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NCT04530565Active, not recruitingPhase 3

Testing the Use of Steroids and Tyrosine Kinase Inhibitors With Blinatumomab or Chemotherapy for Newly Diagnosed BCR-ABL-Positive Acute Lymphoblastic Leukemia in Adults

A Phase III Randomized Trial of Steroids + Tyrosine Kinase Inhibitor (TKI) Induction With Chemotherapy or Blinatumomab for Newly Diagnosed BCR-ABL-Positive Acute Lymphoblastic Leukemia (ALL) in Adults

Source: ClinicalTrials.gov · Last updated 26 Oct 2026

Brief summary (registry, in English)

This phase III trial compares the effect of usual treatment of chemotherapy and steroids and a tyrosine kinase inhibitor (TKI) to the same treatment plus blinatumomab. Blinatumomab is a Bi-specific T-Cell Engager ('BiTE') that may interfere with the ability of cancer cells to grow and spread. The information gained from this study may help researchers determine if combination therapy with steroids, TKIs, and blinatumomab work better than the standard of care.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
348 (estimated)
First submitted
27 Aug 2020
Start date
25 Jan 2021
Primary completion date
1 Jul 2028
Lead sponsor
National Cancer Institute (NCI)
NCT number
NCT04530565

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 348
  • From 25 Jan 2021 to the primary completion date, 1 Jul 2028
  • 211 sites in 3 countries
  • 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

  • ELIGIBILITY CRITERIA FOR PRE-REGISTRATION (TO STEP 0)
  • Patient must be \>= 18 and =\< 75 years of age
  • Patient must have an Eastern Cooperative Oncology Group (ECOG) performance status between 0-3
  • Patient must be newly diagnosed with B acute lymphoblastic leukemia (B-ALL) or is suspected to have acute lymphoblastic leukemia (ALL)
    • Patient must have BCR-ABL1 positive disease. The diagnosis of ALL and the presence of BCR-ABL translocation must be confirmed centrally. Patients can be registered and begin step 1 therapy while awaiting central laboratory eligibility confirmation
    • NOTE: Bone marrow aspirate and/or peripheral blood specimen must be submitted to the ECOG-American College of Radiology Imaging Network (ACRIN) Leukemia Laboratory at MD Anderson Cancer Center to determine patient's eligibility for registration to Step 1 or confirm patient evaluability. Centrally fluorescence-activated cell sorting (FACS) analysis will be performed to determine B-ALL and to exclude acute myeloid leukemia (AML) or acute bi-phenotypic leukemia and baseline BCR-ABL status will be determined by fluorescent in situ hybridization (FISH). The ECOG-ACRIN Leukemia Laboratory will forward results within 48 hours of receipt of the specimen to the submitting institution. Bone marrow aspirate is to be from first pull (initial or re-direct). Specimens must contain sufficient blast cells. In cases where the bone marrow aspiration may be inadequate, or the bone marrow examination has already been performed prior to study consent and enrollment on Step 0, peripheral blood may be submitted, with recommendation that adequate circulating blasts are present (\> 10%). If a diagnosis of BCR-ABL positive B-ALL has already been established by local Clinical Laboratory Improvement Act (CLIA) certified laboratories, the patient may be registered to step 1 without waiting for central confirmation
  • Patient must not have a diagnosis of BCR/ABL T-ALL
  • Patient must not have received chemotherapy for B-ALL. Patients who received up to five days of therapy (hydroxyurea and/or steroids of any kind) with the aim to reduce disease burden prior to study registration to Step 1 are eligible
  • Patient must not have unstable epilepsy that requires treatment
  • Patients with lymphoid blast crisis chronic myeloid leukemia (CML) are not eligible
  • ELIGIBILITY CRITERIA FOR REGISTRATION TO STEP 1
  • Patient must have a diagnosis of Philadelphia chromosome positive (Ph+) ALL that has been determined locally and bone marrow and/or peripheral blood was sent and receipt confirmed for central confirmation or determined centrally by the ECOG-ACRIN Leukemia Laboratory at MD Anderson Cancer Center
