Recruiting

Inotuzumab Ozogamicin and Blinatumomab With or Without Ponatinib in Treating Patients With Newly Diagnosed, Recurrent, or Refractory CD22-Positive B-Lineage Acute Lymphoblastic Leukemia

NCT03739814 · National Cancer Institute (NCI)

Recruiting

In plain English

Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.

Official title

A Phase II Study of Inotuzumab Ozogamicin Followed by Blinatumomab for Ph-Negative, CD22-Positive B-Lineage Acute Lymphoblastic Leukemia in Newly Diagnosed Older Adults or Adults With Relapsed or Refractory Disease

About this study

PRIMARY OBJECTIVES: Ia. For Philadelphia (Ph)-negative B-cell acute lymphoblastic leukemia (ALL), to confirm tolerability of the combination regimen of inotuzumab ozogamicin followed by blinatumomab. Ib. For Ph-positive B-cell ALL, to confirm tolerability of ponatinib in combination with inotuzumab ozogamicin and blinatumomab. II. To estimate the 1-year event-free survival of older, transplant-ineligible patients with newly diagnosed, Ph-negative, CD22-positive, B-cell acute lymphoblastic leukemia (ALL) treated with inotuzumab ozogamicin induction followed by blinatumomab consolidation. (Cohort 1) III. To estimate the 1-year event-free survival of patients with relapsed or refractory Ph-negative, CD22-positive, B-cell ALL treated with inotuzumab ozogamicin induction followed by blinatumomab consolidation. (Cohort 2) IV. To determine the feasibility of the regimen in adult patients with CD22-positive, Ph/BCR-ABL1-positive B-cell ALL. (Cohort 3) SECONDARY OBJECTIVES: I. To estimate the median, 1-year, and 3-year overall survival (OS) in all eligible patients. (Cohort 1) II. To estimate the median, 1-year, and 3-year relapse-free survival (RFS) in all eligible patients. (Cohort 1) III. To estimate the median and 3-year event-free survival (EFS) in all eligible patients. (Cohort 1) IV. To estimate the complete response (CR) rate and overall response rate (ORR, defined as complete response \[CR\] + complete response with incomplete count recovery \[CRi\]) to inotuzumab ozogamicin followed by blinatumomab (regimen CR rate and ORR). (Cohort 1) V. To estimate the CR rate and ORR (CR + CRi) to inotuzumab ozogamicin induction alone (induction CR and ORR). (Cohort 1) VI. To estimate the minimal residual disease (MRD) negativity rate in subjects achieving a CR or CRi. (Cohort 1) VII. To estimate the treatment-related mortality with this regimen. (Cohort 1) VIII. To describe the safety and tolerability of this regimen. (Cohort 1) IX. To estimate the median, 1-year, and 3-year OS in all eligible patients. (Cohort 2) X. To estimate the median, 1-year, and 3-year RFS in all eligible patients. (Cohort 2) XI. To estimate the median and 3-year EFS in all eligible patients. (Cohort 2) XII. To estimate ORR (CR/CRi and CR/complete response with partial hematologic recovery \[CRh\]) to blinatumomab in patients with ALL refractory to inotuzumab ozogamicin. (Cohort 2) XIII. To estimate the CR, CRi, and CRh rates at defined time points and cumulatively for the entire regimen. (Cohort 2) XIV. To determine the MRD negativity (\< 10\^-4) rate at defined time points including prior to allogeneic HCT and cumulatively in patients achieving a CR, CRh, or CRi. (Cohort 2) XV. To determine the allogeneic hematopoietic cell transplantation (HCT) rate in eligible subjects. (Cohort 2) XVI. To estimate the treatment-related mortality with this regimen. (Cohort 2) XVII. To describe the safety and tolerability of this regimen. (Cohort 2) XVIII. To estimate the 24-week complete molecular response rate. (Cohort 3) XIX. To estimate the median, 1-year, and 3-year OS in all eligible patients. (Cohort 3) XX. To estimate the median, 1-year, and 3-year RFS in all eligible patients. (Cohort 3) XXI. To estimate the median and 3-year EFS in all eligible patients. (Cohort 3) XXII. To estimate ORR (CR/CRi and CR/complete response with partial hematologic recovery \[CRh\]) to blinatumomab in patients with ALL refractory to inotuzumab ozogamicin. (Cohort 3) XXIII. To estimate the CR, CRi, and CRh rates at defined time points and cumulatively for the entire regimen. (Cohort 3) XXIV. To determine the complete molecular response rate at defined time points and cumulatively in patients achieving a CR, CRh, or CRi. (Cohort 3) XXV. To estimate the treatment-related mortality with this regimen. (Cohort 3) XXVI. To describe the safety and tolerability of this regimen. (Cohort 3) OTHER OBJECTIVE: I. Results of the primary analysis will be examined for consistency, while accounting for the stratification factors and/or covariates of baseline quality of life (QOL) and fatigue. CORRELATIVE SCIENCE OBJECTIVES: I. To correlate specific karyotype