We've found
31,889
archived clinical trials in
Blood Cancer
We've found
31,889
archived clinical trials in
Blood Cancer
Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
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Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
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Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
Click here to add this to my saved trials
Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
Click here to add this to my saved trials
Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
Click here to add this to my saved trials
Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
Phase 2 Study Adding Pracinostat to a Hypomethylating Agent (HMA) in Patients With MDS Who Failed to Respond to Single Agent HMA
Updated: 2/22/2017
A Phase II Simon Two-Stage Study of the Addition of Pracinostat to a Hypomethylating Agent (HMA) in Patients With Myelodysplastic Syndrome (MDS) Who Have Failed to Respond or Maintain a Response to the HMA Alone
Status: Enrolling
Updated: 2/22/2017
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Granulocyte-colony Stimulating Factor (G-CSF) and Plerixafor Plus Sorafenib for Acute Myelogenous Leukemia (AML) With FLT3 Mutations
Updated: 2/23/2017
G-CSF and Plerixafor With Sorafenib for Acute Myelogenous Leukemia With FLT3 Mutations
Status: Enrolling
Updated: 2/23/2017
Granulocyte-colony Stimulating Factor (G-CSF) and Plerixafor Plus Sorafenib for Acute Myelogenous Leukemia (AML) With FLT3 Mutations
Updated: 2/23/2017
G-CSF and Plerixafor With Sorafenib for Acute Myelogenous Leukemia With FLT3 Mutations
Status: Enrolling
Updated: 2/23/2017
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Study for the Treatment of Transfusional Iron Overload in Myelodysplastic Patients
Updated: 2/28/2017
An Open Label, Safety and Tolerability Study of Deferasirox for Treatment of Transfusional Iron Overload in Low-Risk and INT-1 Myelodysplastic Patients
Status: Enrolling
Updated: 2/28/2017
Study for the Treatment of Transfusional Iron Overload in Myelodysplastic Patients
Updated: 2/28/2017
An Open Label, Safety and Tolerability Study of Deferasirox for Treatment of Transfusional Iron Overload in Low-Risk and INT-1 Myelodysplastic Patients
Status: Enrolling
Updated: 2/28/2017
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Study for the Treatment of Transfusional Iron Overload in Myelodysplastic Patients
Updated: 2/28/2017
An Open Label, Safety and Tolerability Study of Deferasirox for Treatment of Transfusional Iron Overload in Low-Risk and INT-1 Myelodysplastic Patients
Status: Enrolling
Updated: 2/28/2017
Study for the Treatment of Transfusional Iron Overload in Myelodysplastic Patients
Updated: 2/28/2017
An Open Label, Safety and Tolerability Study of Deferasirox for Treatment of Transfusional Iron Overload in Low-Risk and INT-1 Myelodysplastic Patients
Status: Enrolling
Updated: 2/28/2017
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Study for the Treatment of Transfusional Iron Overload in Myelodysplastic Patients
Updated: 2/28/2017
An Open Label, Safety and Tolerability Study of Deferasirox for Treatment of Transfusional Iron Overload in Low-Risk and INT-1 Myelodysplastic Patients
Status: Enrolling
Updated: 2/28/2017
Study for the Treatment of Transfusional Iron Overload in Myelodysplastic Patients
Updated: 2/28/2017
An Open Label, Safety and Tolerability Study of Deferasirox for Treatment of Transfusional Iron Overload in Low-Risk and INT-1 Myelodysplastic Patients
Status: Enrolling
Updated: 2/28/2017
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Phase I/II Study of DFP-10917 in Patients With Acute Leukemia
Updated: 3/2/2017
