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NCT04708418Active, not recruitingPhase 2

A Study Evaluating Whether Pembrolizumab Alone or in Combination With CMP-001 Improves Efficacy of Treatment in Patients With Operable Melanoma

Phase II Randomized Study of Neoadjuvant Pembrolizumab Alone or in Combination With CMP-001 in Patients With Operable Melanoma: Efficacy and Biomarker Study

Source: ClinicalTrials.gov · Last updated 29 Sept 2026

Brief summary (registry, in English)

This phase II trial studies the effect of pembrolizumab alone or in combination with CMP-001 in treating patients with melanoma that can be treated by surgery (operable). Immunotherapy with monoclonal antibodies, such as pembrolizumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Immunotherapy with CMP-001 may induce changes in body's immune system and may interfere with the ability of tumor cells to grow and spread. The addition of CMP-001 to pembrolizumab could improve the ability of the immune system to shrink tumors and to prevent them from returning.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
60 (estimated)
First submitted
13 Jan 2021
Start date
15 Oct 2021
Primary completion date
31 Dec 2026
Lead sponsor
National Cancer Institute (NCI)
Diseases
Melanoma
NCT number
NCT04708418

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 60
  • From 15 Oct 2021 to the primary completion date, 31 Dec 2026
  • 187 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • Patient must be \>= 18 years of age
  • Patient must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Patient must have a histologic diagnosis of melanoma belonging to the following American Joint Committee on Cancer (AJCC) 8th edition TNM stages:
    • T0, Tx or T1-4; and
    • N1b, N2b, N2c, N3b or N3c
  • Patients may have a presentation with primary melanoma with concurrent regional nodal and/or in-transit metastasis; or patients may have a history of primary melanoma or unknown primary melanoma presenting with clinically detected regional nodal and/or in-transit recurrence; and may belong to any of the following groups:
    • Primary cutaneous melanoma with clinically apparent regional lymph node metastases and/or in-transit metastases
    • Clinically detected recurrent melanoma at the proximal regional lymph node(s) basin
    • Primary cutaneous melanoma with concurrent nodal disease involving a single (or multiple) regional nodal group(s) if considered potentially surgically resectable at baseline
    • Clinically detected nodal melanoma (if single site) arising from an unknown primary
    • In-transit cutaneous metastases with or without regional lymph node involvement permitted if considered potentially surgically resectable at baseline
    • NOTE: Patients with mucosal and/or uveal melanoma are not eligible for the study
  • Patient must be a candidate for definitive surgery and have met with the treating surgical oncologist prior to randomization
  • Patient must not have received any live vaccine within 30 days prior to randomization and while participating in the study. Live vaccines include, but are not limited to, the following: measles, mumps, rubella, chicken pox, yellow fever, rabies, Bacillus Calmette-Guerin (BCG), and typhoid (oral) vaccine. Patients are permitted to receive inactivated vaccines and any non-live vaccines including those for the seasonal influenza and COVID-19 (Note: intranasal influenza vaccines, such as Flu-Mist \[registered trademark\] are live attenuated vaccines and are not allowed). If possible, it is recommended to separate study drug administration from vaccine administration by about a week (primarily, in order to minimize an overlap of adverse events)
  • Patient must have the presence of injectable and measurable disease based on Response Evaluation Criteria in Solid Tumors (RECIST) 1.1, documented by scans obtained within 4 weeks prior to randomization
    • NOTE: Injectable disease is defined as an accessible lesion in the skin, subcutaneous tissue or lymph nodes (LN) close to the skin and palpable by physical examination or approachable with ultrasound guidance
  • Absolute neutrophil count (ANC) \>= 1,500 /mcL (obtained within 4 weeks prior to randomization)
  • Hemoglobin (Hgb) \>= 9 g/dL or \>= 5.6 mmol/L (obtained within 4 weeks prior to randomization)
  • Platelets \>= 100,000 / mcL (obtained within 4 weeks prior to randomization)
  • Serum creatinine =\< 1.5 x institutional upper limit of normal (ULN) or measured or calculated creatinine clearance \> 60 mL/min (glomerular filtration rate \[GFR\] can also be used in place of creatinine or creatinine clearance \[CrCl\] for patients with creatinine levels \> 1.5 x institutional ULN) (obtained within 4 weeks prior to randomization)
  • Serum total bilirubin =\< 1.5 x institutional ULN; for total bilirubin level \> 1.5 x ULN but =\< 3 x ULN, the direct bilirubin must be =\< the institutional ULN (obtained within 4 weeks prior to randomization)
  • Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase \[SGOT\]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase \[SGPT\]) =\< 2.5 x institutional ULN (obtained within 4 weeks prior to randomization)
  • International normalized ratio (INR) or prothrombin time (PT) =\< 1.5 x institutional ULN unless patient is receiving anticoagulant therapy as long as PT or partial thromboplastin time (PTT) is within therapeutic range of intended use of anticoagulants (obtained within 4 weeks prior to randomization)
