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NCT04799275Active, not recruitingPhase 2/3

Testing CC-486 (Oral Azacitidine) Plus the Standard Drug Therapy in Patients 75 Years or Older With Newly Diagnosed Diffuse Large B Cell Lymphoma

A Phase II/III Randomized Study of R-MiniCHOP With or Without CC-486 (Oral Azacitidine) in Participants Age 75 Years or Older With Newly Diagnosed Diffuse Large B Cell Lymphoma, Grade IIIB Follicular Lymphoma, Transformed Lymphoma, and High-Grade B-Cell Lymphomas With MYC AND BCL2 and/or BCL6 Rearrangements

Source: ClinicalTrials.gov · Last updated 27 Oct 2026

Brief summary (registry, in English)

This phase II/III trial compares the side effects and activity of oral azacitidine in combination with the standard drug therapy (reduced dose rituximab-cyclophosphamide, doxorubicin, vincristine, and prednisone \[R-miniCHOP\]) versus R-miniCHOP alone in treating patients 75 years or older with newly diagnosed diffuse large B cell lymphoma. R-miniCHOP includes a monoclonal antibody (a type of protein), called rituximab, which attaches to the lymphoma cells and may help the immune system kill these cells. R-miniCHOP also includes prednisone which is an anti-inflammatory medication and a combination of 3 chemotherapy drugs, cyclophosphamide, doxorubicin, and vincristine. These 3 chemotherapy drugs, as well as oral azacitidine, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Combining oral azacitidine with R-miniCHOP may shrink the cancer or extend the time without disease symptoms coming back or extend patient's survival when compared to R-miniCHOP alone.

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
422 (estimated)
First submitted
13 Mar 2021
Start date
20 May 2021
Primary completion date
1 Mar 2027
Lead sponsor
National Cancer Institute (NCI)
NCT number
NCT04799275

What you commit to

  • Study type: Interventional · Phase 2/3
  • Planned participants: 422
  • From 20 May 2021 to the primary completion date, 1 Mar 2027
  • 176 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