A Phase I/II Study of DFP 10917 Given by Continuous Infusion in Patients With Relapsed or Refractory Acute Leukemia
Status: Enrolling
Updated: 3/2/2017
Phase I/II Study of DFP-10917 in Patients With Acute Leukemia
Updated: 3/2/2017
A Phase I/II Study of DFP 10917 Given by Continuous Infusion in Patients With Relapsed or Refractory Acute Leukemia
Status: Enrolling
Updated: 3/2/2017
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Arsenic Trioxide in Combination With Cytarabine in Patients With High-risk MDS and Poor-prognosis AML
Updated: 3/2/2017
Phase I/II Study of Arsenic Trioxide in Combination With Cytosine Arabinoside in Patients With High-risk Myelodysplastic Syndrome and Poor-prognosis Acute Myelogenous Leukemia
Status: Enrolling
Updated: 3/2/2017
Arsenic Trioxide in Combination With Cytarabine in Patients With High-risk MDS and Poor-prognosis AML
Updated: 3/2/2017
Phase I/II Study of Arsenic Trioxide in Combination With Cytosine Arabinoside in Patients With High-risk Myelodysplastic Syndrome and Poor-prognosis Acute Myelogenous Leukemia
Status: Enrolling
Updated: 3/2/2017
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Exergaming Intervention in ALL Patients
Updated: 3/13/2017
The Effect of a Home-based Fitness Intervention on Cardiometabolic Risk Profile in Acute Lymphoblastic Leukemia (ALL) Patients
Status: Enrolling
Updated: 3/13/2017
Exergaming Intervention in ALL Patients
Updated: 3/13/2017
The Effect of a Home-based Fitness Intervention on Cardiometabolic Risk Profile in Acute Lymphoblastic Leukemia (ALL) Patients
Status: Enrolling
Updated: 3/13/2017
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Genomic and Psychosocial Effects of the 3RP on Patients With MGUS and Smoldering Multiple Myeloma
Updated: 3/15/2017
Genomic and Psychosocial Effects of the Relaxation Response Resiliency Program (3RP) on Patients With MGUS and Smoldering Multiple Myeloma
Status: Enrolling
Updated: 3/15/2017
Genomic and Psychosocial Effects of the 3RP on Patients With MGUS and Smoldering Multiple Myeloma
Updated: 3/15/2017
Genomic and Psychosocial Effects of the Relaxation Response Resiliency Program (3RP) on Patients With MGUS and Smoldering Multiple Myeloma
Status: Enrolling
Updated: 3/15/2017
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Genomic and Psychosocial Effects of the 3RP on Patients With MGUS and Smoldering Multiple Myeloma
Updated: 3/15/2017
Genomic and Psychosocial Effects of the Relaxation Response Resiliency Program (3RP) on Patients With MGUS and Smoldering Multiple Myeloma
Status: Enrolling
Updated: 3/15/2017
Genomic and Psychosocial Effects of the 3RP on Patients With MGUS and Smoldering Multiple Myeloma
Updated: 3/15/2017
Genomic and Psychosocial Effects of the Relaxation Response Resiliency Program (3RP) on Patients With MGUS and Smoldering Multiple Myeloma
Status: Enrolling
Updated: 3/15/2017
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Genomic and Psychosocial Effects of the 3RP on Patients With MGUS and Smoldering Multiple Myeloma
Updated: 3/15/2017
Genomic and Psychosocial Effects of the Relaxation Response Resiliency Program (3RP) on Patients With MGUS and Smoldering Multiple Myeloma
Status: Enrolling
Updated: 3/15/2017
Genomic and Psychosocial Effects of the 3RP on Patients With MGUS and Smoldering Multiple Myeloma
Updated: 3/15/2017
Genomic and Psychosocial Effects of the Relaxation Response Resiliency Program (3RP) on Patients With MGUS and Smoldering Multiple Myeloma
Status: Enrolling
Updated: 3/15/2017
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PCI-32765 (Ibrutinib) in Treating Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma, or B-cell Prolymphocytic Leukemia
Updated: 3/20/2017
