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NCT01251861CompletedPhase 2

Bicalutamide With or Without Akt Inhibitor MK2206 in Treating Patients With Previously Treated Prostate Cancer

Androgen Receptor Modulation Phase II, Randomized Study of MK-2206 - Bicalutamide Combination in Patients With Rising PSA at High-Risk of Progression After Primary Therapy

Source: ClinicalTrials.gov · Last updated 25 Jun 2026

Brief summary (registry, in English)

This phase II trial studies how well giving bicalutamide with or without Akt inhibitor MK2206 works in treating patients with previously treated prostate cancer. Androgens can cause the growth of prostate cancer cells. Antihormone therapy, such as bicalutamide, may lessen the amount of androgens made by the body. Akt inhibitor MK2206 may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It is not yet known whether bicalutamide is more effective with or without Akt inhibitor MK2206 in treating prostate cancer.

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
108 (actual)
First submitted
1 Dec 2010
Start date
17 Mar 2011
Primary completion date
17 Jul 2018
Lead sponsor
National Cancer Institute (NCI)
NCT number
NCT01251861

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 108
  • From 17 Mar 2011 to the primary completion date, 17 Jul 2018
  • 198 sites in 2 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

  • Patient must have histologically confirmed diagnosis of prostate cancer
  • Patient must have had previous treatment with definitive surgery or radiation therapy or cryoablation
  • Patient may have prior salvage therapy (surgery, radiation or other local ablative procedures) within 4 weeks prior to randomization if the intent was for cure; prophylactic radiotherapy to prevent gynecomastia within 4 weeks prior to randomization is allowed
  • Patient must have no evidence of metastatic disease on physical exam, computed tomography (CT) abdomen/pelvis (or magnetic resonance imaging \[MRI\]), chest x-ray (or CT chest) and bone scan within 8 weeks prior to randomization
  • Patient may have had prior neoadjuvant and/or adjuvant therapy (chemotherapy, vaccines or experimental agents) within 4 weeks prior to randomization, if the PSA rise and PSA doubling time (PSADT) were documented after the testosterone level was \> 150 ng/dL
  • Patient may not have had therapy modulating testosterone levels (such as luteinizing-hormone, releasing-hormone agonists/antagonists and antiandrogens) within 1 year prior to randomization, unless it was in the neoadjuvant and/or adjuvant setting; agents such as 5 alpha reductase inhibitors, ketoconazole, abiraterone, systemic steroids, or herbal supplements known to decrease PSA levels including any dose of megestrol acetate, finasteride (e.g., Saw Palmetto and PC-SPES, African pygeum extract, lycopene, alanine, glutamic acid and glycine, beta-sitosterol, lycopene, nettle root extract, quercitin, Belizian Man Vine extract, mulra puama extract and epimedium extract campesterol, beta-sitosterol, stigmasterol, sitostanol and brassicasterol) are not permitted at any time during the period that the PSA values are being collected
  • Patient must have hormone-sensitive prostate cancer as evident by a serum total testosterone level \> 150 ng/dL within 12 weeks prior to randomization
  • Patient must have evidence of biochemical failure after primary therapy and subsequent progression
    • Biochemical failure is declared when the PSA reaches a threshold value after primary treatment and it differs for radical prostatectomy or radiation therapy
    • For radical prostatectomy the threshold for this study is PSA \>= 0.4 ng/mL
    • For radiation therapy the threshold is a PSA rise of 2 ng/mL above the nadir PSA achieved post radiation with or without hormone therapy (2006 Radiation Therapy Oncology Group \[RTOG\]-American Society for Radiation Oncology \[ASTRO\] Consensus definition)
    • PSA progression requires a PSA rise above the threshold (PSA1) measured at any time point since the threshold was reached
    • The PSADT must be \< 12 months; requires two consecutive PSA rises (PSA2 and PSA3) above the PSA1; PSA2 and PSA3 must be obtained within 6 months of study entry; all baseline PSAs should be obtained, preferably, at the same reference lab
  • PSADT calculation needs 3 PSA values:
    • PSA1 is any PSA value that is equal or greater than the threshold PSA (0.4 ng/mL for radical prostatectomy or 2 ng/mL above the nadir for primary radiation therapy) indicating biochemical relapse
    • PSA2 must be higher than PSA1, obtained at least 2 weeks after PSA1 and within 6 months or less from randomization
    • PSA3 must be higher than PSA2 and obtained at least 2 weeks after PSA2
    • Baseline PSA must have reached a minimum of 2 ng/mL but be no greater than 50 ng/mL and equal or higher than PSA3; PSA3 may be used as baseline PSA if obtained within 1 week of randomization
