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NCT06470243RecruitingPhase 3

Testing Whether the Addition of Carboplatin Chemotherapy to Cabazitaxel Chemotherapy Will Improve Outcomes Compared to Cabazitaxel Alone in People With Castrate-Resistant Prostate Cancer That Has Spread Beyond the Prostate to Other Parts of the Body

A Phase III Study of Cabazitaxel With or Without Carboplatin in Patients With Metastatic Castrate-Resistant Prostate Cancer (mCRPC), Stratified by Aggressive Variant Signature

Source: ClinicalTrials.gov · Last updated 22 Jan 2026

Brief summary (registry, in English)

This phase III trial compares the effect of adding carboplatin to the standard of care chemotherapy drug cabazitaxel versus cabazitaxel alone in treating prostate cancer that keeps growing even when the amount of testosterone in the body is reduced to very low levels (castrate-resistant) and that has spread from where it first started (primary site) to other places in the body (metastatic). Carboplatin is in a class of medications known as platinum-containing compounds. Carboplatin works by killing, stopping or slowing the growth of tumor cells. Chemotherapy drugs, such as cabazitaxel, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Prednisone is often given together with chemotherapy drugs. Prednisone is in a class of medications called corticosteroids. It is used to reduce inflammation and lower the body's immune response to help lessen the side effects of chemotherapy drugs and to help the chemotherapy work. Giving carboplatin with the standard of care chemotherapy drug cabazitaxel may be better at treating metastatic castrate-resistant prostate cancer.

Status (registry)
Recruiting
Phase (registry)
Phase 3
Study type
Interventional
Enrollment
528 (estimated)
First submitted
17 Jun 2024
Start date
27 Nov 2024
Primary completion date
30 Jun 2029
Lead sponsor
SWOG Cancer Research Network
NCT number
NCT06470243

What you commit to

  • Study type: Interventional · Phase 3
  • Planned participants: 528
  • From 27 Nov 2024 to the primary completion date, 30 Jun 2029
  • 174 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Who the study is looking for