groups (normal or various primary and secondary chromosomal abnormalities) with clinical and laboratory parameters. II. To correlate specific karyotype groups with response rates, response duration, survival, and cure in patients treated with inotuzumab ozogamicin followed by blinatumomab. III. To correlate specific karyotype groups with MRD. IV. To determine karyotype changes at relapse and the influence of the type of change (or no change) in karyotype at relapse. V. To assess the correlation of quantitative MRD post-induction with inotuzumab ozogamicin and at sequential consolidation time points with blinatumomab with RFS, EFS, and OS. VI. To correlate the influence of MRD status (detectable versus \[vs.\] not and as a continuous measure) in relation to EFS, RFS, and OS with other clinical and biological factors (e.g. previously untreated vs. relapsed disease cohorts; age, initial white blood cell \[WBC\] count, cytogenetics). VII. To identify genetic variants and predictors of ex vivo resistance. VIII. To identify genetic variants and predictors of MRD. IX. To identify genetic variants and predictors of relapse. X. To determine inter-patient variability in drug sensitivity of adult ALL. XI. To examine the associations of drug sensitivity with host and leukemia molecular features. XII. To evaluate T-cell populations and T-cell function during therapy using T-cell markers which include the T-cell subset defining markers CD45, CD3, CD4, CD8, CD45RA, CD45RO, CCR7, CD25, CD127, FOXP3, CD 27, CD28, among others, and markers of T cell exhaustion and senescence including CD57, PD-1, Tim-3, LAG-3, TIGIT, CTLA4, CD160, and ICOS among others. XIII. To evaluate cytokine levels, and compare between patients who attain a CR vs. those with stable or progressive disease. EXPLORATORY OBJECTIVES: I. To estimate the median, 1-year, and 3-year RFS, EFS, and OS in patients achieving a CR/CRi to inotuzumab ozogamicin. (Cohort 1) II. To compare the median, 1-year, and 3-year RFS, EFS, and OS among patients achieving MRD-negative vs. MRD-positive CR/CRi to inotuzumab ozogamicin. (Cohort 1) III. To compare the median, 1-year, and 3-year RFS, EFS, and OS among patients achieving MRD-negative vs. MRD-positive CR/CRi at any time. (Cohort 1) IV. To describe the rate, severity, and timing of sinusoidal obstruction syndrome/veno-occlusive disease (SOS/VOD) of the liver after limited inotuzumab ozogamicin exposure and identify risk factors for SOS/VOD. (Cohort 1) V. To estimate the rate of cytokine release syndrome in this population. (Cohort 1) VI. To estimate the median, 1-year, and 3-year RFS from time of CR/CRi to inotuzumab ozogamicin in patients receiving inotuzumab ozogamicin followed by blinatumomab and not undergoing allogeneic hematopoietic cell transplantation (HCT). (Cohort 2) VII. To estimate median, 1-year, and 3-year OS after CR/CRi to inotuzumab ozogamicin in patients not undergoing allogeneic HCT. (Cohort 2) VIII. To compare in a non-randomized fashion median, 1-year, and 3-year OS, median, 1-year, and 3-year RFS, cumulative incidence of relapse (CIR), and non-relapse mortality (NRM) between patients achieving CR/CRi and receiving consolidation with or without allogeneic HCT. (Cohort 2) IX. To describe the rate, severity, and timing of sinusoidal obstruction syndrome/veno-occlusive disease (SOS/VOD) of the liver after limited inotuzumab ozogamicin exposure and identify risk factors for SOS/VOD. (Cohort 2) X. To estimate the rate of cytokine release syndrome in this population. (Cohort 2) XI. To estimate the median, 1-year, and 3-year RFS, EFS, and OS in patients achieving a CR/CRi to inotuzumab ozogamicin. (Cohort 3) XII. To compare the median, 1-year, and 3-year RFS, EFS, and OS among patients with CR/CRi achieving complete molecular response vs. not to inotuzumab ozogamicin. (Cohort 3) XIII. To compare the median, 1-year, and 3-year RFS, EFS, and OS among patients achieving CR/CRi achieving complete molecular response vs. not at any time. (Cohort 3) XIV. To describe the rate, severity, and timing of sinusoidal obstruction syndrome/veno-occlusive disease (SOS/VOD) of the liver after limited inotuzumab ozogamicin exposure and identify risk factors for SOS/VOD. (Cohort 3) XV. To estimate the rate of cytokine release syndrome in this population. (Cohort 3) XVI. To assess ABL1 mutational patterns at relapse. (Cohort 3) OUTLINE: Patients are assigned to 1 of 2 cohorts. COHORT 1: Patients receive inotuzumab ozogamicin intravenously (IV) over 1 hour on day 1, 8, and 15 (Course IA). By the end of Course IA (day 21), patients with adequate ALL cytoreduction continue to Course IB/IC, and patients who fail to achieve ALL cytoreduction continue to Course II. By the end of