  • Patient's PSA doubling time (PSADT) must be less than 12 months
  • Patient must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Granulocytes \>= 1,500/mm\^3
  • Platelet count \>= 100,000/mm\^3
  • Serum creatinine within normal institutional limits or creatinine clearance \>= 50 ml/min for patients with creatinine levels above institutional normal
  • Serum total bilirubin =\< 1.5 times upper limit of normal (ULN)
  • Alkaline phosphatase (ALP) =\< 2.5 x ULN
  • Serum glutamic oxaloacetic transaminase (SGOT) (aspartate aminotransferase \[AST\]) and serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase \[ALT\]) \< 2.5 x institutional upper limit of normal
  • Human immunodeficiency virus (HIV)-positive patients are excluded from this study
  • Patient cannot receive concurrent therapeutic administration of anticoagulant therapy; low dosage aspirin =\< 325 mg per day is allowed
  • Patients with impaired cardiac function including any one of the following will be excluded from entry on study:
    • Baseline corrected QT interval (QTc) \> 450 msec (male) (patients with QTc 450-480 msec will be allowed to participate in this trial if they do not have any of the other cardiac conditions mentioned in this section)
    • Patients with congenital long QT syndrome
    • History of sustained ventricular tachycardia
    • Any history of ventricular fibrillation or torsades de pointes
    • Concomitant use of drugs with a risk of causing torsades de pointes
    • Bradycardia defined as heart rate \< 50 beats per minute; patients with a pacemaker and heart rate \>= 50 beats per minute are eligible
    • Myocardial infarction or unstable angina within 6 months of study entry
    • Congestive heart failure (New York Heart Association class III or IV)
    • Right bundle branch block and left anterior hemi-block (bifascicular block)
  • Patient must not have gastrointestinal (GI) tract disease resulting in an inability to take oral medication, malabsorption syndrome, a requirement for intravenous (IV) alimentation, prior surgical procedures affecting absorption, uncontrolled inflammatory GI disease (e.g., Crohn's, ulcerative colitis)
  • Patient may not be receiving any other investigational agents or receiving concurrent anticancer therapy (chemotherapy, immunotherapy, radiation therapy, surgery for cancer, or experimental medications) at time of randomization
  • Patient may not have a history of allergic reactions attributed to compounds of similar chemical or biologic composition to MK-2206 or bicalutamide
  • Patient must not have any uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
  • Patients with diabetes or at risk for hyperglycemia MUST not be excluded from trials with MK-2206, but the hyperglycemia should be well controlled before the patient enters the trial
  • Patients receiving any medications or substances that are inhibitors or inducers of cytochrome P450, family 3, subfamily A, polypeptide 4 (CYP3A4) are ineligible
  • Patient must NOT have previous or concurrent malignancy; exceptions are made for patients who meet any of the following conditions:
    • Basal cell or squamous cell carcinoma of the skin OR
    • Prior malignancy has been adequately treated and patient has been continuously disease free for \>= 2 years
  • Patient must agree to use barrier contraception during and for 3 months after discontinuation of study treatment; if patient impregnates a woman while on treatment or within 3 months of discontinuing treatment, he should inform his treating physician immediately
  • Patients must discontinue use of enzyme-inducing anti-epileptic drugs (EIAEDs) \>= 14 days prior to study enrollment; the investigator may prescribe non-EIAEDs; patients who must begin EIAED therapy while on study will be allowed to remain
  • Patients must not be taking cytochrome P450 enzyme-inducing antiepileptic drugs (phenytoin, carbamazepine or phenobarbital), St John's Wort, ketoconazole, dexamethasone, the dysrhythmic drugs (terfenadine, quinidine, procainamide, sotalol, probucol, bepridil, indapamide or flecainide), haloperidol, risperidone, rifampin, grapefruit, or grapefruit juice within two weeks of randomization and during the course of therapy
  • Patients may have received targeted agents (angiogenesis inhibitors, epidermal growth factor receptor \[EGFR\] inhibitors, mammalian target of rapamycin \[mTOR\] inhibitors, phosphatidylinositol 3 kinase \[PI3K\] inhibitors, etc.), however patients must have discontinued treatment with the targeted agent(s) at least 4 weeks prior to enrollment; if the patient stopped targeted agent(s) due to unresolved or persistent grade 3 or 4 toxicity, patient cannot be enrolled onto the study regardless of the length of time since discontinuation of treatment with targeted agent(s)