  • STEP 1 SCREENING REGISTRATION: NOTE: All participants must have biopsy tissue submitted to MD Anderson Cancer Center prior to randomization for alteration assessment. Participants must have determination of their AVPC-Molecular Pathologic Signature immunohistochemistry (MSIHC) status from central assessment by the MD Anderson Clinical Pathology Laboratory using Clinical Laboratory Improvement Act (CLIA) certified immunohistochemistry (IHC) assays for TP53, RB1 and PTEN. In addition, while not mandated, CLIA certified next generation sequencing (NGS) of tumor deoxyribonucleic acid (DNA) and/or circulating tumor derived DNA (ctDNA) assessment of AVPC-MS marker status will be collected from participants for whom it is available
  • STEP 1 SCREENING REGISTRATION: Participants must have a histologically confirmed diagnosis of prostate cancer at the time of step 1 registration
  • STEP 1 SCREENING REGISTRATION: Participants must have castrate-resistant prostate cancer and metastatic disease by bone scan and/or CT/MRI (i.e., soft tissue, visceral, lymph node)
  • STEP 1 SCREENING REGISTRATION: Participants may have received any prior therapy, but one must be docetaxel or contain docetaxel in either the castrate-sensitive and/or castrate resistant disease state
  • STEP 1 SCREENING REGISTRATION: Participants must be ≥ 18 years of age at the time of step 1 screening registration
  • STEP 1 SCREENING REGISTRATION: Participants must have solid tumor biopsy material (formalin-fixed paraffin-embedded (FFPE) tissue blocks and/or 10 cut slides on four-micron thick unstained positive charged slides of FFPE tissue) available for submission for alterations in TP53, RB1 and PTEN by IHC using CLIA certified assays in the MD Anderson Clinical Pathology Laboratory. This specimen is required for central assessment of the AVPC-MSIHC regardless of whether the site has already locally evaluated the AVPC-MS status
  • STEP 1 SCREENING REGISTRATION: Tumor samples submitted for analysis must have been collected within 12 months prior to step 1 screening registration. Samples from metastatic lesions collected in the castrate-resistant disease state are preferable but not mandatory. Samples obtained during the hormone-naive disease state are acceptable if collected within 12 months of step 1 screening registration. If more than one tumor sample exists, the sample obtained closest to the date of registration should be submitted to MDACC for analysis
    • NOTE: Sites will receive an email from Southwest Oncology Group (SWOG) Statistics and Data Management Center containing participant results of Aggressive Variant Prostate Cancer Molecular Signature (AVPC-MS) assessment within 5-12 business days after tissue submission to MD Anderson Clinical Pathology Laboratory. The participant's AVPC-MS signature result (positive or negative) is required BEFORE randomization on to step 2. If sites receive a non-evaluable AVPC-MS signature result, SWOG Statistics and Data Management Center will provide instructions for resubmission
  • STEP 1 SCREENING REGISTRATION: NOTE: As a part of the Oncology Patient Enrollment Network (OPEN) registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system
  • STEP 1 SCREENING REGISTRATION: Participants must be informed of the investigational nature of this study and must sign and give informed consent in accordance with institutional and federal guidelines. Documentation of informed consent via remote consent is allowed
    • For participants with impaired decision-making capabilities, legally authorized representatives may sign and give informed consent on behalf of study participants in accordance with applicable federal, local, and Central Institutional Review Board (CIRB) regulations
  • STEP 2 RANDOMIZATION: NOTE: Participants must be registered to step 2 randomization within 70 days after registration to step 1. Participants must plan to start protocol therapy no more than 14 days after step 2 randomization
  • STEP 2 RANDOMIZATION: Participants must have castrate levels of testosterone with a baseline level \< 50ng/dL within 28 days prior to step 2 randomization
  • STEP 2 RANDOMIZATION: Participants must have evidence for metastatic prostate cancer by bone scan and/or CT/MRI (i.e., soft tissue, visceral, lymph node). Visceral and/or soft-tissue metastases must be ≥ 1.0 cm in diameter and lymph nodes must be \> 1.5 cm diameter in the short axis. Scans must be obtained within 28 days prior to randomization
    • NOTE: All disease must be assessed and documented on the baseline/pre-registration tumor assessment form
  • STEP 2 RANDOMZIATION: Participants must have progressive disease (PD) in the opinion of the treating investigator according to any of the following criteria
    • Progression in measurable disease (RECIST 1.1 criteria). Patient with measurable disease must have at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded). Each lesion must be at least 10 mm when measured by computed tomography (CT) \[CT scan thickness no greater than 5 mm\] or magnetic resonance imaging (MRI). Lymph nodes should be ≥ 15 mm in short axis. Previously irradiated lesions, primary prostate lesion and bone lesions will be considered non-measurable disease
