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NCT05136196RecruitingPhase 2

BiCaZO: A Study Combining Two Immunotherapies (Cabozantinib and Nivolumab) to Treat Patients With Advanced Melanoma or Squamous Cell Head and Neck Cancer, an immunoMATCH Pilot Study

Biomarker Stratified CaboZantinib (NSC#761968) and NivOlumab (NSC#748726) (BiCaZO) - A Phase II Study of Combining Cabozantinib and Nivolumab in Participants With Advanced Solid Tumors (IO Refractory Melanoma or HNSCC) Stratified by Tumor Biomarkers - an immunoMATCH Pilot Study

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

This phase II trial studies the good and bad effects of the combination of drugs called cabozantinib and nivolumab in treating patients with melanoma or squamous cell head and neck cancer that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced). Cabozantinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. This trial may help doctors determine how quickly patients can be divided into groups based on biomarkers in their tumors. A biomarker is a biological molecule found in the blood, other body fluids, or in tissues that is a sign of a normal or abnormal process or a sign of a condition or disease. A biomarker may be used to see how well the body responds to a treatment for a disease or condition. The two biomarkers that this trial is studying are "tumor mutational burden" and "tumor inflammation signature." Another purpose of this trial is to help doctors learn if cabozantinib and nivolumab shrink or stabilize the cancer, and whether patients respond differently to the combination depending on the status of the biomarkers.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
150 (estimated)
First submitted
25 Nov 2021
Start date
6 Dec 2022
Primary completion date
1 Jan 2027
Lead sponsor
National Cancer Institute (NCI)
NCT number
NCT05136196

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 150
  • From 6 Dec 2022 to the primary completion date, 1 Jan 2027
  • 232 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

  • STEP 1 - SPECIMEN SUBMISSION
  • Participants must have histologically confirmed melanoma that is stage III or IV, unresectable, recurrent, or metastatic non-uveal melanoma OR Participants must have histologically confirmed squamous cell carcinoma of the head and neck (HNSCC) that is either locally recurrent and non-amendable to curative therapy (e.g., radiation, surgery) or metastatic. The primary tumor location must be the oropharynx, oral cavity, hypopharynx, or larynx. Primary tumor site of nasopharynx (any histology) or unknown primary tumor are not eligible
    • Note: For participants with primary oropharyngeal cancer, human papillomavirus (HPV) or p16 status must be known prior to step 1 registration
  • Participants must have disease presentation consistent with measurable disease. Note: Current disease measurements will not be required until step 2 registration
  • Participants must have had documented progression during or within 12 weeks after the last dose of PD-1 checkpoint inhibition-based therapy. Participants must have been receiving checkpoint inhibition for a minimum of 6 weeks. Participants who recur during adjuvant anti-PD1 treatment or within 12 weeks of completion of adjuvant anti-PD1 treatment are eligible if they have measurable disease and are considered unresectable
  • Participants with known human immunodeficiency virus (HIV)-infection must be receiving anti-retroviral therapy and have an undetectable viral load test within 6 months prior to step 1 registration
  • Participants with evidence of chronic hepatitis B virus (HBV) infection must have undetectable HBV viral load within 28 days prior to step 1 registration
  • Participants with a history of hepatitis C virus (HCV) infection must have no detectable viral load within 28 days prior to step 1 registration
  • Participants must not have an active infection requiring systemic therapy (except HBV, HCV or HIV as mentioned above)
  • Participants must not have experienced myocardial infarction or thromboembolic event requiring anticoagulation within 90 days prior to step 1 registration, unless clinically stable with ongoing medical management
  • Participants must have recovered to baseline or =\< grade 1 Common Terminology Criteria for Adverse Events (CTCAE) version (v) 5 toxicities related to any prior treatments, unless adverse events are deemed clinically nonsignificant by the treating investigator or stable on supportive therapy
  • Participants must not have received more than one prior primary radiotherapy regimen, curative or adjuvant, to the mucosal surfaces of the head and neck, with the additional following criteria:
    • If the primary radiation is combined with chemotherapy, a minimum of 16 weeks will be required to have elapsed between the end of radiotherapy and step 1 registration. If the radiation is given alone, a minimum of 8 weeks will be required to have elapsed between the end of radiotherapy and step 1 registration
    • Additional palliative radiotherapy regimens are permitted but cannot have been administered to previously treated tissue (i.e., overlapping fields are excluded) with the exception of central nervous system (CNS) radiation and must be completed at least 4 weeks prior to step 1 registration
    • Treatment areas should be healed with no sequelae from radiation therapy (RT) that would predispose to fistula formation
