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A Trial of Intratumoral Injections of SD-101 in Combination With Pembrolizumab in Patients With Metastatic Melanoma or Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma

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. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02521870
Recruitment Status : Terminated (A strategic restructuring including the planned conclusion of clinical oncology development programs and no further sponsoring of the development of SD-101.)
First Posted : August 13, 2015
Last Update Posted : June 16, 2020
Sponsor:
Collaborator:
Merck Sharp & Dohme Corp.
Information provided by (Responsible Party):
Dynavax Technologies Corporation

Brief Summary:

This is a phase 1b/2, open-label, multicenter trial designed to evaluate the safety, tolerability, biologic activity, and preliminary efficacy of intratumoral SD-101 injections in combination with intravenous pembrolizumab in patients with metastatic melanoma or recurrent or metastatic head and neck squamous cell carcinoma (HNSCC).

This study will be conducted in 2 phases. Phase 1 evaluates SD-101 given in combination with pembrolizumab in melanoma populations (anti-PD-1/L1 naïve and anti-PD-1/L1 experienced with progressive disease) in up to 4 Dose Escalation cohorts to identify a recommended Phase 2 dose (RP2D) to be evaluated in up to 4 Dose Expansion cohorts in Phase 2. Phase 2 also includes up to 4 Dose Expansion cohorts of patients with HNSCC (anti-PD-1/L1 naïve and anti-PD-1/L1 experienced with progressive disease).


Condition or disease Intervention/treatment Phase
Metastatic Melanoma Head Neck Cancer Drug: SD-101(1) Biological: Pembrolizumab Drug: SD-101(2) Biological: SD-101(3) Phase 1 Phase 2

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 241 participants
Allocation: Non-Randomized
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: A Phase 1b/2, Open-label, Multicenter, Dose-escalation and Expansion Trial of Intratumoral SD-101 in Combination With Pembrolizumab in Patients With Metastatic Melanoma or Recurrent or Metastatic Head and Neck Squamous Cell Carcinoma (SYNERGY-001)
Study Start Date : September 2015
Actual Primary Completion Date : April 2020
Actual Study Completion Date : April 2020


Arm Intervention/treatment
Experimental: Dose Escalation Phase 1b
Determine the maximum tolerated dose (MTD) of escalating doses of SD-101(1) administered in combination with pembrolizumab in patients with melanoma (anti-PD-1/L1 therapy naïve and experienced patients with progressive disease).
Drug: SD-101(1)
SD-101 administered intratumorally at escalating doses (up to 11 doses).

Biological: Pembrolizumab
Pembrolizumab administered intravenously, 200 mg Q3W for two years (up to 35 doses).

Experimental: Dose Expansion Phase 2 (Cohort 1)
Determine the safety and efficacy of SD-101(2) and pembrolizumab in anti-PD-1/L1 therapy naïve patients with recurrent or metastatic melanoma.
Drug: SD-101(2)
Dose Q1W for 4 weeks followed by dose Q3W for 7 weeks, then 9 weeks off, then dose Q1W for 4 weeks followed by dose Q3W for 7 weeks (up to 22 total doses).

Biological: Pembrolizumab
Pembrolizumab administered intravenously, 200mg Q3W for two years (up to 35 doses).

Experimental: Dose Expansion Phase 2 (Cohort 2)
Determine the safety and efficacy of SD-101(2) and pembrolizumab in anti-PD-1/L1 therapy progressing patients with recurrent or metastatic melanoma.
Drug: SD-101(2)
Dose Q1W for 4 weeks followed by dose Q3W for 7 weeks, then 9 weeks off, then dose Q1W for 4 weeks followed by dose Q3W for 7 weeks (up to 22 total doses).

Biological: Pembrolizumab
Pembrolizumab administered intravenously, 200mg Q3W for two years (up to 35 doses).

Experimental: Dose Expansion Phase 2 (Cohort 3)
Determine the safety and efficacy of SD-101(2) and pembrolizumab in anti-PD-1/L1 therapy naïve patients with recurrent head and neck squamous cell carcinoma.
Drug: SD-101(2)
Dose Q1W for 4 weeks followed by dose Q3W for 7 weeks, then 9 weeks off, then dose Q1W for 4 weeks followed by dose Q3W for 7 weeks (up to 22 total doses).

Biological: Pembrolizumab
Pembrolizumab administered intravenously, 200mg Q3W for two years (up to 35 doses).

