Clinical Research Trials Archive – Closed Trials

This is our archive of closed clinical trials, which means that they are no longer accepting new participants or have been concluded. Once a research facility has chosen to close the study, it is sorted into the GPS archive by indication. If you are interested in enrolling in a clinical trial, then please browse our list of active clinical studies.

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We've found
31,889
archived clinical trials in
Blood Cancer

mi
from
Tucson, AZ
Arizona Clinical Research Center
mi
from
Tucson, AZ
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mi
from
Rockville, MD
Associates in Oncology and Hematology
mi
from
Rockville, MD
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mi
from
Dallas, TX
Baylor Charles A. Sammons Cancer Center at Dallas
mi
from
Dallas, TX
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mi
from
Charleston, SC
Charleston Hematology/Oncology Associates, Pa
mi
from
Charleston, SC
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mi
from
Huntsville, AL
Clearview Cancer Institute
mi
from
Huntsville, AL
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mi
from
New York, NY
Mount Sinai Hospital
mi
from
New York, NY
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mi
from
New York, NY
NYU Cancer Center
mi
from
New York, NY
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mi
from
Germantown, TN
The Jones Clinic, PC
mi
from
Germantown, TN
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mi
from
Ann Arbor, MI
University of Michigan Comprehensive Cancer Center
mi
from
Ann Arbor, MI
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mi
from
Nashville, TN
Vanderbilt-Ingram Cancer Center
mi
from
Nashville, TN
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mi
from
Duarte, CA
City of Hope
mi
from
Duarte, CA
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mi
from
Atlanta, GA
Emory University/Winship Cancer Institute
mi
from
Atlanta, GA
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mi
from
Detroit, MI
Karmanos Cancer Institute
mi
from
Detroit, MI
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Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated:  5/5/2016
mi
from
Denver, CO
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated: 5/5/2016
RMCC
mi
from
Denver, CO
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Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated:  5/5/2016
mi
from
Atlanta, GA
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated: 5/5/2016
Emory
mi
from
Atlanta, GA
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Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated:  5/5/2016
mi
from
Chicago, IL
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated: 5/5/2016
Rush
mi
from
Chicago, IL
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Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated:  5/5/2016
IU
mi
from
Indianapolis, IN
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated: 5/5/2016
IU
mi
from
Indianapolis, IN
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Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated:  5/5/2016
mi
from
Hackensack, NJ
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated: 5/5/2016
HUMC
mi
from
Hackensack, NJ
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Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated:  5/5/2016
mi
from
New York City, NY
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated: 5/5/2016
Cornell
mi
from
New York City, NY
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Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated:  5/5/2016
OSU
mi
from
Columbus, OH
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated: 5/5/2016
OSU
mi
from
Columbus, OH
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Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated:  5/5/2016
mi
from
Nashville, TN
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated: 5/5/2016
SCRI
mi
from
Nashville, TN
Click here to add this to my saved trials
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated:  5/5/2016
mi
from
Houston, TX
Phase 1 Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Advanced Hematological Malignancies
Status: Enrolling
Updated: 5/5/2016
MDACC
mi
from
Houston, TX
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Phase 1 Study of TG02 Citrate in Patients With Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Status: Enrolling
Updated:  5/5/2016
GRU
mi
from
Augusta, GA
Phase 1 Study of TG02 Citrate in Patients With Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Status: Enrolling
Updated: 5/5/2016
GRU
mi
from
Augusta, GA
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Phase 1 Study of TG02 Citrate in Patients With Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Status: Enrolling
Updated:  5/5/2016
mi
from
Boston, MA
Phase 1 Study of TG02 Citrate in Patients With Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Status: Enrolling
Updated: 5/5/2016
DFCI
mi
from
Boston, MA
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Phase 1 Study of TG02 Citrate in Patients With Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Status: Enrolling
Updated:  5/5/2016
OSU
mi
from
Columbus, OH
Phase 1 Study of TG02 Citrate in Patients With Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Status: Enrolling
Updated: 5/5/2016
OSU
mi
from
Columbus, OH
Click here to add this to my saved trials
Phase 1 Study of TG02 Citrate in Patients With Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Status: Enrolling
Updated:  5/5/2016
mi
from
Nashville, TN
Phase 1 Study of TG02 Citrate in Patients With Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Status: Enrolling
Updated: 5/5/2016
SCRI
mi
from
Nashville, TN
Click here to add this to my saved trials
Phase 1 Study of TG02 Citrate in Patients With Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Status: Enrolling
Updated:  5/5/2016
mi
from
Houston, TX
Phase 1 Study of TG02 Citrate in Patients With Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Phase 1 Dose-Escalation and Pharmacokinetic Study of TG02 Citrate in Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia and Small Lymphocytic Lymphoma
Status: Enrolling
Updated: 5/5/2016
MDACC
mi
from
Houston, TX
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Ponatinib - Frontline for Chronic Myeloid Leukemia (CML) in Accelerated Phase (AP)
