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NCT05411081Active, not recruitingPhase 2

Testing Cabozantinib With or Without Atezolizumab in Patients With Advanced Papillary Kidney Cancer, PAPMET2 Trial

A Phase II Randomized Trial of Cabozantinib (NSC #761968) With or Without Atezolizumab (NSC #783608) in Patients With Advanced Papillary Renal Cell Carcinoma (PAPMET2)

Source: ClinicalTrials.gov · Last updated 1 Oct 2026

Brief summary (registry, in English)

This phase II trial compares the effect of atezolizumab in combination with usual treatment with cabozantinib to cabozantinib alone in patients with papillary renal cell carcinoma that has spread from where it first started (primary site) to other places in the body (metastatic). Papillary renal cell carcinoma (PRCC) is a type of kidney cancer that forms in the lining of the tiny tubes in the kidney that return filtered substances that the body needs back to the blood and remove extra fluid and waste as urine. Most papillary tumors look like long, thin finger-like growths under a microscope. It is also called papillary kidney cancer or PRCC. Immunotherapy with monoclonal antibodies, such as atezolizumab, may help the body's immune system attack the tumor and may interfere with the ability of tumor cells to grow and spread. Cabozantinib is in a class of medications called kinase inhibitors. It works by blocking the action of an abnormal protein that signals tumor cells to multiply and may also prevent the growth of new blood vessels that tumors need to grow. By these actions it may help slow or stop the spread of tumor cells. Combination therapy with atezolizumab and cabozantinib may shrink the tumor and allow a longer survival time in patients with metastatic renal cell carcinoma.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
200 (estimated)
First submitted
7 Jun 2022
Start date
24 Mar 2023
Primary completion date
1 Jul 2027
Lead sponsor
National Cancer Institute (NCI)
NCT number
NCT05411081

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 200
  • From 24 Mar 2023 to the primary completion date, 1 Jul 2027
  • 198 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