  • Activated partial thromboplastin time (aPTT) =\< 1.5 x institutional ULN unless patient is receiving anticoagulant therapy as long as PT or PTT is within therapeutic range of intended use of anticoagulants (obtained within 4 weeks prior to randomization)
  • Patients must not be pregnant or breast-feeding due to the potential harm to an unborn fetus and possible risk for adverse events in nursing infants with the treatment regimens being used. All patients of childbearing potential must have a blood test or urine study within 14 days prior to randomization to rule out pregnancy. A urine or serum pregnancy test must be repeated within 72 hours prior to receiving the first dose of pembrolizumab if the test done for eligibility/randomization is done outside of this 72 hour window. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required. A patient of childbearing potential is defined as anyone, regardless of whether they have undergone tubal ligation, who meets the following criteria: 1) has achieved menarche at some point, 2) has not undergone a hysterectomy or bilateral oophorectomy; or 3) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months)
  • Patients must not expect to conceive or father children by using accepted and effective method(s) of contraception or abstaining from sexual intercourse from time of randomization, while on study treatment, and continue for 26 weeks after the last dose of protocol treatment
  • Patient must have the ability to understand and the willingness to sign a written informed consent document. Patients with impaired decision-making capacity (IDMC) who have a legally authorized representative (LAR) or caregiver and/or family member available will also be considered eligible
  • Patient must not have received prior systemic therapy for melanoma including systemic therapy with an anti-PD-1, anti-PD-L1, anti-CTLA-4, BRAF/MEK inhibitor combination and/or TLR-9 agonist
  • Patient must not have a diagnosis of immunodeficiency or be receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to randomization, except as noted here
    • Patients who are currently receiving steroids at a dose of prednisone =\< 5 mg daily (or equivalent) are permitted to enroll
    • Patients who require topical, ophthalmologic and inhalational steroids are permitted to enroll
    • Patients with hypothyroidism who are stable on hormone replacement are permitted to enroll
    • Patients who require active immunosuppression with corticosteroids at a dose of prednisone \> 5 mg daily (or equivalent) for any reason are ineligible
    • Patients with adrenal insufficiency are ineligible
    • Patients who have developed autoimmune disorders of grade 4 while on prior immunotherapy are not permitted to enroll on this study. Patients who developed autoimmune disorders of grade =\< 3 may enroll if the disorder has resolved to grade =\< 1 and the patient has been off systemic corticosteroids at doses \> 5 mg for at least 2 weeks prior to randomization
  • Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months prior to randomization are eligible for this trial
  • For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated
  • Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load
  • Patients with a history of brain metastases are not eligible for this study as they do not meet the eligibility staging criteria
  • Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial
  • Patients with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, should have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification. To be eligible for this trial, patients should be class 2B or better
  • Patient must not have had an allogeneic tissue/solid organ transplant
  • Patient must not have a history of (non-infectious) pneumonitis that required steroids or current pneumonitis
  • Patient must not have severe hypersensitivity (\>= grade 3) to pembrolizumab and/or any of its excipients
  • Patient must not have an active infection requiring systemic therapy
  • Patient must not have a known psychiatric or substance abuse disorder that would interfere with the patient's ability to cooperate with the requirements of the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (187)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Providence Regional Cancer System-Aberdeen
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AberdeenUnited StatesUnknown status
Avera Cancer Institute-Aberdeen
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AberdeenUnited StatesUnknown status
Saint Luke's Cancer Center - Allentown
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AllentownUnited StatesUnknown status
Mary Greeley Medical Center
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AmesUnited StatesUnknown status
McFarland Clinic - Ames
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AmesUnited StatesUnknown status
Alaska Breast Care and Surgery LLC
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AnchorageUnited StatesUnknown status
Alaska Oncology and Hematology LLC
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AnchorageUnited StatesUnknown status
Providence Alaska Medical Center
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AnchorageUnited StatesUnknown status
Alaska Women's Cancer Care
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AnchorageUnited StatesUnknown status
Anchorage Oncology Centre
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AnchorageUnited StatesUnknown status
Katmai Oncology Group