Ponatinib as Initial Therapy for Patients With Chronic Myeloid Leukemia in Accelerated Phase
Status: Enrolling
Updated:  5/13/2016
mi
from
Houston, TX
Ponatinib - Frontline for Chronic Myeloid Leukemia (CML) in Accelerated Phase (AP)
Ponatinib as Initial Therapy for Patients With Chronic Myeloid Leukemia in Accelerated Phase
Status: Enrolling
Updated: 5/13/2016
University of Texas M.D. Anderson Cancer Center
mi
from
Houston, TX
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Lestaurtinib With or Without Chemotherapy Agents in Samples From Young Patients With Leukemia
SCOR in Targeted Therapies for Infant Leukemia Project 3: Targeting FLT3 in Infant Leukemia
Status: Enrolling
Updated:  5/17/2016
mi
from
Monrovia, CA
Lestaurtinib With or Without Chemotherapy Agents in Samples From Young Patients With Leukemia
SCOR in Targeted Therapies for Infant Leukemia Project 3: Targeting FLT3 in Infant Leukemia
Status: Enrolling
Updated: 5/17/2016
Children's Oncology Group
mi
from
Monrovia, CA
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Studying Biomarkers as a Diagnostic Tool in Samples From Younger Patients With B-Cell Acute Lymphoblastic Leukemia
OBSERVATIONAL: Replication Profiling as a Diagnostic Tool in B-cell Acute Lymphoblastic Leukemia (ALL)
Status: Enrolling
Updated:  5/17/2016
mi
from
Monrovia, CA
Studying Biomarkers as a Diagnostic Tool in Samples From Younger Patients With B-Cell Acute Lymphoblastic Leukemia
OBSERVATIONAL: Replication Profiling as a Diagnostic Tool in B-cell Acute Lymphoblastic Leukemia (ALL)
Status: Enrolling
Updated: 5/17/2016
Children's Oncology Group
mi
from
Monrovia, CA
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Studying Genes in Samples From Younger Patients With Acute Megakaryoblastic Leukemia
Observational - NUP98/JARID1A as a Recurrent Aberration in Pediatric Acute Megakaryoblastic Leukemia
Status: Enrolling
Updated:  5/17/2016
mi
from
Monrovia, CA
Studying Genes in Samples From Younger Patients With Acute Megakaryoblastic Leukemia
Observational - NUP98/JARID1A as a Recurrent Aberration in Pediatric Acute Megakaryoblastic Leukemia
Status: Enrolling
Updated: 5/17/2016
Children's Oncology Group
mi
from
Monrovia, CA
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Studying DNA in Blood and Bone Marrow Samples From Younger Patients With Acute Myeloid Leukemia
Genetic Predictors of AML Treatment Response
Status: Enrolling
Updated:  5/17/2016
mi
from
Philadelphia, PA
Studying DNA in Blood and Bone Marrow Samples From Younger Patients With Acute Myeloid Leukemia
Genetic Predictors of AML Treatment Response
Status: Enrolling
Updated: 5/17/2016
Children's Oncology Group
mi
from
Philadelphia, PA
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Studying Genes in Samples From Younger Patients With Relapsed Acute Lymphoblastic Leukemia
Molecular Taxonomy of Pediatric Cancer
Status: Enrolling
Updated:  5/17/2016
mi
from
Arcadia, CA
Studying Genes in Samples From Younger Patients With Relapsed Acute Lymphoblastic Leukemia
Molecular Taxonomy of Pediatric Cancer
Status: Enrolling
Updated: 5/17/2016
Children's Oncology Group
mi
from
Arcadia, CA
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Dose Escalation Study of Revlimid With Fludarabine-Rituximab for CLL/SLL
A Phase I Dose Escalation Study of Lenalidomide (Revlimid) in Combination With Fludarabine-Rituximab (Rituxan) for Previously Untreated CLL/SLL
Status: Enrolling
Updated:  5/26/2016
mi
from
Boston, MA
Dose Escalation Study of Revlimid With Fludarabine-Rituximab for CLL/SLL
A Phase I Dose Escalation Study of Lenalidomide (Revlimid) in Combination With Fludarabine-Rituximab (Rituxan) for Previously Untreated CLL/SLL
Status: Enrolling
Updated: 5/26/2016
Massachusetts General Hospital
mi
from
Boston, MA
Click here to add this to my saved trials
Dose Escalation Study of Revlimid With Fludarabine-Rituximab for CLL/SLL
A Phase I Dose Escalation Study of Lenalidomide (Revlimid) in Combination With Fludarabine-Rituximab (Rituxan) for Previously Untreated CLL/SLL
Status: Enrolling
Updated:  5/26/2016
mi
from
Boston, MA
Dose Escalation Study of Revlimid With Fludarabine-Rituximab for CLL/SLL
A Phase I Dose Escalation Study of Lenalidomide (Revlimid) in Combination With Fludarabine-Rituximab (Rituxan) for Previously Untreated CLL/SLL
Status: Enrolling
Updated: 5/26/2016
Dana-Farber Cancer Institute
mi
from
Boston, MA
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Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated:  6/1/2016
mi
from
Monterey, CA
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 6/1/2016
Pacific Cancer Care
mi
from
Monterey, CA
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Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated:  6/1/2016
mi
from
Scarborough, ME
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 6/1/2016
Maine Center for Cancer Medicine
mi
from
Scarborough, ME
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Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated:  6/1/2016
mi
from
Boston, MA
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 6/1/2016
Beth Israel Deaconess Medical Center
mi
from
Boston, MA
Click here to add this to my saved trials
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated:  6/1/2016
mi
from
Boston, MA
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 6/1/2016
Dana-Farber Cancer Institute
mi
from
Boston, MA
Click here to add this to my saved trials
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated:  6/1/2016
mi
from
Boston, MA
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 6/1/2016
Massachusetts General Hospital
mi
from
Boston, MA
Click here to add this to my saved trials
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated:  6/1/2016
mi
from
Southaven, MS
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 6/1/2016
The West Clinic, PC
mi
from
Southaven, MS
Click here to add this to my saved trials
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated:  6/1/2016
mi
from
Albany, NY
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 6/1/2016
New York Oncology Hematology PC
mi
from
Albany, NY
Click here to add this to my saved trials
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated:  6/1/2016
mi
from
Hudson, NY
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 6/1/2016
New York Oncology, Hematology, P.C.