  • Participants must have a histologically confirmed diagnosis of metastatic papillary renal cell carcinoma (PRCC), either type 1 or type 2. (NOTE: A designation of type 1 or type 2 should be made by the local pathologist if possible but is not required). Mixed histologies which contain type 1 or type 2 along with any other RCC histology/histologies will be allowed provided that they contain a papillary component
  • Participants must have measurable disease per RECIST 1.1 criteria. All measurable lesions must be assessed by CT or MRI within 28 days prior to registration. All non-measurable lesions must be assessed by CT or MRI, or nuclear medicine bone scan within 42 days prior to registration. The CT from a combined positron emission tomography (PET)/CT may be used to document only non-measurable disease unless it is of diagnostic quality. If there is clinical suspicion for bone metastases at the time of enrollment (at the discretion of the investigator), bone scan must be performed at baseline (within 42 days prior to registration)
  • Participants with new or progressive brain metastases (active brain metastases) must not require immediate central nervous system (CNS) specific treatment at the time of study registration or anticipated during the first cycle of therapy. Patients with leptomeningeal disease are excluded from enrolling
  • Participants with measurable disease, per RECIST version (v)1.1, must be present outside the CNS
  • Participants must have no history of intracranial hemorrhage or spinal cord hemorrhage
  • Participants must not have undergone stereotactic radiotherapy within 7 days prior to initiation of study treatment, whole-brain radiotherapy within 14 days prior to initiation of study treatment, or neurosurgical resection within 28 days prior to initiation of study treatment
  • Participants must not have ongoing requirements for corticosteroids as therapy for CNS disease
  • Participants, if needed, must receive a stable dose of anti-convulsant therapy
  • Participants must not have cavitating pulmonary lesions
  • Participants must not have uncontrolled pleural effusions, pericardial effusions, or ascites requiring recurrent drainage procedures (once monthly or more frequently). Participants with indwelling catheters (e.g., PleurX \[registered trademark\]) are allowed
  • Participants must not have tumor invading the gastrointestinal (GI) tract or evidence of endotracheal or endobronchial tumor within 28 days prior to registration
  • Participants must not have evidence of tumor invading or encasing any major blood vessels
  • Participants must not have had major surgery within 28 days prior to registration, and participants must have recovered from any adverse effects of surgery
  • Participants must not have had prior treatment with cabozantinib for any reason
  • Participants must not have had prior treatment or adjuvant therapy with PD-1/PD-L1 checkpoint inhibitors for any reason within the past 6 months
  • Participants must not have received more than one prior systemic therapy for advanced or metastatic renal cell carcinoma with the exception of another VEGF inhibitor Food and Drug Administration (FDA)-approved for advanced RCC (i.e., pazopanib, bevacizumab, sorafenib or axitinib). If a participant develops metastatic disease within six months of discontinuation of adjuvant therapy, this will constitute one prior systemic therapy for advanced or metastatic RCC. If a patient develops metastatic disease and more than six months has elapsed since discontinuation of adjuvant therapy, this will not constitute prior systemic therapy for advanced or metastatic RCC
  • Participants must not take within 14 days prior to registration, nor plan to take while on protocol treatment, any strong CYP3A4 inhibitors (e.g. boceprevir, cobicistat, danoprevir, elvitegravir/RIT, fluvoxamine, indinavir, itraconazole, ketoconazole, lopinavir/RIT, nefazodone, nelfinavir, posaconazole, ritonavir, telaprevir, telithromycin, tipranavir/RIT, or voriconazole,); Please refer to https://drug-interactions.medicine.iu.edu/MainTable.aspx for the updated CYP3A4 inhibitors or inducers
  • Participants must not take within 14 days prior to registration, nor plan to take while on protocol treatment, any strong CYP3A4 inducers (e.g. avasimibe, phenytoin, rifampin, rifabutin); Please refer to https://drug-interactions.medicine.iu.edu/MainTable.aspx for the updated CYP3A4 inhibitors or inducers
  • Participants must complete all prior radiation therapy at least 14 days prior to registration. Participants must have recovered to =\< grade 1 from all associated toxicities at the time of registration unless the toxicity is determined to be not clinically significant by the registering investigator
  • Participants must not be receiving or planning to receive any other investigational agents at time of registration
  • Participants must not have been diagnosed with a clinically significant autoimmune disease, exceptions such as diabetes, eczema, and vitiligo are allowed. Other non-clinically significant autoimmune diseases are allowed if approved by the registering investigator
  • Participants must not be on steroid doses \> 10 mg prednisone equivalent. Replacement steroid doses for adrenal insufficiency will be allowed. Also, short duration steroid therapy to prevent allergic reactions are acceptable (e.g. prior to CT imaging)
  • Participants must be \>= 18 years of age
  • Participants must have a complete physical examination and medical history within 28 days prior to registration
  • Participants must have a Zubrod performance status of 0-2
  • White blood count (WBC) \>= 2 x 10\^3/uL (within 28 days prior to registration)
