New drug cocktail aims to boost mesothelioma surgery success
NCT ID NCT03228537
First seen Jun 27, 2026 · Last updated Aug 05, 2026 · Updated 4 times
Summary
This early-phase trial is testing whether adding the immunotherapy drug atezolizumab to standard chemotherapy (cisplatin and pemetrexed) before and after surgery can help people with resectable pleural mesothelioma. The study includes 28 participants with stage I-III disease. The main goals are to see if the treatment plan is feasible and safe, not yet to prove it works better than existing options.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- atezolizumab (immunotherapy) plus cisplatin and pemetrexed (chemotherapy)
- What this could lead to
- If this approach works, it could improve outcomes for people with resectable mesothelioma by shrinking tumors before surgery and clearing remaining cancer cells afterward.
- What could go wrong
- This is a very early, small phase 1 trial focused on feasibility and safety, not effectiveness. The combination may cause serious immune-related side effects, and results may not apply to all mesothelioma types.
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
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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28 people
The number who actually took part.
- Started
-
Jul 2018
- Expected to finish
-
Sep 2026
An estimate. End dates often move.
- Lead sponsor
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A government research agency
The lead sponsor is the US National Institutes of Health.
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: * STEP 1: NEOADJUVANT * Patient must have stage I-III malignant pleural mesothelioma that is deemed resectable and must be planning to undergo pleurectomy decortication (P/D) or extrapleural pneumonectomy (EPP) * Patient must have epithelioid or biphasic histology (sarcomatoid histology is excluded); histologic diagnosis and typing of mesothelioma requires at least a core needle biopsy or surgical biopsy of the pleura via thoracoscopy and small thoracotomy; cytology only will not be regarded as sufficient for the diagnosis * Patient must have computed tomography (CT) chest/abdomen/pelvis with contrast or fludeoxyglucose F-18 (FDG)-positron emission tomography (PET)/CT scan performed within 28 days prior to step 1 registration * Patients must have non-measurable or measurable disease documented by CT or magnetic resonance imaging (MRI); the CT from a combined PET/CT may be used to document only non-measurable disease unless it is of diagnostic quality; measurable disease must be assessed within 28 days prior to step 1 registration; non-measurable disease must be assessed within 42 days prior to step 1 registration; all disease must be assessed and documented on the RECIST 1.1 and modified RECIST baseline tumor assessment form * Patient must have undergone extended surgical staging including mediastinoscopy or endobronchial ultrasound; at minimum, samples must be obtained from the mediastinal stations 4R, 7 (subcarinal), and 4L; this surgical staging must be performed within 42 days prior to step 1 registration; patient must be T1-3 and N0-N2 (single station) * Patient must undergo video-assisted thoracoscopic surgery and diagnostic laparoscopy within 28 days prior to step 1 registration to rule out peritoneal disease spread * Patient must have consultation with a surgeon within 21 days prior to step 1 registration; the surgeon must confirm that the patient's disease is resectable by pleurectomy decortication (P/D) or extrapleural pneumonectomy (EPP) and that the patient is an appropriate candidate for the surgical procedures * Patient must not have had prior immunotherapy or chemotherapy for malignant pleural mesothelioma * Patient must have Zubrod performance status 0 or 1 documented within 28 days prior to step 1 registration * Patients requiring hearing aids or reporting hearing loss must have audiogram performed within 28 days prior to step 1 registration * Patient must have not had any major surgery or radiation within 28 days prior to step 1 registration; diagnostic thoracotomies and laparoscopies are not considered major surgeries * Patients must not have any anticancer therapy or investigational agent within 28 days prior to step 1 registration * Absolute neutrophil count (ANC) \>= 1,500/mcl (documented within 28 days prior to step 1 registration) * Hemoglobin \>= 9 g/dl (documented within 28 days prior to step 1 registration) * Platelets \>= 100,000/mcl (documented within 28 days prior to step 1 registration) * Creatinine =\< 1.5 x upper limit of normal (ULN) (documented within 28 days prior to step 1 registration) * Creatinine clearance \>= 45 ml/min (documented within 28 days prior to step 1 registration) * Total bilirubin =\< 1.5 x upper limit of normal (ULN) (within 28 days prior to step 1 registration) * Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =\< 3 x ULN (within 28 days prior to step 1 registration) * No other prior malignancy is allowed except for the following: adequately treated basal cell or squamous cell skin cancer, in situ cervical cancer, adequately treated stage I or II cancer from which the patient is currently in complete remission, or any other cancer from which the patient has been disease free for three years * Patients must not be pregnant or nursing due to the potential teratogenic side effects of the protocol treatment; women of reproductive potential and men must have agreed to use an effective contraceptive method for the duration of study treatment and for 5 months (150 days) after the last dose of atezolizumab; a woman is considered to be of "reproductive potential" if she has had menses at any time in the preceding 12 consecutive months; in