Course II, patients with CR-CRi to Course IB/IC and Course II continue to Course IIIA, patients without adequate ALL cytoreduction to Course IA or refractory to Course IB/IC but CR/CRi to Course II continue to Course IIIB. Patients undergo bone marrow aspiration and biopsy and blood sample collection throughout the study. Patients undergo lumbar puncture with cerebrospinal fluid sample collection at baseline and may undergo additionally throughout the study. COHORT 2: Patients receive inotuzumab ozogamicin IV over 1 hour on day 1, 8, and 15 (Course IA). By the end of Course IA (day 21), patients with adequate ALL cytoreduction continue to Course IB/IC, and patients who fail to achieve ALL cytoreduction continue to Course II. Patients with CR/CRi at the end of Course II continue to Course IIIB. COURSE IB/IC: Patients receive inotuzumab ozogamicin IV over 1 hour on days 1, 8, and 15. Treatment continues for 1 course (28 days) in the absence of disease progression or unacceptable toxicity. COURSE II: Patients receive blinatumomab IV continuously on days 1-28 and 43-70. Treatment continues for 1 course (84 days) in the absence of disease progression or unacceptable toxicity. COURSE IIIA: Patients receive blinatumomab IV continuously on days 1-28 and 43-70. Treatment continues for 1 course (84 days) in the absence of disease progression or unacceptable toxicity. COURSE IIIB: Patients receive blinatumomab IV continuously on days 1-28, 43-70, and 85-112. Treatment continues for 1 course (126 days) in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow aspiration and biopsy and blood sample collection throughout the study. Patients undergo lumbar puncture with cerebrospinal fluid sample collection at baseline and may undergo additionally throughout the study. COHORT 3: INDUCTION: COURSE I: Patients receive ponatinib orally (PO) daily (QD) on day 1-35, dexamethasone PO QD on days 1-7 and 15-21 and methotrexate intrathecally (IT) on day 1, 15 and 29 for 1 course (35 days) in the absence of disease progression or unacceptable toxicity. Patients with CR or CRi continue to consolidation course IIA or end the study treatment to receive allogenic HCT per the treating physician. Patients without CR or CRi with but adequate ALL cytoreduction (defined as ≥ 50% reduction in bone marrow lymphoblasts from the pre-registration bone marrow aspirate/biopsy and/or ≤ 20% marrow cellularity at the end of Course I bone marrow aspirate/biopsy) also proceed to consolidation course IIA. Patients with progression or failure to achieve adequate ALL cytoreduction are removed from study treatment. CONSOLIDATION: COURSE IIA: Patients receive ponatinib PO QD on days 1-21, inotuzumab ozogamicin IV over 1 hour on days 1, 8 and 15 and methotrexate IT on day 1 for 1 course (21 days) in the absence of disease progression or unacceptable toxicity. Patients with CR or CRi continue to consolidation course IIB or end the study treatment to receive allogenic HCT per the treating physician. Patients without CR or CRi and without progressive disease proceed to course IIC. Patients with progression are removed from study treatment. COURSE IIB/C: Patients receive ponatinib PO QD on days 1-28, inotuzumab ozogamicin IV over 1 hour on days 1, 8 and 15 and methotrexate IT on day 1 for 1 course (28 days) in the absence of disease progression or unacceptable toxicity. Patients with CR or CRi end the study treatment to receive allogenic HCT per the treating physician. Patients with progression are removed from study treatment. All other patients proceed to course III. COURSE III: Patients receive ponatinib PO QD on days 1-84 and receive blinatumomab IV continuously on days 1-28 and 43-70. Treatment continues for 1 course (84 days) in the absence of disease progression or unacceptable toxicity. Patients in CR/CRi proceed to course IV. Patients not in CR/CRi are removed from study treatment. COURSE IV: Patients receive ponatinib PO QD on days 1-84 and receive blinatumomab IV continuously on days 1-28 and 43-70. Treatment continues for 1 course (84 days) in the absence of disease progression or unacceptable toxicity. Patients in CR/CRi proceed to maintenance. Patients not in CR/CRi are removed from study treatment. MAINTENANCE: Patients receive ponatinib PO QD for 24 months in the absence of disease progression or unacceptable toxicity. Patients undergo bone marrow aspiration and biopsy and blood sample collection throughout the study. Patients undergo lumbar puncture with cerebrospinal fluid sample collection at baseline and may undergo additionally throughout the study. After completion of study treatment, patients are followed up every 3 months for 3 years, and then every 6 months for up to 10 years.