  • Absolute neutrophil count (ANC) \>= 1.5 x 10\^3/uL (within 28 days prior to registration)
  • Platelet count \>= 100 x 10\^3/uL (within 28 days prior to registration)
  • Lymphocyte count \>= 0.5 x 10\^3/uL (within 28 days prior to registration)
  • Hemoglobin (\>= 9 g/dL) (within 28 days prior to registration). Participants may be transfused to meet this criterion
  • Total serum bilirubin =\< 1.5 x the institutional upper limit of normal (ULN) unless history of Gilbert's disease (within 28 days prior to registration). Participants with history of Gilbert's disease must have total bilirubin =\< 5 x institutional ULN
  • Aspartate aminotransferase (AST) must be =\< 3 x the institutional ULN unless the liver is involved with the tumor, in which case serum transaminase (SGOT) must be =\< 5 x the institutional ULN (within 28 days prior to registration)
  • Alanine aminotransferase (ALT), must be =\< 3 x the institutional ULN unless the liver is involved with the tumor, in which case serum transaminase (SGPT) must be =\< 5 x the institutional ULN (within 28 days prior to registration)
  • Participants must have serum creatinine =\< 2 x the institutional ULN OR creatinine clearance (either measured or calculated) \> 30 mL/min and obtained within 28 days prior to registration
  • Participants must not have any clinical evidence of congestive heart failure (CHF) (specifically, New York Heart Association \[NYHA\] class III \[moderate\] or class IV \[severe\]) at the time of registration
  • Participants must not have known history of congenital long QT syndrome and must not have experienced unstable angina pectoris, clinically significant cardiac arrhythmias, or stroke (transient ischemic attack \[TIA\] or other ischemic event) within 90 days prior to registration
  • Participants must not have experienced myocardial infarction or thromboembolic event requiring anticoagulation within 90 days of registration, unless clinically stable with ongoing medical management
  • Participants must have urine protein \< 3+ within 28 days prior to registration. If urine protein is 3+ or greater, then urine protein by 24-hour collection must show less than 3 grams of protein
  • Participants must have documented blood pressure of systolic blood pressure (SBP) \< 150 mm Hg or diastolic blood pressure (DBP) \< 100 mm Hg within 14 days prior to registration
  • Participants with known human immunodeficiency virus (HIV) must be on effective anti-retroviral therapy at registration and have undetectable viral load within 6 months of registration
  • Participants with evidence of chronic hepatitis B virus (HBV) infection must have undetectable HBV viral load while on suppressive therapy within 6 months prior to registration, if indicated
  • Participants with a history of hepatitis C virus (HCV) infection must have been treated and cured. Participants currently being treated for HCV infection must have undetectable HCV viral load within 6 months prior to registration
  • Participants must be able to take oral medications (i.e., swallow pills whole). Participants must not have gastrointestinal tract disease resulting in an inability to take oral medication or a requirement for IV alimentation, prior surgical procedures that could in the opinion of the treating investigator affect absorption, or active peptic ulcer disease. Participants with intractable nausea or vomiting are not eligible
  • Participants must not have had any clinically-significant GI bleeding within 3 months prior to registration and participants must not have a GI disorder which (at the discretion of the investigator) bears a high risk of perforation or fistula (e.g. Crohn's disease)
  • Participants must not have had hemoptysis of \>= (2.5 mL) of red blood, and do not demonstrate any other signs indicative of pulmonary hemorrhage within 3 months prior registration
  • Participants 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
  • Participants must not be pregnant or nursing, due to VEGF therapy being toxic to embryogenesis. Individuals who are of reproductive potential must have agreed to use an effective contraceptive method with details provided as a part of the consent process. A person who has had menses at any time in the preceding 12 consecutive months or who has semen likely to contain sperm is considered to be of "reproductive potential." In addition to routine contraceptive methods, "effective contraception" also includes refraining from sexual activity that might result in pregnancy and surgery intended to prevent pregnancy (or with a side-effect of pregnancy prevention) including hysterectomy, bilateral oophorectomy, bilateral tubal ligation/occlusion, and vasectomy with testing showing no sperm in the semen
  • Participants must not be on warfarin, at therapeutic doses. Low dose aspirin for cardio-protection (per local applicable guidelines) and low molecular weight heparin (LMWH) are allowed
  • Participants must be offered the opportunity to participate in specimen banking. With participant consent, specimens must be collected and submitted via the Southwest Oncology Group (SWOG) Specimen Tracking System
  • Participants must be informed of the investigational nature of this study and must sign and give informed consent in accordance with institutional and federal guidelines
    • NOTE: For participants with impaired decision-making capabilities, legally authorized representatives may sign and give informed consent on behalf of study participants in accordance with applicable federal, local, and Central Institutional Review Board (CIRB) regulations
  • As a part of the OPEN registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system