addition to routine contraceptive methods, "effective contraception" also includes heterosexual celibacy and surgery intended to prevent pregnancy (or with a side effect of pregnancy prevention) defined as a hysterectomy, bilateral oophorectomy or bilateral tubal ligation; however, if at any point a previously celibate patient chooses to become heterosexually active during the time period for use of contraceptive measures outlined in the protocol, he/she is responsible for beginning contraceptive measures * Patient must NOT have a history of severe allergic, anaphylactic, or other hypersensitivity reactions to chimeric or humanized antibodies or fusion proteins * Patient must NOT have a known hypersensitivity or allergy to biopharmaceuticals produced in Chinese hamster ovary cells or any component of the atezolizumab formulation * Patients must not have severe infections within 28 days prior to step 1 registration, including but not limited to hospitalization for complications of infection, bacteremia, or severe pneumonia * Patients must not have active autoimmune disease that has required systemic treatment in past two years (i.e., with use of disease modifying agents, corticosteroids or immunosuppressive drugs); replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment; autoimmune diseases include, but are not limited to, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, vascular thrombosis associated with antiphospholipid syndrome, Wegener's granulomatosis, Sjogren's syndrome, Bell's palsy, Guillain-Barre syndrome, multiple sclerosis, autoimmune thyroid disease, vasculitis, or glomerulonephritis; this protocol includes an immunotherapy agent which can precipitate known autoimmune diseases * Patients must not have undergone prior allogeneic bone marrow transplantation or prior solid organ transplantation * Patient must not have active tuberculosis * Patient must not have history of idiopathic pulmonary fibrosis, pneumonitis (including drug induced), organizing pneumonia (i.e., bronchiolitis obliterans, cryptogenic organizing pneumonia, etc.), or evidence of active pneumonitis; this protocol includes an immunotherapy agent which can precipitate known pneumonitis * Patient must not have active (chronic or acute) hepatitis B virus (HBV) infection as evidenced by testing performed within 28 days prior to registration; patients with past or resolved HBV infection are eligible; active HBV is defined as having a positive hepatitis B surface antigen (HBsAg) test; past or resolved HBV is defined as having a negative HBsAG test and a positive total hepatitis B core antibody (HBcAb) test; patient must not have active hepatitis C virus (HCV) infection as evidenced by testing performed within 28 days prior to registration; active HCV is defined as having a positive HCV antibody test followed by a positive HCV RNA test * Patient must NOT have a known positive test for human immunodeficiency virus (HIV); patients do not need to be screened for HIV; patients with HIV are excluded due to a potential incompetent immune system and need for medications that could interfere with the treatment and immunotherapy * Patient must not have significant cardiovascular disease, such as New York Heart Association cardiac disease (class II or greater), myocardial infarction within 3 months prior to initiation of treatment, unstable arrhythmias, or unstable angina given the higher risks associated with surgical resection * Patient must not receive live, attenuated influenza vaccine within 4 weeks prior to registration or at any time during the study and until 5 months after the last dose of atezolizumab * Patient must be willing to have tissue specimens submitted for translational medicine studies * Patient must be offered the opportunity to participate in tissue and blood banking for future studies * Patient must be informed of the investigational nature of this study and must sign and give written informed consent in accordance with institutional and federal guidelines * 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 2: SURGERY * Patient must have a CT of chest/abdomen with contrast or FDG-PET/CT scan within 28 days prior to step 2 registration; patients must not have evidence of progression per RECIST 1.1 or modified RECIST for pleural tumors * Patients planning to receive EPP must also be evaluated for appropriateness of radiation therapy (RT) by a radiation oncologist within 14 days prior to step 2 registration * Patients must have a Zubrod performance status of 0-1 documented within 28 days prior to step 2 registration * Patients must have postoperative predicted forced expiratory volume in 1 second (FEV1) \> 35% prior to surgery obtained within 28 days prior to step 2 registration; pulmonary function tests to ascertain these values must be obtained within 28 days prior to Step 2 registration * Patients must have postoperative predicted carbon monoxide diffusing capability (DLCO) \> 35% prior to surgery obtained within 28 days prior to step 2 registration; pulmonary function tests to ascertain these values must be obtained within 28 days prior to Step 2 registration * Patient must have received at least two cycles of triplet neoadjuvant therapy (all three drugs) during step 1 * Patient must be registered to step 2 no less than 21 days and no more than 90 days after the end of their final cycle of neoadjuvant therapy * STEP 3: MAINTENANCE * Patient must have received either P/D or EPP and must have recovered from all effects of surgery with adequate wound healing; patients who received radiation therapy (RT) must be registered to step 3 within 90 days after discontinuing RT; patients who did not receive RT must be registered to step 3 within 90 days after surgery * Patient must have a CT