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NCT06732401Active, not recruitingPhase 3

Testing the Addition of AZD6738 (Ceralasertib) to Immunotherapy to Increase Time Without Cancer for Patients With Non-Small Cell Lung Cancer

A Randomized Phase III Trial of Checkpoint Blockade in Lung CancEr Patients in the Adjuvant Setting Based on Pathologic Response Following Neoadjuvant Therapy (CLEAR)

Source: ClinicalTrials.gov · Last updated 21 Sept 2026

Brief summary (registry, in English)

This phase III trial compares the effect of adding AZD6738 to durvalumab versus durvalumab alone to increase time without cancer in patients with non-small cell lung cancer, following treatment with chemotherapy and surgery. AZD6738 may stop the growth of tumor cells and may kill them by blocking some of the enzymes needed for cell growth. Durvalumab is a monoclonal antibody that may interfere with the ability of tumor cells to grow and spread. A monoclonal antibody is a type of protein that can bind to certain targets in the body, such as molecules that cause the body to make an immune response (antigens). Adding AZD6738 to durvalumab may increase time without cancer in patients with non-small cell lung cancer, following treatment with chemotherapy and surgery.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
630 (estimated)
First submitted
12 Dec 2024
Start date
7 Aug 2025
Primary completion date
30 Jun 2028
Lead sponsor
National Cancer Institute (NCI)
Diseases
Lung cancer
NCT number
NCT06732401