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

Full criteria on ClinicalTrials.gov

Sites (198)

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

SiteCityCountrySite status
Cork University Hospital
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CorkIrelandUnknown status
Tallaght University Hospital
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DublinIrelandUnknown status
Mater Misericordiae University Hospital
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DublinIrelandUnknown status
Mater Private Hospital
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DublinIrelandUnknown status
Saint Vincent's University Hospital
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DublinIrelandUnknown status
University College Hospital Galway
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GalwayIrelandUnknown status
Hickman Cancer Center
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AdrianUnited StatesUnknown status
Bixby Medical Center
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AdrianUnited StatesUnknown status
University of New Mexico Cancer Center
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AlbuquerqueUnited StatesUnknown status
Hematology Oncology Associates
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AlbuquerqueUnited StatesUnknown status
McFarland Clinic - Ames
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AmesUnited StatesUnknown status
Michigan Cancer Research Consortium NCORP
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Ann ArborUnited StatesUnknown status
Trinity Health Saint Joseph Mercy Hospital Ann Arbor
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Ann ArborUnited StatesUnknown status
Emory University Hospital/Winship Cancer Institute
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AtlantaUnited StatesUnknown status
The Medical Center of Aurora
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AuroraUnited StatesUnknown status
Rush-Copley Medical Center
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AuroraUnited StatesUnknown status
Johns Hopkins University/Sidney Kimmel Cancer Center
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BaltimoreUnited StatesUnknown status
OSF Saint Joseph Medical Center
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BloomingtonUnited StatesUnknown status
Saint Alphonsus Cancer Care Center-Boise
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BoiseUnited StatesUnknown status
Tufts Medical Center
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BostonUnited StatesUnknown status
Boulder Community Foothills Hospital
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BoulderUnited StatesUnknown status
Toledo Clinic Cancer Centers-Bowling Green
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Bowling GreenUnited StatesUnknown status
Essentia Health Saint Joseph's Medical Center
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BrainerdUnited StatesUnknown status
Fairview Ridges Hospital
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BurnsvilleUnited StatesUnknown status
Butler Memorial Hospital
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ButlerUnited StatesUnknown status
Cooper Hospital University Medical Center
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CamdenUnited StatesUnknown status
Graham Hospital Association
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CantonUnited StatesUnknown status
Saint Francis Medical Center
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Cape GirardeauUnited StatesUnknown status
Memorial Hospital
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CarthageUnited StatesUnknown status
John H Stroger Jr Hospital of Cook County
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ChicagoUnited StatesUnknown status
MetroHealth Medical Center
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ClevelandUnited StatesUnknown status
UI Health Care Mission Cancer and Blood - West Des Moines Clinic
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CliveUnited StatesUnknown status
North Coast Cancer Care-Clyde
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ClydeUnited StatesUnknown status
Penrose-Saint Francis Healthcare
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Colorado SpringsUnited StatesUnknown status
Mercy Hospital
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Coon RapidsUnited StatesUnknown status
UT Southwestern/Simmons Cancer Center-Dallas
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DallasUnited StatesUnknown status
Parkland Memorial Hospital
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DallasUnited StatesUnknown status
Geisinger Medical Center
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DanvilleUnited StatesUnknown status
Corewell Health Dearborn Hospital
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DearbornUnited StatesUnknown status
Heartland Cancer Research NCORP
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DecaturUnited StatesUnknown status
Atlanta VA Medical Center
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DecaturUnited StatesUnknown status
Decatur Memorial Hospital
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DecaturUnited StatesUnknown status
Saint Joseph Hospital - Cancer Centers of Colorado
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DenverUnited StatesUnknown status
Western States Cancer Research NCORP
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DenverUnited StatesUnknown status
Rose Medical Center
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DenverUnited StatesUnknown status
Presbyterian - Saint Lukes Medical Center - Health One
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DenverUnited StatesUnknown status
AdventHealth Porter
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DenverUnited StatesUnknown status
UI Health Care Mission Cancer and Blood - Laurel Clinic
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Des MoinesUnited StatesUnknown status
Iowa-Wide Oncology Research Coalition NCORP
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Des MoinesUnited StatesUnknown status