  • Participants must not have received prior treatment with anti-VEGF therapies for any reason
  • Participants must be \>= 18 years of age
  • Participants must have a Zubrod Performance Status 0 or 1
  • Participants must have adequate cardiac function. Participants with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, must have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification and must be class 2B or better to be eligible for this trial
  • Participants must not have any known significant organ disfunction that, in the opinion of the treating investigator, may impact suitability for receiving combination nivolumab/cabozantinib treatment
  • Participants must be able to take oral medication without breaking, opening, crushing, dissolving or chewing capsules
  • Participants must not have malabsorption syndrome
  • Participants must not have active autoimmune disease requiring systemic steroids (equivalent of \> 10mg of prednisone) or other immune suppression. Exceptions:
    • Type 1 diabetes mellitus
    • Endocrinopathy only requiring hormone replacement
    • Skin disorders (e.g., vitiligo, psoriasis, or alopecia) not requiring systemic treatment
    • Conditions not expected to recur in the absence of an external trigger
  • Participants must not have received an organ allograft
  • Participants must not have a history of hemoptysis (defined as \>= 1/2 tsp of bright red blood per day) or tumor bleeding within 90 days prior to step 1 registration
  • Participants must not have any of the following criteria due to the possibility of increased risk for tumor bleeding with cabozantinib therapy:
    • Prior carotid bleeding
    • Tumors that invade major vessels (e.g., the carotid) as shown unequivocally by imaging studies
    • Central (e.g., within 2 cm from the hilum) lung metastases that are cavitary as shown unequivocally by imaging studies
    • Any prior history of bleeding related to the current head and neck cancer
    • History of gross hemoptysis (bright red blood of 1/2 teaspoon or more per episode of coughing) within 3 months
  • Participants must not require concomitant anticoagulation with coumarin agents (e.g., warfarin), direct thrombin inhibitors (e.g., dabigatran), direct factor Xa inhibitor betrixaban, or platelet inhibitors (e.g., clopidogrel)
    • Participants must not require anticoagulants except for the following:
    • Prophylactic use of low-dose aspirin for cardio-protection (per local applicable guidelines) and low-dose low molecular weight heparins (LMWH).
    • Therapeutic doses of LMWH or anticoagulation with direct factor Xa inhibitors, rivaroxaban, edoxaban, or apixaban in participants without known brain metastases who are on a stable dose of the anticoagulant for at least 1 week prior to step 1 registration without clinically significant hemorrhagic complications from the anticoagulation regimen or the tumor
  • Participants must not have evidence of preexisting uncontrolled hypertension 28 days prior to step 1 registration as documented by baseline blood pressure reading with systolic blood pressure \> 150 mmHg and/or diastolic blood pressure \> 90 mmHg. Participants on antihypertensive therapies with controlled blood pressure are eligible
  • Participants must not have a prior or concurrent malignancy whose natural history or treatment (in the opinion of the treating physician) has the potential to interfere with the safety or efficacy assessment of the investigational regimen
  • Participants must not be pregnant or nursing due to the known safety profiles of the drugs in this study. 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
  • Have an adequate archival tissue specimen verified by the local pathologist and documented on the Pathology Review Form from a procedure obtained after the development of resistance to anti-PD-1/L1 therapy. Archival tissue must consist of tumor block or at least 1 hematoxylin and eosin (H\&E)-stained 4-5 micron slide and 20 freshly cut serially sectioned and numbered 4-5 micron unstained, uncharged slides OR
    • Be willing to undergo research biopsy AND have tumor accessible for biopsy based on the following criteria:
  • Mediastinal, laparoscopic, gastrointestinal, or bronchial endoscopic biopsies can be obtained incidentally to a clinically necessary procedure and NOT for the sole purpose of the clinical trial
  • Acceptable biopsy procedures are:
    • Percutaneous biopsy with local anesthetic and/or sedation with an expected risk of severe complications \< 2%
    • Direct transoral biopsy (with or without local anesthetic and/or sedation) with an expected risk of severe complications \< 2%
    • Excisional cutaneous biopsy with local anesthetic and/or sedation with an expected risk of severe complications \< 2%
    • Biopsy with removal of additional tumor tissue during a medically necessary mediastinoscopy, laparoscopy, gastrointestinal endoscopy, bronchoscopy or craniotomy. No open surgical, laparoscopic or endoscopic procedure should be performed solely to obtain a biopsy for this protocol
    • Removal of additional tumor tissue during a medically necessary surgical procedure
    • Participants must submit whole blood for germline genomic analysis
    • Participants must have been offered the opportunity to participate in specimen banking
    • Note: As a part of the Oncology Patient Enrollment Network (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
