Can stronger radiation beat brain cancer? new trial aims to find out
NCT ID NCT02179086
First seen Jun 26, 2026 · Last updated Aug 28, 2026 · Updated 2 times
Summary
This phase 2 trial compares two types of higher-dose radiation (IMRT or proton beam) plus the chemotherapy drug temozolomide against standard radiation plus temozolomide in 606 people with newly diagnosed glioblastoma. The goal is to see if the higher-dose approaches improve overall survival. The study is active but no longer recruiting new participants.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- temozolomide
- What this could lead to
- If successful, this could show that higher-dose radiation (IMRT or proton beam) combined with temozolomide extends survival for people with newly diagnosed glioblastoma.
- What could go wrong
- This is a phase 2 trial, so results are still preliminary. Higher radiation doses may increase side effects, and it's not yet known if they are more effective than standard treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
624 people
The number who actually took part.
- Started
-
Dec 2014
- Expected to finish
-
Dec 2026
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * PRIOR TO STEP 1 REGISTRATION * A diagnostic contrast-enhanced MRI (no other scan type allowed) of the brain must be performed postoperatively; the residual enhancing tumor and/or resection cavity must have a maximal diameter of 5 cm or less; the tumor diameter will be the greatest diameter as measured on the contrast-enhanced postoperative MRI and will include residual disease and/or the postoperative surgical cavity as appropriate * The postoperative brain MRI should be obtained within 72 hours of resection; if it is not obtained within 72 hours post-resection, then an MRI obtained 2 weeks or longer after surgery is required and can be utilized to ensure maximal diameter of residual tumor and/or resection cavity is 5 cm or less * For cases where a gross total resection of enhancing tumor is performed, but postoperative surgical cavity is NOT identifiable, the patient will be excluded from the trial * Tumor tissue must be available for submission for central pathology review * Timing requirements: * If MGMT has been assessed locally by LabCorps or MD Anderson Cancer Center Molecular Diagnostics Lab (MDACC-MDL): * Tissue for central pathology review and central MGMT assessment and the official LabCorps or MDACC-MDL MGMT result must be received by the NRG Oncology Biospecimen Bank on or before postoperative calendar day 40 * The site's local MGMT report from LabCorp or MDACC-MDL will then be used to stratify the patient; a post-stratification MGMT central review will be performed, but step 2 registration and protocol treatment can proceed without central review of MGMT * Patients whose tissue for central pathology review and official LabCorps or MDACC-MDL MGMT result cannot be received by NRG Oncology Biospecimen Bank on or before 40 calendar days after surgery may NOT enroll on this trial, as central pathology review and stratification will not be complete in time for the patient to start treatment within 49 calendar days following surgery * If MGMT has not been assessed locally by LabCorps or MDACC-MDL: * Tissue for central pathology review and central MGMT assessment must be received by the NRG Oncology Biospecimen Bank on or before postoperative calendar day 30 * Central MGMT analysis will be performed at MDACC-MDL and used for patient stratification; results will be conveyed to NRG Oncology within 10 business days of receipt of the tissue * Patients who have not had local MGMT assessment by LabCorps or MDACC-MDL and whose tissue for central pathology review cannot be received by NRG Oncology Biospecimen Bank on or before 30 calendar days after surgery may NOT enroll on this trial, as central pathology review and stratification will not be complete in time for the patient to start treatment within 49 calendar days following surgery * Tissue Requirements: * Patients must have at least 1 block of tumor tissue; submission of 2 blocks is strongly encouraged to maximize the chances of eligibility; in total, at least 1 cubic centimeter of tissue composed primarily of tumor must be present * Submission of an accompanying hematoxylin and eosin H\&E slide(s) is MANDATORY * Diagnosis must be made by surgical excision, either partial or complete; stereotactic biopsy and cavitronic ultrasonic surgical (CUSA) techniques are not allowed * The tumor must be located in the supratentorial compartment only (any component involving the brain stem or cerebellum is not allowed) * Patients must provide study-specific informed consent prior to step 1 registration * PRIOR TO STEP 2 REGISTRATION * Histologically proven diagnosis of glioblastoma (World Health Organization \[WHO\] grade IV) confirmed by central review prior to step 2 registration * Tumor tissue that is determined by central pathology review prior to step 2 registration to be of sufficient quantity for central analysis of MGMT status * History/physical examination within 28 days prior to step 2 registration * The patient must have recovered from effects of surgery, postoperative infection, and other complications within 28 days prior to step 2 registration * Documentation of steroid doses within 28 days prior to step 2 registration * Karnofsky performance status \>= 70 within 28 days prior