  • 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 registration to rule out pregnancy. A patient of childbearing potential is defined as any woman, regardless of whether they have undergone tubal ligation, who meets the following criteria: 1) has achieved menarche at some point, 2) has not undergone a hysterectomy or bilateral oophorectomy, or 3) has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months)
  • Patients must not expect to conceive or father children by using accepted and effective method(s) of contraception or by abstaining from sexual intercourse from the time of step 1 registration, while on study treatment, and until at least six months after the last dose of study treatment
  • Total bilirubin =\< 3 mg/dL (patients with Gilbert's syndrome must have a total bilirubin =\< 5 mg/dL) (obtained =\< 28 days prior to step 1 registration)
  • Aspartate aminotransferase (AST) (serum glutamic-oxaloacetic transaminase \[SGOT\]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase \[SGPT\]) =\< 2.5 X the institutional upper limit of normal (ULN) (obtained =\< 28 days prior to step 1 registration)
  • Estimated creatinine clearance \> 45 mL/min (based on Cockcroft-Gault equation) (obtained =\< 28 days prior to step 1 registration)
  • Patients with acute organ dysfunction at step 1 registration, which may be attributed to leukemia can be registered regardless of lab results at presentation. Such patients will be allowed to register and can start Arm A steroid + TKI therapy but will only be allowed to proceed to step 2 randomization if the eligibility criteria outlined is met
  • Patients who presented with no evidence of acute organ dysfunction but during step 0 experienced a rise in liver enzymes which investigator suspects to be a side effect of any of prescribed drugs, are allowed to be registered regardless of the level of liver enzymes. Step 2 randomization must be withheld until the eligibility criteria outline is met but no more than 14 days after concluding Arm A therapy
  • Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial
  • For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable or on suppressive therapy, if indicated
  • Patients with a history of hepatitis C virus (HCV) infection must have an undetectable HCV viral load and if indicated, on treatment
  • Patients with a prior 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
  • Patient must not have active concomitant malignancy. Patients on chronic hormonal therapy for breast or prostate cancer or patients treated with maintenance with targeted agents but are in remission with no evidence for the primary malignancies are eligible
  • Patient must not have complaints of symptoms and/or have clinical and/or radiological signs that indicate an uncontrolled infection or any other concurrent medical condition that could be exacerbated by the treatment or would seriously complicate compliance with the protocol
  • 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 must be class 2B or better
  • Investigators must confirm which TKI patient is to receive
    • NOTE: Patients with known T315I mutation status should receive ponatinib treatment
    • NOTE: In situations due to insurance coverage issues and the pre-selected TKI is not immediately available, patients can receive dasatinib or imatinib during step 1. The investigator must re-specify dasatinib or ponatinib prior to step 2 randomization and from then on patients must receive the pre-selected TKI only
  • ELIGIBILITY CRITERIA FOR RANDOMIZATION TO STEP 2
  • Patient must have completed at least 7 and no more than 21 days of protocol-treatment on Arm A prior to step 2 randomization. (Days in which arm A therapy was withheld for any reason are not counted)
    • NOTE: First day of steroids prescription after registration will be considered as the first day of study therapy. The selected TKI must be initiated prior to randomization
  • Patients who presented with acute organ dysfunction within 2 weeks of registration to step 1 must have total bilirubin =\< 2 X institutional upper limit of normal (ULN)
  • AST(SGOT) and ALT(SGPT) =\< 2 X the institutional upper limit of normal (ULN)
  • Estimated creatinine clearance \> 45 mL/min (based on Cockcroft-Gault equation)
  • Investigators must confirm which TKI patient is to receive.
