months. ]
    Evaluate pre-and post-treatment Translational biomarkers of T-cell receptor (TCR) sequencing in blood samples and correlate with ORR, PFS, and OS



Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Be willing and able to provide written informed consent/assent for the trial.
  2. Histologically confirmed metastatic pancreatic ductal adenocarcinoma, via archived or fresh core biopsy of either primary tumor or metastatic site.
  3. Available tumor tissue (formalin-fixed paraffin-embedded [FFPE] block preferred) with enough tumor to make a minimum of 5-10 unstained, consecutive FFPE slides (10 slides are preferred) of 1 archival block that meets specific tissue sample requirements. Archived or fresh tissue from the primary lesion or a metastatic lesion is required. Note: Fine needle aspirates or brushing biopsies will not be acceptable. This tumor tissue requirement is for the determination of the HA-high or -low expression status.
  4. Subjects must be determined to be HA-high based on archival or fresh tumor biopsy that meets the requirements noted in the previous inclusion criterion.
  5. 18 years of age on day of signing informed consent.
  6. Have measurable metastatic disease based on RECIST 1.1.
  7. Life expectancy ≥ 12 weeks.
  8. Have a performance status of 0 or 1 on the ECOG Performance Scale.
  9. Received no more than 2 prior lines of systemic therapy for metastatic disease (1 or 2 prior lines of therapy for metastatic disease are allowed)
  10. Be willing to provide tumor tissue from newly obtained tumor cores or excisional biopsy for research purposes. Newly-obtained is defined as a specimen obtained within 2 weeks (14 days) prior to initiation of treatment on Day 1.
  11. Be willing to provide tumor tissue from tumor biopsy after 6 weeks of treatment (mandatory, if safe and feasible), and at the time of tumor progression (optional, if safe and feasible). Note: Fine needle aspirates or brushing biopsies will not be acceptable.
  12. Demonstrate adequate organ function, all screening labs should be performed within 14 days of treatment initiation.
  13. Female subjects of childbearing potential should have a negative urine or serum pregnancy within 72 hours prior to receiving the first dose of study medication. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.
  14. Female subjects of childbearing potential must be willing to use an adequate method of contraception for the course of the study through 120 days after the last dose of study medication.

    Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the subject.

  15. Male subjects of childbearing potential must agree to use an adequate method of contraception starting with the first dose of study therapy through 120 days after the last dose of study therapy.

    Note: Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the subject.

  16. No history of acute DVT/PE or CVA/TIA (new within 4 weeks of study registration) or clinical significant carotid artery disease.
  17. If prior history of DVT/PE the patient needs to be on stable doses of anticoagulation with low molecular weight heparins.

    • Patients should have all eligibility criteria met, before undergoing the baseline research biopsy.

Exclusion Criteria:

  1. Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 2 weeks of the first dose of treatment.
  2. Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy (equivalent of > 20 mg of hydrocortisone per day) or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatment.
  3. Has a known history of active tuberculosis (TB).
  4. Hypersensitivity to pembrolizumab or any of its excipients.
  5. Known allergy to PEGPH20 (hyaluronidase).
  6. Current use of megestrol acetate (use within 10 days of Day 1).
  7. Contraindication to heparin as per institutional guidelines.
  8. Has had a prior anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to agents administered more than 2 weeks earlier.
  9. Has had prior chemotherapy, targeted small molecule therapy, or radiation therapy within 2 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to a previously administered agent.

    • Note: Subjects with ≤ Grade 2 neuropathy are an exception to this criterion and may qualify for the study.
    • Note: If subject received major surgery, they must have recovered adequately from the toxicity and/or complications from the intervention prior to starting therapy.
  10. Has a known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer.
  11. Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis. Subjects with previously treated brain metastases may participate provided they are stable (without evidence of progression by imaging for at least four weeks prior to the first dose of trial treatment and any neurologic symptoms have returned to baseline), have no evidence of new or enlarging brain metastases, and are not using steroids for at least 7 days prior to trial treatment. This exception does not include carcinomatous meningitis which is excluded regardless of clinical stability.
  12. Has active autoimmune disease that has required systemic treatment in the past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs), or documented history of clinically severe autoimmune disease (e.g., colitis, Crohns' disease)*. Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.