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

Who cannot take part

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

Who the study is looking for

  • Participants must have histologically or cytologically confirmed diffuse large B-cell lymphoma (DLBCL), Ann Arbor Stage IIX (bulky), III or IV. Participants with DLBCL transformed from follicular lymphoma (FL) or marginal zone lymphoma (MZL, including mucosa-associated lymphoid tissue \[MALT\] lymphomas), lymphoplasmacytic lymphoma (LPL), or nodular lymphocyte-predominant Hodgkin Lymphoma (NLPHL) are eligible. Participants with Grade IIIB follicular lymphoma (FL) or high-grade B-cell lymphomas with MYC and BCL2 and/or BCL6 rearrangements are also eligible. Participants with DLBCL that arose from prior CLL (Richter's transformation) are not eligible.
  • As defined by the World Health Organization (WHO), eligible lymphoma subtypes include the following:
    • DLBCL, not otherwise specified (NOS)
    • DLBCL, germinal-center B-cell type (GCB)
    • DLBCL, activated B-cell type (ABC)
    • T-cell histiocyte-rich B-cell lymphomas (THRBCL)
    • Primary cutaneous DLBCL, leg type
    • Intravascular large B cell lymphoma
    • EBV+ DLBCL, NOS
    • DLBCL associated with chronic inflammation
    • HHV8+ DLBCL, NOS
    • High-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements
    • High grade B-cell lymphoma, NOS
    • Follicular lymphoma grade 3b
  • Participants must have staging imaging performed within 28 days prior to registration, as follows. PET-CT baseline scans are strongly preferred; diagnostic quality magnetic resonance imaging (MRI), contrast-enhanced CT, or contrast-enhanced MRI scans are also acceptable if PET-CT is not feasible at baseline. Note: PET-CT will be required at end of treatment (EOT) and progression for response assessment. Participants must have measurable disease (at least one lesion with longest diameter ≥ 1.5 cm). All measurable lesions (longest diameter \>= 1.5 cm) must be assessed within 28 days prior to registration. Tests to assess non-measurable disease must be performed within 42 days prior to registration.
  • Participants with known human immunodeficiency virus (HIV)-infection are eligible providing they are on effective anti-retroviral therapy and have undetectable viral load at their most recent viral load test (must be within 26 weeks prior to registration). Participants with known HIV must have a CD4 count checked within 28 days prior to registration, but may proceed with therapy regardless of CD4 count.
  • All participants must be screened for chronic hepatitis B virus (HBV) within 28 days prior to registration. Participants with known HBV infection (positive serology) must also have a HBV viral load performed within 28 days prior to registration, and participants must have an undetectable HBV viral load on suppressive therapy within 28 days prior to registration. Participants found to be HBV carriers during screening are eligible and must receive standard of care prophylaxis. Participants with active hepatitis B (HBV viral load \> 500 IU/mL) within 28 days prior to registration are not eligible
  • Participants with a known history of hepatitis C virus (HCV) infection must have an undetectable HCV viral load within in 28 days prior to registration
  • Participants must not have known lymphomatous involvement of the central nervous system (CNS)
  • Participants must not have active inflammatory bowel disease (such as, Crohn's disease, ulcerative colitis), celiac disease (i.e., sprue), prior gastrectomy or upper bowel removal, or any other gastrointestinal disorder or defect that would interfere with the absorption, distribution, metabolism, or excretion of the study drug and/or predispose the subject to an increased risk of gastrointestinal toxicity
  • Participants must not have a history of acute leukemia having been treated with intensive induction therapy. Participants with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial
  • Participants must not have received any prior cytotoxic chemotherapy or rituximab for treatment of the newly diagnosed DLBCL except for the pre-phase treatment (within specified dose range) that may have either started before or may start after registration to S1918. Inhaled, nasal, and topical steroid use is allowed. Prior cytotoxic chemotherapy and/or antibody therapy for an indolent lymphoma prior to transformation is allowed. Up to 4 doses of intrathecal (IT) chemotherapy administered for central nervous system (CNS) prophylaxis is allowed in addition to protocol therapy. High-dose intravenous methotrexate is not allowed.
  • Participants must not have received more than a cumulative of dose 250 mg/m\^2 of prior doxorubicin (or equivalent dose of another anthracycline, such as epirubicin) therapy (at any time prior to registration).
  • Participants must not currently be receiving any other investigational agents
  • Participant must not have a history of allergic reactions attributed to azacitidine, mannitol, or other hypomethylating agents
  • Participants must be age ≥ 75
  • Participants must have a Zubrod performance status of 0-2
  • Participants must have adequate renal function, as demonstrated by a creatinine clearance, calculated by the Cockcroft and Gault formula, of \>= 30 ml/min that was obtained within 28 days prior to registration
  • Aspartate aminotransferase (AST) =\< 2.5 x institutional upper limit of normal (IULN), alanine aminotransferase (ALT) =\< 2.5 x IULN (within 28 days prior to registration)
  • Total bilirubin =\< 2 x institutional upper limit of normal (IULN), unless due to Gilbert's disease, hemolysis, or lymphomatous involvement of liver (within 28 days prior to registration). Note: If total bilirubin is elevated, and direct bilirubin is subsequently performed (within 28 days prior to registration) and resulted to be =\< 2 x IULN, the participant will be considered eligible
  • Absolute neutrophil count (ANC) \>= 1000/mcL (within 28 days prior to registration)
  • Platelets \>= 75,000/mcL (within 28 days prior to registration)
  • Hemoglobin (Hgb) \>= 8 g/ dL (within 28 days prior to registration)
  • If there is a documented lymphomatous involvement of the bone marrow, bone marrow function within 28 days prior to registration, as evidenced by:
    • ANC \>= 500/mcL
    • Platelets \>= 50,000/mcL
    • Hgb \>= 8 g/ dL
  • Participants must have a left ventricular ejection (LVEF) fraction \>= 45% as measured by echocardiogram or radionuclide (multigated acquisition scan \[MUGA\]) ventriculography within 56 days prior to registration
  • For the duration of the study treatment period and for at least 4 months following the last dose of study drug, male participants must agree to use effective contraceptive methods during sexual contact with a female of childbearing potential (FCBP) and must agree to refrain from semen or sperm donation during the same timeframe. Effective contraceptive methods include a history of vasectomy, use of hormonal contraception or an intrauterine device (IUD) by the female partner, or use of condoms
    • A FCBP is a sexually mature woman who: 1) has not undergone a hysterectomy or bilateral oophorectomy; or 2) has not been naturally postmenopausal for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months)
  • Participants must not have active infection (systemic fungal, bacterial, or viral infection) that is not controlled (defined as ongoing signs/symptoms related the infection without improvement despite appropriate antibiotics, antiviral therapy, and/or other treatment)
  • Participants must not have active cardiac disease within 26 weeks prior to registration, including: symptomatic congestive heart failure (New York Heart Association \[NYHA\] class 4), unstable angina pectoris, hemodynamically unstable cardiac arrhythmia, or myocardial infarction
  • Participants must not have \>= grade 2 neuropathy, by Common Terminology Criteria for Adverse Events (CTCAE) version (v.) 5.0, within 28 days prior to registration
  • Participants must not have any other known uncontrolled intercurrent illness including, but not limited to ongoing psychiatric illness/social situations that would limit compliance with study requirements
  • Participants must not have a concurrent primary malignancy undergoing active therapy. Exceptions: participants may have non-melanomatous skin cancers requiring only surgical intervention. Participants may have a history of early stage breast cancer or prostate cancer in remission after surgical and/or radiation therapy on adjuvant hormonal therapy only