UI Health Care Mission Cancer and Blood - Des Moines Clinic
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Des MoinesUnited StatesUnknown status
Iowa Methodist Medical Center
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Des MoinesUnited StatesUnknown status
Mercy Medical Center - Des Moines
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Des MoinesUnited StatesUnknown status
Iowa Lutheran Hospital
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Des MoinesUnited StatesUnknown status
Henry Ford Health Saint John Hospital
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DetroitUnited StatesUnknown status
Essentia Health Saint Mary's Medical Center
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DuluthUnited StatesUnknown status
Essentia Health Cancer Center
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DuluthUnited StatesUnknown status
Miller-Dwan Hospital
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DuluthUnited StatesUnknown status
University of Maryland Shore Medical Center at Easton
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EastonUnited StatesUnknown status
Veterans Adminstration New Jersey Health Care System
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East OrangeUnited StatesUnknown status
Fairview Southdale Hospital
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EdinaUnited StatesUnknown status
Elkhart General Hospital
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ElkhartUnited StatesUnknown status
Christiana Care - Union Hospital
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ElktonUnited StatesUnknown status
Mercy Cancer Center-Elyria
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ElyriaUnited StatesUnknown status
Hematology Oncology Center Incorporated
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ElyriaUnited StatesUnknown status
Swedish Medical Center
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EnglewoodUnited StatesUnknown status
Eureka Hospital
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EurekaUnited StatesUnknown status
NorthShore University HealthSystem-Evanston Hospital
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EvanstonUnited StatesUnknown status
Lake Region Healthcare Corporation-Cancer Care
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Fergus FallsUnited StatesUnknown status
Genesys Regional Medical Center-West Flint Campus
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FlintUnited StatesUnknown status
Genesys Hurley Cancer Institute
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FlintUnited StatesUnknown status
Hurley Medical Center
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FlintUnited StatesUnknown status
Poudre Valley Hospital
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Fort CollinsUnited StatesUnknown status
Fredericksburg Oncology Inc
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FredericksburgUnited StatesUnknown status
Unity Hospital
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FridleyUnited StatesUnknown status
Illinois CancerCare-Galesburg
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GalesburgUnited StatesUnknown status
Saint Mary's Hospital and Regional Medical Center
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Grand JunctionUnited StatesUnknown status
Banner North Colorado Medical Center
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GreeleyUnited StatesUnknown status
Saint Vincent Hospital Cancer Center Green Bay
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Green BayUnited StatesUnknown status
UPMC Pinnacle Cancer Center/Community Osteopathic Campus
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HarrisburgUnited StatesUnknown status
Smilow Cancer Hospital Care Center at Saint Francis
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HartfordUnited StatesUnknown status
Mason District Hospital
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HavanaUnited StatesUnknown status
Geisinger Medical Center-Cancer Center Hazleton
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HazletonUnited StatesUnknown status
Hinsdale Hematology Oncology Associates Incorporated
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HinsdaleUnited StatesUnknown status
Hutchinson Area Health Care
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HutchinsonUnited StatesUnknown status
Indiana University/Melvin and Bren Simon Cancer Center
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IndianapolisUnited StatesUnknown status
IU Health Methodist Hospital
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IndianapolisUnited StatesUnknown status
Sidney and Lois Eskenazi Hospital
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IndianapolisUnited StatesUnknown status
Richard L. Roudebush Veterans Affairs Medical Center
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IndianapolisUnited StatesUnknown status
IU Health Central Indiana Cancer Centers-East
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IndianapolisUnited StatesUnknown status
Allegiance Health
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JacksonUnited StatesUnknown status
Mayo Clinic in Florida
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JacksonvilleUnited StatesUnknown status
Bronson Methodist Hospital
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KalamazooUnited StatesUnknown status
West Michigan Cancer Center
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KalamazooUnited StatesUnknown status
Beacon Kalamazoo
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KalamazooUnited StatesUnknown status
Community Howard Regional Health
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KokomoUnited StatesUnknown status
Horizon Oncology Research LLC
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LafayetteUnited StatesUnknown status
CommonSpirit Saint Anthony Hospital Cancer Center
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LakewoodUnited StatesUnknown status
Saint Mary Medical and Regional Cancer Center
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LanghorneUnited StatesUnknown status
University of Michigan Health - Sparrow Lansing