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 630
  • From 7 Aug 2025 to the primary completion date, 30 Jun 2028
  • 192 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 0: Patient must be \>= 18 years of age
  • STEP 0: Patient must have stage II to select stage IIIB (N2 but excluding N3) non-small cell lung cancer (NSCLC) of any histology using International Association for the Study of Lung Cancer (IASLC) 8th edition. Stage is assessed at time of initiating pre-operative chemo-immunotherapy
  • STEP 0: Patient must fall into one of the following categories:
    • Planning to undergo, be currently undergoing, or recently completed any standard of care neoadjuvant chemo-immunotherapy with plans to undergo surgical resection
    • Recently completed any standard of care neoadjuvant chemo-immunotherapy AND completed surgical resection and are awaiting pCR status.
    • Recently completed any standard of care neoadjuvant chemo-immunotherapy AND completed surgical resection with confirmed non-path complete response (CR) status.
    • NOTES:
  • Patient must have completed at least 3 cycles of neoadjuvant chemo-immunotherapy before surgery in order to be eligible for Step 1 randomization.
  • Patients who have completed their surgical resection prior to enrollment in step 0 registration must have their surgery date within a window that will allow initiation of EA5231 treatment (cycle 1 day 1) to commence within 4-12 weeks following surgery
    • STEP 1: EA5231 CLEAR randomization for patients without a pCR post-surgery. Patient's with pCR after surgery will be offered to enroll in the SWOG study S2414 INSIGHT instead
    • STEP 1: Patient must have completed R0 resection after standard of care neoadjuvant chemo-immunotherapy (minimum three cycles completed) for stage II to select stage IIIB (N2 but excluding N3) non-small cell lung cancer (NSCLC) of any histology using IASLC 8th Edition
    • STEP 1: Patient must have non-pathological CR status post-surgery. The pathological CR/non-pathological CR status will be determined by local pathology using IASLC criteria and using the surgical sample tissue
    • STEP 1: Patient must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 - ≤ 2 (or Karnofsky ≥ 60%)
    • STEP 1: Patient must not have any known EGFR or ALK genetic alterations. Mutation negative status will be determined per local institutional practices and consistent with National Comprehensive Cancer Network (NCCN) guidelines
    • STEP 1: Patient must have undergone a chest CT after surgery and within 28 days prior to step 1 randomization
    • STEP 1: Patient must have recovered from clinically significant adverse events of their most recent therapy/intervention prior to step 1 randomization
    • STEP 1: Patient must not have experienced a toxicity that led to the permanent discontinuation of prior immunotherapy
    • STEP 1: Patient must not be receiving ongoing steroids at a dose of prednisone 10 mg or higher (or equivalent) at the time of step 1 randomization. Steroids as premedication for hypersensitivity reactions (e.g., CT scan premedication) are allowed. Intranasal, inhaled, topical steroids, or local steroid injections (e.g., intra articular injection) are allowed
    • STEP 1: Patient must not have received or have a plan to receive post-operative radiation therapy (PORT)
    • STEP 1: Patient must not have a history of treatment-related pneumonitis requiring ongoing steroids or supplemental oxygen use
    • STEP 1: Patient must not have a history of interstitial lung disease (ILD)
    • STEP 1: Patient must not have diagnosis of ataxia telangiectasia
    • STEP 1: Patient must not have history of active primary immunodeficiency
    • STEP 1: Patient must not have history of allogenic organ transplantation
    • STEP 1: Patient must have body weight \> 30 kg
    • STEP 1: Patient 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 Step 1 randomization to rule out pregnancy. A patient of childbearing potential is defined as anyone, regardless of whether they have undergone tubal ligation, who meets the following criteria:
  • Has achieved menarche at some point
  • Has not undergone a hysterectomy or bilateral oophorectomy
  • 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)
    • STEP 1: Patient must not expect to conceive or father children by using highly accepted and effective method(s) of contraception or by abstaining from sexual intercourse for the duration of their participation in the study. Patients of childbearing potential must use at least 1 highly effective method of contraception in addition to a condom and continue to use it throughout their time on protocol treatment. Male patients must use a condom plus spermicide throughout their time on while on protocol treatment. In addition, all patients must continue contraception use for at least 6 months after the last dose of protocol treatment. Patients must also not breastfeed while on protocol treatment and for at least 6 months after the last dose of protocol treatment. Patients must not donate sperm while on protocol treatment and for 6 months after the last dose of protocol treatment
    • STEP 1: Patient must not donate blood while on protocol treatment
    • STEP 1: 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
    • STEP 1: Leukocytes ≥ 3,000/mcL (these labs must be obtained ≤ 28 days prior to step 1 randomization)
    • STEP 1: Hemoglobin ≥ 9.0 g/dL (these labs must be obtained ≤ 28 days prior to step 1 randomization)
    • STEP 1: Absolute neutrophil count (ANC) ≥ 1,500/mcL (these labs must be obtained ≤ 28 days prior to step 1 randomization)
    • STEP 1: Platelets ≥ 100,000/mcL (these labs must be obtained ≤ 28 days prior to step 1 randomization)
    • STEP 1: Total bilirubin ≤ institutional upper limit of normal (ULN) (these labs must be obtained ≤ 28 days prior to step 1 randomization)
    • STEP 1: Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase \[SGOT\]) and alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase \[SGPT\]) ≤ 3.0 × institutional ULN (these labs must be obtained ≤ 28 days prior to step 1 randomization)
    • STEP 1: Creatinine clearance ≥ 50 mL/min (estimated using Cockcroft-Gault method or measured) (these labs must be obtained ≤ 28 days prior to step 1 randomization)
    • STEP 1: Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months of step 1 randomization are eligible for this trial
    • STEP 1: For patients with known chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated
    • STEP 1: 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
    • STEP 1: 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
    • STEP 1: 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
    • STEP 1: Patient must not have received live attenuated vaccine within 30 days prior to the step 1 randomization, while on protocol treatment and within 30 days after the last dose of durvalumab

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

Full criteria on ClinicalTrials.gov

Sites (192)