Experimental: Dose Expansion Phase 2 (Cohort 4)
Determine the safety and efficacy of SD-101(2) and pembrolizumab in anti-PD-1/L1 therapy progressing patients with recurrent head and neck squamous cell carcinoma.
Drug: SD-101(2)
Dose Q1W for 4 weeks followed by dose Q3W for 7 weeks, then 9 weeks off, then dose Q1W for 4 weeks followed by dose Q3W for 7 weeks (up to 22 total doses).

Biological: Pembrolizumab
Pembrolizumab administered intravenously, 200mg Q3W for two years (up to 35 doses).

Experimental: Dose Expansion Phase 2 (Cohort 5)
Determine the safety and efficacy of SD-101(3) and pembrolizumab in anti-PD-1/L1 therapy naïve patients with recurrent or metastatic melanoma.
Biological: SD-101(3)
Dose Q1W for 4 weeks followed by dose Q3W for 16 additional weeks (up to 20 total doses).

Biological: Pembrolizumab
Pembrolizumab administered intravenously, 200mg Q3W for two years (up to 35 doses).

Experimental: Dose Expansion Phase 2 (Cohort 6)
Determine the safety and efficacy of SD-101(3) and pembrolizumab in anti-PD-1/L1 therapy naïve patients with recurrent head and neck squamous cell carcinoma.
Biological: SD-101(3)
Dose Q1W for 4 weeks followed by dose Q3W for 16 additional weeks (up to 20 total doses).

Biological: Pembrolizumab
Pembrolizumab administered intravenously, 200mg Q3W for two years (up to 35 doses).

Experimental: Dose Expansion Phase 2 (Cohort 7)
Determine the safety and efficacy of SD-101(3) and pembrolizumab in anti-PD-1/L1 therapy refractory or resistant patients with recurrent head and neck squamous cell carcinoma.
Biological: SD-101(3)
Dose Q1W for 4 weeks followed by dose Q3W for 16 additional weeks (up to 20 total doses).

Biological: Pembrolizumab
Pembrolizumab administered intravenously, 200mg Q3W for two years (up to 35 doses).

Experimental: Dose Expansion Phase 2 (Cohort 8)
Determine the safety and efficacy of SD-101(3) and pembrolizumab in anti-PD-1/L1 therapy refractory or resistant patients with recurrent or metastatic melanoma.
Biological: SD-101(3)
Dose Q1W for 4 weeks followed by dose Q3W for 16 additional weeks (up to 20 total doses).

Biological: Pembrolizumab
Pembrolizumab administered intravenously, 200mg Q3W for two years (up to 35 doses).




Primary Outcome Measures :
  1. Phase 1b - Number of participants with dose-limiting toxicities (DLTs) [ Time Frame: Day 29 ]
    DLTs evaluated through 7 days after last dose.

  2. Phase 2 - Overall response rate (ORR) per RECIST v1.1 [ Time Frame: Day 743 or EOS ]
    Evaluated through Day 743 or EOS

  3. Phase 1b - Number of participants with injection-site reactions [ Time Frame: Day 743 or EOS ]
    Evaluated through Day 743 or EOS

  4. Phase 1b - Number of participants with adverse events (AEs) [ Time Frame: Day 743 or EOS ]
    Evaluated through Day 743 or EOS

  5. Phase 1b - Number of participants with serious adverse events (SAEs) [ Time Frame: Day 743 or EOS ]
    Evaluated through Day 743 or EOS

  6. Phase 1b - Changes in the expression of IFN-inducible genes in whole blood [ Time Frame: Days 0, 8, and 9 ]
    Evaluated through Day 9


Secondary Outcome Measures :
  1. Phase 2 - Number of participants with injection-site reactions [ Time Frame: Day 743 or EOS ]
    Evaluated through Day 743 or EOS

  2. Phase 2 - Number of participants with AEs [ Time Frame: Day 743 or EOS ]
    Evaluated through Day 743 or EOS

  3. Phase 2 - Number of participants with SAEs [ Time Frame: Day 743 or EOS ]
    Evaluated through Day 743 or EOS

  4. Phase 2 - Time to objective response (TOR) per RECIST v1.1 [ Time Frame: Day 743 or EOS ]
    Evaluated through Day 743 or EOS

  5. Phase 2 - Duration of response per RECIST v1.1 [ Time Frame: Day 743 or EOS ]
    Evaluated through Day 743 or EOS

  6. Phase 2 - Duration of radiographic progression-free survival (PFS) per RECIST v1.1 [ Time Frame: Day 743 or EOS ]
    Evaluated through Day 743 or EOS