    • NOTE: Patients with known T315I mutation status should receive ponatinib treatment
  • For patients under age 70, intended chemotherapy regimen must have been determined prior to randomization
  • Patient must not have active central nervous system (CNS) involvement by leukemic blasts. Patients with signs of CNS involvement at presentation are eligible for randomization if clearance of blasts from the cerebrospinal fluid (CSF) is demonstrated
  • Patients must have resolved any serious infectious complications related to therapy
  • Any significant medical complications related to therapy must have resolved
  • ELIGIBILITY CRITERIA FOR REGISTRATION TO STEP 3 (RE-INDUCTION)
  • Institution has received centralized MRD results confirming positive status
  • Patients who presented with acute organ dysfunction within 2 weeks of registration to step 1 must have total bilirubin =\< 2 X institutional ULN
  • Patients who presented with acute organ dysfunction must have AST (SGOT)/ALT (SGPT) =\< 2 X institutional upper limit of normal (ULN)
  • Patients who presented with acute organ dysfunction must have an estimated creatinine clearance \> 45 mL/min (based on Cockcroft-Gault equation)
  • Investigators must confirm which TKI patient is to receive
    • NOTE: Patients with known T315I mutation status should receive ponatinib treatment
  • For patients under age 70 and previously assigned to Arm C, intended chemotherapy regimen must have been determined
  • Step 3 (Re-Induction): Patients must have resolved any serious infectious complications related to therapy
  • Step 3 (Re-Induction): Any significant medical complications related to therapy must have resolved

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (211)

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

SiteCityCountrySite status
Rambam Medical Center
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HaifaIsraelUnknown status
Shaare Zedek Medical Center
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JerusalemIsraelUnknown status
Centro Comprensivo de Cancer de UPR
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San JuanPuerto RicoUnknown status
San Juan City Hospital
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San JuanPuerto RicoUnknown status
Providence Regional Cancer System-Aberdeen
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AberdeenUnited StatesUnknown status
Hawaii Cancer Care - Westridge
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‘AieaUnited StatesUnknown status
Pali Momi Medical Center
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‘AieaUnited StatesUnknown status
The Cancer Center of Hawaii-Pali Momi
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‘AieaUnited StatesUnknown status
Queen's Cancer Center - Pearlridge
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‘AieaUnited StatesUnknown status
University of New Mexico Cancer Center
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AlbuquerqueUnited StatesUnknown status
Lehigh Valley Hospital-Cedar Crest
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AllentownUnited StatesUnknown status
OSF Saint Anthony's Health Center
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AltonUnited StatesUnknown status
Mary Greeley Medical Center
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AmesUnited StatesUnknown status
McFarland Clinic - Ames
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AmesUnited StatesUnknown status
Katmai Oncology Group
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AnchorageUnited StatesUnknown status
Anchorage Radiation Therapy Center
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AnchorageUnited StatesUnknown status
Alaska Breast Care and Surgery LLC
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AnchorageUnited StatesUnknown status
Alaska Oncology and Hematology LLC
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AnchorageUnited StatesUnknown status
Providence Alaska Medical Center
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AnchorageUnited StatesUnknown status
Anchorage Oncology Centre
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AnchorageUnited StatesUnknown status
Alaska Women's Cancer Care
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AnchorageUnited StatesUnknown status
Anchorage Associates in Radiation Medicine
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AnchorageUnited StatesUnknown status
University of Michigan Rogel Cancer Center
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Ann ArborUnited StatesUnknown status
Trinity Health Saint Joseph Mercy Hospital Ann Arbor
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Ann ArborUnited StatesUnknown status
Augusta University Medical Center
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AugustaUnited StatesUnknown status
Mercy Oncology and Hematology - Clayton-Clarkson
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BallwinUnited StatesUnknown status
Johns Hopkins University/Sidney Kimmel Cancer Center
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BaltimoreUnited StatesUnknown status
PeaceHealth Saint Joseph Medical Center
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BellinghamUnited StatesUnknown status
Saint Charles Health System
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BendUnited StatesUnknown status
Walter Reed National Military Medical Center
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BethesdaUnited StatesUnknown status