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

SiteCityCountrySite status
Lehigh Valley Hospital-Cedar Crest
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AllentownUnited StatesUnknown status
Community Hospital of Anaconda
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AnacondaUnited StatesUnknown status
Aspirus Cancer Care-Antigo-Volm Cancer Center
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AntigoUnited StatesUnknown status
ThedaCare Regional Cancer Center
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AppletonUnited StatesUnknown status
Duluth Clinic Ashland
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AshlandUnited StatesUnknown status
Emory University Hospital Midtown
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AtlantaUnited StatesUnknown status
Emory University Hospital/Winship Cancer Institute
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AtlantaUnited StatesUnknown status
Emory Saint Joseph's Hospital
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AtlantaUnited StatesUnknown status
University of Maryland/Greenebaum Cancer Center
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BaltimoreUnited StatesUnknown status
Bronson Battle Creek
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Battle CreekUnited StatesUnknown status
Lehigh Valley Hospital - Muhlenberg
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BethlehemUnited StatesUnknown status
Beverly Hospital
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BeverlyUnited StatesUnknown status
Tower Cancer Research Foundation
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Beverly HillsUnited 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 Luke's Cancer Institute - Boise
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BoiseUnited StatesUnknown status
Bozeman Health Deaconess Hospital
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BozemanUnited StatesUnknown status
Essentia Health Saint Joseph's Medical Center
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BrainerdUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology - Brighton
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BrightonUnited StatesUnknown status
Bryn Mawr Hospital
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Bryn MawrUnited StatesUnknown status
Lahey Clinic
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BurlingtonUnited StatesUnknown status
Aultman Health Foundation
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CantonUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology - Canton
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CantonUnited StatesUnknown status
Illinois CancerCare-Canton
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CantonUnited StatesUnknown status
Saint Francis Medical Center
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Cape GirardeauUnited StatesUnknown status
Illinois CancerCare-Carthage
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CarthageUnited StatesUnknown status
University of Virginia Cancer Center
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CharlottesvilleUnited 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
Kootenai Health - Coeur d'Alene
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Coeur d'AleneUnited StatesUnknown status
Baptist Memorial Hospital and Cancer Center-Collierville
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ColliervilleUnited StatesUnknown status
Baptist Memorial Hospital and Cancer Center-Golden Triangle
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ColumbusUnited StatesUnknown status
Ohio State University Comprehensive Cancer Center
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ColumbusUnited StatesUnknown status
New Hampshire Oncology Hematology PA-Concord
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ConcordUnited StatesUnknown status
Mercy Hospital
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Coon RapidsUnited StatesUnknown status
Decatur Memorial Hospital
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DecaturUnited StatesUnknown status
Emory Decatur Hospital
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DecaturUnited StatesUnknown status
Cancer Care Specialists of Illinois - Decatur
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DecaturUnited StatesUnknown status
Essentia Health - Deer River Clinic
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Deer RiverUnited StatesUnknown status
Northwestern Medicine Cancer Center Kishwaukee
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DeKalbUnited StatesUnknown status
Illinois CancerCare-Dixon
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DixonUnited StatesUnknown status
Essentia Health Cancer Center
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DuluthUnited StatesUnknown status
Pocono Medical Center
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East StroudsburgUnited StatesUnknown status
Fairview Southdale Hospital
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EdinaUnited StatesUnknown status
Crossroads Cancer Center
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EffinghamUnited StatesUnknown status
Cancer Center of Kansas - El Dorado
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El DoradoUnited StatesUnknown status
UPMC Hillman Cancer Center Erie
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ErieUnited StatesUnknown status
Illinois CancerCare-Eureka
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EurekaUnited StatesUnknown status
Essentia Health Cancer Center-South University Clinic
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FargoUnited StatesUnknown status
Parkland Health Center - Farmington
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FarmingtonUnited StatesUnknown status
Hunterdon Medical Center
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FlemingtonUnited 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
Cancer Hematology Centers - Flint
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FlintUnited StatesUnknown status
Hematology Oncology Associates of Fredericksburg Inc
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FredericksburgUnited 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
Tidelands Georgetown Memorial Hospital