to step 2 registration * Age \>= 18 * Complete blood count (CBC)/differential obtained within 28 days prior to step 2 registration * Absolute neutrophil count (ANC) \>= 1,500 cells/mm\^3 (obtained within 28 days prior to step 2 registration) * Platelets \>= 100,000 cells/mm\^3 (obtained within 28 days prior to step 2 registration) * Hemoglobin \>= 10.0 g/dl (obtained within 28 days prior to step 2 registration) (note: the use of transfusion or other intervention to achieve hemoglobin \[Hgb\] \>= 10.0 g/dl is acceptable) * Bilirubin =\< 1.5 upper limit of normal (ULN) (within 28 days prior to step 2 registration) * Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) =\< 3 x ULN (within 28 days prior to step 2 registration) * Negative serum pregnancy test obtained for females of child-bearing potential within 28 days prior to step 2 registration * As of Amendment 2, if the registering site is a photon center (registering patients to group I), the patient must agree to participate in the advanced imaging sub-study Exclusion Criteria: * Prior invasive malignancy (except non-melanomatous skin cancer) unless disease-free for a minimum of 3 years; (for example, carcinoma in situ of the breast, oral cavity, or cervix are all permissible) * Recurrent or multifocal malignant gliomas * Any site of distant disease (for example, drop metastases from the GBM tumor site) * Prior chemotherapy or radiosensitizers for cancers of the head and neck region; note that prior chemotherapy for a different cancer is allowable (except temozolomide) * Prior use of Gliadel wafers or any other intratumoral or intracavitary treatment are not permitted * Prior radiotherapy to the head or neck (except for T1 glottic cancer), resulting in overlap of radiation fields * Severe, active co-morbidity, defined as follows: * Unstable angina at step 2 registration * Transmural myocardial infarction within the last 6 months prior to step 2 registration * Evidence of recent myocardial infarction or ischemia by the findings of S-T elevations of \>= 2 mm using the analysis of an electrocardiogram (EKG) performed within 28 days prior to step 2 registration (Note: EKG to be performed only if clinical suspicion of cardiac issue) * New York Heart Association grade II or greater congestive heart failure requiring hospitalization within 12 months prior to step 2 registration * Serious and inadequately controlled arrhythmia at step 2 registration * Serious or non-healing wound, ulcer or bone fracture or history of abdominal fistula, intra-abdominal abscess requiring major surgical procedure, open biopsy or significant traumatic injury within 28 days prior to step 2 registration, with the exception of the craniotomy for surgical resection * Acute bacterial or fungal infection requiring intravenous antibiotics at the time of step 2 registration * Hepatic insufficiency resulting in clinical jaundice and/or coagulation defects; note, however, that laboratory tests for coagulation parameters are not required for entry into this protocol * Chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy at the time of step 2 registration * Acquired immune deficiency syndrome (AIDS) based upon current Centers for Disease Control and Prevention (CDC) definition; note, however, that human immunodeficiency virus (HIV) testing is not required for entry into this protocol; the need to exclude patients with AIDS from this protocol is because the treatments involved in this protocol may be significantly immunosuppressive with potentially fatal outcomes in patients already immunosuppressed * Any other severe immunocompromised condition * Active connective tissue disorders, such as lupus or scleroderma, that in the opinion of the treating physician may put the patient at high risk for radiation toxicity * End-stage renal disease (ie, on dialysis or dialysis has been recommended) * Any other major medical illnesses or psychiatric treatments that in the investigator's opinion will prevent administration or completion of protocol therapy * Pregnancy or women of childbearing potential and men who are sexually active and not willing/able to use medically acceptable forms of contraception; this exclusion is necessary because the treatment involved in this study may be significantly teratogenic * Patients treated on any other therapeutic clinical protocols within 30 days prior to step 2 registration * Inability to undergo MRI (e.g., due to safety reasons, such as presence of a pacemaker, or severe claustrophobia) * Postoperative tumor plus surgical bed size exceeds 5 cm in maximum diameter
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Get notified about this study
Sign up to get updates when this study changes or when new studies for Glioblastoma are added.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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AIS Cancer Center at San Joaquin Community Hospital
Bakersfield, California, 93301, United States
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Adams Cancer Center
Gettysburg, Pennsylvania, 17325, United States
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Advocate Lutheran General Hospital
Park Ridge, Illinois, 60068, United States
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Alta Bates Summit Medical Center-Herrick Campus
Berkeley, California, 94704, United States