Lehigh Valley Hospital - Muhlenberg
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BethlehemUnited StatesUnknown status
University of Alabama at Birmingham Cancer Center
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BirminghamUnited StatesUnknown status
Prisma Health Cancer Institute - Spartanburg
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Boiling SpringsUnited StatesUnknown status
Saint Luke's Cancer Institute - Boise
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BoiseUnited StatesUnknown status
Central Care Cancer Center - Bolivar
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BolivarUnited StatesUnknown status
McFarland Clinic - Boone
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BooneUnited StatesUnknown status
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
Henry Ford Cancer Institute-Downriver
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BrownstownUnited StatesUnknown status
Providence Saint Joseph Medical Center/Disney Family Cancer Center
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BurbankUnited StatesUnknown status
University of Vermont and State Agricultural College
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BurlingtonUnited StatesUnknown status
University of Vermont Medical Center
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BurlingtonUnited StatesUnknown status
Loyola Center for Health at Burr Ridge
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Burr RidgeUnited StatesUnknown status
Trinity Health Medical Center - Canton
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CantonUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology - Canton
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CantonUnited StatesUnknown status
Providence Regional Cancer System-Centralia
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CentraliaUnited StatesUnknown status
UNC Lineberger Comprehensive Cancer Center
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Chapel HillUnited StatesUnknown status
Medical University of South Carolina
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CharlestonUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology - Chelsea Hospital
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ChelseaUnited StatesUnknown status
Chelsea Hospital
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ChelseaUnited StatesUnknown status
Northwestern University
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ChicagoUnited StatesUnknown status
University of Cincinnati Cancer Center-UC Medical Center
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CincinnatiUnited StatesUnknown status
Siteman Cancer Center at Saint Peters Hospital
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City of Saint PetersUnited StatesUnknown status
Clackamas Radiation Oncology Center
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ClackamasUnited StatesUnknown status
Providence Cancer Institute Clackamas Clinic
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ClackamasUnited StatesUnknown status
Hematology Oncology Consultants-Clarkston
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ClarkstonUnited StatesUnknown status
Newland Medical Associates-Clarkston
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ClarkstonUnited StatesUnknown status
Case Western Reserve University
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ClevelandUnited StatesUnknown status
MetroHealth Medical Center
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ClevelandUnited StatesUnknown status
Henry Ford Macomb Hospital-Clinton Township
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Clinton TownshipUnited StatesUnknown status
Community Cancer Institute
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ClovisUnited StatesUnknown status
University Oncology Associates
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ClovisUnited StatesUnknown status
Ohio State University Comprehensive Cancer Center
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ColumbusUnited StatesUnknown status
Bay Area Hospital
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Coos BayUnited 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
Geisinger Medical Center
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DanvilleUnited StatesUnknown status
Henry Ford Medical Center-Fairlane
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DearbornUnited StatesUnknown status
Wayne State University/Karmanos Cancer Institute
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DetroitUnited StatesUnknown status
Henry Ford Hospital
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DetroitUnited StatesUnknown status
City of Hope Comprehensive Cancer Center
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DuarteUnited StatesUnknown status
Duke University Medical Center
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DurhamUnited StatesUnknown status
Prisma Health Cancer Institute - Easley
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EasleyUnited StatesUnknown status
Pocono Medical Center
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East StroudsburgUnited StatesUnknown status
Marshfield Medical Center-EC Cancer Center
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Eau ClaireUnited StatesUnknown status
Swedish Cancer Institute-Edmonds
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EdmondsUnited StatesUnknown status
NorthShore University HealthSystem-Evanston Hospital