Eligibility criteria

Inclusion Criteria: * STEP 0: Submission of bone marrow aspirate and peripheral blood for MRD analysis is mandatory prior to registration; the bone marrow sample should be from the first aspiration (i.e. first pull). Aspirate needle should be redirected if needed to get first pull bone marrow aspirate. It should be initiated as soon as possible after pre-registration. The specimens should be sent to the HEME Biobank. * Lumbar Puncture (Spinal Tap) and Intrathecal Methotrexate: * Patients may receive the day 1 of course IA dose of intrathecal (IT) methotrexate during the prior-to-registration lumbar puncture (or the venous line placement) to avoid a second lumbar puncture. If the dose is administered prior to registration, then systemic chemotherapy must begin within 7 days of this IT chemotherapy. * STEP 1: Morphologic diagnosis of precursor B-cell acute lymphoblastic leukemia (ALL) based on World Health Organization (WHO) criteria. Patients with Burkitt lymphoma/leukemia are not eligible. * STEP 1: CD22-positive disease defined as CD22 expression by \>= 20% of lymphoblasts by local hematopathology evaluation. * STEP 1: Philadelphia chromosome/BCR-ABL1-negative or Philadelphia chromosome/BCR-ABL1-positive B-cell ALL by cytogenetics, fluorescence in situ hybridization (FISH), and/or polymerase chain reaction (PCR). * STEP 1: No active central nervous system (CNS) leukemia (i.e. only CNS-1 disease allowed). Active CNS leukemia is defined as morphologic evidence of lymphoblasts in the cerebrospinal fluid (CSF), use of CNS-directed local treatment for active disease within 28 days prior to registration, symptomatic CNS leukemia (i.e. cranial nerve palsies or other significant neurological dysfunction) within the 28 days prior to registration, and/or known asymptomatic parenchymal CNS mass lesions; see below for additional guidance. Prophylactic intrathecal medication alone is not an exclusion. * Categories of CNS Involvement for CNS Evaluation Prior to Registration: * CNS 1: CSF has \< 5 WBC/uL with cytospin negative for blasts; or \>= 10 red blood cell (RBC)/uL with cytospin negative for blasts. * CNS 2: CSF has \< 5 WBC/uL with cytospin positive for blasts; or \>= 10 RBC/uL with cytospin positive for blasts; or \>= 10 RBC/uL, WBC/uL \>= 5 but less than Steinherz/Bleyer algorithm with cytospin positive for blasts (see below). * CNS 3: CSF has \>= 5 WBC/uL with cytospin positive for blasts; or \>= 10 RBC/uL, \>= 5 WBC/uL and positive by Steinherz/Bleyer algorithm (see below); or clinical signs of CNS leukemia (such as facial nerve palsy, brain/eye involvement or hypothalamic syndrome). Steinherz/Bleyer Method of Evaluating Initial Traumatic Lumbar Punctures: * If the patient has leukemia cells in the peripheral blood and the lumbar puncture is traumatic and contains \>= 5 WBC/uL with blasts, the following algorithm should be used to define CNS disease: CSF WBC/CSF RBC \> 2 x (Blood WBC/Blood RBC count) * STEP 1: Patients with known or suspected testicular involvement by leukemia are allowed provided that the patient receives concomitant scrotal/testicular radiotherapy. * Unilateral or bilateral testicular enlargement should be assessed by ultrasound or other imaging technique. Biopsy is recommended if clinical findings are equivocal or suggestive of hydrocele or a non-leukemic mass, but further assessments are per treating physician discretion. * STEP 1: Not pregnant and not nursing. * This study involves agents that have known genotoxic, mutagenic, and teratogenic effects. Therefore, for women of childbearing potential only, a negative pregnancy test done =\< 7 days prior to registration is required. * STEP 1: Eastern Cooperative Oncology Group (ECOG) performance status: 0-2 * STEP 1: No unstable cardiac disease such as myocardial infarction, angina pectoris, uncontrolled heart failure, or uncontrolled cardiac arrhythmia within 6 months of registration. * STEP 1: No impaired cardiac function, defined as left ventricular ejection fraction (LVEF) \< 45% or New York Heart Association (NYHA) stage III or IV congestive heart failure (CHF). * STEP 1: Patients with known human immunodeficiency virus (HIV) infection are eligible if they have been on effective antiretroviral therapy with an undetectable viral load tested within 6 months of registration. * STEP 1: Patients with hepatitis B virus (HBV) are eligible only if they meet all the following: * On HBV-suppressive therapy. * No evidence of active virus. * No evidence of HBV-related liver damage. * STEP 1: Patients with hepatitis C virus (HCV) are eligible only if they meet all the following: * Successfully completed complete-eradication