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AnchorageUnited StatesUnknown status
Anchorage Associates in Radiation Medicine
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AnchorageUnited StatesUnknown status
Rocky Mountain Cancer Centers-Aurora
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AuroraUnited StatesUnknown status
The Medical Center of Aurora
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AuroraUnited StatesUnknown status
UM Sylvester Comprehensive Cancer Center at Aventura
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AventuraUnited StatesUnknown status
Mercy Oncology and Hematology - Clayton-Clarkson
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BallwinUnited StatesUnknown status
Mary Bird Perkins Cancer Center
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Baton RougeUnited StatesUnknown status
Louisiana Hematology Oncology Associates LLC
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Baton RougeUnited StatesUnknown status
Bronson Battle Creek
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Battle CreekUnited StatesUnknown status
Indu and Raj Soin Medical Center
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BeavercreekUnited StatesUnknown status
PeaceHealth Saint Joseph Medical Center
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BellinghamUnited StatesUnknown status
Saint Charles Health System
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BendUnited StatesUnknown status
Central Vermont Medical Center/National Life Cancer Treatment
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Berlin CornersUnited StatesUnknown status
Saint Luke's University Hospital-Bethlehem Campus
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BethlehemUnited StatesUnknown status
Illinois CancerCare-Bloomington
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BloomingtonUnited StatesUnknown status
Saint Luke's Cancer Institute - Boise
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BoiseUnited StatesUnknown status
Central Care Cancer Center - Bolivar
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BolivarUnited StatesUnknown status
McFarland Clinic - Boone
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BooneUnited StatesUnknown status
Rocky Mountain Cancer Centers-Boulder
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BoulderUnited StatesUnknown status
Providence Saint Joseph Medical Center/Disney Family Cancer Center
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BurbankUnited StatesUnknown status
University of Vermont Medical Center
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BurlingtonUnited StatesUnknown status
Illinois CancerCare-Canton
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CantonUnited StatesUnknown status
Saint Francis Medical Center
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Cape GirardeauUnited StatesUnknown status
Mercy Cancer Center - Cape Girardeau
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Cape GirardeauUnited StatesUnknown status
Memorial Hospital of Carbondale
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CarbondaleUnited StatesUnknown status
SIH Cancer Institute
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CartervilleUnited StatesUnknown status
Illinois CancerCare-Carthage
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CarthageUnited StatesUnknown status
Rocky Mountain Cancer Centers - Centennial
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CentennialUnited StatesUnknown status
Miami Valley Hospital South
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CentervilleUnited StatesUnknown status
Dayton Physicians LLC-Miami Valley South
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CentervilleUnited StatesUnknown status
Centralia Oncology Clinic
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CentraliaUnited StatesUnknown status
Providence Regional Cancer System-Centralia
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CentraliaUnited StatesUnknown status
University of Virginia Cancer Center
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CharlottesvilleUnited StatesUnknown status
University of Illinois
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ChicagoUnited StatesUnknown status
Oncology Hematology Care Inc-Kenwood
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CincinnatiUnited StatesUnknown status
Clackamas Radiation Oncology Center
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ClackamasUnited StatesUnknown status
Providence Cancer Institute Clackamas Clinic
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ClackamasUnited StatesUnknown status
Bay Area Hospital
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Coos BayUnited StatesUnknown status
UM Sylvester Comprehensive Cancer Center at Coral Gables
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Coral GablesUnited StatesUnknown status
Miami Valley Hospital North
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DaytonUnited StatesUnknown status
Miami Valley Hospital
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DaytonUnited StatesUnknown status
Dayton Physician LLC - Englewood
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DaytonUnited StatesUnknown status
Cancer Care Specialists of Illinois - Decatur
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DecaturUnited StatesUnknown status
Decatur Memorial Hospital
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DecaturUnited StatesUnknown status
UM Sylvester Comprehensive Cancer Center at Deerfield Beach