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 (Phase 1 and Phase 2)]

  1. Willing and able to provide written informed consent for the trial
  2. Aged 18 years and older
  3. Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 or 1
  4. Patient must have adequate organ function as indicated by the following laboratory values:

    1. Hematological:

      • Absolute neutrophil count (ANC) ≥ 1,500 /mcL
      • Platelet count ≥ 100,000 /mcL
      • Hemoglobin ≥ 9 g/dL or ≥ 5.6 mmol/L
    2. Renal:

      • Serum creatinine ≤ 1.5 × upper limit of normal (ULN) OR
      • Measured or calculated creatinine clearance (GFR can also be used in place of creatinine or CrCl) ≥ 60 mL/min for subject with creatinine levels > 1.5 × institutional ULN
    3. Hepatic:

      • Serum total bilirubin:
      • ≤ 1.5 × ULN OR
      • < 3 × ULN for persons with Gilbert's syndrome OR
      • Direct bilirubin ≤ ULN for patients with total bilirubin levels > 1.5 × ULN
      • Aspartate transaminase (AST) and alanine transaminase (ALT) (also known as serum glutamic oxaloacetic transaminase and serum glutamic pyruvic transaminase)
      • ≤ 2.5 × ULN OR
      • ≤ 5 × ULN for patients with liver metastases
    4. Coagulation:

      • International normalized ratio or prothrombin time (PT) ≤ 1.5 × ULN unless patient is receiving anticoagulant therapy, and as long as PT or partial thromboplastin time (PTT) is within therapeutic range of intended use of anticoagulants
      • Activated partial thromboplastin time (aPTT) ≤ 1.5 × ULN unless patient is receiving anticoagulant therapy, and as long as PT or PTT is within therapeutic range of intended use of anticoagulants
  5. Have provided 2 tissue biopsy samples taken of the target lesion (Lesion A) as a single biopsy split into 2 samples or 2 separate biopsies that meet the minimal sample size requirement per the study laboratory manual. One sample is for determining PD-L1 expression level by immunohistochemistry and can be an archival sample of the anticipated target lesion that has been collected within 3 months of screening. The other sample is for RNA expression profiling and must be a fresh biopsy.
  6. Life expectancy of at least 6 months
  7. Female patients of childbearing potential, as defined in Section 5.2.1, must have a negative urine or serum pregnancy test within 72 hours prior to taking the first dose of trial treatment. If the urine test is positive or cannot be confirmed as negative then a serum test is required which must be negative for the patient to enroll. Women of childbearing potential (WOCBP) must be willing to use 2 medically acceptable methods of contraceptive from Day 1 through 120 days after the last dose of trial treatment. The 2 medically acceptable birth control methods can be either 2 barrier methods or a barrier method plus a hormonal method to prevent pregnancy. The following are considered adequate barrier methods of contraception: diaphragm, condom (by the partner), copper intrauterine device, sponge, or spermicide as per local regulations or guidelines. Appropriate hormonal contraceptives will include any registered and marketed contraceptive agent that contains an estrogen and/or a progestational agent (including oral, subcutaneous, intrauterine, or intramuscular agents).

    Male patients of reproductive potential, as described in Section 5.2.1, must agree to use an adequate method of contraception from Day 1 through 120 days after the last dose of trial treatment.

    Abstinence is acceptable if this is the usual lifestyle and preferred contraception for the patient.

    [Inclusion Criteria (Phase 1 only: Melanoma)]

  8. Histologically or cytologically confirmed unresectable or metastatic (stage IV) melanoma
  9. For Phase 1 Escalation Cohorts 1-4, must have at least 1 lesion that qualifies as a target lesion per RECIST v1.1 except for the minimum measurement of 10 mm in diameter for superficial lesions, is easily accessible (palpable or can be visualized by ultrasound), and is amenable to multiple intratumoral injections. If superficial, the target lesion must be documented photographically.