    • Progression in bone as evidenced by:
    • Appearance of 2 or more new bone lesions on bone scan (BS). If equivocal, they must be confirmed by other imaging modalities (CT; MRI), and/or repeat BS \> 4 weeks later
    • Appearance of a new lytic lesion(s) and/or increasing size of an existing lesion by CT/MRI, since AVPC tumors may produce lytic bone lesions that are not detected on conventional bone scans
    • Rising prostate-specific antigen (PSA) defined (Prostate Cancer Working Group 2 \[PCWG2\]) as at least two consecutive rises in PSA to be documented over a reference value (measure 1) taken at least one week apart. The first rising PSA (measure 2) should be taken at least 7 days after the reference value. A third confirmatory PSA measure is required (2nd beyond the reference level) to be greater than the second measure and it must be obtained at least 7 days after the 2nd measure. If this is not the case, a fourth PSA measure is required to be taken and be greater than the 2nd measure. In case of progression based on rising PSA only, the first rising PSA (measure 2) must be obtained within 6 months of initiation of androgen receptor (AR) targeted therapy (≤ 6 months)
    • Clinical progression. Increasing symptoms unequivocally attributed to disease progression as judged by the treating physician
  • STEP 2 RANDOMIZATION: Participants must not have received prior cabazitaxel or carboplatin
  • STEP 2 RANDOMIZATION: Participants must not be receiving treatment on another therapeutic clinical trial at the time of randomization. Chemotherapies, bone targeting therapies, immunotherapies and clinical trial agents must be discontinued ≥ 21 days prior to randomization. Stereotactic radiation (SART) must be discontinued ≥ 3 days prior to randomization
  • STEP 2 RANDOMIZATION: Participants must not be receiving radiation therapy or kyphoplasty-vertebroplasty within 14 days prior to randomization or major surgery (e.g., open abdominal, pelvic, thoracic, orthopedic or neurosurgery) within 28 days prior to step 2 randomization
  • STEP 2 RANDOMIZATION: Participants must not have untreated fractures and/or cord compression
  • STEP 2 RANDOMIZATION: Participants must not have symptomatic uncontrolled brain metastases. Properly treated brain metastases (i.e., with stereotactic radiation) within 14 days are allowed
  • STEP 2 RANDOMIZATION: Participants must have Zubrod performance status of 0 - 2 within 28 days prior to step 2 randomization
  • STEP 2 RANDOMIZATION: Participants must have a complete medical history and physical exam within 28 days prior to step 2 randomization
  • STEP 2 RANDOMIZATION: Absolute neutrophil count ≥ 1.5 x 10\^3/uL (within 28 days prior to step 2 randomization)
  • STEP 2 RANDOMIZATION: Platelets ≥ 100 x 10\^3/uL (unless clinical evidence of bone marrow infiltration by tumor in which case \> 75 x 10\^3/uL are allowed) (within 28 days prior to step 2 randomization)
  • STEP 2 RANDOMIZATION: Total bilirubin ≤ institutional upper limit of normal (ULN) with the exception of isolated hyperbilirubinemia due to Gilbert's syndrome or if the participant has liver metastases and/or acute tumor associated illness \< 4x ULN (within 28 days prior to step 2 randomization)
  • STEP 2 RANDOMIZATION: Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) ≤ 3 × institutional ULN (or if participant has liver metastases and/or acute tumor-associated illness, ≤ 4x institutional ULN) (within 28 days prior to step 2 randomization)
  • STEP 2 REGISTRATION: Participants must have a calculated creatinine clearance ≥ 30 mL/min using the Cockcroft-Gault Formula. This specimen must have been drawn and processed within 28 days prior to step 2 randomization
  • STEP 2 RANDOMIZATION: Participants with peripheral neuropathy must have ≤ grade 2 peripheral neuropathy (Common Terminology Criteria for Adverse Events \[CTCAE\] version 5.0) (within 28 days prior to step 2 randomization)
  • STEP 2 RANDOMIZATION: Participants who are of reproductive potential must have agreed to use an effective contraceptive method with details provided as a part of the consent process. A person who has semen likely to contain sperm is considered to be of "reproductive potential." In addition to routine contraceptive methods, "effective contraception" also includes refraining from sexual activity that might result in pregnancy and surgery intended to prevent pregnancy (or with a side-effect of pregnancy prevention) including vasectomy with testing showing no sperm in the semen
  • STEP 2 RANDOMIZATION: Participants must not have a prior or concurrent malignancy whose natural history or treatment (in the opinion of the treating physician) has the potential to interfere with the safety or efficacy assessment of the treatment regimen
  • STEP 2 RANDOMIZATION: Participants with known human immunodeficiency virus (HIV)-infection must be on effective anti-retroviral therapy at registration and have undetectable viral load test on the most recent test results obtained within 6 months prior to registration
  • STEP 2 RANDOMIZATION: Participants must be offered the opportunity to participate in specimen banking. With participant consent, specimens must be collected and submitted via the SWOG Specimen Tracking System