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Deerfield BeachUnited StatesUnknown status
Rocky Mountain Cancer Centers-Midtown
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DenverUnited StatesUnknown status
Rocky Mountain Cancer Centers-Rose
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DenverUnited StatesUnknown status
Presbyterian - Saint Lukes Medical Center - Health One
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DenverUnited StatesUnknown status
Illinois CancerCare-Dixon
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DixonUnited StatesUnknown status
Epic Care-Dublin
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DublinUnited StatesUnknown status
Saint Luke's Hospital-Anderson Campus
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EastonUnited StatesUnknown status
Marshfield Medical Center-EC Cancer Center
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Eau ClaireUnited StatesUnknown status
Swedish Cancer Institute-Edmonds
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EdmondsUnited StatesUnknown status
Crossroads Cancer Center
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EffinghamUnited StatesUnknown status
Bay Area Breast Surgeons Inc
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EmeryvilleUnited StatesUnknown status
Epic Care Partners in Cancer Care
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EmeryvilleUnited StatesUnknown status
Rocky Mountain Cancer Centers - Swedish
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EnglewoodUnited StatesUnknown status
Swedish Medical Center
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EnglewoodUnited StatesUnknown status
The Melanoma and Skin Cancer Institute
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EnglewoodUnited StatesUnknown status
Mountain Blue Cancer Care Center - Swedish
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EnglewoodUnited StatesUnknown status
Illinois CancerCare-Eureka
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EurekaUnited StatesUnknown status
Providence Regional Cancer Partnership
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EverettUnited StatesUnknown status
Fairbanks Memorial Hospital
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FairbanksUnited StatesUnknown status
Parkland Health Center - Farmington
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FarmingtonUnited StatesUnknown status
Blanchard Valley Hospital
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FindlayUnited StatesUnknown status
Armes Family Cancer Center
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FindlayUnited StatesUnknown status
Orion Cancer Care
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FindlayUnited StatesUnknown status
McFarland Clinic - Trinity Cancer Center
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Fort DodgeUnited StatesUnknown status
Mercy Hospital Fort Smith
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Fort SmithUnited StatesUnknown status
Atrium Medical Center-Middletown Regional Hospital
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FranklinUnited StatesUnknown status
Dayton Physicians LLC-Atrium
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FranklinUnited StatesUnknown status
Saint Luke's Cancer Institute - Fruitland
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FruitlandUnited StatesUnknown status
Western Illinois Cancer Treatment Center
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GalesburgUnited StatesUnknown status
Illinois CancerCare-Galesburg
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GalesburgUnited StatesUnknown status
Central Care Cancer Center - Garden City
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Garden CityUnited StatesUnknown status
Corewell Health Grand Rapids Hospitals - Butterworth Hospital
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Grand RapidsUnited StatesUnknown status
Corewell Health Grand Rapids Hospitals - Helen DeVos Children's Hospital
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Grand RapidsUnited StatesUnknown status
Trinity Health Grand Rapids Hospital
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Grand RapidsUnited StatesUnknown status
Central Care Cancer Center - Great Bend
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Great BendUnited StatesUnknown status
Banner North Colorado Medical Center
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GreeleyUnited StatesUnknown status
Dayton Physicians LLC-Wayne
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GreenvilleUnited StatesUnknown status
Wayne Hospital
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GreenvilleUnited StatesUnknown status
Terrebonne General Medical Center
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HoumaUnited StatesUnknown status
Swedish Cancer Institute-Issaquah
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IssaquahUnited StatesUnknown status
McFarland Clinic - Jefferson
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JeffersonUnited StatesUnknown status
MU Health Care Goldschmidt Cancer Center
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Jefferson CityUnited StatesUnknown status
Freeman Health System
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JoplinUnited StatesUnknown status
Mercy Hospital Joplin
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JoplinUnited StatesUnknown status
Beacon Kalamazoo
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KalamazooUnited StatesUnknown status
