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Therapeutic Areas: Oncology | Hematology

Myelodysplastic Syndromes (MDS) Clinical Trials

A listing of Myelodysplastic Syndromes (MDS) medical research trials actively recruiting patient volunteers. Use the filters below to narrow your search results.

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Alabama

Research Site
Mobile Alabama 36608

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

California

Alta Bates Comprehensive Cancer Center
Berkeley California 94704
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

California Cancer Associates for Research and Excellence (cCARE)
Escondido California 92025
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Marin Oncology Associates
Greenbrae California 94904-2007
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

UCSD-Thornton Hospital
La Jolla California 44106-5000
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Research Site
Los Angeles California 90033

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

Colorado

Research Site
Denver Colorado 80218

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

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Rocky Mountain Cancer Centers
Denver Colorado 80218

Patients are needed to participate in a clinical research study evaluating Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg and Sotatercept 0.5 mg/kg for the treatment of Anemia, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Low to Intermediate-1 MDS

Florida

Research Site
Fort Myers Florida 33916

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

Research Site
St. Petersburg Florida 33705

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

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H. Lee Moffitt Cancer Center
Tampa Florida 33602

Patients are needed to participate in a clinical research study evaluating Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg and Sotatercept 0.5 mg/kg for the treatment of Anemia, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Low to Intermediate-1 MDS

Georgia

Phoebe Cancer Center of Phoebe Putney Memorial Hospital
Albany Georgia 31701
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Illinois

University of Chicago Medical Center
Chicago Illinois 60637
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Robert H Lurie Comprehensive Cancer Center/ NW Univ
Chicago Illinois 60611
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Research Site
Chicago Illinois 60601

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

Louisiana

Hematology and Oncology Specialists, LLC
Metairie Louisiana 70006
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Maryland

Johns Hopkins University
Baltimore Maryland 21231

Patients are needed to participate in a clinical research study evaluating Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg and Sotatercept 0.5 mg/kg for the treatment of Anemia, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Low to Intermediate-1 MDS

Massachusetts

UMASS Memorial Hospital
Worcester Massachusetts 1655
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

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Dana-Farber Cancer Institute/Brigham and Women's Hospital
Boston Massachusetts 02215

Patients are needed to participate in a clinical research study evaluating Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg and Sotatercept 0.5 mg/kg for the treatment of Anemia, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Low to Intermediate-1 MDS

Minnesota

Mayo Clinic - Rochester
Rochester Minnesota 55905
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Mississippi

Jackson Oncology Associates PLLC
Jackson Mississippi 39202
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Missouri

Kansas City VA Medical Center/University of Kansas Medical Center
Kansas City Missouri 64128
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Saint Luke's Cancer Institute
Kansas City Missouri 64111
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Nebraska

University of Nebraska Medical Center
Omaha Nebraska 68198-6805
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

New Jersey

Research Site
Hackensak New Jersey 07601

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

New York

Mount Sinai Medical Center
New York New York 10029
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

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North Shore-LIJ Health System Monter Cancer Center
Lake Success New York 11020

Patients are needed to participate in a clinical research study evaluating Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg and Sotatercept 0.5 mg/kg for the treatment of Anemia, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Low to Intermediate-1 MDS

Columbia University Medical Center
New York New York 10032

Patients are needed to participate in a clinical research study evaluating Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg and Sotatercept 0.5 mg/kg for the treatment of Anemia, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Low to Intermediate-1 MDS

North Carolina

Eastern Institute of Medical Sciences
Greenville North Carolina 27834
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

North Dakota

Ohio

Research Site
Cincinnati Ohio 45242

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

University Hospitals of Cleveland Case Medical Center
Cleveland Ohio 44106-5000
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Research Site
Cleveland Ohio 44195

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

View More »

Cleveland Clinic Foundation
Cleveland Ohio 44195

Patients are needed to participate in a clinical research study evaluating Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg and Sotatercept 0.5 mg/kg for the treatment of Anemia, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Low to Intermediate-1 MDS

Oregon

Kaiser Permanente Northwest Oncology/Hematology
Portland Oregon 97227
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Pennsylvania

University of Pennsylvania
Philadelphia Pennsylvania 19104
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Tennessee

Research Site
Chattanooga Tennessee 37404

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

Research Site
Nashville Tennessee 37203

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

View More »

Sarah Cannon Research Institute
Nashville Tennessee 37203

Patients are needed to participate in a clinical research study evaluating Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg and Sotatercept 0.5 mg/kg for the treatment of Anemia, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Low to Intermediate-1 MDS

Texas

Research Site
Dallas Texas 75246

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

Brooke Army Medical Center Francis Street Medical Center
Fort Sam Houston Texas 78235-8200
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

MD Anderson Cancer Center The University of Texas
Houston Texas 77030
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Michael Debakey VA Medical Center
Houston Texas 77030
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Millenium Oncology
Houston Texas 77090
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

Research Site
Houston Texas 77030

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

Research Site
San Antonio Texas 78229

Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients with MDS Who Failed to Respond to Single Agent HMA

View More »

The University of Texas, MD Anderson Cancer Center
Houston Texas 77030

Patients are needed to participate in a clinical research study evaluating Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg and Sotatercept 0.5 mg/kg for the treatment of Anemia, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Low to Intermediate-1 MDS

Texas Oncology
Tyler Texas 75702

Patients are needed to participate in a clinical research study evaluating Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg and Sotatercept 0.5 mg/kg for the treatment of Anemia, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Low to Intermediate-1 MDS

Virginia

VA Commonwealth University Massey Cancer Center
Richmond Virginia 23298-0037
New

A Phase 3, Multicenter, Randomized, Double-Blind study to compare the efficacy and safety to oral azacitidine plus best supportive care versus placebo plus best supportive care in subjects with low red blood cells requiring transfusions and low platelets due to IPSS lower-risk Myledoysplastic Syndromes (MDS).

View More »

Virginia Oncology Associates
Norfolk Virginia 23502

Patients are needed to participate in a clinical research study evaluating Sotatercept 0.1 mg/kg, Sotatercept 0.3 mg/kg and Sotatercept 0.5 mg/kg for the treatment of Anemia, Myelodysplastic Syndromes (MDS), Chronic Myelomonocytic Leukemia (CMML) or Low to Intermediate-1 MDS

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