Age in the registry: 75 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (176)

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

SiteCityCountrySite status
Hawaii Cancer Care - Westridge
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‘AieaUnited StatesUnknown status
Pali Momi Medical Center
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‘AieaUnited StatesUnknown status
McFarland Clinic - Ames
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AmesUnited StatesUnknown status
Kaiser Permanente-Anaheim
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AnaheimUnited StatesUnknown status
UI Health Care Mission Cancer and Blood - Ankeny Clinic
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AnkenyUnited StatesUnknown status
Trinity Health Saint Joseph Mercy Hospital Ann Arbor
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Ann ArborUnited StatesUnknown status
Duluth Clinic Ashland
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AshlandUnited StatesUnknown status
Emory Saint Joseph's Hospital
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AtlantaUnited StatesUnknown status
Emory University Hospital Midtown
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AtlantaUnited StatesUnknown status
Emory University Hospital/Winship Cancer Institute
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AtlantaUnited StatesUnknown status
Augusta University Medical Center
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AugustaUnited StatesUnknown status
Kaiser Permanente-Baldwin Park
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Baldwin ParkUnited StatesUnknown status
Memorial Sloan Kettering Basking Ridge
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Basking RidgeUnited StatesUnknown status
FHCC Overlake
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BellevueUnited StatesUnknown status
Kaiser Permanente-Bellflower
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BellflowerUnited StatesUnknown status
Tower Cancer Research Foundation
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Beverly HillsUnited StatesUnknown status
Tufts Medical Center
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BostonUnited StatesUnknown status
Trinity Health Medical Center - Brighton
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BrightonUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology - Brighton
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BrightonUnited StatesUnknown status
Roswell Park Cancer Institute
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BuffaloUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology - Canton
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CantonUnited StatesUnknown status
Trinity Health Medical Center - Canton
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CantonUnited StatesUnknown status
Saint Francis Medical Center
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Cape GirardeauUnited StatesUnknown status
Centralia Oncology Clinic
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CentraliaUnited StatesUnknown status
UNC Lineberger Comprehensive Cancer Center
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Chapel HillUnited StatesUnknown status
Vandalia Health/CAMC Institute for Academic Medicine
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CharlestonUnited StatesUnknown status
Medical University of South Carolina
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CharlestonUnited StatesUnknown status
University of Virginia Cancer Center
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CharlottesvilleUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology - Chelsea Hospital
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ChelseaUnited StatesUnknown status
Chelsea Hospital
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ChelseaUnited StatesUnknown status
Saint Luke's Hospital
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ChesterfieldUnited StatesUnknown status
Northwestern University
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ChicagoUnited StatesUnknown status
University of Chicago Comprehensive Cancer Center
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ChicagoUnited StatesUnknown status
University of Illinois
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ChicagoUnited StatesUnknown status
Siteman Cancer Center at Saint Peters Hospital
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City of Saint PetersUnited StatesUnknown status
Cleveland Clinic Foundation
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ClevelandUnited StatesUnknown status
Cleveland Clinic Cancer Center/Fairview Hospital
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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
Ohio State University Comprehensive Cancer Center
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ColumbusUnited StatesUnknown status
Memorial Sloan Kettering Commack
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CommackUnited StatesUnknown status
UC Irvine Health Cancer Center-Newport
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Costa MesaUnited StatesUnknown status
Siteman Cancer Center at West County Hospital
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Creve CoeurUnited StatesUnknown status
Carle at The Riverfront
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DanvilleUnited StatesUnknown status
Dayton Physician LLC - Englewood
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DaytonUnited StatesUnknown status
Decatur Memorial Hospital
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DecaturUnited StatesUnknown status
Cancer Care Specialists of Illinois - Decatur
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DecaturUnited StatesUnknown status
Essentia Health - Deer River Clinic
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Deer RiverUnited StatesUnknown status
Northwestern Medicine Cancer Center Kishwaukee
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DeKalbUnited StatesUnknown status
UI Health Care Mission Cancer and Blood - Laurel Clinic
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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
City of Hope Comprehensive Cancer Center
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DuarteUnited StatesUnknown status
Essentia Health Cancer Center
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DuluthUnited StatesUnknown status
Marshfield Medical Center-EC Cancer Center
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Eau ClaireUnited StatesUnknown status
Carle Physician Group-Effingham
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EffinghamUnited StatesUnknown status
Crossroads Cancer Center
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EffinghamUnited StatesUnknown status
Englewood Hospital and Medical Center
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EnglewoodUnited StatesUnknown status
NorthShore University HealthSystem-Evanston Hospital
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EvanstonUnited StatesUnknown status
Inova Schar Cancer Institute
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FairfaxUnited StatesUnknown status
Kaiser Permanente-Fontana
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FontanaUnited StatesUnknown status
Northwestern Medicine Cancer Center Delnor