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

Full criteria on ClinicalTrials.gov

Sites (174)

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 StatesRecruiting
Community Hospital of Anaconda
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AnacondaUnited StatesRecruiting
Trinity Health Saint Joseph Mercy Hospital Ann Arbor
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Ann ArborUnited StatesRecruiting
Saint Alphonsus Cancer Care Center-Baker City
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Baker CityUnited StatesRecruiting
Indu and Raj Soin Medical Center
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BeavercreekUnited StatesRecruiting
Nebraska Medicine-Bellevue
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BellevueUnited StatesRecruiting
Lehigh Valley Hospital - Muhlenberg
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BethlehemUnited StatesRecruiting
Billings Clinic Cancer Center
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BillingsUnited StatesRecruiting
Illinois CancerCare-Bloomington
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BloomingtonUnited StatesRecruiting
Saint Elizabeth Boardman Hospital
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BoardmanUnited StatesRecruiting
Saint Alphonsus Cancer Care Center-Boise
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BoiseUnited StatesRecruiting
Bozeman Health Deaconess Hospital
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BozemanUnited StatesRecruiting
Trinity Health IHA Medical Group Hematology Oncology - Brighton
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BrightonUnited StatesRecruiting
Trinity Health Medical Center - Brighton
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BrightonUnited StatesRecruiting
Minnesota Oncology - Burnsville
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BurnsvilleUnited StatesRecruiting
Saint Alphonsus Cancer Care Center-Caldwell
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CaldwellUnited StatesRecruiting
Cambridge Medical Center
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CambridgeUnited StatesRecruiting
Illinois CancerCare-Canton
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CantonUnited StatesRecruiting
Trinity Health Medical Center - Canton
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CantonUnited StatesRecruiting
Trinity Health IHA Medical Group Hematology Oncology - Canton
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CantonUnited StatesRecruiting
Southeast Cancer Center
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Cape GirardeauUnited StatesRecruiting
Saint Francis Medical Center
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Cape GirardeauUnited StatesRecruiting
Memorial Hospital of Carbondale
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CarbondaleUnited StatesRecruiting
Caro Cancer Center
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CaroUnited StatesRecruiting
SIH Cancer Institute
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CartervilleUnited StatesRecruiting
Illinois CancerCare-Carthage
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CarthageUnited StatesRecruiting
Oncology Associates at Mercy Medical Center
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Cedar RapidsUnited StatesRecruiting
Mercy Hospital
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Cedar RapidsUnited StatesRecruiting
Dayton Physicians LLC-Miami Valley South
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CentervilleUnited StatesRecruiting
Centralia Oncology Clinic
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CentraliaUnited StatesRecruiting
Christiana Care Health System-Concord Health Center
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Chadds FordUnited StatesRecruiting
Trinity Health IHA Medical Group Hematology Oncology - Chelsea Hospital
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ChelseaUnited StatesRecruiting
Chelsea Hospital
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ChelseaUnited StatesRecruiting
University of Illinois
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ChicagoUnited StatesRecruiting
Northwestern University
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ChicagoUnited StatesRecruiting
Oncology Hematology Care Inc-Kenwood
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CincinnatiUnited StatesRecruiting
Newland Medical Associates-Clarkston
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ClarkstonUnited StatesRecruiting
Hematology Oncology Consultants-Clarkston
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ClarkstonUnited StatesRecruiting
Billings Clinic-Cody
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CodyUnited StatesRecruiting
Kootenai Health - Coeur d'Alene
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Coeur d'AleneUnited StatesRecruiting
MD Anderson in The Woodlands
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ConroeUnited StatesRecruiting
Mercy Hospital
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Coon RapidsUnited StatesRecruiting
Dayton Physician LLC - Englewood
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DaytonUnited StatesRecruiting
Decatur Memorial Hospital
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DecaturUnited StatesRecruiting
Cancer Care Specialists of Illinois - Decatur
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DecaturUnited StatesRecruiting
Northwestern Medicine Cancer Center Kishwaukee
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DeKalbUnited StatesRecruiting
Henry Ford Health Saint John Hospital
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DetroitUnited StatesRecruiting
Illinois CancerCare-Dixon
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DixonUnited StatesRecruiting
Great Lakes Cancer Management Specialists-Doctors Park
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East China TownshipUnited StatesRecruiting
Pocono Medical Center
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East StroudsburgUnited StatesRecruiting
Fairview Southdale Hospital
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EdinaUnited StatesRecruiting
Crossroads Cancer Center
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EffinghamUnited StatesRecruiting
Christiana Care - Union Hospital
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ElktonUnited StatesRecruiting
Illinois CancerCare-Eureka
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EurekaUnited StatesRecruiting
Parkland Health Center - Farmington
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FarmingtonUnited StatesRecruiting
Highlands Oncology Group - Fayetteville
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FayettevilleUnited StatesRecruiting
Armes Family Cancer Center
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FindlayUnited StatesRecruiting
Orion Cancer Care
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FindlayUnited StatesRecruiting