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GeorgetownUnited StatesUnknown status
UM Baltimore Washington Medical Center/Tate Cancer Center
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Glen BurnieUnited StatesUnknown status
Glens Falls Hospital
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Glens FallsUnited StatesUnknown status
Northwestern Medicine Glenview Outpatient Center
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GlenviewUnited StatesUnknown status
Addison Gilbert Hospital
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GloucesterUnited StatesUnknown status
Trinity Health Grand Rapids Hospital
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Grand RapidsUnited 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
UPMC Cancer Centers - Arnold Palmer Pavilion
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GreensburgUnited StatesUnknown status
Baptist Cancer Center-Grenada
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GrenadaUnited StatesUnknown status
UPMC Pinnacle Cancer Center/Community Osteopathic Campus
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HarrisburgUnited StatesUnknown status
Hartford Hospital
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HartfordUnited StatesUnknown status
Essentia Health-Hayward Clinic
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HaywardUnited StatesUnknown status
Lehigh Valley Hospital-Hazleton
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HazletonUnited StatesUnknown status
Essentia Health Hibbing Clinic
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HibbingUnited StatesUnknown status
Edwards Comprehensive Cancer Center
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HuntingtonUnited StatesUnknown status
Indiana University/Melvin and Bren Simon Cancer Center
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IndianapolisUnited StatesUnknown status
Emory Johns Creek Hospital
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Johns CreekUnited StatesUnknown status
NEA Baptist Memorial Hospital and Fowler Family Cancer Center - Jonesboro
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JonesboroUnited StatesUnknown status
West Michigan Cancer Center
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KalamazooUnited StatesUnknown status
Bronson Methodist Hospital
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KalamazooUnited StatesUnknown status
Illinois CancerCare-Kewanee Clinic
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KewaneeUnited StatesUnknown status
Gundersen Lutheran Medical Center
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La CrosseUnited 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
Lawrence Memorial Hospital
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LawrenceUnited StatesUnknown status
Trinity Health Saint Mary Mercy Livonia Hospital
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LivoniaUnited StatesUnknown status
Cedars-Sinai Medical Center
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Los AngelesUnited StatesUnknown status
Illinois CancerCare-Macomb
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MacombUnited StatesUnknown status
Solinsky Center for Cancer Care
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ManchesterUnited StatesUnknown status
Loyola University Medical Center
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MaywoodUnited StatesUnknown status
UPMC Hillman Cancer Center at Rocco And Nancy Ortenzio Cancer Pavilion
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MechanicsburgUnited StatesUnknown status
Aspirus Medford Hospital
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MedfordUnited StatesUnknown status
Riddle Memorial Hospital
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MediaUnited StatesUnknown status
Baptist Memorial Hospital and Cancer Center-Memphis
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MemphisUnited StatesUnknown status
Midstate Medical Center
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MeridenUnited StatesUnknown status
Saint Luke's Cancer Institute - Meridian
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MeridianUnited StatesUnknown status
Beebe South Coastal Health Campus
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MillvilleUnited StatesUnknown status
Minneapolis VA Medical Center
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MinneapolisUnited StatesUnknown status
Abbott-Northwestern Hospital
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MinneapolisUnited StatesUnknown status
Community Medical Center
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MissoulaUnited StatesUnknown status
UPMC Hillman Cancer Center - Monroeville
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MonroevilleUnited StatesUnknown status
West Virginia University Healthcare
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MorgantownUnited StatesUnknown status
ProHealth D N Greenwald Center
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MukwonagoUnited 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
Vanderbilt University/Ingram Cancer Center
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NashvilleUnited StatesUnknown status
Baptist Memorial Hospital and Cancer Center-Union County
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New AlbanyUnited StatesUnknown status
Medical Oncology Hematology Consultants PA
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NewarkUnited StatesUnknown status
Helen F Graham Cancer Center
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NewarkUnited StatesUnknown status
Providence Newberg Medical Center
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NewbergUnited StatesUnknown status
The Hospital of Central Connecticut
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New BritainUnited StatesUnknown status
Cancer Center of Kansas - Newton
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NewtonUnited 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
Northwestern Medicine Oak Brook
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Oak BrookUnited StatesUnknown status
ProHealth Oconomowoc Memorial Hospital
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OconomowocUnited StatesUnknown status
HSHS Saint Elizabeth's Hospital