    [Inclusion Criteria (Phase 2 only: Melanoma)]

  10. Histologically or cytologically confirmed recurrent or unresectable or metastatic (stage IV) melanoma
  11. Must have at least 2 lesions that qualify as a target lesion per RECIST v1.1, and 1 of the qualifying lesions must be easily accessible (palpable or can be visualized by ultrasound) and amenable to multiple intratumoral injections. The target lesion should be of sufficient size such that the required tumor biopsies do not significantly affect tumor assessment per RECIST v1.1. If superficial, the target lesion must measure at least 10 mm in diameter, be measured by calipers, and be documented photographically. Tumor lesions situated in a previously irradiated area, or in an area subjected to other loco-regional therapy, are usually not considered measurable unless there has been demonstrated progression in the lesion. Approval from the Medical Monitor is required to inject a previously radiated lesion.
  12. Expansion Cohort 2: Must have documented PD per RECIST v1.1 on a prior treatment regimen containing an anti-PD-1/L1 drug (see Appendix 6 for definition of PD per RECIST v1.1)
  13. Expansion Cohort 8: Must have all of the following:

    1. Received at least 2 doses of an anti-PD-1/L1 therapy
    2. PD occurred within 3 months after last dose of anti-PD-1/L1 therapy
    3. Documented PD per RECIST v.1.1, which has been confirmed by a second assessment at least 4 weeks from the date of the first documented PD, in the absence of rapid clinical progression

    [Inclusion Criteria (Phase 2 only: HNSCC)]

  14. Histologically or cytologically confirmed recurrent or metastatic HNSCC that could not be treated with curative intent
  15. Must have at least 1 lesion that qualifies as a target lesion per RECIST v1.1, and which must be easily accessible (palpable or can be visualized by ultrasound) and amenable to multiple intratumoral injections. The target lesion should be of sufficient size such that the required tumor biopsies do not significantly affect tumor assessment per RECIST v1.1. Tumor lesions situated in a previously irradiated area, or in an area subjected to other loco-regional therapy, are usually not considered measurable unless there has been demonstrated progression in the lesion. Approval from the Medical Monitor is required to inject a previously radiated lesion.
  16. Expansion Cohort 4: Must have documented confirmed PD per RECIST v1.1 on a prior treatment regimen containing an anti-PD-1/L1 drug (see Appendix 6 for definition of PD per RECIST v1.1)
  17. Expansion Cohort 7: Must have all of the following:

    1. Received at least 2 doses of an anti-PD-1/L1 therapy, where the last dose of anti-PD-1/L1 therapy was within 6 months of study enrollment (Day 1)
    2. Refractory response, ie, PD occurred within 3 months duration of the start of treatment on anti-PD-1/L1 therapy; OR resistant response, ie, PD occurred beyond 3 months duration of treatment on anti-PD-1/L1 therapy and within 6 months after the last dose of treatment on anti-PD-1/L1 therapy
    3. Documented PD per RECIST v.1.1, which has been confirmed by a second assessment at least 4 weeks from the date of the first documented PD, in the absence of rapid clinical progression

[Exclusion Criteria (Phase 1 and Phase 2)]

  1. Received systemic chemotherapy or biological cancer therapy (except anti-PD-1/L1 therapy) within 3 weeks prior to study enrollment
  2. Received prior radiotherapy within 2 weeks of start of study therapy. A shorter washout period may be permitted after approval by the Medical Monitor.
  3. Received small molecule inhibitor targeted therapy, such as tyrosine kinase inhibitors, within 2 weeks prior to study enrollment
  4. Has not recovered to CTCAE Grade 1 or better from the AEs due to cancer therapeutics prior to study enrollment

    NOTE: Patients with ≤ Grade 2 neuropathy or ≤ Grade 2 alopecia or Grade 2 AEs that qualify as Grade 2 due to replacement hormonal or steroid therapy are exceptions to this criterion and may qualify for the study with approval by a Dynavax Medical Monitor.

    If a patient received major surgery, they must have recovered adequately from the toxicity and/or complications from the intervention prior to enrollment.

  5. Received a transfusion of blood products (including platelets or red blood cells) or colony-stimulating factors (including G-CSF, GM-CSF or recombinant erythropoietin) within 4 weeks prior to study enrollment
  6. Is expected to require any other form of anti-cancer therapy while in the trial
  7. Diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy (including immune modulators or systemic corticosteroids) within 7 days prior to study enrollment
  8. Positive for active hepatitis B, hepatitis C, or human immunodeficiency virus (HIV) infection as determined by laboratory tests for HBsAg, anti-HBc, and anti-HBs; anti-HCV; and anti-HIV -1/2, respectively
  9. History of or current uveal or ocular or mucosal melanoma
  10. Active infection including cytomegalovirus
  11. Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial through 120 days after the last dose of trial treatment
  12. Active autoimmune disease requiring systemic treatment in the past 2 years or a disease that requires immunosuppressive medication including systemic lupus erythematosus, rheumatoid arthritis, multiple sclerosis, Sjogren's syndrome, or autoimmune thrombocytopenia. Replacement therapy (eg, thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency) is not considered a form of systemic treatment.
  13. Current pneumonitis or history of (non-infectious) pneumonitis that required steroids
  14. An immune-related AE from a previous immunotherapeutic agent that has not resolved to Grade 1 or less prior to study enrollment. The exception is a Grade 2 AE which qualifies as Grade 2 due to replacement steroid therapy which may be allowed with approval by a Dynavax Medical Monitor.
  15. Known active central nervous system metastases or carcinomatous meningitis