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Arizona Oncology Associates-West Orange Grove
Tucson, Arizona, 85704, United States
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Aspirus Regional Cancer Center
Wausau, Wisconsin, 54401, United States
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Austin Cancer Centers-Central Austin
Austin, Texas, 78702, United States
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Austin Cancer Centers-North
Austin, Texas, 78758, United States
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BCCA-Vancouver Island Cancer Centre
Victoria, British Columbia, V8R 6V5, Canada
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Banner University Medical Center - Tucson
Tucson, Arizona, 85719, United States
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Baptist MD Anderson Cancer Center
Jacksonville, Florida, 32207, United States
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Baptist Medical Center South
Jacksonville, Florida, 32258, United States
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Billings Clinic Cancer Center
Billings, Montana, 59101, United States
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Boca Raton Regional Hospital
Boca Raton, Florida, 33486, United States
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Boston Medical Center
Boston, Massachusetts, 02118, United States
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CHU de Quebec-L'Hotel-Dieu de Quebec (HDQ)
Québec, Quebec, G1R 2J6, Canada
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CHUM - Centre Hospitalier de l'Universite de Montreal
Montreal, Quebec, H2X 3E4, Canada
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California Pacific Medical Center-Pacific Campus
San Francisco, California, 94115, United States
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Capital Health Medical Center-Hopewell
Pennington, New Jersey, 08534, United States
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Case Western Reserve University
Cleveland, Ohio, 44106, United States
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Cedars Sinai Medical Center
Los Angeles, California, 90048, United States
-
Central Maryland Radiation Oncology in Howard County
Columbia, Maryland, 21044, United States
-
Central Vermont Medical Center/National Life Cancer Treatment
Berlin Corners, Vermont, 05602, United States
-
Cleveland Clinic Akron General
Akron, Ohio, 44307, United States
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Cleveland Clinic Cancer Center Independence
Independence, Ohio, 44131, United States
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Cleveland Clinic Cancer Center Strongsville
Strongsville, Ohio, 44136, United States
-
Cleveland Clinic Cancer Center/Fairview Hospital
Cleveland, Ohio, 44111, United States
-
Cleveland Clinic Foundation
Cleveland, Ohio, 44195, United States
-
Cleveland Clinic Wooster Family Health and Surgery Center
Wooster, Ohio, 44691, United States
-
Coborn Cancer Center at Saint Cloud Hospital
Saint Cloud, Minnesota, 56303, United States
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Community Cancer Center East
Indianapolis, Indiana, 46219, United States
-
Community Cancer Center North
Indianapolis, Indiana, 46256, United States
-
Community Cancer Center South
Indianapolis, Indiana, 46227, United States
-
Compass Oncology Vancouver
Vancouver, Washington, 98684, United States
-
Comprehensive Cancer Centers of Nevada
Las Vegas, Nevada, 89148, United States
-
Corewell Health Beaumont Troy Hospital
Troy, Michigan, 48085, United States
-
Corewell Health Dearborn Hospital
Dearborn, Michigan, 48124, United States
-
Corewell Health Grand Rapids Hospitals - Butterworth Hospital
Grand Rapids, Michigan, 49503, United States
-
Corewell Health Lakeland Hospitals - Saint Joseph Hospital
Saint Joseph, Michigan, 49085, United States
-
Corewell Health William Beaumont University Hospital
Royal Oak, Michigan, 48073, United States
-
Covenant Medical Center-Lakeside
Lubbock, Texas, 79410, United States
-
Dartmouth Cancer Center - North
Saint Johnsbury, Vermont, 05819, United States
-
Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center
Lebanon, New Hampshire, 03756, United States
-
Decatur Memorial Hospital
Decatur, Illinois, 62526, United States
-
Dell Seton Medical Center at The University of Texas
Austin, Texas, 78701, United States
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Eden Hospital Medical Center
Castro Valley, California, 94546, United States
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Emory Proton Therapy Center
Atlanta, Georgia, 30308, United States
-
Emory University Hospital Midtown
Atlanta, Georgia, 30308, United States
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Emory University Hospital/Winship Cancer Institute
Atlanta, Georgia, 30322, United States
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Ephrata Cancer Center
Ephrata, Pennsylvania, 17522, United States
-
FHCC Proton Therapy Center
Seattle, Washington, 98133, United States
-
FHCC at Northwest Hospital
Seattle, Washington, 98133, United States
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Fremont - Rideout Cancer Center
Marysville, California, 95901, United States
-
Fresno Cancer Center
Fresno, California, 93720, United States
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Froedtert Menomonee Falls Hospital