therapy with undetectable viral load. * No evidence of HCV-related liver damage. * STEP 1: No history of clinically relevant neurologic disorder such as epilepsy, seizure, aphasia, stroke, severe brain injury, structural brain abnormality, benign brain tumor, dementia, Parkinson's disease, movement disorder, cerebellar disease, or other significant CNS abnormalities. * STEP 1: No prior additional malignancy (i.e. in addition to ALL) except adequately treated basal- or squamous-cell skin cancer, in situ cervical cancer, stage I or II cancer from which the patient is currently in complete remission, or any other cancer from which the patient has been disease-free for \>= 2 years. * STEP 1: No history of clinically significant ventricular arrhythmia, unexplained non-vasovagal syncope, or chronic bradycardic states such as sinoatrial block or higher degree of atrioventricular block unless a permanent pacemaker has been implanted. * STEP 1: No history of chronic liver disease, including cirrhosis. * STEP 1: No history of sinusoidal occlusion syndrome/veno-occlusive disease of the liver. * STEP 1: No uncontrolled infection or recent history (within 4 months prior to registration) of deep tissue infections such as fasciitis or osteomyelitis. * STEP 1: Total bilirubin, serum =\< 1.5 x upper limit of normal (ULN)\* * Except in the event of: 1) Gilbert disease, in which case total bilirubin must be =\< 2 x ULN, or 2) elevated bilirubin believed by investigator to be due to leukemic infiltration, in which case total bilirubin must be =\< 2 x ULN. * STEP 1: Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) =\< 2.5 x ULN * STEP 1: Creatinine, serum =\< 1.5 ULN OR creatinine clearance \>= 40 mL/min * STEP 1: QT interval by Fridericia's correction formula (QTcF) =\< 470 msec * COHORT 1: Age \>= 60 years. * COHORT 1: Diagnosis of Philadelphia chromosome/BCR-ABL1-negative B-cell ALL. * COHORT 1: No prior treatment for ALL except a single dose of intrathecal chemotherapy, corticosteroids, hydroxyurea, and/or leukapheresis to reduce peripheral blast count and prevent ALL complications. Allowed therapy may be administered for no more than 14 days and must be completed \>= 24 hours prior to the initiation of protocol therapy. * COHORT 1: No plan for allogeneic or autologous hematopoietic cell transplantation (HCT). * COHORT 2: Age \>= 18 years. * COHORT 2: Diagnosis of Philadelphia chromosome/BCR-ABL1-negative B-cell ALL. * COHORT 2: Relapsed or refractory disease in salvage 1 or 2. * COHORT 2: No isolated extramedullary relapse. * COHORT 2: Prior allogeneic HCT permitted. * COHORT 2: Patients with prior allogeneic HCT must have completed transplantation \>= 4 months prior to registration. * COHORT 2: Patients with prior allogeneic HCT must have no evidence of graft-versus-host disease and must have completed immunosuppressive therapy \>= 30 days prior to registration. * COHORT 2: Prior treatment with inotuzumab ozogamicin, blinatumomab, other CD22-directed therapy, or other CD19-directed therapy is not allowed. * COHORT 2: Prior treatment with rituximab must be completed \>= 7 days prior to registration. * COHORT 2: Prior treatment with other monoclonal antibodies must be completed \>= 6 weeks prior to registration. * COHORT 2: Prior treatment for ALL must be completed \>= 14 days prior to registration with the following exceptions: intrathecal chemotherapy, hydroxyurea, corticosteroids, 6-mercaptopurine, methotrexate, vincristine, and/or leukapheresis to reduce circulating absolute lymphoblast count to =\< 10,000/uL or prevent complications related to ALL are allowed but must be completed \>= 24 hours prior to the initiation of protocol therapy. * COHORT 2: Patients should have resolution of any acute non-hematologic toxicities of prior therapy to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version (v)5.0 grade =\< 1. * COHORT 2: Peripheral blood absolute lymphoblast count =\< 10,000/uL (treatment allowed as above to reduce blast count to =\< 10,000/uL) * COHORT 3: Age ≥ 75 years OR age ≥ 18 years AND ineligible for hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (HyperCVAD) regimens * COHORT 3: Diagnosis of Philadelphia chromosome/BCR-ABL1-positive B-cell ALL * COHORT 3: No prior treatment for ALL except a single dose of intrathecal chemotherapy, corticosteroids, hydroxyurea, BCR-ABL1-targeted tyrosine kinase inhibitor, and/or leukapheresis to reduce peripheral blast count and prevent ALL complications. Allowed non-protocol therapy may be administered for no more than 14 days and must be completed ≥ 24 hours prior to the initiation of protocol therapy. * COHORT 3: No chronic, strong CYP3A4 inducers