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LansingUnited StatesUnknown status
IU Health La Porte Hospital
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La PorteUnited StatesUnknown status
Memorial Medical Center-Las Cruces
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Las CrucesUnited StatesUnknown status
Nevada Cancer Research Foundation NCORP
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Las VegasUnited StatesUnknown status
Beebe Medical Center
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LewesUnited StatesUnknown status
Lima Memorial Hospital
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LimaUnited StatesUnknown status
AdventHealth Littleton
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LittletonUnited StatesUnknown status
Trinity Health Saint Mary Mercy Livonia Hospital
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LivoniaUnited StatesUnknown status
Sky Ridge Medical Center
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Lone TreeUnited StatesUnknown status
Longmont United Hospital
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LongmontUnited StatesUnknown status
Banner North Colorado Medical Center - Loveland Campus
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LovelandUnited StatesUnknown status
Mcdonough District Hospital
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MacombUnited StatesUnknown status
Holy Family Memorial Hospital
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ManitowocUnited StatesUnknown status
Minnesota Oncology Hematology PA-Maplewood
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MaplewoodUnited StatesUnknown status
Saint John's Hospital - Healtheast
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MaplewoodUnited StatesUnknown status
Bay Area Medical Center
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MarinetteUnited StatesUnknown status
Toledo Clinic Cancer Centers-Maumee
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MaumeeUnited StatesUnknown status
Saint Luke's Hospital
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MaumeeUnited StatesUnknown status
Franciscan Saint Anthony Health-Michigan City
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Michigan CityUnited StatesUnknown status
Hennepin County Medical Center
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MinneapolisUnited StatesUnknown status
Abbott-Northwestern Hospital
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MinneapolisUnited StatesUnknown status
Saint Joseph Regional Medical Center-Mishawaka
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MishawakaUnited StatesUnknown status
Trinity Medical Center
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MolineUnited StatesUnknown status
Mercy Memorial Hospital
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MonroeUnited StatesUnknown status
Toledo Clinic Cancer Centers-Monroe
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MonroeUnited StatesUnknown status
Christiana Care Health System-Christiana Hospital
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NewarkUnited StatesUnknown status
Rutgers Cancer Institute of New Jersey
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New BrunswickUnited StatesUnknown status
Cancer Center of Western Wisconsin
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New RichmondUnited StatesUnknown status
New Ulm Medical Center
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New UlmUnited StatesUnknown status
Laura and Isaac Perlmutter Cancer Center at NYU Langone
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New YorkUnited StatesUnknown status
Mount Sinai Union Square
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New YorkUnited StatesUnknown status
Carle Cancer Institute Normal
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NormalUnited StatesUnknown status
Carle BroMenn Medical Center
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NormalUnited StatesUnknown status
Fisher-Titus Medical Center
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NorwalkUnited StatesUnknown status
ProHealth Oconomowoc Memorial Hospital
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OconomowocUnited StatesUnknown status
Toledo Clinic Cancer Centers-Oregon
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OregonUnited StatesUnknown status
Saint Charles Hospital
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OregonUnited StatesUnknown status
Ottawa Regional Hospital and Healthcare Center
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OttawaUnited StatesUnknown status
Stanford Cancer Institute Palo Alto
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Palo AltoUnited StatesUnknown status
VA Palo Alto Health Care System
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Palo AltoUnited StatesUnknown status
AdventHealth Parker
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ParkerUnited StatesUnknown status
OSF Saint Francis Radiation Oncology at Pekin
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PekinUnited StatesUnknown status
Methodist Medical Center of Illinois
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PeoriaUnited StatesUnknown status
OSF Saint Francis Medical Center
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PeoriaUnited StatesUnknown status
Illinois CancerCare-Peoria
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PeoriaUnited StatesUnknown status
Proctor Hospital
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PeoriaUnited StatesUnknown status
Illinois Valley Hospital
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PeruUnited StatesUnknown status
University of Pennsylvania/Abramson Cancer Center
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PhiladelphiaUnited StatesUnknown status
Fox Chase Cancer Center
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PhiladelphiaUnited StatesUnknown status
Thomas Jefferson University Hospital
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PhiladelphiaUnited StatesUnknown status
University of Pittsburgh Cancer Institute (UPCI)