Menomonee Falls, Wisconsin, 53051, United States
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Geauga Hospital
Chardon, Ohio, 44024, United States
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Gundersen Lutheran Medical Center
La Crosse, Wisconsin, 54601, United States
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Hartford Hospital
Hartford, Connecticut, 06102, United States
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Henry Ford Hospital
Detroit, Michigan, 48202, United States
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Hillcrest Hospital Cancer Center
Mayfield Heights, Ohio, 44124, United States
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Huntsman Cancer Institute/University of Utah
Salt Lake City, Utah, 84112, United States
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IU Health Ball Memorial Hospital
Muncie, Indiana, 47303, United States
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IU Health Methodist Hospital
Indianapolis, Indiana, 46202, United States
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Intermountain Medical Center
Murray, Utah, 84107, United States
-
Iowa Methodist Medical Center
Des Moines, Iowa, 50309, United States
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Jefferson Torresdale Hospital
Philadelphia, Pennsylvania, 19114, United States
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John H Stroger Jr Hospital of Cook County
Chicago, Illinois, 60612, United States
-
John Muir Medical Center-Walnut Creek
Walnut Creek, California, 94598, United States
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Kaiser Permanente Cancer Treatment Center
South San Francisco, California, 94080, United States
-
Kaiser Permanente Oakland-Broadway
Oakland, California, 94611, United States
-
Kaiser Permanente-Rancho Cordova Cancer Center
Rancho Cordova, California, 95670, United States
-
Langlade Hospital and Cancer Center
Antigo, Wisconsin, 54409, United States
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Laura and Isaac Perlmutter Cancer Center at NYU Langone
New York, New York, 10016, United States
-
Legacy Good Samaritan Hospital and Medical Center
Portland, Oregon, 97210, United States
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Legacy Mount Hood Medical Center
Gresham, Oregon, 97030, United States
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Legacy Salmon Creek Hospital
Vancouver, Washington, 98686, United States
-
Lewis Cancer and Research Pavilion at Saint Joseph's/Candler
Savannah, Georgia, 31405, United States
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Logan Regional Hospital
Logan, Utah, 84321, United States
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Loma Linda University Medical Center
Loma Linda, California, 92354, United States
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Los Angeles General Medical Center
Los Angeles, California, 90033, United States
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Lowell General Hospital
Lowell, Massachusetts, 01854, United States
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M D Anderson Cancer Center
Houston, Texas, 77030, United States
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Marin General Hospital
Greenbrae, California, 94904, United States
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Maryland Proton Treatment Center
Baltimore, Maryland, 21201, United States
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Mass General/North Shore Cancer Center
Danvers, Massachusetts, 01923, United States
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Massachusetts General Hospital Cancer Center
Boston, Massachusetts, 02114, United States
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Mayo Clinic Hospital in Arizona
Phoenix, Arizona, 85054, United States
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Mayo Clinic in Arizona
Scottsdale, Arizona, 85259, United States
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Mayo Clinic in Rochester
Rochester, Minnesota, 55905, United States
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McKay-Dee Hospital Center
Ogden, Utah, 84403, United States
-
McLaren Cancer Institute-Bay City
Bay City, Michigan, 48706, United States
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McLaren Cancer Institute-Central Michigan
Mount Pleasant, Michigan, 48858, United States
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McLaren Cancer Institute-Flint
Flint, Michigan, 48532, United States
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McLaren Cancer Institute-Lapeer Region
Lapeer, Michigan, 48446, United States
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McLaren Cancer Institute-Macomb
Mount Clemens, Michigan, 48043, United States
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McLaren Cancer Institute-Northern Michigan
Petoskey, Michigan, 49770, United States
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McLaren Cancer Institute-Owosso
Owosso, Michigan, 48867, United States
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Medical College of Wisconsin
Milwaukee, Wisconsin, 53226, United States
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Medical University of South Carolina
Charleston, South Carolina, 29425, United States
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Memorial Hermann Memorial City Medical Center