mi
from
Hudson, NY
Click here to add this to my saved trials
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated:  6/1/2016
mi
from
Memphis, TN
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 6/1/2016
The West Clinic, PC
mi
from
Memphis, TN
Click here to add this to my saved trials
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated:  6/1/2016
mi
from
Tampa, FL
Open-label Study of TH-302 and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
A Phase 1/2 Open-label Study to Assess the Safety, Tolerability and Preliminary Efficacy of TH-302, A Hypoxia-Activated Prodrug, and Dexamethasone With or Without Bortezomib or Pomalidomide in Subjects With Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 6/1/2016
Moffitt Cancer Center
mi
from
Tampa, FL
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Comprehensive Frailty Assessment
Comprehensive Frailty Assessment
Status: Enrolling
Updated:  6/1/2016
mi
from
Columbus, OH
Comprehensive Frailty Assessment
Comprehensive Frailty Assessment
Status: Enrolling
Updated: 6/1/2016
Ohio State University Hospital East
mi
from
Columbus, OH
Click here to add this to my saved trials
Comprehensive Frailty Assessment
Comprehensive Frailty Assessment
Status: Enrolling
Updated:  6/1/2016
mi
from
Columbus, OH
Comprehensive Frailty Assessment
Comprehensive Frailty Assessment
Status: Enrolling
Updated: 6/1/2016
Ohio State University
mi
from
Columbus, OH
Click here to add this to my saved trials
Melphalan, Peripheral Stem Cell Transplantation, and Interleukin-2 Followed by Interferon Alfa in Treating Patients With Advanced Multiple Myeloma
Immunotherapy for Autologous/Syngeneic Peripheral Blood Stem Cell (PBSC) Transplant Patients as Treatment for Advanced Multiple Myeloma
Status: Enrolling
Updated:  6/1/2016
mi
from
Seattle, WA
Melphalan, Peripheral Stem Cell Transplantation, and Interleukin-2 Followed by Interferon Alfa in Treating Patients With Advanced Multiple Myeloma
Immunotherapy for Autologous/Syngeneic Peripheral Blood Stem Cell (PBSC) Transplant Patients as Treatment for Advanced Multiple Myeloma
Status: Enrolling
Updated: 6/1/2016
Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium
mi
from
Seattle, WA
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Risk of Psychopathology and Neurocognitive Impairment in Leukemia Survivors
Risk of Psychopathology and Neurocognitive Impairment in Leukemia Survivors
Status: Enrolling
Updated:  6/6/2016
mi
from
Memphis, TN
Risk of Psychopathology and Neurocognitive Impairment in Leukemia Survivors
Risk of Psychopathology and Neurocognitive Impairment in Leukemia Survivors
Status: Enrolling
Updated: 6/6/2016
St. Jude Children's Research Hospital
mi
from
Memphis, TN
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Enhancing Graft vs Leukemia Via Delayed Ex-Vivo Co-Stimulated DLI After Non-Myeloablative Stem Cell Transplantation
Non-Myeloablative Conditioning With Allogeneic Peripheral Blood Progenitor Cell Transplantation Followed by Prophylactic Activated Donor Lymphocyte Infusion (DLI) for the Treatment of High Risk Acute Leukemia/MDS
Status: Enrolling
Updated:  6/7/2016
mi
from
Philadelphia, PA
Enhancing Graft vs Leukemia Via Delayed Ex-Vivo Co-Stimulated DLI After Non-Myeloablative Stem Cell Transplantation
Non-Myeloablative Conditioning With Allogeneic Peripheral Blood Progenitor Cell Transplantation Followed by Prophylactic Activated Donor Lymphocyte Infusion (DLI) for the Treatment of High Risk Acute Leukemia/MDS
Status: Enrolling
Updated: 6/7/2016
Abramson Cancer Center of the University of Pennsylvania
mi
from
Philadelphia, PA
Click here to add this to my saved trials