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EvanstonUnited StatesUnknown status
Providence Regional Cancer Partnership
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EverettUnited StatesUnknown status
Weisberg Cancer Treatment Center
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Farmington HillsUnited StatesUnknown status
Hurley Medical Center
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FlintUnited StatesUnknown status
Cancer Hematology Centers - Flint
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FlintUnited StatesUnknown status
Genesee Hematology Oncology PC
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FlintUnited StatesUnknown status
Genesys Hurley Cancer Institute
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FlintUnited StatesUnknown status
McFarland Clinic - Trinity Cancer Center
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Fort DodgeUnited StatesUnknown status
Mercy Hospital Fort Smith
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Fort SmithUnited StatesUnknown status
Vanderbilt-Ingram Cancer Center Cool Springs
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FranklinUnited StatesUnknown status
Saint Luke's Cancer Institute - Fruitland
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FruitlandUnited StatesUnknown status
Central Care Cancer Center - Garden City
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Garden CityUnited StatesUnknown status
NorthShore University HealthSystem-Glenbrook Hospital
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GlenviewUnited StatesUnknown status
Central Care Cancer Center - Great Bend
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Great BendUnited StatesUnknown status
Prisma Health Cancer Institute - Faris
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GreenvilleUnited StatesUnknown status
Prisma Health Greenville Memorial Hospital
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GreenvilleUnited StatesUnknown status
Prisma Health Cancer Institute - Eastside
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GreenvilleUnited StatesUnknown status
Prisma Health Cancer Institute - Butternut
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GreenvilleUnited StatesUnknown status
Prisma Health Cancer Institute - Greer
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GreerUnited StatesUnknown status
Lehigh Valley Hospital-Hazleton
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HazletonUnited StatesUnknown status
NorthShore University HealthSystem-Highland Park Hospital
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Highland ParkUnited StatesUnknown status
Loyola Medicine Homer Glen
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Homer GlenUnited StatesUnknown status
Kuakini Medical Center
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HonoluluUnited StatesUnknown status
Kapiolani Medical Center for Women and Children
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HonoluluUnited StatesUnknown status
Hawaii Cancer Care Inc - Waterfront Plaza
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HonoluluUnited StatesUnknown status
Hawaii Cancer Care Inc-Liliha
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HonoluluUnited StatesUnknown status
Queen's Medical Center
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HonoluluUnited StatesUnknown status
Queen's Cancer Center - Kuakini
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HonoluluUnited StatesUnknown status
Queen's Cancer Cenrer - POB I
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HonoluluUnited StatesUnknown status
Straub Clinic and Hospital
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HonoluluUnited StatesUnknown status
The Cancer Center of Hawaii-Liliha
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HonoluluUnited StatesUnknown status
University of Hawaii Cancer Center
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HonoluluUnited StatesUnknown status
Houston Methodist Hospital
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HoustonUnited StatesUnknown status
Indiana University/Melvin and Bren Simon Cancer Center
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IndianapolisUnited StatesUnknown status
UCI Health - Chao Family Comprehensive Cancer Center and Ambulatory Care
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IrvineUnited StatesUnknown status
Swedish Cancer Institute-Issaquah
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IssaquahUnited StatesUnknown status
Allegiance Health
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JacksonUnited StatesUnknown status
McFarland Clinic - Jefferson
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JeffersonUnited StatesUnknown status
Mercy Hospital Joplin
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JoplinUnited StatesUnknown status
Freeman Health System
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JoplinUnited StatesUnknown status
University of Kansas Cancer Center
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Kansas CityUnited StatesUnknown status
Research Medical Center
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Kansas CityUnited StatesUnknown status
Kadlec Clinic Hematology and Oncology
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KennewickUnited StatesUnknown status
Providence Regional Cancer System-Lacey
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LaceyUnited StatesUnknown status