Study design

Enrollment target: 84 participants

Allocation: non_randomized

Masking: none

Age groups: adult, older_adult

Timeline

Starts: 2019-05-08

Estimated completion: 2027-02-01

Last updated: 2026-06-03

Interventions

Procedure: Biospecimen CollectionBiological: BlinatumomabProcedure: Bone Marrow AspirationProcedure: Bone Marrow BiopsyBiological: Inotuzumab OzogamicinProcedure: Lumbar PunctureDrug: Ponatinib

Primary outcomes

• Event-free survival (At 1 year)
• Completion of protocol treatment (cohort 3) (Up to 10 years)

Sponsor

National Cancer Institute (NCI) · nih

Contacts & investigators

InvestigatorMatthew J Wieduwilt · principal_investigator, Alliance for Clinical Trials in Oncology

All locations (276)

University of Alabama at Birmingham Cancer CenterActive Not Recruiting

Birmingham, Alabama, United States

Anchorage Associates in Radiation MedicineSuspended

Anchorage, Alaska, United States

Anchorage Radiation Therapy CenterSuspended

Anchorage, Alaska, United States

Alaska Breast Care and Surgery LLCSuspended

Anchorage, Alaska, United States

Alaska Oncology and Hematology LLCSuspended

Anchorage, Alaska, United States

Alaska Women's Cancer CareSuspended

Anchorage, Alaska, United States

Anchorage Oncology CentreSuspended

Anchorage, Alaska, United States

Katmai Oncology GroupSuspended

Anchorage, Alaska, United States

Providence Alaska Medical CenterSuspended

Anchorage, Alaska, United States

Kingman Regional Medical CenterSuspended

Kingman, Arizona, United States

Mercy Hospital Fort SmithSuspended

Fort Smith, Arkansas, United States

PCR OncologySuspended

Arroyo Grande, California, United States

Providence Saint Joseph Medical Center/Disney Family Cancer CenterSuspended

Burbank, California, United States

Community Cancer InstituteActive Not Recruiting

Clovis, California, United States

University Oncology AssociatesActive Not Recruiting

Clovis, California, United States

City of Hope Comprehensive Cancer CenterRecruiting

Duarte, California, United States

UCI Health - Chao Family Comprehensive Cancer Center and Ambulatory CareRecruiting