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GenevaUnited StatesUnknown status
Glens Falls Hospital
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Glens FallsUnited StatesUnknown status
NorthShore University HealthSystem-Glenbrook Hospital
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GlenviewUnited StatesUnknown status
Northwestern Medicine Glenview Outpatient Center
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GlenviewUnited StatesUnknown status
Lutheran Hospital - Cancer Centers of Colorado
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GoldenUnited StatesUnknown status
Northwestern Medicine Grayslake Outpatient Center
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GrayslakeUnited StatesUnknown status
Saint Vincent Hospital Cancer Center Green Bay
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Green BayUnited StatesUnknown status
Saint Vincent Hospital Cancer Center at Saint Mary's
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Green BayUnited StatesUnknown status
Saint Francis Cancer Center
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GreenvilleUnited StatesUnknown status
Saint Francis Hospital
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GreenvilleUnited StatesUnknown status
Kaiser Permanente South Bay
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Harbor CityUnited StatesUnknown status
Memorial Sloan Kettering Westchester
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HarrisonUnited StatesUnknown status
Essentia Health Hibbing Clinic
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HibbingUnited StatesUnknown status
NorthShore University HealthSystem-Highland Park Hospital
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Highland ParkUnited StatesUnknown status
Hawaii Cancer Care Inc - Waterfront Plaza
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HonoluluUnited StatesUnknown status
Queen's Cancer Center - Kuakini
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HonoluluUnited StatesUnknown status
Queen's Medical Center
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HonoluluUnited StatesUnknown status
Queen's Cancer Cenrer - POB I
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HonoluluUnited StatesUnknown status
Straub Clinic and Hospital
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HonoluluUnited StatesUnknown status
City of Hope Seacliff
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Huntington BeachUnited StatesUnknown status
Cleveland Clinic Cancer Center Independence
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IndependenceUnited StatesUnknown status
City of Hope at Irvine Lennar
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IrvineUnited StatesUnknown status
Kaiser Permanente-Irvine
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IrvineUnited StatesUnknown status
Greater Dayton Cancer Center
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KetteringUnited StatesUnknown status
FHCC at EvergreenHealth
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KirklandUnited StatesUnknown status
Gundersen Lutheran Medical Center
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La CrosseUnited StatesUnknown status
Northwestern Medicine Lake Forest Hospital
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Lake ForestUnited StatesUnknown status
Monmouth Medical Center Southern Campus
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LakewoodUnited StatesUnknown status
City of Hope Antelope Valley
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LancasterUnited StatesUnknown status
Cancer Centers of Southwest Oklahoma Research
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LawtonUnited StatesUnknown status
Cancer Partners of Nebraska
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LincolnUnited StatesUnknown status
University of Arkansas for Medical Sciences
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Little RockUnited StatesUnknown status
Hope Cancer Clinic
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LivoniaUnited StatesUnknown status
Trinity Health Saint Mary Mercy Livonia Hospital
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LivoniaUnited StatesUnknown status
Tibor Rubin VA Medical Center
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Long BeachUnited StatesUnknown status
City of Hope at Long Beach Elm
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Long BeachUnited StatesUnknown status
Monmouth Medical Center
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Long BranchUnited StatesUnknown status
Cedars-Sinai Medical Center
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Los AngelesUnited StatesUnknown status
Kaiser Permanente West Los Angeles
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Los AngelesUnited StatesUnknown status
Kaiser Permanente Los Angeles Medical Center
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Los AngelesUnited StatesUnknown status
Cleveland Clinic Cancer Center Mansfield
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MansfieldUnited StatesUnknown status
Marshfield Medical Center-Marshfield
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MarshfieldUnited StatesUnknown status
Carle Physician Group-Mattoon/Charleston
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MattoonUnited StatesUnknown status
Hillcrest Hospital Cancer Center
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Mayfield HeightsUnited StatesUnknown status
Baptist Memorial Hospital and Cancer Center-Memphis
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MemphisUnited StatesUnknown status
University of Miami Miller School of Medicine-Sylvester Cancer Center
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MiamiUnited StatesUnknown status
Memorial Sloan Kettering Monmouth
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MiddletownUnited StatesUnknown status
NYU Langone Hospital - Long Island
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MineolaUnited StatesUnknown status
Marshfield Medical Center - Minocqua
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MinocquaUnited StatesUnknown status
Ochsner LSU Health Monroe Medical Center
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MonroeUnited StatesUnknown status
Memorial Sloan Kettering Bergen
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MontvaleUnited StatesUnknown status
Helen F Graham Cancer Center
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NewarkUnited StatesUnknown status
Delaware Clinical and Laboratory Physicians PA
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NewarkUnited StatesUnknown status
Newark Beth Israel Medical Center
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NewarkUnited StatesUnknown status
Medical Oncology Hematology Consultants PA
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NewarkUnited StatesUnknown status
Rutgers Cancer Institute of New Jersey
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New BrunswickUnited StatesUnknown status
UC Comprehensive Cancer Center at Silver Cross
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New LenoxUnited StatesUnknown status
City of Hope Newport Beach
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Newport BeachUnited StatesUnknown status
NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center
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New YorkUnited StatesUnknown status