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

Full criteria on ClinicalTrials.gov

Sites (198)

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

SiteCityCountrySite status
Mary Greeley Medical Center
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AmesUnited StatesUnknown status
McFarland Clinic - Ames
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AmesUnited StatesUnknown status
Community Hospital of Anaconda
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AnacondaUnited StatesUnknown status
Kaiser Permanente-Anaheim
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AnaheimUnited StatesUnknown status
UI Health Care Mission Cancer and Blood - Ankeny Clinic
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AnkenyUnited StatesUnknown status
Trinity Health Saint Joseph Mercy Hospital Ann Arbor
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Ann ArborUnited StatesUnknown status
UH Seidman Cancer Center at UH Avon Health Center
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AvonUnited StatesUnknown status
Kaiser Permanente-Baldwin Park
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Baldwin ParkUnited StatesUnknown status
Johns Hopkins University/Sidney Kimmel Cancer Center
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BaltimoreUnited StatesUnknown status
Bronson Battle Creek
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Battle CreekUnited StatesUnknown status
UHHS-Chagrin Highlands Medical Center
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BeachwoodUnited StatesUnknown status
Kaiser Permanente-Bellflower
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BellflowerUnited StatesUnknown status
Saint Vincent Frontier Cancer Center
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BillingsUnited StatesUnknown status
Billings Clinic Cancer Center
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BillingsUnited StatesUnknown status
Illinois CancerCare-Bloomington
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BloomingtonUnited StatesUnknown status
Saint Alphonsus Cancer Care Center-Boise
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BoiseUnited StatesUnknown status
Saint Luke's Cancer Institute - Boise
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BoiseUnited StatesUnknown status
McFarland Clinic - Boone
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BooneUnited StatesUnknown status
Bozeman Health Deaconess Hospital
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BozemanUnited StatesUnknown status
Trinity Health Medical Center - Brighton
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BrightonUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology - Brighton
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BrightonUnited StatesUnknown status
Saint Alphonsus Cancer Care Center-Caldwell
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CaldwellUnited StatesUnknown status
Illinois CancerCare-Canton
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CantonUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology - Canton
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CantonUnited StatesUnknown status
Trinity Health Medical Center - Canton
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CantonUnited StatesUnknown status
Saint Francis Medical Center
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Cape GirardeauUnited StatesUnknown status
Caro Cancer Center
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CaroUnited StatesUnknown status
Illinois CancerCare-Carthage
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CarthageUnited StatesUnknown status
Duke Cancer Center Cary
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CaryUnited StatesUnknown status
Miami Valley Hospital South
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CentervilleUnited StatesUnknown status
Vandalia Health/CAMC Institute for Academic Medicine
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CharlestonUnited StatesUnknown status
Chelsea Hospital
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ChelseaUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology - Chelsea Hospital
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ChelseaUnited StatesUnknown status
Northwestern University
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ChicagoUnited StatesUnknown status
Siteman Cancer Center at Saint Peters Hospital
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City of Saint PetersUnited StatesUnknown status
Case Western Reserve University
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ClevelandUnited StatesUnknown status
Southeastern Medical Oncology Center-Clinton
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ClintonUnited StatesUnknown status
UI Health Care Mission Cancer and Blood - West Des Moines Clinic
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CliveUnited StatesUnknown status
Kootenai Health - Coeur d'Alene
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Coeur d'AleneUnited StatesUnknown status
Mercy Hospital
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Coon RapidsUnited StatesUnknown status
Siteman Cancer Center at West County Hospital
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Creve CoeurUnited StatesUnknown status
UT Southwestern/Simmons Cancer Center-Dallas
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DallasUnited StatesUnknown status
UT Southwestern Simmons Cancer Center - RedBird
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DallasUnited StatesUnknown status
Carle at The Riverfront
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DanvilleUnited StatesUnknown status
Premier Blood and Cancer Center
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DaytonUnited StatesUnknown status
Miami Valley Hospital
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DaytonUnited StatesUnknown status
Miami Valley Hospital North
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DaytonUnited StatesUnknown status
Dayton Physician LLC - Englewood