Blanchard Valley Hospital
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FindlayUnited StatesRecruiting
Hurley Medical Center
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FlintUnited StatesRecruiting
Genesys Hurley Cancer Institute
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FlintUnited StatesRecruiting
Genesee Cancer and Blood Disease Treatment Center
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FlintUnited StatesRecruiting
Genesee Hematology Oncology PC
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FlintUnited StatesRecruiting
Holy Cross Hospital
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Fort LauderdaleUnited StatesRecruiting
Dayton Physicians LLC-Atrium
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FranklinUnited StatesRecruiting
Western Illinois Cancer Treatment Center
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GalesburgUnited StatesRecruiting
Illinois CancerCare-Galesburg
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GalesburgUnited StatesRecruiting
Northwestern Medicine Cancer Center Delnor
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GenevaUnited StatesRecruiting
The West Clinic - Wolf River
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GermantownUnited StatesRecruiting
Northwestern Medicine Glenview Outpatient Center
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GlenviewUnited StatesRecruiting
Northwestern Medicine Grayslake Outpatient Center
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GrayslakeUnited StatesRecruiting
Great Falls Clinic
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Great FallsUnited StatesRecruiting
Benefis Sletten Cancer Institute
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Great FallsUnited StatesRecruiting
Wayne Hospital
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GreenvilleUnited StatesRecruiting
Dayton Physicians LLC-Wayne
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GreenvilleUnited StatesRecruiting
Great Lakes Cancer Management Specialists-Van Elslander Cancer Center
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Grosse Pointe WoodsUnited StatesRecruiting
Henry Ford Saint John Hospital - Academic
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Grosse Pointe WoodsUnited StatesRecruiting
Henry Ford Saint John Hospital - Breast
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Grosse Pointe WoodsUnited StatesRecruiting
Lehigh Valley Hospital-Hazleton
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HazletonUnited StatesRecruiting
MD Anderson West Houston
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HoustonUnited StatesRecruiting
Lyndon Baines Johnson General Hospital
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HoustonUnited StatesRecruiting
M D Anderson Cancer Center
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HoustonUnited StatesRecruiting
University of Mississippi Medical Center
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JacksonUnited StatesRecruiting
Kalispell Regional Medical Center
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KalispellUnited StatesRecruiting
Greater Dayton Cancer Center
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KetteringUnited StatesRecruiting
Kettering Medical Center
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KetteringUnited StatesRecruiting
Illinois CancerCare-Kewanee Clinic
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KewaneeUnited StatesRecruiting
Northwestern Medicine Lake Forest Hospital
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Lake ForestUnited StatesRecruiting
University of Michigan Health - Sparrow Lansing
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LansingUnited StatesRecruiting
MD Anderson League City
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League CityUnited StatesRecruiting
Beebe Medical Center
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LewesUnited StatesRecruiting
Trinity Health Saint Mary Mercy Livonia Hospital
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LivoniaUnited StatesRecruiting
Tibor Rubin VA Medical Center
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Long BeachUnited StatesRecruiting
Henry Ford Warren Hospital - Breast Macomb
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MacombUnited StatesRecruiting
Great Lakes Cancer Management Specialists-Macomb Medical Campus
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MacombUnited StatesRecruiting
Illinois CancerCare-Macomb
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MacombUnited StatesRecruiting
Fairview Clinics and Surgery Center Maple Grove
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Maple GroveUnited StatesRecruiting
Saint John's Hospital - Healtheast
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MaplewoodUnited StatesRecruiting
Minnesota Oncology Hematology PA-Maplewood
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MaplewoodUnited StatesRecruiting
Saint Mary's Oncology/Hematology Associates of Marlette
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MarletteUnited StatesRecruiting
Idaho Urologic Institute-Meridian
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MeridianUnited StatesRecruiting
Beebe South Coastal Health Campus
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MillvilleUnited StatesRecruiting
Health Partners Inc
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MinneapolisUnited StatesRecruiting
Hennepin County Medical Center
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MinneapolisUnited StatesRecruiting
Abbott-Northwestern Hospital
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MinneapolisUnited StatesRecruiting
Community Medical Center
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MissoulaUnited StatesRecruiting
Monticello Cancer Center
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MonticelloUnited StatesRecruiting
Saint Alphonsus Cancer Care Center-Nampa
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NampaUnited StatesRecruiting
Christiana Care Health System-Christiana Hospital
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NewarkUnited StatesRecruiting
Medical Oncology Hematology Consultants PA
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NewarkUnited StatesRecruiting
Helen F Graham Cancer Center
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NewarkUnited StatesRecruiting
Cancer Center of Western Wisconsin
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New RichmondUnited StatesRecruiting
New Ulm Medical Center
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New UlmUnited StatesRecruiting
HSHS Saint Elizabeth's Hospital
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O'FallonUnited StatesRecruiting
Cancer Care Center of O'Fallon
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O'FallonUnited StatesRecruiting
University of Oklahoma Health Sciences Center
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Oklahoma CityUnited StatesRecruiting