Houston, Texas, 77024, United States
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Memorial Medical Center
Modesto, California, 95355, United States
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Memorial Sloan Kettering Basking Ridge
Basking Ridge, New Jersey, 07920, United States
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Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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Memorial Sloan Kettering Commack
Commack, New York, 11725, United States
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Memorial Sloan Kettering Westchester
East White Plains, New York, 10604, United States
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Mercy Cancer Center-Elyria
Elyria, Ohio, 44035, United States
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Mercy Hospital
Cedar Rapids, Iowa, 52403, United States
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Miami Cancer Institute
Miami, Florida, 33176, United States
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Mission Hospital
Asheville, North Carolina, 28801, United States
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Moffitt Cancer Center
Tampa, Florida, 33612, United States
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Montefiore Medical Center - Moses Campus
The Bronx, New York, 10467, United States
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NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center
New York, New York, 10032, United States
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New York-Presbyterian/Brooklyn Methodist Hospital
Brooklyn, New York, 11215, United States
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North Coast Cancer Care
Sandusky, Ohio, 44870, United States
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North Kansas City Hospital
Kansas City, Missouri, 64116, United States
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Northeast Radiation Oncology Center
Dunmore, Pennsylvania, 18512, United States
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Northwell Health/Center for Advanced Medicine
Lake Success, New York, 11042, United States
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Northwestern Medicine Cancer Center Delnor
Geneva, Illinois, 60134, United States
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Northwestern Medicine Cancer Center Kishwaukee
DeKalb, Illinois, 60115, United States
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Northwestern Medicine Cancer Center Warrenville
Warrenville, Illinois, 60555, United States
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Northwestern University
Chicago, Illinois, 60611, United States
-
Norton Hospital Pavilion and Medical Campus
Louisville, Kentucky, 40202, United States
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Novant Health Forsyth Medical Center
Winston-Salem, North Carolina, 27103, United States
-
OSF Saint Francis Medical Center
Peoria, Illinois, 61637, United States
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Ochsner Medical Center Jefferson
New Orleans, Louisiana, 70121, United States
-
Ohio State University Comprehensive Cancer Center
Columbus, Ohio, 43210, United States
-
Ottawa Hospital and Cancer Center-General Campus
Ottawa, Ontario, K1H 8L6, Canada
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Palo Alto Medical Foundation Health Care
Palo Alto, California, 94301, United States
-
Palo Alto Medical Foundation-Santa Cruz
Santa Cruz, California, 95065, United States
-
Palo Alto Medical Foundation-Sunnyvale
Sunnyvale, California, 94086, United States
-
Parkview Hospital Randallia
Fort Wayne, Indiana, 46805, United States
-
Parkview Regional Medical Center
Fort Wayne, Indiana, 46845, United States
-
Pomona Valley Hospital Medical Center
Pomona, California, 91767, United States
-
Poudre Valley Hospital
Fort Collins, Colorado, 80524, United States
-
Prisma Health Cancer Institute - Eastside
Greenville, South Carolina, 29615, United States
-
Prisma Health Cancer Institute - Faris
Greenville, South Carolina, 29605, United States
-
Prisma Health Cancer Institute - Greer
Greer, South Carolina, 29650, United States
-
Prisma Health Cancer Institute - Seneca
Seneca, South Carolina, 29672, United States
-
Prisma Health Cancer Institute - Spartanburg
Boiling Springs, South Carolina, 29316, United States
-
ProCure Proton Therapy Center-Somerset
Somerset, New Jersey, 08873, United States
-
Radiation Oncology Associates PC
Fort Wayne, Indiana, 46804, United States
-
Reading Hospital
West Reading, Pennsylvania, 19611, United States
-
Regions Hospital
Saint Paul, Minnesota, 55101, United States
-
Renown Regional Medical Center
Reno, Nevada, 89502, United States
-
Riverside Methodist Hospital
Columbus, Ohio, 43214, United States
-
Rohnert Park Cancer Center
Rohnert Park, California, 94928, United States
-
Rush MD Anderson Cancer Center
Chicago, Illinois, 60612, United States
-
Rutgers Cancer Institute of New Jersey
New Brunswick, New Jersey, 08903, United States
-
Rutgers Cancer Institute of New Jersey-Robert Wood Johnson University Hospital
New Brunswick, New Jersey, 08903, United States
-
Saint Alphonsus Cancer Care Center-Boise
Boise, Idaho, 83706, United States
-
Saint George Regional Medical Center
St. George, Utah, 84770, United States
-
Saint Joseph Hospital - Orange
Orange, California, 92868, United States