    *Any relevant diseases that are not listed as examples of exclusionary diseases are to be discussed with the Sponsor-Investigator.

  13. Has known history of, or any evidence of active, non-infectious pneumonitis.
  14. Has a history of (non-infectious) pneumonitis that required steroids or has current pneumonitis.
  15. Has known hepatobiliary diseases (e.g., primary biliary cholangitis, primary sclerosing cholangitis, immune mediated cholangitis); patients with cholangitis attributed to infectious etiology (e.g., ascending cholangitis, bacterial cholangitis) are eligible if the infection has been fully recovered prior to the screening visit.
  16. Has known history of drug-induced hepatobiliary toxicities
  17. Has an active infection requiring systemic therapy.
  18. Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject's participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.
  19. Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial.
  20. Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the pre-screening or screening visit through 120 days after the last dose of trial treatment.
  21. Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent, or any other immune checkpoint inhibitors.
  22. Has received prior therapy with PEGPH20, or has participated in the Halozyme HALO 301 phase III study.
  23. Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).
  24. Has known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C (e.g., HCV RNA [qualitative] is detected).
  25. Has received a live vaccine within 30 days of planned start of study therapy. Note: Seasonal influenza vaccines for injection are generally inactivated flu vaccines and are allowed; however intranasal influenza vaccines (e.g., Flu-Mist®) are live attenuated vaccines, and are not allowed.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03634332


Contacts
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Contact: Amy Stoll-Dastice, MS 206-816-4239 amys@crab.org
Contact: Stephanie Edwards 206-652-4452 stephe@crab.org

Locations
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United States, Arizona
Banner Health - MD Anderson Cancer Center Not yet recruiting
Gilbert, Arizona, United States, 85234
Contact: Jana Bergelin    480-256-5168    Jana.bergelin@bannerhealth.com   
Principal Investigator: Tomislav Dragovich, MD, PhD         
United States, California
Cedars Sinai Medical Center Not yet recruiting
Los Angeles, California, United States, 80048
Contact: Virginia Naessig, MA    310-423-0721    virginia.naessig@cshs.org   
Principal Investigator: Andrew Hendifar, MD         
United States, New Jersey
Rutgers - Cancer Institute of New Jersey (CINJ) Active, not recruiting
New Brunswick, New Jersey, United States, 08901
United States, Washington
University of Washington--Seattle Cancer Care Alliance Recruiting
Seattle, Washington, United States, 98101
Contact: Samantha Elliot, CCRP    206-606-6387    tellio@seattlecca.org   
Contact: Tracey Pierce    206-606-7603    pierct@seattlecca.org   
Sub-Investigator: Elena G Chiorean, MD         
Principal Investigator: David B Zhen, MD         
United States, Wisconsin
Medical College of Wisconsin Recruiting
Milwaukee, Wisconsin, United States, 53226
Contact: Barbara Dion       badion@mcw.edu   
Principal Investigator: Paul Ritch, MD         
Sponsors and Collaborators
Pancreatic Cancer Research Team
Merck Sharp & Dohme Corp.
Halozyme Therapeutics
University of Washington
Investigators
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Principal Investigator: Gabriella Chiorean, MD Seattle Cancer Care Alliance--University of Washington
Publications:
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Responsible Party: Pancreatic Cancer Research Team
ClinicalTrials.gov Identifier: NCT03634332    
Other Study ID Numbers: PCRT 16-001
First Posted: August 16, 2018    Key Record Dates
Last Update Posted: May 7, 2019
Last Verified: May 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: Yes
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by Pancreatic Cancer Research Team:
pancreatic
pancreas
cancer
adenocarcinoma
Additional relevant MeSH terms:
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Adenocarcinoma
Pancreatic Neoplasms
Carcinoma
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms
Digestive System Neoplasms
Neoplasms by Site
Endocrine Gland Neoplasms
Digestive System Diseases
Pancreatic Diseases
Endocrine System Diseases
Pembrolizumab
Antineoplastic Agents, Immunological
Antineoplastic Agents