  • 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
  • Participants with impaired decision-making capacity are eligible as long as their neurological or psychological condition does not preclude their safe participation in the study (e.g., tracking pill consumption and reporting adverse events to the investigator)
    • STEP 2 TREATMENT REGISTRATION
  • Note: No tests or exams are required to be repeated for step 2 registration (Treatment). However, participants who are known to have a change in eligibility status after step 1 registration are not eligible for step 2 registration
    • Participants must continue to meet eligibility for step 1 registration prior to step 2 registration
    • Participants must have had their tumor tissue submitted via the Southwest Oncology Group (SWOG) Specimen Tracking System prior to step 2 registration
    • Participants registered during stage II of the protocol must have received assignment to an open cohort from the SWOG Statistics and Data Management Center based on their biomarker screening profile (not applicable for patients registered during stage I of the protocol)
    • Participants must have measurable disease. All measurable disease must be assessed within 28 days prior to step 2 registration. All non-measurable disease must be assessed within 42 days prior to step 2 registration. Note: All disease must be assessed and documented on the Baseline Tumor Assessment Form (Response Evaluation Criteria in Solid Tumors \[RECIST\] 1.1)
    • For melanoma participants, CT chest, abdomen and pelvis must be obtained. For HNSCC participants, CT neck and chest must be obtained. Further imaging (i.e., MR brain, CT abdomen/pelvis or extremities, bone scan) will be performed as deemed appropriate by the treating physician
    • Participants with treated brain metastases must have no evidence of progression on the follow-up brain imaging after central nervous system (CNS)-directed therapy
    • Participants must not have experienced any significant health changes that, in the opinion of the treating investigator, may impact continued suitability for receiving combination nivolumab/cabozantinib treatment
    • Participants with treated brain metastases must have discontinued steroid treatment at least 14 days prior to step 2 registration
    • Participants must not have received investigational agents or monoclonal antibodies (except Food and Drug Administration \[FDA\] approved supportive care antibodies, such as denosumab) within 28 days prior to step 2 registration
    • Participants must not have received surgery, chemotherapy, radiation therapy, biologic agents, or steroids within 14 days prior to step 2 registration
    • Participants must not have received administration of a live, attenuated vaccine within 30 days prior to step 2 registration. Note: Participants may have received a messenger ribonucleic acid (mRNA) or viral vector-based coronavirus disease 2019 (COVID-19) vaccine within 30 days prior to step 2 registration
    • Participants must not have received administration of any strong CYP3A4 inducers, such as but not limited to rifampin, carbamazepine, enzalutamide, mitotane, phenytoin and St. John's wort, within 14 days prior to step 2 registration
    • Participants must not have received administration of any strong CYP3A4 inhibitors, such as but not limited to clarithromycin, itraconazole, ketoconazole, grapefruit juice, indinavir, nelfinavir, ritonavir, nefazodone, saquinavir, and telithromycin, within 5 times the half-life of the CYP3A inhibitor prior to step 2 registration
    • Participants must have a history and physical examination performed within 28 days prior to step 2 registration
    • Leukocytes \>= 3,000/uL (within 28 days prior to step 2 registration)
    • Absolute neutrophil count \>= 1,500/uL (within 28 days prior to step 2 registration)
    • Platelets \>= 100,000/uL (within 28 days prior to step 2 registration)
    • Total bilirubin =\< 1.5 x institutional upper limit of normal (ULN) or =\< 3 x ULN for participants with Gilbert's disease (within 28 days prior to step 2 registration)
    • Aspartate aminotransferase (AST) =\< 3 x institutional ULN (within 28 days prior to step 2 registration)
    • Alanine aminotransferase (ALT) =\< 3 x institutional ULN (within 28 days prior to step 2 registration)
    • Urinalysis: For baseline value (no required value for eligibility)
    • Measured (OR calculated) creatinine clearance \>= 30 mL/min using the following Cockcroft-Gault Formula. This specimen must have been drawn and processed within 28 days prior to step 2 registration

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

Full criteria on ClinicalTrials.gov

Sites (232)

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

SiteCityCountrySite status
Hawaii Cancer Care - Westridge
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‘AieaUnited StatesSuspended
University of New Mexico Cancer Center
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AlbuquerqueUnited StatesRecruiting
Inova Alexandria Hospital
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AlexandriaUnited StatesRecruiting
Mary Greeley Medical Center
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AmesUnited StatesRecruiting
McFarland Clinic - Ames
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AmesUnited StatesRecruiting