-
Saint Joseph's Hospital and Medical Center
Phoenix, Arizona, 85013, United States
-
Saint Luke's Hospital of Duluth
Duluth, Minnesota, 55805, United States
-
Saint Luke's University Hospital-Bethlehem Campus
Bethlehem, Pennsylvania, 18015, United States
-
Saint Mary's Regional Medical Center
Reno, Nevada, 89503, United States
-
Sanford Bismarck Medical Center
Bismarck, North Dakota, 58501, United States
-
Sanford Joe Lueken Cancer Center
Bemidji, Minnesota, 56601, United States
-
Sanford Roger Maris Cancer Center
Fargo, North Dakota, 58122, United States
-
Sanford USD Medical Center - Sioux Falls
Sioux Falls, South Dakota, 57117-5134, United States
-
Saskatoon Cancer Centre
Saskatoon, Saskatchewan, S7N 4H4, Canada
-
Sechler Family Cancer Center
Lebanon, Pennsylvania, 17042, United States
-
Self Regional Healthcare
Greenwood, South Carolina, 29646, United States
-
South Sacramento Cancer Center
Sacramento, California, 95823, United States
-
Springfield Memorial Hospital
Springfield, Illinois, 62781, United States
-
Sutter Cancer Centers Radiation Oncology Services-Auburn
Auburn, California, 95603, United States
-
Sutter Cancer Centers Radiation Oncology Services-Cameron Park
Cameron Park, California, 95682, United States
-
Sutter Cancer Centers Radiation Oncology Services-Roseville
Roseville, California, 95661, United States
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Sutter Medical Center Sacramento
Sacramento, California, 95816, United States
-
Tennessee Cancer Specialists-Dowell Springs
Knoxville, Tennessee, 37909, United States
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Texas Oncology - Central Austin Cancer Center
Austin, Texas, 78731, United States
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Texas Oncology - Denison Cancer Center
Denison, Texas, 75020, United States
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Texas Oncology - Fort Worth Cancer Center
Fort Worth, Texas, 76104, United States
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Texas Oncology - Round Rock Cancer Center
Round Rock, Texas, 78681, United States
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Texas Oncology - South Austin Cancer Center
Austin, Texas, 78745, United States
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Texas Oncology - Tyler
Tyler, Texas, 75702, United States
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Texas Oncology Cancer Center Sugar Land
Sugar Land, Texas, 77479, United States
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Texas Oncology-Austin Midtown
Austin, Texas, 78705, United States
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Texas Oncology-Flower Mound
Flower Mound, Texas, 75028, United States
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Texas Oncology-Seton Williamson
Round Rock, Texas, 78665, United States
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The Permanente Medical Group-Roseville Radiation Oncology
Roseville, California, 95678, United States
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The Research Institute of the McGill University Health Centre (MUHC)
Montreal, Quebec, H3H 2R9, Canada
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Thomas Jefferson University Hospital
Philadelphia, Pennsylvania, 19107, United States
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Trinity Health Grand Rapids Hospital
Grand Rapids, Michigan, 49503, United States
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Trinity Health Saint Joseph Mercy Hospital Ann Arbor
Ann Arbor, Michigan, 48106, United States
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Trinity Health Saint Joseph Mercy Oakland Hospital
Pontiac, Michigan, 48341, United States
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Trinity Health Saint Mary Mercy Livonia Hospital
Livonia, Michigan, 48154, United States
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Tufts Medical Center
Boston, Massachusetts, 02111, United States
-
UC Comprehensive Cancer Center at Silver Cross
New Lenox, Illinois, 60451, United States
-
UC Irvine Health/Chao Family Comprehensive Cancer Center
Orange, California, 92868, United States
-
UCHealth Memorial Hospital Central
Colorado Springs, Colorado, 80909, United States
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UF Health Cancer Institute - Gainesville
Gainesville, Florida, 32610, United States
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UH Seidman Cancer Center at Firelands Regional Medical Center
Sandusky, Ohio, 44870, United States
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UH Seidman Cancer Center at Lake Health Mentor Campus
Mentor, Ohio, 44060, United States
-
UH Seidman Cancer Center at Southwest General Hospital
Middleburg Heights, Ohio, 44130, United States
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UHHS-Chagrin Highlands Medical Center
Beachwood, Ohio, 44122, United States
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UHHS-Westlake Medical Center
Westlake, Ohio, 44145, United States
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UM Baltimore Washington Medical Center/Tate Cancer Center
Glen Burnie, Maryland, 21061, United States
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UM Upper Chesapeake Medical Center
Bel Air, Maryland, 21014, United States
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UPMC Pinnacle Cancer Center/Community Osteopathic Campus