    NOTE: Patients with previously treated brain metastases may participate provided they are stable (without evidence of progression by imaging [using the identical imaging modality for each assessment, either MRI or CT scan] for at least 4 weeks prior to the first dose of trial treatment and with any neurologic symptoms 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.

  16. Use of any investigational agent within the last 28 days prior to study enrollment
  17. Has received a live-virus vaccination within 30 days of planned treatment start. Seasonal flu vaccines that do not contain live virus are permitted.
  18. Any other significant medical or psychiatric condition, laboratory abnormality, or difficulty complying with protocol requirements that may increase the risk associated with trial participation or trial drug administration that may interfere with the interpretation of trial results and, in the judgment of the investigator, would make the patient inappropriate for this trial
  19. History of sensitivity to any component of SD-101 or hypersensitivity reaction to treatment with a monoclonal antibody and/or any of its excipients
  20. Any known additional malignancy that is progressing or requires active treatment. Exceptions are cutaneous melanoma or HNSCC under study per protocol, or basal cell carcinoma of the skin, squamous cell carcinoma of the skin or in situ cervical cancer that has undergone potentially curative therapy.

    [Exclusion Criteria (Phase 2, Melanoma Expansion Cohorts 1 and 5 only)]

  21. Melanoma considered resectable with curative intent
  22. Prior therapy with an anti-PD-1/L1 agent
  23. Has severe hypersensitivity (≥ Grade 3) to pembrolizumab and/or any of its excipients

    [Exclusion Criteria (Phase 2, Melanoma Expansion Cohorts 2 and 8 only)]

  24. Melanoma considered resectable with curative intent
  25. Any prior combination therapy involving agents given by intratumoral injection that target the innate immune pathway or system such as oncolytic viral or microbial therapy (eg, T-VEC [talimogene laherparepvec]), toll-like receptors (TLR) agonists, STING or RIG-1 and an anti-PD-1/L1 inhibitor

    [Exclusion Criteria (Phase 2, HNSCC Expansion Cohorts 3 and 6 only)]

  26. HNSCC considered resectable with curative intent
  27. Prior therapy with an anti-PD-1/L1 agent
  28. Require anticoagulation therapy

    [Exclusion Criteria (Phase 2, HNSCC Expansion Cohorts 4 and 7 only)]

  29. HNSCC considered resectable with curative intent
  30. Any prior combination therapy involving agents given by intratumoral injection that target the innate immune pathway or system such as oncolytic viral or microbial therapy (eg, T-VEC), TLR agonists, STING or RIG-1 and an anti-PD-1/L1 inhibitor
  31. Require treatment on anticoagulation therapy