Community Hospital of Anaconda
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AnacondaUnited StatesRecruiting
UI Health Care Mission Cancer and Blood - Ankeny Clinic
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AnkenyUnited StatesRecruiting
University of Michigan Rogel Cancer Center
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Ann ArborUnited StatesRecruiting
Trinity Health Saint Joseph Mercy Hospital Ann Arbor
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Ann ArborUnited StatesRecruiting
Duluth Clinic Ashland
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AshlandUnited StatesRecruiting
Rocky Mountain Regional VA Medical Center
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AuroraUnited StatesActive, not recruiting
Rush-Copley Medical Center
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AuroraUnited StatesSuspended
Bronson Battle Creek
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Battle CreekUnited StatesRecruiting
Nebraska Medicine-Bellevue
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BellevueUnited StatesRecruiting
Sanford Joe Lueken Cancer Center
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BemidjiUnited StatesRecruiting
Saint Charles Health System
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BendUnited StatesRecruiting
Tower Cancer Research Foundation
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Beverly HillsUnited StatesRecruiting
Billings Clinic Cancer Center
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BillingsUnited StatesRecruiting
Sanford Bismarck Medical Center
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BismarckUnited StatesRecruiting
Illinois CancerCare-Bloomington
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BloomingtonUnited StatesRecruiting
Saint Luke's Cancer Institute - Boise
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BoiseUnited StatesRecruiting
Saint Alphonsus Cancer Care Center-Boise
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BoiseUnited StatesRecruiting
McFarland Clinic - Boone
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BooneUnited StatesSuspended
Tufts Medical Center
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BostonUnited StatesActive, not recruiting
Bozeman Health Deaconess Hospital
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BozemanUnited StatesRecruiting
Essentia Health Saint Joseph's Medical Center
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BrainerdUnited StatesRecruiting
Trinity Health Medical Center - Brighton
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BrightonUnited StatesRecruiting
Trinity Health IHA Medical Group Hematology Oncology - Brighton
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BrightonUnited StatesRecruiting
Minnesota Oncology - Burnsville
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BurnsvilleUnited StatesRecruiting
Saint Alphonsus Cancer Care Center-Caldwell
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CaldwellUnited StatesRecruiting
Trinity Health IHA Medical Group Hematology Oncology - Canton
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CantonUnited StatesRecruiting
Illinois CancerCare-Canton
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CantonUnited StatesRecruiting
Trinity Health Medical Center - Canton
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CantonUnited StatesRecruiting
Saint Francis Medical Center
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Cape GirardeauUnited StatesRecruiting
Illinois CancerCare-Carthage
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CarthageUnited StatesRecruiting
Mercy Hospital
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Cedar RapidsUnited StatesRecruiting
Oncology Associates at Mercy Medical Center
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Cedar RapidsUnited StatesRecruiting
Miami Valley Hospital South
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CentervilleUnited StatesRecruiting
Centralia Oncology Clinic
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CentraliaUnited StatesRecruiting
Minnesota Oncology Hematology PA-Chaska
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ChaskaUnited StatesRecruiting
Chelsea Hospital
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ChelseaUnited StatesRecruiting
Trinity Health IHA Medical Group Hematology Oncology - Chelsea Hospital
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ChelseaUnited StatesRecruiting
Northwestern University
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ChicagoUnited StatesRecruiting
University of Illinois
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ChicagoUnited StatesRecruiting
Siteman Cancer Center at Saint Peters Hospital
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City of Saint PetersUnited StatesRecruiting
Clackamas Radiation Oncology Center
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ClackamasUnited StatesRecruiting
Southeastern Medical Oncology Center-Clinton
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ClintonUnited StatesRecruiting
UI Health Care Mission Cancer and Blood - West Des Moines Clinic
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CliveUnited StatesRecruiting
Mercy Cancer Center-West Lakes
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CliveUnited StatesRecruiting
Kootenai Health - Coeur d'Alene