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DaytonUnited StatesUnknown status
Decatur Memorial Hospital
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DecaturUnited StatesUnknown status
Cancer Care Specialists of Illinois - Decatur
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DecaturUnited StatesUnknown status
Northwestern Medicine Cancer Center Kishwaukee
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DeKalbUnited StatesUnknown status
UI Health Care Mission Cancer and Blood - Des Moines Clinic
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Des MoinesUnited StatesUnknown status
UI Health Care Mission Cancer and Blood - Laurel Clinic
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Des MoinesUnited StatesUnknown status
Mercy Medical Center - Des Moines
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Des MoinesUnited StatesUnknown status
Wayne State University/Karmanos Cancer Institute
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DetroitUnited StatesUnknown status
Illinois CancerCare-Dixon
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DixonUnited StatesUnknown status
City of Hope Comprehensive Cancer Center
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DuarteUnited StatesUnknown status
Epic Care-Dublin
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DublinUnited StatesUnknown status
Duke University Medical Center
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DurhamUnited StatesUnknown status
Marshfield Medical Center-EC Cancer Center
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Eau ClaireUnited StatesUnknown status
Fairview Southdale Hospital
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EdinaUnited StatesUnknown status
Carle Physician Group-Effingham
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EffinghamUnited StatesUnknown status
Crossroads Cancer Center
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EffinghamUnited StatesUnknown status
Epic Care Partners in Cancer Care
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EmeryvilleUnited StatesUnknown status
Illinois CancerCare-Eureka
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EurekaUnited StatesUnknown status
Farmington Health Center
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FarmingtonUnited StatesUnknown status
Parkland Health Center - Farmington
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FarmingtonUnited StatesUnknown status
Weisberg Cancer Treatment Center
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Farmington HillsUnited StatesUnknown status
Cancer Hematology Centers - Flint
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FlintUnited StatesUnknown status
Genesee Hematology Oncology PC
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FlintUnited StatesUnknown status
Hurley Medical Center
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FlintUnited StatesUnknown status
Genesys Hurley Cancer Institute
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FlintUnited StatesUnknown status
Kaiser Permanente-Fontana
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FontanaUnited StatesUnknown status
McFarland Clinic - Trinity Cancer Center
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Fort DodgeUnited StatesUnknown status
UT Southwestern/Simmons Cancer Center-Fort Worth
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Fort WorthUnited StatesUnknown status
Atrium Medical Center-Middletown Regional Hospital
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FranklinUnited StatesUnknown status
Saint Luke's Cancer Institute - Fruitland
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FruitlandUnited StatesUnknown status
Illinois CancerCare-Galesburg
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GalesburgUnited StatesUnknown status
Northwestern Medicine Cancer Center Delnor
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GenevaUnited StatesUnknown status
Banner MD Anderson Cancer Center
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GilbertUnited StatesUnknown status
Northwestern Medicine Glenview Outpatient Center
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GlenviewUnited StatesUnknown status
Southeastern Medical Oncology Center-Goldsboro
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GoldsboroUnited StatesUnknown status
Corewell Health Grand Rapids Hospitals - Butterworth Hospital
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Grand RapidsUnited StatesUnknown status
Northwestern Medicine Grayslake Outpatient Center
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GrayslakeUnited StatesUnknown status
Benefis Sletten Cancer Institute
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Great FallsUnited StatesUnknown status
Miami Valley Cancer Care and Infusion
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GreenvilleUnited StatesUnknown status
Hackensack University Medical Center
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HackensackUnited StatesUnknown status
Kaiser Permanente South Bay
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Harbor CityUnited StatesUnknown status
Kaiser Permanente-Irvine
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IrvineUnited StatesUnknown status
University of Mississippi Medical Center
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JacksonUnited StatesUnknown status
Southeastern Medical Oncology Center-Jacksonville
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JacksonvilleUnited StatesUnknown status
McFarland Clinic - Jefferson
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JeffersonUnited StatesUnknown status
Bronson Methodist Hospital
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KalamazooUnited StatesUnknown status
Beacon Kalamazoo Cancer Center
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KalamazooUnited StatesUnknown status
West Michigan Cancer Center
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KalamazooUnited StatesUnknown status
Logan Health Medical Center