Harrisburg, Pennsylvania, 17109, United States
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USC / Norris Comprehensive Cancer Center
Los Angeles, California, 90033, United States
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UT Southwestern/Simmons Cancer Center-Dallas
Dallas, Texas, 75390, United States
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UTMB Cancer Center at Victory Lakes
League City, Texas, 77573, United States
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UW Cancer Center at ProHealth Care
Waukesha, Wisconsin, 53188, United States
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University Hospitals Parma Medical Center
Parma, Ohio, 44129, United States
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University of Alabama at Birmingham Cancer Center
Birmingham, Alabama, 35233, United States
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University of Arkansas for Medical Sciences
Little Rock, Arkansas, 72205, United States
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University of California Davis Comprehensive Cancer Center
Sacramento, California, 95817, United States
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University of Chicago Comprehensive Cancer Center
Chicago, Illinois, 60637, United States
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University of Cincinnati Cancer Center-UC Medical Center
Cincinnati, Ohio, 45219, United States
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University of Cincinnati Cancer Center-West Chester
West Chester, Ohio, 45069, United States
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University of Florida Health Science Center - Jacksonville
Jacksonville, Florida, 32209, United States
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University of Kansas Cancer Center
Kansas City, Kansas, 66160, United States
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University of Kansas Cancer Center - North
Kansas City, Missouri, 64154, United States
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University of Kansas Cancer Center-Overland Park
Overland Park, Kansas, 66210, United States
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University of Maryland/Greenebaum Cancer Center
Baltimore, Maryland, 21201, United States
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University of Michigan Rogel Cancer Center
Ann Arbor, Michigan, 48109, United States
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University of Mississippi Medical Center
Jackson, Mississippi, 39216, United States
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University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, 73104, United States
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University of Pennsylvania/Abramson Cancer Center
Philadelphia, Pennsylvania, 19104, United States
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University of Texas Health Science Center at San Antonio
San Antonio, Texas, 78229, United States
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University of Texas Medical Branch
Galveston, Texas, 77555-0565, United States
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University of Toledo
Toledo, Ohio, 43614, United States
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University of Vermont Medical Center
Burlington, Vermont, 05401, United States
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University of Washington Medical Center - Montlake
Seattle, Washington, 98195, United States
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University of Wisconsin Carbone Cancer Center - University Hospital
Madison, Wisconsin, 53792, United States
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Utah Valley Regional Medical Center
Provo, Utah, 84604, United States
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VCU Massey Comprehensive Cancer Center
Richmond, Virginia, 23298, United States
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Virtua Voorhees
Voorhees Township, New Jersey, 08043, United States
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Wake Forest University Health Sciences
Winston-Salem, North Carolina, 27157, United States
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Washington University School of Medicine
St Louis, Missouri, 63110, United States
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WellSpan Health-York Cancer Center
York, Pennsylvania, 17403, United States
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West Michigan Cancer Center
Kalamazoo, Michigan, 49007, United States
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Wheeling Hospital/Schiffler Cancer Center
Wheeling, West Virginia, 26003, United States
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Willamette Valley Cancer Center
Eugene, Oregon, 97401, United States
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Willis-Knighton Medical and Cancer Center
Shreveport, Louisiana, 71103, United States
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Windsor Regional Cancer Centre
Windsor, Ontario, N8W 2X3, Canada
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Other studies related to the condition(s) this trial covers.
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- Can repeated MRI scans reveal how tumors respond to radiation?