Irvine, California, United States

UC San Diego Moores Cancer CenterRecruiting

La Jolla, California, United States

UC Irvine Health/Chao Family Comprehensive Cancer CenterRecruiting

Orange, California, United States

Stanford Cancer Institute Palo AltoActive Not Recruiting

Palo Alto, California, United States

Beebe Medical CenterSuspended

Lewes, Delaware, United States

Beebe South Coastal Health CampusSuspended

Millville, Delaware, United States

Delaware Clinical and Laboratory Physicians PASuspended

Newark, Delaware, United States

Helen F Graham Cancer CenterRecruiting

Newark, Delaware, United States

Medical Oncology Hematology Consultants PARecruiting

Newark, Delaware, United States

Christiana Care Health System-Christiana HospitalSuspended

Newark, Delaware, United States

Beebe Health CampusSuspended

Rehoboth Beach, Delaware, United States

TidalHealth Nanticoke / Allen Cancer CenterSuspended

Seaford, Delaware, United States

Christiana Care Health System-Wilmington HospitalSuspended

Wilmington, Delaware, United States

MedStar Georgetown University HospitalRecruiting

Washington D.C., District of Columbia, United States

Holy Cross HospitalSuspended

Fort Lauderdale, Florida, United States

Jupiter Medical CenterRecruiting

Jupiter, Florida, United States

Emory University Hospital/Winship Cancer InstituteRecruiting

Atlanta, Georgia, United States

Emory Saint Joseph's HospitalRecruiting

Atlanta, Georgia, United States

Saint Luke's Cancer Institute - BoiseSuspended

Boise, Idaho, United States

Saint Luke's Cancer Institute - FruitlandSuspended

Fruitland, Idaho, United States

Saint Luke's Cancer Institute - MeridianSuspended

Meridian, Idaho, United States

Saint Alphonsus Cancer Care Center-NampaRecruiting

Nampa, Idaho, United States

Saint Luke's Cancer Institute - NampaSuspended

Nampa, Idaho, United States

Saint Luke's Cancer Institute - Twin FallsSuspended

Twin Falls, Idaho, United States

OSF Saint Anthony's Health CenterSuspended

Alton, Illinois, United States

Illinois CancerCare-BloomingtonSuspended

Bloomington, Illinois, United States

Loyola Center for Health at Burr RidgeSuspended

Burr Ridge, Illinois, United States

Illinois CancerCare-CantonSuspended

Canton, Illinois, United States

Memorial Hospital of CarbondaleSuspended

Carbondale, Illinois, United States

SIH Cancer InstituteSuspended

Carterville, Illinois, United States

Illinois CancerCare-CarthageSuspended

Carthage, Illinois, United States

Centralia Oncology ClinicSuspended

Centralia, Illinois, United States

Northwestern UniversityRecruiting

Chicago, Illinois, United States

University of IllinoisRecruiting

Chicago, Illinois, United States

University of Chicago Comprehensive Cancer CenterSuspended

Chicago, Illinois, United States

Cancer Care Specialists of Illinois - DecaturRecruiting

Decatur, Illinois, United States

Decatur Memorial HospitalSuspended

Decatur, Illinois, United States

Illinois CancerCare-DixonSuspended

Dixon, Illinois, United States

Crossroads Cancer CenterRecruiting

Effingham, Illinois, United States

Illinois CancerCare-EurekaSuspended

Eureka, Illinois, United States

Illinois CancerCare-GalesburgSuspended

Galesburg, Illinois, United States

Western Illinois Cancer Treatment CenterSuspended

Galesburg, Illinois, United States

Loyola Medicine Homer GlenSuspended

Homer Glen, Illinois, United States

Illinois CancerCare-Kewanee ClinicSuspended

Kewanee, Illinois, United States

Northwestern Medicine Lake Forest HospitalActive Not Recruiting

Lake Forest, Illinois, United States

Illinois CancerCare-MacombSuspended

Macomb, Illinois, United States

Loyola University Medical CenterRecruiting

Maywood, Illinois, United States

Marjorie Weinberg Cancer Center at Loyola-GottliebSuspended

Melrose Park, Illinois, United States

SSM Health Good SamaritanSuspended

Mount Vernon, Illinois, United States

UC Comprehensive Cancer Center at Silver CrossRecruiting

New Lenox, Illinois, United States

Cancer Care Center of O'FallonSuspended

O'Fallon, Illinois, United States

University of Chicago Medicine-Orland ParkRecruiting

Orland Park, Illinois, United States

Illinois CancerCare-Ottawa ClinicSuspended

Ottawa, Illinois, United States

Illinois CancerCare-PekinSuspended

Pekin, Illinois, United States

OSF Saint Francis Radiation Oncology at PekinSuspended

Pekin, Illinois, United States

Illinois CancerCare-PeoriaRecruiting

Peoria, Illinois, United States

OSF Saint Francis Radiation Oncology at Peoria Cancer CenterSuspended

Peoria, Illinois, United States

Methodist Medical Center of IllinoisSuspended

Peoria, Illinois, United States

OSF Saint Francis Medical CenterSuspended

Peoria, Illinois, United States

Illinois CancerCare-PeruSuspended

Peru, Illinois, United States

Valley Radiation OncologySuspended

Peru, Illinois, United States

Illinois CancerCare-PrincetonSuspended

Princeton, Illinois, United States

Southern Illinois University School of MedicineSuspended

Springfield, Illinois, United States

Springfield ClinicSuspended

Springfield, Illinois, United States

Springfield Memorial HospitalSuspended

Springfield, Illinois, United States

Illinois CancerCare - WashingtonSuspended

Washington, Illinois, United States

Central Care Cancer Center - Garden CitySuspended

Garden City, Kansas, United States

Central Care Cancer Center - Great BendSuspended

Great Bend, Kansas, United States

University of Kansas Cancer CenterRecruiting

Kansas City, Kansas, United States

University of Kansas Hospital-Westwood Cancer CenterRecruiting

Westwood, Kansas, United States

Ochsner Medical Center JeffersonActive Not Recruiting

New Orleans, Louisiana, United States

University of Maryland/Greenebaum Cancer CenterActive Not Recruiting

Baltimore, Maryland, United States

Mercy Medical CenterSuspended

Springfield, Massachusetts, United States

Trinity Health Saint Joseph Mercy Hospital Ann ArborRecruiting

Ann Arbor, Michigan, United States

Trinity Health IHA Medical Group Hematology Oncology - BrightonRecruiting

Brighton, Michigan, United States

Trinity Health Medical Center - BrightonRecruiting

Brighton, Michigan, United States

Trinity Health IHA Medical Group Hematology Oncology - CantonRecruiting

Canton, Michigan, United States

Trinity Health Medical Center - CantonRecruiting

Canton, Michigan, United States

Caro Cancer CenterSuspended

Caro, Michigan, United States

Chelsea HospitalRecruiting

Chelsea, Michigan, United States

Trinity Health IHA Medical Group Hematology Oncology - Chelsea HospitalRecruiting