Nebraska Medicine-Village Pointe
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OmahaUnited StatesRecruiting
University of Nebraska Medical Center
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OmahaUnited StatesRecruiting
Saint Alphonsus Cancer Care Center-Ontario
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OntarioUnited StatesRecruiting
Northwestern Medicine Orland Park
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Orland ParkUnited StatesRecruiting
Illinois CancerCare-Ottawa Clinic
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OttawaUnited StatesRecruiting
Illinois CancerCare-Pekin
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PekinUnited StatesRecruiting
Methodist Medical Center of Illinois
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PeoriaUnited StatesRecruiting
Illinois CancerCare-Peoria
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PeoriaUnited StatesRecruiting
Valley Radiation Oncology
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PeruUnited StatesRecruiting
Illinois CancerCare-Peru
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PeruUnited StatesRecruiting
Trinity Health Saint Joseph Mercy Oakland Hospital
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PontiacUnited StatesRecruiting
Newland Medical Associates-Pontiac
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PontiacUnited StatesRecruiting
Michigan Healthcare Professionals Pontiac
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PontiacUnited StatesRecruiting
Hope Cancer Center
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PontiacUnited StatesRecruiting
Kootenai Clinic Cancer Services - Post Falls
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Post FallsUnited StatesRecruiting
Illinois CancerCare-Princeton
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PrincetonUnited StatesRecruiting
Fairview Northland Medical Center
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PrincetonUnited StatesRecruiting
Beebe Health Campus
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Rehoboth BeachUnited StatesRecruiting
Reid Health
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RichmondUnited StatesRecruiting
VCU Massey Cancer Center at Stony Point
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RichmondUnited StatesRecruiting
Virginia Commonwealth University/Massey Cancer Center
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RichmondUnited StatesRecruiting
North Memorial Medical Health Center
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RobbinsdaleUnited StatesRecruiting
Highlands Oncology Group - Rogers
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RogersUnited StatesRecruiting
MyMichigan Medical Center Saginaw
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SaginawUnited StatesRecruiting
Oncology Hematology Associates of Saginaw Valley PC
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SaginawUnited StatesRecruiting
Sainte Genevieve County Memorial Hospital
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Sainte GenevieveUnited StatesRecruiting
Park Nicollet Clinic - Saint Louis Park
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Saint Louis ParkUnited StatesRecruiting
United Hospital
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Saint PaulUnited StatesRecruiting
Regions Hospital
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Saint PaulUnited StatesRecruiting
Kootenai Clinic Cancer Services - Sandpoint
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SandpointUnited StatesRecruiting
Saint Francis Regional Medical Center
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ShakopeeUnited StatesRecruiting
Welch Cancer Center
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SheridanUnited StatesRecruiting
Highlands Oncology Group
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SpringdaleUnited StatesRecruiting
Southern Illinois University School of Medicine
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SpringfieldUnited StatesRecruiting
Springfield Clinic
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SpringfieldUnited StatesRecruiting
Memorial Medical Center
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SpringfieldUnited StatesRecruiting
Lakeview Hospital
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StillwaterUnited StatesRecruiting
Missouri Baptist Medical Center
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St LouisUnited StatesRecruiting
MD Anderson in Sugar Land
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Sugar LandUnited StatesRecruiting
Missouri Baptist Sullivan Hospital
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SullivanUnited StatesRecruiting
BJC Outpatient Center at Sunset Hills
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Sunset HillsUnited StatesRecruiting
MyMichigan Medical Center Tawas
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Tawas CityUnited StatesRecruiting
Dayton Physicians LLC - Troy
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TroyUnited StatesRecruiting
Ridgeview Medical Center
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WaconiaUnited StatesRecruiting
Saint Joseph Warren Hospital
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WarrenUnited StatesRecruiting
Great Lakes Cancer Management Specialists-Macomb Professional Building
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WarrenUnited StatesRecruiting
Henry Ford Madison Heights Hospital - Breast
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WarrenUnited StatesRecruiting
Saint John Macomb-Oakland Hospital
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WarrenUnited StatesRecruiting
Northwestern Medicine Cancer Center Warrenville
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WarrenvilleUnited StatesRecruiting
Illinois CancerCare - Washington
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WashingtonUnited StatesRecruiting
Saint Mary's Oncology/Hematology Associates of West Branch
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West BranchUnited StatesRecruiting
Rice Memorial Hospital
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WillmarUnited StatesRecruiting
Christiana Care Health System-Wilmington Hospital
Coordinator of this site? Confirm its status
WilmingtonUnited StatesRecruiting
Minnesota Oncology Hematology PA-Woodbury
Coordinator of this site? Confirm its status
WoodburyUnited StatesRecruiting
Fairview Lakes Medical Center
Coordinator of this site? Confirm its status
WyomingUnited StatesRecruiting
Saint Elizabeth Youngstown Hospital
Coordinator of this site? Confirm its status
YoungstownUnited StatesRecruiting
Huron Gastroenterology PC
Coordinator of this site? Confirm its status
YpsilantiUnited StatesRecruiting
Trinity Health IHA Medical Group Hematology Oncology Ann Arbor Campus
Coordinator of this site? Confirm its status
YpsilantiUnited StatesRecruiting

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