Gundersen Lutheran Medical Center
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La CrosseUnited StatesUnknown status
UC San Diego Moores Cancer Center
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La JollaUnited StatesUnknown status
Northwestern Medicine Lake Forest Hospital
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Lake ForestUnited StatesUnknown status
Wilcox Memorial Hospital and Kauai Medical Clinic
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LihueUnited StatesUnknown status
Trinity Health Saint Mary Mercy Livonia Hospital
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LivoniaUnited StatesUnknown status
Monmouth Medical Center
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Long BranchUnited StatesUnknown status
PeaceHealth Saint John Medical Center
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LongviewUnited StatesUnknown status
UofL Health Medical Center Northeast
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LouisvilleUnited StatesUnknown status
The James Graham Brown Cancer Center at University of Louisville
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LouisvilleUnited StatesUnknown status
Henry Ford Saint John Hospital - Macomb Medical
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MacombUnited StatesUnknown status
University of Wisconsin Carbone Cancer Center - Eastpark Medical Center
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MadisonUnited StatesUnknown status
University of Wisconsin Carbone Cancer Center - University Hospital
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MadisonUnited StatesUnknown status
McFarland Clinic - Marshalltown
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MarshalltownUnited StatesUnknown status
Marshfield Medical Center-Marshfield
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MarshfieldUnited StatesUnknown status
Loyola University Medical Center
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MaywoodUnited StatesUnknown status
Marjorie Weinberg Cancer Center at Loyola-Gottlieb
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Melrose ParkUnited StatesUnknown status
Baptist Memorial Hospital and Cancer Center-Memphis
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MemphisUnited StatesUnknown status
Saint Luke's Cancer Institute - Meridian
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MeridianUnited StatesUnknown status
Medical College of Wisconsin
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MilwaukeeUnited StatesUnknown status
Marshfield Medical Center - Minocqua
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MinocquaUnited StatesUnknown status
Saint Patrick Hospital - Community Hospital
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MissoulaUnited StatesUnknown status
SSM Health Good Samaritan
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Mount VernonUnited StatesUnknown status
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
Vanderbilt Breast Center at One Hundred Oaks
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NashvilleUnited StatesUnknown status
Providence Newberg Medical Center
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NewbergUnited StatesUnknown status
Rutgers Cancer Institute of New Jersey
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New BrunswickUnited StatesUnknown status
Yale University
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New HavenUnited StatesUnknown status
Henry Ford Medical Center-Columbus
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NoviUnited StatesUnknown status
University of Oklahoma Health Sciences Center
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Oklahoma CityUnited StatesUnknown status
Mercy Hospital Oklahoma City
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Oklahoma CityUnited StatesUnknown status
UC Irvine Health- Chao Family Comprehensive Cancer Center
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OrangeUnited StatesUnknown status
Providence Willamette Falls Medical Center
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Oregon CityUnited StatesUnknown status
University of Kansas Hospital-Indian Creek Campus
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Overland ParkUnited StatesUnknown status
Thomas Jefferson University Hospital
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PhiladelphiaUnited StatesUnknown status
University of Pennsylvania/Abramson Cancer Center
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PhiladelphiaUnited StatesUnknown status
UPMC Hillman Cancer Center
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PittsburghUnited StatesUnknown status
Trinity Health IHA Medical Group-Alice Gustafson Center
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PontiacUnited StatesUnknown status
Michigan Healthcare Professionals Pontiac
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PontiacUnited 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
Saint Charles Health System-Redmond
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RedmondUnited StatesUnknown status
Marshfield Medical Center-Rice Lake
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Rice LakeUnited StatesUnknown status
VCU Massey Comprehensive Cancer Center
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RichmondUnited StatesUnknown status
University of Rochester
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RochesterUnited StatesUnknown status
Mayo Clinic in Rochester