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PittsburghUnited StatesUnknown status
Trinity Health Saint Joseph Mercy Oakland Hospital
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PontiacUnited StatesUnknown status
Lake Huron Medical Center
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Port HuronUnited StatesUnknown status
Perry Memorial Hospital
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PrincetonUnited StatesUnknown status
Saint Mary Corwin Medical Center
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PuebloUnited StatesUnknown status
North Memorial Medical Health Center
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RobbinsdaleUnited StatesUnknown status
Mayo Clinic in Rochester
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RochesterUnited StatesUnknown status
Swedish American Hospital
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RockfordUnited StatesUnknown status
MyMichigan Medical Center Saginaw
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SaginawUnited StatesUnknown status
Corewell Health Lakeland Hospitals - Marie Yeager Cancer Center
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Saint JosephUnited StatesUnknown status
Corewell Health Lakeland Hospitals - Saint Joseph Hospital
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Saint JosephUnited StatesUnknown status
Park Nicollet Clinic - Saint Louis Park
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Saint Louis ParkUnited StatesUnknown status
Metro-Minnesota Community Oncology Research Consortium
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Saint Louis ParkUnited StatesUnknown status
Regions Hospital
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Saint PaulUnited StatesUnknown status
United Hospital
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Saint PaulUnited StatesUnknown status
North Coast Cancer Care
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SanduskyUnited StatesUnknown status
Lewis Cancer and Research Pavilion at Saint Joseph's/Candler
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SavannahUnited StatesUnknown status
Saint Francis Regional Medical Center
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ShakopeeUnited StatesUnknown status
HSHS Saint Nicholas Hospital
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SheboyganUnited StatesUnknown status
Saint Luke's Regional Medical Center
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Sioux CityUnited StatesUnknown status
Siouxland Regional Cancer Center
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Sioux CityUnited StatesUnknown status
Mercy Medical Center-Sioux City
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Sioux CityUnited StatesUnknown status
Memorial Hospital of South Bend
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South BendUnited StatesUnknown status
South Bend Clinic
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South BendUnited StatesUnknown status
Northern Indiana Cancer Research Consortium
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South BendUnited StatesUnknown status
Baystate Medical Center
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SpringfieldUnited StatesUnknown status
Springfield Memorial Hospital
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SpringfieldUnited StatesUnknown status
Geisinger Medical Group
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State CollegeUnited StatesUnknown status
Trinity's Tony Teramana Cancer Center
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SteubenvilleUnited StatesUnknown status
Lakeview Hospital
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StillwaterUnited StatesUnknown status
ProMedica Flower Hospital
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SylvaniaUnited StatesUnknown status
North Suburban Medical Center
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ThorntonUnited StatesUnknown status
Mercy Hospital of Tiffin
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TiffinUnited StatesUnknown status
Mercy Health - Saint Anne Hospital
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ToledoUnited StatesUnknown status
ProMedica Toledo Hospital/Russell J Ebeid Children's Hospital
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ToledoUnited StatesUnknown status
Toledo Clinic Cancer Centers-Toledo
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ToledoUnited StatesUnknown status
University of Toledo
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ToledoUnited StatesUnknown status
Mercy Health - Saint Vincent Hospital
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ToledoUnited StatesUnknown status
Toledo Community Hospital Oncology Program CCOP
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ToledoUnited StatesUnknown status
Carle Cancer Center
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UrbanaUnited StatesUnknown status
Ridgeview Medical Center
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WaconiaUnited StatesUnknown status
Henry Ford Health Warren Hospital
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WarrenUnited StatesUnknown status
Sibley Memorial Hospital
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Washington D.C.United StatesUnknown status
ProHealth Waukesha Memorial Hospital
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WaukeshaUnited StatesUnknown status
Fulton County Health Center
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WauseonUnited StatesUnknown status
Intermountain Health Lutheran Hospital
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Wheat RidgeUnited StatesUnknown status
Geisinger Wyoming Valley/Henry Cancer Center
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Wilkes-BarreUnited StatesUnknown status
Rice Memorial Hospital
Coordinator of this site? Confirm its status
WillmarUnited StatesUnknown status
Aspirus Cancer Care - Wisconsin Rapids
Coordinator of this site? Confirm its status
Wisconsin RapidsUnited StatesUnknown status
Minnesota Oncology Hematology PA-Woodbury
Coordinator of this site? Confirm its status
WoodburyUnited StatesUnknown status

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