of chest/abdomen/pelvis with contrast or FDG-PET/CT scan within 28 days prior to step 3 registration; patient must not have evidence of progression per RECIST 1.1 or modified RECIST for pleural tumors * Patient may have discontinued RT early due to toxicity or other reasons * Patients must have a Zubrod performance status of 0-1 documented within 28 days prior to step 3 registration * ANC \> 1,500/mcl (documented within 28 days prior to step 3 registration) * Hemoglobin \> 9 g/dl (documented within 28 days prior to step 3 registration) * Platelets \> 100,000/mcl (documented within 28 days prior to step 3 registration) * Creatinine \< 1.5 x ULN (documented within 28 days prior to step 3 registration) * Total bilirubin =\< 1.5 x upper limit of normal (ULN) (within 28 days prior to step 3 registration) * Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =\< 3 x ULN (within 28 days prior to step 3 registration)
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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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AdventHealth Littleton
Littleton, Colorado, 80122, United States
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AdventHealth Parker
Parker, Colorado, 80138, United States
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AdventHealth Porter
Denver, Colorado, 80210, United States
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Alegent Health Bergan Mercy Medical Center
Omaha, Nebraska, 68124, United States
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Alegent Health Immanuel Medical Center
Omaha, Nebraska, 68122, United States
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Alegent Health Lakeside Hospital
Omaha, Nebraska, 68130, United States
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Alegent Health Mercy Hospital
Council Bluffs, Iowa, 51503, United States
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Allegiance Health
Jackson, Michigan, 49201, United States
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Alliance for Childhood Diseases/Cure 4 the Kids Foundation
Las Vegas, Nevada, 89135, United States
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Ascension Via Christi Hospitals Wichita
Wichita, Kansas, 67214, United States
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Baptist MD Anderson Cancer Center
Jacksonville, Florida, 32207, United States
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Benefis Sletten Cancer Institute
Great Falls, Montana, 59405, United States
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Bethesda North Hospital
Cincinnati, Ohio, 45242, United States
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Billings Clinic Cancer Center
Billings, Montana, 59101, United States
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Billings Clinic-Cody
Cody, Wyoming, 82414, United States
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Bozeman Health Deaconess Hospital
Bozeman, Montana, 59715, United States
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CHI Health Good Samaritan
Kearney, Nebraska, 68847, United States
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CHI Saint Vincent Cancer Center Hot Springs
Hot Springs, Arkansas, 71913, United States
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Cancer Care Center of O'Fallon
O'Fallon, Illinois, 62269, United States
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Cancer Care Specialists of Illinois - Decatur
Decatur, Illinois, 62526, United States
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Cancer Center of Kansas - Wichita
Wichita, Kansas, 67214, United States
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Cancer Center of Kansas-Wichita Medical Arts Tower
Wichita, Kansas, 67208, United States
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Cancer Centers of Southwest Oklahoma Research
Lawton, Oklahoma, 73505, United States
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Carle Cancer Center
Urbana, Illinois, 61801, United States
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Carle Physician Group-Effingham
Effingham, Illinois, 62401, United States
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Carle Physician Group-Mattoon/Charleston
Mattoon, Illinois, 61938, United States
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Carle at The Riverfront
Danville, Illinois, 61832, United States
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Centralia Oncology Clinic
Centralia, Illinois, 62801, United States
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City of Hope Comprehensive Cancer Center
Duarte, California, 91010, United States
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CommonSpirit Cancer Center Mercy
Durango, Colorado, 81301, United States
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CommonSpirit Saint Anthony Hospital Cancer Center
Lakewood, Colorado, 80228, United States
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CommonSpirit Saint Joseph Hospital - Bardstown
Bardstown, Kentucky, 40004, United States
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CommonSpirit Saint Joseph Hospital London
London, Kentucky, 40741, United States
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CommonSpirit Saint Joseph Medical Center - East Lexington
Lexington, Kentucky, 40509, United States
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Commonwealth Cancer Center-Corbin
Corbin, Kentucky, 40701, United States
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Community Hospital of Anaconda
Anaconda, Montana, 59711, United States
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Community Medical Center
Missoula, Montana, 59804, United States