Memorial Sloan-Kettering Cancer Center
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New YorkUnited StatesUnknown status
NYP/Weill Cornell Medical Center
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New YorkUnited StatesUnknown status
Laura and Isaac Perlmutter Cancer Center at NYU Langone
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New YorkUnited StatesUnknown status
Saint Vincent Hospital Cancer Center at Oconto Falls
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Oconto FallsUnited StatesUnknown status
Cancer Care Center of O'Fallon
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O'FallonUnited StatesUnknown status
University of Oklahoma Health Sciences Center
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Oklahoma CityUnited StatesUnknown status
Kaiser Permanente-Ontario
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OntarioUnited StatesUnknown status
UC Irvine Health- Chao Family Comprehensive Cancer Center
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OrangeUnited StatesUnknown status
University of Chicago Medicine-Orland Park
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Orland ParkUnited StatesUnknown status
Northwestern Medicine Orland Park
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Orland ParkUnited StatesUnknown status
Upstate Cancer Center at Oswego
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OswegoUnited StatesUnknown status
Baptist Memorial Hospital and Cancer Center-Oxford
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OxfordUnited StatesUnknown status
Stanford Cancer Institute Palo Alto
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Palo AltoUnited StatesUnknown status
Kaiser Permanente - Panorama City
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Panorama CityUnited StatesUnknown status
Illinois CancerCare-Peoria
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PeoriaUnited StatesUnknown status
Providence Saint Vincent Medical Center
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PortlandUnited StatesUnknown status
Portland VA Medical Center
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PortlandUnited StatesUnknown status
Marshfield Medical Center-Rice Lake
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Rice LakeUnited StatesUnknown status
VCU Massey Comprehensive Cancer Center
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RichmondUnited StatesUnknown status
Kaiser Permanente-Riverside
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RiversideUnited StatesUnknown status
Heartland Regional Medical Center
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Saint JosephUnited StatesUnknown status
Huntsman Cancer Institute/University of Utah
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Salt Lake CityUnited StatesUnknown status
George E. Wahlen Department of Veterans Affairs Medical Center
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Salt Lake CityUnited StatesUnknown status
Kaiser Permanente-San Diego Zion
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San DiegoUnited StatesUnknown status
Essentia Health Sandstone
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SandstoneUnited StatesUnknown status
North Coast Cancer Care
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SanduskyUnited StatesUnknown status
Kaiser Permanente-San Marcos
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San MarcosUnited StatesUnknown status
UCSF Cancer Center - San Mateo
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San MateoUnited StatesUnknown status
FHCC at Northwest Hospital
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SeattleUnited StatesUnknown status
Saint Vincent Hospital Cancer Center at Sheboygan
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SheboyganUnited StatesUnknown status
Memorial Hospital East
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ShilohUnited StatesUnknown status
LSU Health Sciences Center at Shreveport
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ShreveportUnited StatesUnknown status
Baptist Memorial Hospital and Cancer Center-Desoto
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SouthhavenUnited StatesUnknown status
City of Hope South Pasadena
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South PasadenaUnited StatesUnknown status
Marshfield Medical Center-River Region at Stevens Point
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Stevens PointUnited StatesUnknown status
Siteman Cancer Center at Christian Hospital
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St LouisUnited StatesUnknown status
Siteman Cancer Center-South County
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St LouisUnited StatesUnknown status
Washington University School of Medicine
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St LouisUnited StatesUnknown status
Cleveland Clinic Cancer Center Strongsville
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StrongsvilleUnited StatesUnknown status
Saint Vincent Hospital Cancer Center at Sturgeon Bay
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Sturgeon BayUnited StatesUnknown status
State University of New York Upstate Medical University
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SyracuseUnited StatesUnknown status
Community Medical Center
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Toms RiverUnited StatesUnknown status
City of Hope South Bay
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TorranceUnited StatesUnknown status
University of Arizona Cancer Center-North Campus
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TucsonUnited StatesUnknown status
Banner University Medical Center - Tucson
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TucsonUnited StatesUnknown status
Memorial Sloan Kettering Nassau
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UniondaleUnited StatesUnknown status
City of Hope Upland
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UplandUnited StatesUnknown status
Carle Cancer Center
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UrbanaUnited StatesUnknown status
Upstate Cancer Center at Verona
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VeronaUnited StatesUnknown status
Essentia Health Virginia Clinic
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VirginiaUnited StatesUnknown status
South Pointe Hospital
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Warrensville HeightsUnited StatesUnknown status
Northwestern Medicine Cancer Center Warrenville
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WarrenvilleUnited StatesUnknown status
Marshfield Medical Center - Weston
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WestonUnited StatesUnknown status
Kaiser Permanente-Woodland Hills
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Woodland HillsUnited StatesUnknown status
Cleveland Clinic Wooster Family Health and Surgery Center
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WoosterUnited StatesUnknown status
Huron Gastroenterology PC
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YpsilantiUnited StatesUnknown status
Trinity Health IHA Medical Group Hematology Oncology Ann Arbor Campus
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YpsilantiUnited StatesUnknown status

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