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): NCT02521870


Locations
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United States, Alabama
University of Alabama School of Medicine
Birmingham, Alabama, United States, 35294
University of Alabama
Birmingham, Alabama, United States, 35294
United States, Arizona
University of Arizona Cancer Center
Tucson, Arizona, United States, 85721
United States, California
University of California, Los Angeles
Los Angeles, California, United States, 90095
Stanford Hospitals and Clinics
Palo Alto, California, United States, 94305
University of California, San Diego
San Diego, California, United States, 92093
University of California San Francisco
San Francisco, California, United States, 94158
United States, Colorado
University of Colorado
Aurora, Colorado, United States, 80045
United States, Florida
Mount Sinai Comprehensive Cancer Center
Miami Beach, Florida, United States, 33140
United States, Georgia
Georgia Cancer Center - Northside Hospital Central Research Department
Atlanta, Georgia, United States, 30341
United States, Illinois
Northwestern University
Chicago, Illinois, United States, 60208
United States, Iowa
University of Iowa Healthcare
Iowa City, Iowa, United States, 52242
United States, Michigan
University of Michigan
Ann Arbor, Michigan, United States, 48109
Barbara Ann Karmanos Cancer Institute
Detroit, Michigan, United States, 48201
United States, Minnesota
University of Minnesota Masonic Cancer Center
Minneapolis, Minnesota, United States, 55455
United States, Nebraska
Nebraska Methodist Hospital
Omaha, Nebraska, United States, 68130
United States, New Jersey
Atlantic Health
Morristown, New Jersey, United States, 07962
United States, New York
Roswell Park Cancer Institute
Buffalo, New York, United States, 14263
United States, North Carolina
Levine Cancer Institute
Charlotte, North Carolina, United States, 28204
Duke University Medical Center
Durham, North Carolina, United States, 27710
United States, Ohio
The Christ Hospital
Cincinnati, Ohio, United States, 45219
University Hospitals Cleveland Medical Center - Seidman Cancer center
Cleveland, Ohio, United States, 44106
United States, Oklahoma
University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, United States, 73104
United States, Oregon
Providence Portland Medical Center
Portland, Oregon, United States, 97213
United States, Pennsylvania
Penn State Hershey Medical Center
Hershey, Pennsylvania, United States, 17033
United States, South Carolina
Medical University of South Carolina
Charleston, South Carolina, United States, 29425
United States, Texas
Mary Crowley Cancer Research Center
Dallas, Texas, United States, 75230
United States, Utah
University of Utah Health Care - Huntsman Cancer institute
Salt Lake City, Utah, United States, 84112
United States, Virginia
Inova Schar Cancer Institute
Fairfax, Virginia, United States, 22031
United States, West Virginia
West Virginia University
Morgantown, West Virginia, United States, 26506
Australia, New South Wales
The Tweed Hospital
Tweed Heads, New South Wales, Australia, 2485
Liverpool Hospital
Westmead, New South Wales, Australia, 2170
Melanoma Institute
Wollstonecraft, New South Wales, Australia, 2065
Australia, South Australia
Adelaide Cancer Centre - Ashford Cancer Centre
Kurralta Park, South Australia, Australia, 5037
Australia, Western Australia
Hollywood Private Hospital / Affinity Research
Nedlands, Western Australia, Australia
Germany
Charité - Universitätsmedizin Berlin
Berlin, Germany
Klinikum BuxtehudeDermato-Onkologie Studienzentrale
Buxtehude, Germany
Uniklinikum Dresden Klinik und Poliklinik für Dermatologie
Dresden, Germany
Universitätshautklinik Frankfurt
Frankfurt, Germany
Medizinische Hochschule Hannover
Hannover, Germany
HNO-Universitätsklinik Jena
Jena, Germany
Universitätshautklinik Magdeburg
Magdeburg, Germany
Universitätsklinikum Regensburg
Regensburg, Germany
Universitätsklinikum Tübingen
Tubingen, Germany
New Zealand
Auckland City Hospital
Auckland, New Zealand, 1023
Christchurch Hospital
Christchurch, New Zealand, 4710
Waikato Hospital
Hamilton, New Zealand, 3204
Sponsors and Collaborators
Dynavax Technologies Corporation
Merck Sharp & Dohme Corp.
Investigators
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Principal Investigator: Antoni Ribas, MD UCLA School of Medicine (Melanoma)
Principal Investigator: Ezra Cohen, MD UCSD Moores Cancer Center (HNSCC)
Principal Investigator: Thomas Tüting, MD University Hospital Magdeburg
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Dynavax Technologies Corporation
ClinicalTrials.gov Identifier: NCT02521870    
Other Study ID Numbers: DV3-MEL-01
Keynote 184 ( Other Identifier: Merck )
SYNERGY-001 ( Other Identifier: Dynavax )
First Posted: August 13, 2015    Key Record Dates
Last Update Posted: June 16, 2020
Last Verified: June 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: Yes
Plan Description: Data will be shared under guidance of the New Rule - FDAAA 801 eff. Jan 2017. 3/2017 - additional changes forthcoming.
Keywords provided by Dynavax Technologies Corporation:
Skin Cancer
Skin Tumors
Head and Neck Squamous Cell Carcinoma
Cancer Immunotherapy
Additional relevant MeSH terms:
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Carcinoma
Melanoma
Carcinoma, Squamous Cell
Head and Neck Neoplasms
Squamous Cell Carcinoma of Head and Neck
Neoplasms, Glandular and Epithelial
Neoplasms by Histologic Type
Neoplasms
Neuroendocrine Tumors
Neuroectodermal Tumors
Neoplasms, Germ Cell and Embryonal
Neoplasms, Nerve Tissue
Nevi and Melanomas
Neoplasms, Squamous Cell
Neoplasms by Site
Pembrolizumab
Antineoplastic Agents, Immunological
Antineoplastic Agents