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Comprehensive Cancer Centers of Nevada
Las Vegas, Nevada, 89148, United States
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Comprehensive Cancer Centers of Nevada - Central Valley
Las Vegas, Nevada, 89169, United States
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Comprehensive Cancer Centers of Nevada - Henderson
Henderson, Nevada, 89052, United States
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Comprehensive Cancer Centers of Nevada - Northwest
Las Vegas, Nevada, 89128, United States
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Comprehensive Cancer Centers of Nevada-Summerlin
Las Vegas, Nevada, 89144, United States
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Crossroads Cancer Center
Effingham, Illinois, 62401, United States
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Decatur Memorial Hospital
Decatur, Illinois, 62526, United States
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Franciscan Research Center-Northwest Medical Plaza
Tacoma, Washington, 98405, United States
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Fred Hutchinson Cancer Center
Seattle, Washington, 98109, United States
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Fred and Pamela Buffett Cancer Center - Kearney
Kearney, Nebraska, 68845, United States
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Good Samaritan Hospital - Cincinnati
Cincinnati, Ohio, 45220, United States
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Great Falls Clinic
Great Falls, Montana, 59405, United States
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Greater Regional Medical Center
Creston, Iowa, 50801, United States
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Harrison HealthPartners Hematology and Oncology-Poulsbo
Poulsbo, Washington, 98370, United States
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Hematology and Oncology Consultants PC
Omaha, Nebraska, 68122, United States
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Henry Ford Cancer Institute-Downriver
Brownstown, Michigan, 48183, United States
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Henry Ford Hospital
Detroit, Michigan, 48202, United States
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Henry Ford Macomb Health Center - Shelby Township
Shelby, Michigan, 48315, United States
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Henry Ford Macomb Hospital-Clinton Township
Clinton Township, Michigan, 48038, United States
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Henry Ford West Bloomfield Hospital
West Bloomfield, Michigan, 48322, United States
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Highline Medical Center-Main Campus
Burien, Washington, 98166, United States
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Idaho Urologic Institute-Meridian
Meridian, Idaho, 83642, United States
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Illinois CancerCare-Bloomington
Bloomington, Illinois, 61704, United States
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Illinois CancerCare-Canton
Canton, Illinois, 61520, United States
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Illinois CancerCare-Carthage
Carthage, Illinois, 62321, United States
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Illinois CancerCare-Eureka
Eureka, Illinois, 61530, United States
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Illinois CancerCare-Galesburg
Galesburg, Illinois, 61401, United States
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Illinois CancerCare-Kewanee Clinic
Kewanee, Illinois, 61443, United States
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Illinois CancerCare-Macomb
Macomb, Illinois, 61455, United States
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Illinois CancerCare-Ottawa Clinic
Ottawa, Illinois, 61350, United States
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Illinois CancerCare-Pekin
Pekin, Illinois, 61554, United States
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Illinois CancerCare-Peoria
Peoria, Illinois, 61615, United States
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Illinois CancerCare-Peru
Peru, Illinois, 61354, United States
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Illinois CancerCare-Princeton
Princeton, Illinois, 61356, United States
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Jewish Hospital
Louisville, Kentucky, 40202, United States
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Jewish Hospital Medical Center South
Shepherdsville, Kentucky, 40165, United States
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Kootenai Clinic Cancer Services - Post Falls
Post Falls, Idaho, 83854, United States
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Kootenai Clinic Cancer Services - Sandpoint
Sandpoint, Idaho, 83864, United States
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Kootenai Health - Coeur d'Alene
Coeur d'Alene, Idaho, 83814, United States
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Lawrence Memorial Hospital
Lawrence, Kansas, 66044, United States
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Logan Health Medical Center
Kalispell, Montana, 59901, United States
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Longmont United Hospital
Longmont, Colorado, 80501, United States
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Lyndon Baines Johnson General Hospital
Houston, Texas, 77026-1967, United States
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MU Health Care Goldschmidt Cancer Center
Jefferson City, Missouri, 65109, United States
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Mary Greeley Medical Center