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Coeur d'AleneUnited StatesRecruiting
Memorial Hospital North
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Colorado SpringsUnited StatesRecruiting
UCHealth Memorial Hospital Central
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Colorado SpringsUnited StatesRecruiting
Mercy Hospital
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Coon RapidsUnited StatesRecruiting
Siteman Cancer Center at West County Hospital
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Creve CoeurUnited StatesRecruiting
Carle at The Riverfront
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DanvilleUnited StatesRecruiting
Miami Valley Hospital North
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DaytonUnited StatesRecruiting
Premier Blood and Cancer Center
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DaytonUnited StatesRecruiting
Cancer Care Specialists of Illinois - Decatur
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DecaturUnited StatesRecruiting
Decatur Memorial Hospital
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DecaturUnited StatesRecruiting
Essentia Health - Deer River Clinic
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Deer RiverUnited StatesRecruiting
Northwestern Medicine Cancer Center Kishwaukee
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DeKalbUnited StatesRecruiting
UI Health Care Mission Cancer and Blood - Laurel Clinic
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Des MoinesUnited StatesRecruiting
UI Health Care Mission Cancer and Blood - Des Moines Clinic
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Des MoinesUnited StatesRecruiting
Mercy Medical Center - Des Moines
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Des MoinesUnited StatesRecruiting
Wayne State University/Karmanos Cancer Institute
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DetroitUnited StatesActive, not recruiting
Essentia Health Saint Mary's - Detroit Lakes Clinic
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Detroit LakesUnited StatesRecruiting
Illinois CancerCare-Dixon
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DixonUnited StatesRecruiting
Essentia Health Cancer Center
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DuluthUnited StatesRecruiting
Marshfield Medical Center-EC Cancer Center
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Eau ClaireUnited StatesRecruiting
Fairview Southdale Hospital
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EdinaUnited StatesRecruiting
Minnesota Oncology - Edina
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EdinaUnited StatesRecruiting
Carle Physician Group-Effingham
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EffinghamUnited StatesRecruiting
Crossroads Cancer Center
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EffinghamUnited StatesRecruiting
OSF Saint Francis Hospital and Medical Group
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EscanabaUnited StatesRecruiting
Illinois CancerCare-Eureka
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EurekaUnited StatesRecruiting
Inova Schar Cancer Institute
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FairfaxUnited StatesRecruiting
Inova Fair Oaks Hospital
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FairfaxUnited StatesRecruiting
Inova Fairfax Hospital
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Falls ChurchUnited StatesRecruiting
Essentia Health Cancer Center-South University Clinic
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FargoUnited StatesRecruiting
Sanford Roger Maris Cancer Center
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FargoUnited StatesRecruiting
Sanford Broadway Medical Center
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FargoUnited StatesRecruiting
Weisberg Cancer Treatment Center
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Farmington HillsUnited StatesActive, not recruiting
Hurley Medical Center
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FlintUnited StatesRecruiting
Genesee Hematology Oncology PC
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FlintUnited StatesSuspended
Cancer Hematology Centers - Flint
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FlintUnited StatesRecruiting
Genesys Hurley Cancer Institute
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FlintUnited StatesRecruiting
Cancer Care and Hematology-Fort Collins
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Fort CollinsUnited StatesRecruiting
Poudre Valley Hospital
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Fort CollinsUnited StatesRecruiting
McFarland Clinic - Trinity Cancer Center
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Fort DodgeUnited StatesRecruiting
Essentia Health - Fosston
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FosstonUnited StatesRecruiting
Atrium Medical Center-Middletown Regional Hospital
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FranklinUnited StatesRecruiting
Unity Hospital
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FridleyUnited StatesActive, not recruiting
Saint Luke's Cancer Institute - Fruitland
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FruitlandUnited StatesRecruiting
Illinois CancerCare-Galesburg
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GalesburgUnited StatesRecruiting
Northwestern Medicine Cancer Center Delnor