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RochesterUnited StatesUnknown status
Mercy Clinic-Rolla-Cancer and Hematology
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RollaUnited StatesUnknown status
Phelps Health Delbert Day Cancer Institute
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RollaUnited StatesUnknown status
Oncology Hematology Associates of Saginaw Valley PC
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SaginawUnited StatesUnknown status
MyMichigan Medical Center Saginaw
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SaginawUnited StatesUnknown status
Heartland Regional Medical Center
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Saint JosephUnited StatesUnknown status
Huntsman Cancer Institute/University of Utah
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Salt Lake CityUnited StatesUnknown status
Swedish Medical Center-Cherry Hill
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SeattleUnited StatesUnknown status
Swedish Medical Center-First Hill
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SeattleUnited StatesUnknown status
Pacific Gynecology Specialists
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SeattleUnited StatesUnknown status
Swedish Medical Center-Ballard Campus
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SeattleUnited StatesUnknown status
PeaceHealth United General Medical Center
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Sedro-WoolleyUnited StatesUnknown status
Prisma Health Cancer Institute - Seneca
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SenecaUnited StatesUnknown status
Henry Ford Macomb Health Center - Shelby Township
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ShelbyUnited StatesUnknown status
Providence Regional Cancer System-Shelton
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SheltonUnited StatesUnknown status
LSU Health Sciences Center at Shreveport
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ShreveportUnited StatesUnknown status
Baptist Memorial Hospital and Cancer Center-Desoto
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SouthhavenUnited StatesUnknown status
CoxHealth South Hospital
Coordinator of this site? Confirm its status
SpringfieldUnited StatesUnknown status
Mercy Hospital Springfield
Coordinator of this site? Confirm its status
SpringfieldUnited StatesUnknown status
Marshfield Medical Center-River Region at Stevens Point
Coordinator of this site? Confirm its status
Stevens PointUnited StatesUnknown status
Siteman Cancer Center-South County
Coordinator of this site? Confirm its status
St LouisUnited StatesUnknown status
Washington University School of Medicine
Coordinator of this site? Confirm its status
St LouisUnited StatesUnknown status
Siteman Cancer Center at Christian Hospital
Coordinator of this site? Confirm its status
St LouisUnited StatesUnknown status
Mercy Hospital South
Coordinator of this site? Confirm its status
St LouisUnited StatesUnknown status
Mercy Infusion Center - Chippewa
Coordinator of this site? Confirm its status
St LouisUnited StatesUnknown status
Mercy Hospital Saint Louis
Coordinator of this site? Confirm its status
St LouisUnited StatesUnknown status
MyMichigan Medical Center Tawas
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Tawas CityUnited StatesUnknown status
Montefiore Medical Center-Einstein Campus
Coordinator of this site? Confirm its status
The BronxUnited StatesUnknown status
Montefiore Medical Center - Moses Campus
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The BronxUnited StatesUnknown status
Saint Luke's Cancer Institute - Twin Falls
Coordinator of this site? Confirm its status
Twin FallsUnited StatesUnknown status
PeaceHealth Southwest Medical Center
Coordinator of this site? Confirm its status
VancouverUnited StatesUnknown status
Providence Saint Mary Regional Cancer Center
Coordinator of this site? Confirm its status
Walla WallaUnited StatesUnknown status
Mercy Hospital Washington
Coordinator of this site? Confirm its status
WashingtonUnited StatesUnknown status
Henry Ford West Bloomfield Hospital
Coordinator of this site? Confirm its status
West BloomfieldUnited StatesUnknown status
Saint Mary's Oncology/Hematology Associates of West Branch
Coordinator of this site? Confirm its status
West BranchUnited StatesUnknown status
University of Cincinnati Cancer Center-West Chester
Coordinator of this site? Confirm its status
West ChesterUnited StatesUnknown status
Marshfield Medical Center - Weston
Coordinator of this site? Confirm its status
WestonUnited StatesUnknown status
University of Kansas Hospital-Westwood Cancer Center
Coordinator of this site? Confirm its status
WestwoodUnited StatesUnknown status
Geisinger Wyoming Valley/Henry Cancer Center
Coordinator of this site? Confirm its status
Wilkes-BarreUnited StatesUnknown status
Wake Forest University Health Sciences
Coordinator of this site? Confirm its status
Winston-SalemUnited StatesUnknown status
Henry Ford Wyandotte Hospital
Coordinator of this site? Confirm its status
WyandotteUnited StatesUnknown status
Providence Regional Cancer System-Yelm
Coordinator of this site? Confirm its status
YelmUnited StatesUnknown status
Huron Gastroenterology PC
Coordinator of this site? Confirm its status
YpsilantiUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology Ann Arbor Campus
Coordinator of this site? Confirm its status
YpsilantiUnited StatesUnknown status

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