Ames, Iowa, 50010, 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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McFarland Clinic - Ames
Ames, Iowa, 50010, United States
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McFarland Clinic - Boone
Boone, Iowa, 50036, United States
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McFarland Clinic - Jefferson
Jefferson, Iowa, 50129, United States
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McFarland Clinic - Marshalltown
Marshalltown, Iowa, 50158, United States
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McFarland Clinic - Trinity Cancer Center
Fort Dodge, Iowa, 50501, United States
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Medical University of South Carolina
Charleston, South Carolina, 29425, United States
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Memorial GYN Plus
Ooltewah, Tennessee, 37363, United States
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Memorial Hospital
Chattanooga, Tennessee, 37404, United States
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Memorial Hospital of Carbondale
Carbondale, Illinois, 62902, United States
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Mercy Cancer Center - Cape Girardeau
Cape Girardeau, Missouri, 63703, United States
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Mercy Cancer Center-West Lakes
Clive, Iowa, 50325, United States
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Mercy Medical Center
Durango, Colorado, 81301, United States
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Mercy Medical Center - Des Moines
Des Moines, Iowa, 50314, United States
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Mercy Medical Center-West Lakes
West Des Moines, Iowa, 50266, United States
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Methodist Medical Center of Illinois
Peoria, Illinois, 61636, United States
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Midlands Community Hospital
Papillion, Nebraska, 68046, United States
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Missouri Baptist Medical Center
St Louis, Missouri, 63131, United States
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Missouri Baptist Sullivan Hospital
Sullivan, Missouri, 63080, United States
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Mountain Blue Cancer Care Center
Golden, Colorado, 80401, United States
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Nebraska Cancer Specialists/Oncology Hematology West PC
Grand Island, Nebraska, 68803, United States
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Northwest Medical Specialties PLLC
Tacoma, Washington, 98405, United States
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OSF Saint Francis Medical Center
Peoria, Illinois, 61637, United States
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OSF Saint Francis Radiation Oncology at Pekin
Pekin, Illinois, 61554, United States
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OSF Saint Francis Radiation Oncology at Peoria Cancer Center
Peoria, Illinois, 61615, United States
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Ochsner Medical Center Jefferson
New Orleans, Louisiana, 70121, United States
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Oncology Las Vegas - Henderson
Henderson, Nevada, 89074, United States
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OptumCare Cancer Care at Charleston
Las Vegas, Nevada, 89102, United States
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OptumCare Cancer Care at Fort Apache
Las Vegas, Nevada, 89183, United States
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OptumCare Cancer Care at MountainView
Las Vegas, Nevada, 89128, United States
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Overlake Medical Center
Bellevue, Washington, 98004, United States
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PCR Oncology
Arroyo Grande, California, 93420, United States
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Parkland Health Center-Bonne Terre
Bonne Terre, Missouri, 63628, United States
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Penrose-Saint Francis Healthcare
Colorado Springs, Colorado, 80907, United States
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Pulmonary Medicine Center of Chattanooga-Hixson
Hixson, Tennessee, 37343, United States
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Radiation Oncology Associates
Reno, Nevada, 89509, United States
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Radiation Oncology Centers of Nevada Central
Las Vegas, Nevada, 89106, United States
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Radiation Oncology Centers of Nevada Southeast
Las Vegas, Nevada, 89119, United States
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Renown Regional Medical Center
Reno, Nevada, 89502, United States
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Rocky Mountain Cancer Centers - Pueblo
Pueblo, Colorado, 81008, United States
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Rocky Mountain Cancer Centers-Lakewood
Lakewood, Colorado, 80228, United States
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Rocky Mountain Cancer Centers-Longmont
Longmont, Colorado, 80501, United States
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Rocky Mountain Cancer Centers-Parker
Parker, Colorado, 80138, United States
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Rocky Mountain Cancer Centers-Penrose
Colorado Springs, Colorado, 80907, United States
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Rocky Mountain Cancer Centers-Thornton
Thornton, Colorado, 80260, United States
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Rush-Copley Healthcare Center
Yorkville, Illinois, 60560, United States