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GenevaUnited StatesRecruiting
Northwestern Medicine Glenview Outpatient Center
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GlenviewUnited StatesRecruiting
Southeastern Medical Oncology Center-Goldsboro
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GoldsboroUnited StatesRecruiting
Trinity Health Grand Rapids Hospital
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Grand RapidsUnited StatesRecruiting
Corewell Health Grand Rapids Hospitals - Butterworth Hospital
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Grand RapidsUnited StatesRecruiting
Northwestern Medicine Grayslake Outpatient Center
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GrayslakeUnited StatesRecruiting
Benefis Sletten Cancer Institute
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Great FallsUnited StatesRecruiting
UCHealth Greeley Hospital
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GreeleyUnited StatesRecruiting
Saint Vincent Hospital Cancer Center at Saint Mary's
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Green BayUnited StatesRecruiting
Saint Vincent Hospital Cancer Center Green Bay
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Green BayUnited StatesRecruiting
Miami Valley Cancer Care and Infusion
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GreenvilleUnited StatesRecruiting
Essentia Health Hibbing Clinic
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HibbingUnited StatesRecruiting
Queen's Cancer Center - Kuakini
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HonoluluUnited StatesSuspended
Queen's Cancer Cenrer - POB I
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HonoluluUnited StatesSuspended
Queen's Medical Center
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HonoluluUnited StatesSuspended
Hawaii Cancer Care Inc - Waterfront Plaza
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HonoluluUnited StatesSuspended
UCI Health - Chao Family Comprehensive Cancer Center and Ambulatory Care
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IrvineUnited StatesRecruiting
Southeastern Medical Oncology Center-Jacksonville
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JacksonvilleUnited StatesRecruiting
Mayo Clinic in Florida
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JacksonvilleUnited StatesRecruiting
Essentia Health - Jamestown Clinic
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JamestownUnited StatesRecruiting
McFarland Clinic - Jefferson
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JeffersonUnited StatesSuspended
Bronson Methodist Hospital
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KalamazooUnited StatesRecruiting
West Michigan Cancer Center
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KalamazooUnited StatesRecruiting
Beacon Kalamazoo Cancer Center
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KalamazooUnited StatesRecruiting
Logan Health Medical Center
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KalispellUnited StatesRecruiting
Illinois CancerCare-Kewanee Clinic
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KewaneeUnited StatesRecruiting
Gundersen Lutheran Medical Center
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La CrosseUnited StatesRecruiting
Northwestern Medicine Lake Forest Hospital
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Lake ForestUnited StatesRecruiting
Northwell Health/Center for Advanced Medicine
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Lake SuccessUnited StatesActive, not recruiting
University of Michigan Health - Sparrow Lansing
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LansingUnited StatesRecruiting
Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center
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LebanonUnited StatesRecruiting
University of Arkansas for Medical Sciences
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Little RockUnited StatesRecruiting
Trinity Health Saint Mary Mercy Livonia Hospital
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LivoniaUnited StatesRecruiting
Cedars-Sinai Medical Center
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Los AngelesUnited StatesRecruiting
The Angeles Clinic and Research Institute - West Los Angeles Office
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Los AngelesUnited StatesRecruiting
Los Angeles General Medical Center
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Los AngelesUnited StatesRecruiting
USC / Norris Comprehensive Cancer Center
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Los AngelesUnited StatesRecruiting
Medical Center of the Rockies
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LovelandUnited StatesRecruiting
Centra Alan B Pearson Regional Cancer Center
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LynchburgUnited StatesRecruiting
Illinois CancerCare-Macomb
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MacombUnited StatesRecruiting
Saint John's Hospital - Healtheast
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MaplewoodUnited StatesRecruiting
McFarland Clinic - Marshalltown
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MarshalltownUnited StatesRecruiting
Marshfield Medical Center-Marshfield
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MarshfieldUnited StatesRecruiting
Carle Physician Group-Mattoon/Charleston