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O'FallonUnited 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
The University of Kansas Cancer Center - Olathe
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OlatheUnited 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
Baptist Memorial Hospital and Cancer Center-Oxford
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OxfordUnited StatesUnknown status
Paoli Memorial Hospital
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PaoliUnited StatesUnknown status
Camden Clark Medical Center
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ParkersburgUnited StatesUnknown status
Lahey Clinic Peabody
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PeabodyUnited 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
University of Pennsylvania/Abramson Cancer Center
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PhiladelphiaUnited StatesUnknown status
FirstHealth of the Carolinas-Moore Regional Hospital
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PinehurstUnited StatesUnknown status
UPMC Hillman Cancer Center
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PittsburghUnited StatesUnknown status
UPMC-Saint Clair Hospital Cancer Center
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PittsburghUnited 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
Corewell Health Reed City Hospital
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Reed CityUnited StatesUnknown status
Beebe Health Campus
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Rehoboth BeachUnited StatesUnknown status
Aspirus Cancer Care-Rhinelander-James Beck Cancer Center
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RhinelanderUnited StatesUnknown status
VCU Massey Comprehensive Cancer Center
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RichmondUnited StatesUnknown status
VCU Massey Cancer Center at Stony Point
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RichmondUnited StatesUnknown status
Virginia Cancer Institute
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RichmondUnited 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
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
Salina Regional Health Center
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SalinaUnited StatesUnknown status
Kootenai Clinic Cancer Services - Sandpoint
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SandpointUnited StatesUnknown status
Essentia Health Sandstone
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SandstoneUnited StatesUnknown status
Baptist Memorial Hospital and Cancer Center-Desoto
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SouthhavenUnited StatesUnknown status
VCU Community Memorial Health Center
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South HillUnited StatesUnknown status
Essentia Health-Spooner Clinic
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SpoonerUnited StatesUnknown status
Southern Illinois University School of Medicine
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SpringfieldUnited StatesUnknown status
Springfield Clinic
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SpringfieldUnited StatesUnknown status
Baystate Medical Center
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SpringfieldUnited StatesUnknown status
Springfield Memorial Hospital
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SpringfieldUnited StatesUnknown status
Aspirus Cancer Care - Stevens Point
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Stevens PointUnited StatesUnknown status
Mercy Hospital South
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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
Essentia Health Saint Mary's Hospital - Superior
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SuperiorUnited StatesUnknown status
Cedars-Sinai Cancer - Tarzana
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TarzanaUnited StatesUnknown status
Montefiore Medical Center-Einstein Campus
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The BronxUnited StatesUnknown status
University of Kansas Health System Saint Francis Campus
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TopekaUnited StatesUnknown status
Torrance Memorial Physician Network - Cancer Care
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TorranceUnited StatesUnknown status
Munson Medical Center
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Traverse CityUnited StatesUnknown status
Essentia Health Virginia Clinic
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VirginiaUnited 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 Washington Hospital Center
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Washington D.C.United StatesUnknown status
MedStar Georgetown University Hospital
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Washington D.C.United StatesUnknown status
UW Cancer Center at ProHealth Care
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WaukeshaUnited StatesUnknown status
Aspirus Cancer Care-Wausau
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WausauUnited StatesUnknown status
Cancer Center of Kansas - Wellington
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WellingtonUnited StatesUnknown status
Reading Hospital
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West ReadingUnited StatesUnknown status
Cancer Center of Kansas - Wichita
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WichitaUnited StatesUnknown status
Cancer Center of Kansas-Wichita Medical Arts Tower
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WichitaUnited StatesUnknown status
Ascension Via Christi Hospitals Wichita
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WichitaUnited StatesUnknown status
Cancer Center of Kansas - Winfield
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WinfieldUnited StatesUnknown status
Aspirus Cancer Care - Wisconsin Rapids
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Wisconsin RapidsUnited StatesUnknown status
Lankenau Medical Center
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WynnewoodUnited StatesUnknown status
University of Michigan Health - West
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WyomingUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology Ann Arbor Campus
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