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Rush-Copley Medical Center
Aurora, Illinois, 60504, United States
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SIH Cancer Institute
Carterville, Illinois, 62918, United States
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Saint Alphonsus Cancer Care Center-Boise
Boise, Idaho, 83706, United States
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Saint Alphonsus Cancer Care Center-Caldwell
Caldwell, Idaho, 83605, United States
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Saint Alphonsus Cancer Care Center-Nampa
Nampa, Idaho, 83687, United States
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Saint Clare Hospital
Lakewood, Washington, 98499, United States
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Saint Elizabeth Hospital
Enumclaw, Washington, 98022, United States
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Saint Elizabeth Regional Medical Center
Lincoln, Nebraska, 68510, United States
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Saint Francis Hospital
Federal Way, Washington, 98003, United States
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Saint Francis Medical Center
Cape Girardeau, Missouri, 63703, United States
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Saint Joseph Medical Center Hematology and Oncology - Silverdale
Silverdale, Washington, 98383, United States
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Saint Joseph Radiation Oncology Resource Center
Lexington, Kentucky, 40504, United States
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Saint Joseph Regional Cancer Center
Bryan, Texas, 77802, United States
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Saint Mary Corwin Medical Center
Pueblo, Colorado, 81004, United States
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Saint Mary's Regional Medical Center
Reno, Nevada, 89503, United States
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Saint Peter's Community Hospital
Helena, Montana, 59601, United States
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Sainte Genevieve County Memorial Hospital
Sainte Genevieve, Missouri, 63670, United States
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Saints Mary and Elizabeth Hospital
Louisville, Kentucky, 40215, United States
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Southern Illinois University School of Medicine
Springfield, Illinois, 62702, United States
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Southwest Illinois Health Services LLP
Swansea, Illinois, 62226, United States
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Springfield Clinic
Springfield, Illinois, 62702, United States
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Springfield Memorial Hospital
Springfield, Illinois, 62781, United States
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The Carle Foundation Hospital
Urbana, Illinois, 61801, United States
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TriHealth Cancer Institute-Anderson
Cincinnati, Ohio, 45255, United States
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TriHealth Cancer Institute-Westside
Cincinnati, Ohio, 45247, United States
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UI Health Care Mission Cancer and Blood - Laurel Clinic
Des Moines, Iowa, 50314, United States
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UI Health Care Mission Cancer and Blood - West Des Moines Clinic
Clive, Iowa, 50325, United States
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UPMC Hillman Cancer Center
Pittsburgh, Pennsylvania, 15232, United States
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UT MD Anderson - League City
League City, Texas, 77573, United States
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UT MD Anderson - Sugar Land
Sugar Land, Texas, 77478, United States
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UT MD Anderson - The Woodlands
Conroe, Texas, 77384, United States
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UT MD Anderson - West Houston
Houston, Texas, 77079, United States
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UT MD Anderson Cancer Center
Houston, Texas, 77030, United States
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UT Southwestern Clinical Center at Richardson/Plano
Richardson, Texas, 75080, United States
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UT Southwestern/Simmons Cancer Center-Dallas
Dallas, Texas, 75390, United States
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University of California Davis Comprehensive Cancer Center
Sacramento, California, 95817, United States
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University of Oklahoma Health Sciences Center
Oklahoma City, Oklahoma, 73104, United States
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University of Virginia Cancer Center
Charlottesville, Virginia, 22908, United States
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University of Washington Medical Center - Montlake
Seattle, Washington, 98195, United States
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UofL Health Medical Center Northeast
Louisville, Kentucky, 40245, United States
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Valley Medical Center
Renton, Washington, 98055, United States
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Valley Radiation Oncology
Peru, Illinois, 61354, United States
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Welch Cancer Center
Sheridan, Wyoming, 82801, United States
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Western Illinois Cancer Treatment Center
Galesburg, Illinois, 61401, United States
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