Chelsea, Michigan, United States

Hematology Oncology Consultants-ClarkstonSuspended

Clarkston, Michigan, United States

Newland Medical Associates-ClarkstonSuspended

Clarkston, Michigan, United States

Henry Ford Health Saint John HospitalRecruiting

Detroit, Michigan, United States

Henry Ford River District HospitalRecruiting

East China Township, Michigan, United States

Cancer Hematology Centers - FlintRecruiting

Flint, Michigan, United States

Genesee Hematology Oncology PCSuspended

Flint, Michigan, United States

Genesys Hurley Cancer InstituteRecruiting

Flint, Michigan, United States

Hurley Medical CenterRecruiting

Flint, Michigan, United States

Henry Ford Saint John Hospital - AcademicRecruiting

Grosse Pointe Woods, Michigan, United States

Henry Ford Saint John Hospital - BreastSuspended

Grosse Pointe Woods, Michigan, United States

Henry Ford Saint John Hospital - Van ElslanderRecruiting

Grosse Pointe Woods, Michigan, United States

University of Michigan Health - Sparrow LansingSuspended

Lansing, Michigan, United States

Hope Cancer ClinicSuspended

Livonia, Michigan, United States

Trinity Health Saint Mary Mercy Livonia HospitalRecruiting

Livonia, Michigan, United States

Henry Ford Saint John Hospital - Macomb MedicalRecruiting

Macomb, Michigan, United States

Henry Ford Warren Hospital - Breast MacombSuspended

Macomb, Michigan, United States

Saint Mary's Oncology/Hematology Associates of MarletteSuspended

Marlette, Michigan, United States

Hope Cancer CenterSuspended

Pontiac, Michigan, United States

Michigan Healthcare Professionals PontiacSuspended

Pontiac, Michigan, United States

Newland Medical Associates-PontiacSuspended

Pontiac, Michigan, United States

Trinity Health Saint Joseph Mercy Oakland HospitalRecruiting

Pontiac, Michigan, United States

Henry Ford Rochester HospitalSuspended

Rochester Hills, Michigan, United States

MyMichigan Medical Center SaginawRecruiting

Saginaw, Michigan, United States

Oncology Hematology Associates of Saginaw Valley PCSuspended

Saginaw, Michigan, United States

Bhadresh Nayak MD PC-Sterling HeightsSuspended

Sterling Heights, Michigan, United States

MyMichigan Medical Center TawasRecruiting

Tawas City, Michigan, United States

Advanced Breast Care Center PLLCSuspended

Warren, Michigan, United States

Henry Ford Health Warren HospitalRecruiting

Warren, Michigan, United States

Henry Ford Madison Heights Hospital - BreastSuspended

Warren, Michigan, United States

Henry Ford Warren Hospital - GLCMSRecruiting

Warren, Michigan, United States

Macomb Hematology Oncology PCSuspended

Warren, Michigan, United States

Saint Mary's Oncology/Hematology Associates of West BranchSuspended

West Branch, Michigan, United States

Huron Gastroenterology PCRecruiting

Ypsilanti, Michigan, United States

Trinity Health IHA Medical Group Hematology Oncology Ann Arbor CampusRecruiting

Ypsilanti, Michigan, United States

Mayo Clinic in RochesterCompleted

Rochester, Minnesota, United States

Mercy Oncology and Hematology - Clayton-ClarksonSuspended

Ballwin, Missouri, United States

Central Care Cancer Center - BolivarSuspended

Bolivar, Missouri, United States

Cox Cancer Center BransonSuspended

Branson, Missouri, United States

Mercy Cancer Center - Cape GirardeauSuspended

Cape Girardeau, Missouri, United States

Saint Francis Medical CenterSuspended

Cape Girardeau, Missouri, United States

Siteman Cancer Center at Saint Peters HospitalRecruiting

City of Saint Peters, Missouri, United States

Siteman Cancer Center at West County HospitalRecruiting

Creve Coeur, Missouri, United States

Parkland Health Center - FarmingtonSuspended

Farmington, Missouri, United States

MU Health Care Goldschmidt Cancer CenterSuspended

Jefferson City, Missouri, United States

Freeman Health SystemSuspended

Joplin, Missouri, United States

Mercy Hospital JoplinSuspended

Joplin, Missouri, United States

Mercy Clinic-Rolla-Cancer and HematologySuspended

Rolla, Missouri, United States

Phelps Health Delbert Day Cancer InstituteSuspended

Rolla, Missouri, United States

Heartland Regional Medical CenterSuspended

Saint Joseph, Missouri, United States

Sainte Genevieve County Memorial HospitalSuspended

Sainte Genevieve, Missouri, United States

Mercy Hospital SpringfieldSuspended

Springfield, Missouri, United States

CoxHealth South HospitalSuspended

Springfield, Missouri, United States

Mercy Infusion Center - ChippewaSuspended

St Louis, Missouri, United States

Washington University School of MedicineRecruiting

St Louis, Missouri, United States

Mercy Hospital SouthRecruiting

St Louis, Missouri, United States

Siteman Cancer Center-South CountyRecruiting

St Louis, Missouri, United States

Missouri Baptist Medical CenterSuspended

St Louis, Missouri, United States

Siteman Cancer Center at Christian HospitalRecruiting

St Louis, Missouri, United States

Mercy Hospital Saint LouisRecruiting

St Louis, Missouri, United States

Missouri Baptist Sullivan HospitalSuspended

Sullivan, Missouri, United States

BJC Outpatient Center at Sunset HillsSuspended

Sunset Hills, Missouri, United States

Mercy Hospital WashingtonSuspended

Washington, Missouri, United States

Saint Patrick Hospital - Community HospitalSuspended

Missoula, Montana, United States

Nebraska Medicine-Village PointeActive Not Recruiting

Omaha, Nebraska, United States

University of Nebraska Medical CenterActive Not Recruiting

Omaha, Nebraska, United States

Carson Tahoe Regional Medical CenterSuspended

Carson City, Nevada, United States

Cancer and Blood Specialists-HendersonSuspended

Henderson, Nevada, United States

Comprehensive Cancer Centers of Nevada - HendersonSuspended

Henderson, Nevada, United States

Comprehensive Cancer Centers of Nevada-Horizon RidgeSuspended

Henderson, Nevada, United States

Las Vegas Cancer Center-HendersonSuspended

Henderson, Nevada, United States

Comprehensive Cancer Centers of Nevada-Southeast HendersonSuspended

Henderson, Nevada, United States

Las Vegas Urology - Green ValleySuspended

Henderson, Nevada, United States

Las Vegas Urology - PebbleSuspended

Henderson, Nevada, United States

Oncology Las Vegas - HendersonSuspended

Henderson, Nevada, United States

Urology Specialists of Nevada - Green ValleySuspended

Henderson, Nevada, United States

Las Vegas Urology - PecosSuspended