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KalispellUnited StatesUnknown status
Kettering Medical Center
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KetteringUnited StatesUnknown status
Illinois CancerCare-Kewanee Clinic
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KewaneeUnited StatesUnknown status
Northwestern Medicine Lake Forest Hospital
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Lake ForestUnited StatesUnknown status
University of Michigan Health - Sparrow Lansing
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LansingUnited StatesUnknown status
OptumCare Cancer Care at Charleston
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Las VegasUnited StatesUnknown status
OptumCare Cancer Care at Fort Apache
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Las VegasUnited StatesUnknown status
University of Arkansas for Medical Sciences
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Little RockUnited StatesUnknown status
Trinity Health Saint Mary Mercy Livonia Hospital
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LivoniaUnited StatesUnknown status
Kaiser Permanente West Los Angeles
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Los AngelesUnited StatesUnknown status
Kaiser Permanente Los Angeles Medical Center
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Los AngelesUnited StatesUnknown status
Illinois CancerCare-Macomb
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MacombUnited StatesUnknown status
Saint John's Hospital - Healtheast
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MaplewoodUnited StatesUnknown status
Saint Mary's Oncology/Hematology Associates of Marlette
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MarletteUnited 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
Carle Physician Group-Mattoon/Charleston
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MattoonUnited StatesUnknown status
Loyola University Medical Center
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MaywoodUnited StatesUnknown status
Saint Luke's Cancer Institute - Meridian
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MeridianUnited StatesUnknown status
East Jefferson General Hospital
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MetairieUnited StatesUnknown status
Mary Bird Perkins Cancer Center - Metairie
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MetairieUnited StatesUnknown status
LSU Healthcare Network / Metairie Multi-Specialty Clinic
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MetairieUnited StatesUnknown status
Abbott-Northwestern Hospital
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MinneapolisUnited StatesUnknown status
Marshfield Medical Center - Minocqua
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MinocquaUnited StatesUnknown status
Community Medical Center
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MissoulaUnited 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
Saint Alphonsus Cancer Care Center-Nampa
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NampaUnited StatesUnknown status
Providence Newberg Medical Center
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NewbergUnited StatesUnknown status
Touro Infirmary
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New OrleansUnited StatesUnknown status
University Medical Center New Orleans
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New OrleansUnited 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
Cancer Care Center of O'Fallon
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O'FallonUnited StatesUnknown status
University of Oklahoma Health Sciences Center
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Oklahoma CityUnited StatesUnknown status
Saint Alphonsus Cancer Care Center-Ontario
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OntarioUnited StatesUnknown status
Kaiser Permanente-Ontario
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OntarioUnited StatesUnknown status
Providence Willamette Falls Medical Center
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Oregon CityUnited StatesUnknown status
Northwestern Medicine Orland Park
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Orland ParkUnited StatesUnknown status
Illinois CancerCare-Ottawa Clinic
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OttawaUnited StatesUnknown status
Kaiser Permanente - Panorama City
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Panorama CityUnited StatesUnknown status
Illinois CancerCare-Pekin
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PekinUnited StatesUnknown status
Illinois CancerCare-Peoria
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PeoriaUnited StatesUnknown status
Illinois CancerCare-Peru
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PeruUnited StatesUnknown status
Cancer Center at Saint Joseph's
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PhoenixUnited StatesUnknown status
FirstHealth of the Carolinas-Moore Regional Hospital
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PinehurstUnited StatesUnknown status
Trinity Health Saint Joseph Mercy Oakland Hospital
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PontiacUnited StatesUnknown status
Providence Saint Vincent Medical Center
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PortlandUnited StatesUnknown status
Providence Portland Medical Center
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PortlandUnited StatesUnknown status
Oregon Health and Science University
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PortlandUnited StatesUnknown status
Kootenai Clinic Cancer Services - Post Falls
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Post FallsUnited StatesUnknown status
Illinois CancerCare-Princeton
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PrincetonUnited StatesUnknown status
Duke Cancer Center Raleigh
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RaleighUnited StatesUnknown status
Marshfield Medical Center-Rice Lake