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MattoonUnited StatesRecruiting
Loyola University Medical Center
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MaywoodUnited StatesRecruiting
Saint Luke's Cancer Institute - Meridian
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MeridianUnited StatesRecruiting
Medical College of Wisconsin
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MilwaukeeUnited StatesRecruiting
NYU Langone Hospital - Long Island
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MineolaUnited StatesRecruiting
Abbott-Northwestern Hospital
Coordinator of this site? Confirm its status
MinneapolisUnited StatesRecruiting
Marshfield Medical Center - Minocqua
Coordinator of this site? Confirm its status
MinocquaUnited StatesRecruiting
Community Medical Center
Coordinator of this site? Confirm its status
MissoulaUnited StatesRecruiting
ProHealth D N Greenwald Center
Coordinator of this site? Confirm its status
MukwonagoUnited StatesRecruiting
Trinity Health Muskegon Hospital
Coordinator of this site? Confirm its status
MuskegonUnited StatesSuspended
Saint Luke's Cancer Institute - Nampa
Coordinator of this site? Confirm its status
NampaUnited StatesRecruiting
Saint Alphonsus Cancer Care Center-Nampa
Coordinator of this site? Confirm its status
NampaUnited StatesRecruiting
Helen F Graham Cancer Center
Coordinator of this site? Confirm its status
NewarkUnited StatesRecruiting
Medical Oncology Hematology Consultants PA
Coordinator of this site? Confirm its status
NewarkUnited StatesRecruiting
Providence Newberg Medical Center
Coordinator of this site? Confirm its status
NewbergUnited StatesRecruiting
Cancer Center of Western Wisconsin
Coordinator of this site? Confirm its status
New RichmondUnited StatesRecruiting
Laura and Isaac Perlmutter Cancer Center at NYU Langone
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Corewell Health Lakeland Hospitals - Niles Hospital
Coordinator of this site? Confirm its status
NilesUnited StatesRecruiting
Carle Cancer Institute Normal
Coordinator of this site? Confirm its status
NormalUnited StatesRecruiting
Carle BroMenn Medical Center
Coordinator of this site? Confirm its status
NormalUnited StatesRecruiting
Cancer and Hematology Centers of Western Michigan - Norton Shores
Coordinator of this site? Confirm its status
Norton ShoresUnited StatesRecruiting
ProHealth Oconomowoc Memorial Hospital
Coordinator of this site? Confirm its status
OconomowocUnited StatesRecruiting
Saint Vincent Hospital Cancer Center at Oconto Falls
Coordinator of this site? Confirm its status
Oconto FallsUnited StatesRecruiting
Cancer Care Center of O'Fallon
Coordinator of this site? Confirm its status
O'FallonUnited StatesRecruiting
University of Oklahoma Health Sciences Center
Coordinator of this site? Confirm its status
Oklahoma CityUnited StatesRecruiting
Nebraska Medicine-Village Pointe
Coordinator of this site? Confirm its status
OmahaUnited StatesRecruiting
University of Nebraska Medical Center
Coordinator of this site? Confirm its status
OmahaUnited StatesRecruiting
Saint Alphonsus Cancer Care Center-Ontario
Coordinator of this site? Confirm its status
OntarioUnited StatesRecruiting
UC Irvine Health- Chao Family Comprehensive Cancer Center
Coordinator of this site? Confirm its status
OrangeUnited StatesRecruiting
Providence Willamette Falls Medical Center
Coordinator of this site? Confirm its status
Oregon CityUnited StatesRecruiting
AdventHealth Orlando
Coordinator of this site? Confirm its status
OrlandoUnited StatesRecruiting
Northwestern Medicine Orland Park
Coordinator of this site? Confirm its status
Orland ParkUnited StatesRecruiting
Illinois CancerCare-Ottawa Clinic
Coordinator of this site? Confirm its status
OttawaUnited StatesRecruiting
Essentia Health - Park Rapids
Coordinator of this site? Confirm its status
Park RapidsUnited StatesRecruiting
Illinois CancerCare-Pekin
Coordinator of this site? Confirm its status
PekinUnited StatesRecruiting
Illinois CancerCare-Peoria
Coordinator of this site? Confirm its status
PeoriaUnited StatesRecruiting
Illinois CancerCare-Peru
Coordinator of this site? Confirm its status
PeruUnited StatesRecruiting
Thomas Jefferson University Hospital
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesActive, not recruiting
Jefferson Torresdale Hospital
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesActive, not recruiting
Mayo Clinic Hospital in Arizona
Coordinator of this site? Confirm its status
PhoenixUnited StatesRecruiting
Trinity Health Saint Joseph Mercy Oakland Hospital
Coordinator of this site? Confirm its status
PontiacUnited StatesRecruiting
Providence Saint Vincent Medical Center
Coordinator of this site? Confirm its status
PortlandUnited StatesRecruiting
Providence Portland Medical Center
Coordinator of this site? Confirm its status
PortlandUnited StatesRecruiting
Kootenai Clinic Cancer Services - Post Falls
Coordinator of this site? Confirm its status
Post FallsUnited StatesRecruiting
Illinois CancerCare-Princeton
Coordinator of this site? Confirm its status
PrincetonUnited StatesRecruiting
Rapid City Regional Hospital
Coordinator of this site? Confirm its status
Rapid CityUnited StatesRecruiting
Corewell Health Reed City Hospital
Coordinator of this site? Confirm its status
Reed CityUnited StatesRecruiting
Marshfield Medical Center-Rice Lake
Coordinator of this site? Confirm its status
Rice LakeUnited StatesRecruiting
VCU Massey Comprehensive Cancer Center