West Michigan Cancer Center
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KalamazooUnited StatesUnknown status
Beacon Kalamazoo Cancer Center
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KalamazooUnited StatesUnknown status
Bronson Methodist Hospital
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KalamazooUnited StatesUnknown status
Kadlec Clinic Hematology and Oncology
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KennewickUnited StatesUnknown status
Kettering Medical Center
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KetteringUnited StatesUnknown status
Greater Dayton Cancer Center
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KetteringUnited StatesUnknown status
Illinois CancerCare-Kewanee Clinic
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KewaneeUnited StatesUnknown status
Providence Regional Cancer System-Lacey
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LaceyUnited StatesUnknown status
Rocky Mountain Cancer Centers-Littleton
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LittletonUnited StatesUnknown status
Sky Ridge Medical Center
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Lone TreeUnited StatesUnknown status
Rocky Mountain Cancer Centers-Sky Ridge
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Lone TreeUnited StatesUnknown status
PeaceHealth Saint John Medical Center
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LongviewUnited StatesUnknown status
Banner North Colorado Medical Center - Loveland Campus
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LovelandUnited StatesUnknown status
Illinois CancerCare-Macomb
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MacombUnited StatesUnknown status
McFarland Clinic - Marshalltown
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MarshalltownUnited StatesUnknown status
Marshfield Medical Center-Marshfield
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MarshfieldUnited StatesUnknown status
Contra Costa Regional Medical Center
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MartinezUnited StatesUnknown status
Saint Luke's Cancer Institute - Meridian
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MeridianUnited StatesUnknown status
University of Miami Miller School of Medicine-Sylvester Cancer Center
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MiamiUnited StatesUnknown status
Medical College of Wisconsin
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MilwaukeeUnited StatesUnknown status
Marshfield Medical Center - Minocqua
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MinocquaUnited StatesUnknown status
Saint Patrick Hospital - Community Hospital
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MissoulaUnited StatesUnknown status
SSM Health Good Samaritan
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Mount VernonUnited StatesUnknown status
Trinity Health Muskegon Hospital
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MuskegonUnited StatesUnknown status
Saint Luke's Cancer Institute - Nampa
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NampaUnited StatesUnknown status
Providence Newberg Medical Center
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NewbergUnited StatesUnknown status
Corewell Health Lakeland Hospitals - Niles Hospital
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NilesUnited StatesUnknown status
Cancer and Hematology Centers of Western Michigan - Norton Shores
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Norton ShoresUnited StatesUnknown status
Alta Bates Summit Medical Center - Summit Campus
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OaklandUnited StatesUnknown status
Bay Area Tumor Institute
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OaklandUnited StatesUnknown status
Cancer Care Center of O'Fallon
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O'FallonUnited StatesUnknown status
Mercy Hospital Oklahoma City
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Oklahoma CityUnited StatesUnknown status
Saint Joseph Hospital - Orange
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OrangeUnited StatesUnknown status
UC Irvine Health- Chao Family Comprehensive Cancer Center
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OrangeUnited StatesUnknown status
Illinois CancerCare-Ottawa Clinic
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OttawaUnited StatesUnknown status
Illinois CancerCare-Pekin
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PekinUnited StatesUnknown status
Methodist Medical Center of Illinois
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PeoriaUnited StatesUnknown status
Illinois CancerCare-Peoria
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PeoriaUnited StatesUnknown status
Illinois CancerCare-Peru
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PeruUnited StatesUnknown status
Valley Radiation Oncology
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PeruUnited StatesUnknown status
UPMC Hillman Cancer Center
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PittsburghUnited StatesUnknown status
UM Sylvester Comprehensive Cancer Center at Plantation
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PlantationUnited StatesUnknown status
Providence Portland Medical Center
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PortlandUnited StatesUnknown status
Providence Saint Vincent Medical Center
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PortlandUnited StatesUnknown status
Jefferson Healthcare