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Rice LakeUnited StatesUnknown status
UT Southwestern Clinical Center at Richardson/Plano
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RichardsonUnited StatesUnknown status
VCU Massey Cancer Center at Stony Point
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RichmondUnited StatesUnknown status
VCU Massey Comprehensive Cancer Center
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RichmondUnited StatesUnknown status
Kaiser Permanente-Riverside
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RiversideUnited StatesUnknown status
UW Health Carbone Cancer Center Rockford
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RockfordUnited StatesUnknown status
University of California Davis Comprehensive Cancer Center
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SacramentoUnited StatesUnknown status
MyMichigan Medical Center Saginaw
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SaginawUnited StatesUnknown status
Oncology Hematology Associates of Saginaw Valley PC
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SaginawUnited 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
Park Nicollet Clinic - Saint Louis Park
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Saint Louis ParkUnited StatesUnknown status
Regions Hospital
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Saint PaulUnited StatesUnknown status
United Hospital
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Saint PaulUnited StatesUnknown status
Huntsman Cancer Institute/University of Utah
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Salt Lake CityUnited StatesUnknown status
University of Texas Health Science Center at San Antonio
Coordinator of this site? Confirm its status
San AntonioUnited StatesUnknown status
Kaiser Permanente-San Diego Zion
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San DiegoUnited StatesUnknown status
Kootenai Clinic Cancer Services - Sandpoint
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SandpointUnited StatesUnknown status
Kaiser Permanente-San Marcos
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San MarcosUnited StatesUnknown status
Memorial Hospital East
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ShilohUnited StatesUnknown status
Springfield Memorial Hospital
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SpringfieldUnited StatesUnknown status
Southern Illinois University School of Medicine
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SpringfieldUnited StatesUnknown status
Springfield Clinic
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SpringfieldUnited StatesUnknown status
Marshfield Medical Center-River Region at Stevens Point
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Stevens PointUnited StatesUnknown status
Missouri Baptist Medical Center
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St LouisUnited StatesUnknown status
Siteman Cancer Center at Christian Hospital
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St LouisUnited StatesUnknown status
Mercy Hospital South
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St LouisUnited StatesUnknown status
Washington University School of Medicine
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St LouisUnited StatesUnknown status
Siteman Cancer Center-South County
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St LouisUnited StatesUnknown status
Mercy Hospital Saint Louis
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St LouisUnited StatesUnknown status
Missouri Baptist Sullivan Hospital
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SullivanUnited StatesUnknown status
MyMichigan Medical Center Tawas
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Tawas CityUnited StatesUnknown status
Cotton O'Neil Cancer Center / Stormont Vail Health
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TopekaUnited StatesUnknown status
Munson Medical Center
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Traverse CityUnited StatesUnknown status
Upper Valley Medical Center
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TroyUnited StatesUnknown status
Oklahoma Cancer Specialists and Research Institute-Tulsa
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TulsaUnited StatesUnknown status
Saint Luke's Cancer Institute - Twin Falls
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Twin FallsUnited StatesUnknown status
Carle Cancer Center
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UrbanaUnited StatesUnknown status
Epic Care Cyberknife Center
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Walnut CreekUnited StatesUnknown status
Northwestern Medicine Cancer Center Warrenville
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WarrenvilleUnited StatesUnknown status
Illinois CancerCare - Washington
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WashingtonUnited StatesUnknown status
MedStar Georgetown University Hospital
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Washington D.C.United StatesUnknown status
UI Health Care Mission Cancer and Blood - Waukee Clinic
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WaukeeUnited StatesUnknown status
Saint Mary's Oncology/Hematology Associates of West Branch
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West BranchUnited StatesUnknown status
Marshfield Medical Center - Weston
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WestonUnited StatesUnknown status
Kaiser Permanente-Woodland Hills
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Woodland HillsUnited StatesUnknown status
University of Michigan Health - West
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WyomingUnited StatesUnknown status
Huron Gastroenterology PC
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YpsilantiUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology Ann Arbor Campus
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YpsilantiUnited StatesUnknown status

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