Coordinator of this site? Confirm its status
RichmondUnited StatesRecruiting
Virginia Cancer Institute
Coordinator of this site? Confirm its status
RichmondUnited StatesRecruiting
VCU Massey Cancer Center at Stony Point
Coordinator of this site? Confirm its status
RichmondUnited StatesRecruiting
Mayo Clinic in Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesRecruiting
Dartmouth Cancer Center - North
Coordinator of this site? Confirm its status
Saint JohnsburyUnited StatesRecruiting
Corewell Health Lakeland Hospitals - Marie Yeager Cancer Center
Coordinator of this site? Confirm its status
Saint JosephUnited StatesRecruiting
Park Nicollet Clinic - Saint Louis Park
Coordinator of this site? Confirm its status
Saint Louis ParkUnited StatesRecruiting
United Hospital
Coordinator of this site? Confirm its status
Saint PaulUnited StatesRecruiting
Regions Hospital
Coordinator of this site? Confirm its status
Saint PaulUnited StatesRecruiting
Huntsman Cancer Institute/University of Utah
Coordinator of this site? Confirm its status
Salt Lake CityUnited StatesRecruiting
Kootenai Clinic Cancer Services - Sandpoint
Coordinator of this site? Confirm its status
SandpointUnited StatesRecruiting
Essentia Health Sandstone
Coordinator of this site? Confirm its status
SandstoneUnited StatesRecruiting
Saint Vincent Hospital Cancer Center at Sheboygan
Coordinator of this site? Confirm its status
SheboyganUnited StatesRecruiting
Memorial Hospital East
Coordinator of this site? Confirm its status
ShilohUnited StatesRecruiting
Sanford Cancer Center Oncology Clinic
Coordinator of this site? Confirm its status
Sioux FallsUnited StatesRecruiting
Sanford USD Medical Center - Sioux Falls
Coordinator of this site? Confirm its status
Sioux FallsUnited StatesRecruiting
Springfield Clinic
Coordinator of this site? Confirm its status
SpringfieldUnited StatesRecruiting
Southern Illinois University School of Medicine
Coordinator of this site? Confirm its status
SpringfieldUnited StatesRecruiting
Springfield Memorial Hospital
Coordinator of this site? Confirm its status
SpringfieldUnited StatesRecruiting
Baystate Medical Center
Coordinator of this site? Confirm its status
SpringfieldUnited StatesRecruiting
Marshfield Medical Center-River Region at Stevens Point
Coordinator of this site? Confirm its status
Stevens PointUnited StatesRecruiting
Siteman Cancer Center at Christian Hospital
Coordinator of this site? Confirm its status
St LouisUnited StatesRecruiting
Mercy Hospital South
Coordinator of this site? Confirm its status
St LouisUnited StatesRecruiting
Siteman Cancer Center-South County
Coordinator of this site? Confirm its status
St LouisUnited StatesRecruiting
Washington University School of Medicine
Coordinator of this site? Confirm its status
St LouisUnited StatesRecruiting
Tufts Medical Center Cancer Center Stoneham
Coordinator of this site? Confirm its status
StonehamUnited StatesActive, not recruiting
Saint Vincent Hospital Cancer Center at Sturgeon Bay
Coordinator of this site? Confirm its status
Sturgeon BayUnited StatesRecruiting
Essentia Health Saint Mary's Hospital - Superior
Coordinator of this site? Confirm its status
SuperiorUnited StatesRecruiting
VCU Health Tappahannock Hospital
Coordinator of this site? Confirm its status
TappahannockUnited StatesRecruiting
Munson Medical Center
Coordinator of this site? Confirm its status
Traverse CityUnited StatesRecruiting
Upper Valley Medical Center
Coordinator of this site? Confirm its status
TroyUnited StatesRecruiting
Saint Luke's Cancer Institute - Twin Falls
Coordinator of this site? Confirm its status
Twin FallsUnited StatesRecruiting
Carle Cancer Center
Coordinator of this site? Confirm its status
UrbanaUnited StatesRecruiting
Essentia Health Virginia Clinic
Coordinator of this site? Confirm its status
VirginiaUnited StatesRecruiting
Ridgeview Medical Center
Coordinator of this site? Confirm its status
WaconiaUnited StatesRecruiting
Northwestern Medicine Cancer Center Warrenville
Coordinator of this site? Confirm its status
WarrenvilleUnited StatesRecruiting
Illinois CancerCare - Washington
Coordinator of this site? Confirm its status
WashingtonUnited StatesRecruiting
UI Health Care Mission Cancer and Blood - Waukee Clinic
Coordinator of this site? Confirm its status
WaukeeUnited StatesRecruiting
UW Cancer Center at ProHealth Care
Coordinator of this site? Confirm its status
WaukeshaUnited StatesRecruiting
ProHealth Waukesha Memorial Hospital
Coordinator of this site? Confirm its status
WaukeshaUnited StatesRecruiting
Marshfield Medical Center - Weston
Coordinator of this site? Confirm its status
WestonUnited StatesRecruiting
Asplundh Cancer Pavilion
Coordinator of this site? Confirm its status
Willow GroveUnited StatesActive, not recruiting
Minnesota Oncology Hematology PA-Woodbury
Coordinator of this site? Confirm its status
WoodburyUnited StatesRecruiting
University of Michigan Health - West
Coordinator of this site? Confirm its status
WyomingUnited StatesRecruiting
Rush-Copley Healthcare Center
Coordinator of this site? Confirm its status
YorkvilleUnited StatesSuspended
Huron Gastroenterology PC
Coordinator of this site? Confirm its status
YpsilantiUnited StatesRecruiting
Trinity Health IHA Medical Group Hematology Oncology Ann Arbor Campus
Coordinator of this site? Confirm its status
YpsilantiUnited StatesRecruiting

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