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Port TownsendUnited StatesUnknown status
Illinois CancerCare-Princeton
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PrincetonUnited StatesUnknown status
Saint Luke's Hospital-Quakertown Campus
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QuakertownUnited StatesUnknown status
Corewell Health Reed City Hospital
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Reed CityUnited StatesUnknown status
Marshfield Medical Center-Rice Lake
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Rice LakeUnited StatesUnknown status
Reid Health
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RichmondUnited StatesUnknown status
VCU Massey Comprehensive Cancer Center
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RichmondUnited StatesUnknown status
Phelps Health Delbert Day Cancer Institute
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RollaUnited StatesUnknown status
Mercy Clinic-Rolla-Cancer and Hematology
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RollaUnited StatesUnknown status
Sainte Genevieve County Memorial Hospital
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Sainte GenevieveUnited StatesUnknown status
Corewell Health Lakeland Hospitals - Marie Yeager Cancer Center
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Saint JosephUnited StatesUnknown status
Corewell Health Lakeland Hospitals - Saint Joseph Hospital
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Saint JosephUnited StatesUnknown status
Heartland Regional Medical Center
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Saint JosephUnited StatesUnknown status
Huntsman Cancer Institute/University of Utah
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Salt Lake CityUnited StatesUnknown status
Guthrie Medical Group PC-Robert Packer Hospital
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SayreUnited StatesUnknown status
Swedish Medical Center-First Hill
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SeattleUnited StatesUnknown status
Swedish Medical Center-Ballard Campus
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SeattleUnited StatesUnknown status
PeaceHealth United General Medical Center
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Sedro-WoolleyUnited StatesUnknown status
Avera Cancer Institute
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Sioux FallsUnited StatesUnknown status
Mercy Hospital Springfield
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SpringfieldUnited StatesUnknown status
CoxHealth South Hospital
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SpringfieldUnited StatesUnknown status
Springfield Regional Cancer Center
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SpringfieldUnited StatesUnknown status
Springfield Clinic
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SpringfieldUnited StatesUnknown status
Springfield Regional Medical Center
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SpringfieldUnited StatesUnknown status
Southern Illinois University School of Medicine
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SpringfieldUnited StatesUnknown status
Springfield Memorial Hospital
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SpringfieldUnited StatesUnknown status
Marshfield Medical Center-River Region at Stevens Point
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Stevens PointUnited StatesUnknown status
Mercy Hospital South
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St LouisUnited StatesUnknown status
Mercy Hospital Saint Louis
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St LouisUnited StatesUnknown status
Missouri Baptist Medical Center
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St LouisUnited StatesUnknown status
Missouri Baptist Sullivan Hospital
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SullivanUnited StatesUnknown status
Rocky Mountain Cancer Centers-Thornton
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ThorntonUnited StatesUnknown status
Munson Medical Center
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Traverse CityUnited StatesUnknown status
Upper Valley Medical Center
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TroyUnited StatesUnknown status
Dayton Physicians LLC - Troy
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TroyUnited StatesUnknown status
University of Arizona Cancer Center-North Campus
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TucsonUnited StatesUnknown status
Banner University Medical Center - Tucson
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TucsonUnited StatesUnknown status
Saint Luke's Cancer Institute - Twin Falls
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Twin FallsUnited StatesUnknown status
PeaceHealth Southwest Medical Center
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VancouverUnited StatesUnknown status
Providence Saint Mary Regional Cancer Center
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Walla WallaUnited StatesUnknown status
Epic Care Cyberknife Center
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Walnut CreekUnited StatesUnknown status
Illinois CancerCare - Washington
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WashingtonUnited StatesUnknown status
Marshfield Medical Center - Weston
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WestonUnited StatesUnknown status
University of Michigan Health - West
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WyomingUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.