A Phase 2 Study of the Bruton's Tyrosine Kinase (Btk) Inhibitor, PCI-32765(Ibrutinib), in Relapsed and Refractory Patients With Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL) and B-cell Prolymphocytic Leukemia (B-PLL)
Status: Enrolling
Updated: 3/20/2017
PCI-32765 (Ibrutinib) in Treating Patients With Relapsed or Refractory Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma, or B-cell Prolymphocytic Leukemia
Updated: 3/20/2017
A Phase 2 Study of the Bruton's Tyrosine Kinase (Btk) Inhibitor, PCI-32765(Ibrutinib), in Relapsed and Refractory Patients With Chronic Lymphocytic Leukemia (CLL)/Small Lymphocytic Lymphoma (SLL) and B-cell Prolymphocytic Leukemia (B-PLL)
Status: Enrolling
Updated: 3/20/2017
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Sorafenib Maintenance Therapy for Patients With AML After Allogeneic Stem Cell Transplant
Updated: 3/21/2017
Phase I Trial of Sorafenib Maintenance Therapy for Patients With FLT3-ITD AML After Allogeneic Stem Cell Transplantation
Status: Enrolling
Updated: 3/21/2017
Sorafenib Maintenance Therapy for Patients With AML After Allogeneic Stem Cell Transplant
Updated: 3/21/2017
Phase I Trial of Sorafenib Maintenance Therapy for Patients With FLT3-ITD AML After Allogeneic Stem Cell Transplantation
Status: Enrolling
Updated: 3/21/2017
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Sorafenib Maintenance Therapy for Patients With AML After Allogeneic Stem Cell Transplant
Updated: 3/21/2017
Phase I Trial of Sorafenib Maintenance Therapy for Patients With FLT3-ITD AML After Allogeneic Stem Cell Transplantation
Status: Enrolling
Updated: 3/21/2017
Sorafenib Maintenance Therapy for Patients With AML After Allogeneic Stem Cell Transplant
Updated: 3/21/2017
Phase I Trial of Sorafenib Maintenance Therapy for Patients With FLT3-ITD AML After Allogeneic Stem Cell Transplantation
Status: Enrolling
Updated: 3/21/2017
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Busulfan/Clofarabine + Allogeneic Stem Cell Transplantation
Updated: 3/21/2017
Phase II Study of Reduced Intensity Conditioning With Busulfan/Clofarabine Followed by Allogeneic Stem Cell Transplantation
Status: Enrolling
Updated: 3/21/2017
Busulfan/Clofarabine + Allogeneic Stem Cell Transplantation
Updated: 3/21/2017
Phase II Study of Reduced Intensity Conditioning With Busulfan/Clofarabine Followed by Allogeneic Stem Cell Transplantation
Status: Enrolling
Updated: 3/21/2017
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Busulfan/Clofarabine + Allogeneic Stem Cell Transplantation
Updated: 3/21/2017
Phase II Study of Reduced Intensity Conditioning With Busulfan/Clofarabine Followed by Allogeneic Stem Cell Transplantation
Status: Enrolling
Updated: 3/21/2017
Busulfan/Clofarabine + Allogeneic Stem Cell Transplantation
Updated: 3/21/2017
Phase II Study of Reduced Intensity Conditioning With Busulfan/Clofarabine Followed by Allogeneic Stem Cell Transplantation
Status: Enrolling
Updated: 3/21/2017
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Busulfan/Clofarabine + Allogeneic Stem Cell Transplantation
Updated: 3/21/2017
Phase II Study of Reduced Intensity Conditioning With Busulfan/Clofarabine Followed by Allogeneic Stem Cell Transplantation
Status: Enrolling
Updated: 3/21/2017
Busulfan/Clofarabine + Allogeneic Stem Cell Transplantation
Updated: 3/21/2017
Phase II Study of Reduced Intensity Conditioning With Busulfan/Clofarabine Followed by Allogeneic Stem Cell Transplantation
Status: Enrolling
Updated: 3/21/2017
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Bendamustine Hydrochloride, Clofarabine, and Etoposide in Treating Younger Patients With Relapsed or Refractory Hematologic Malignancies
Updated: 3/21/2017
A Phase I Trial of Bendamustine in Combination With Clofarabine and Etoposide in Pediatric Patients With Relapsed or Refractory Hematologic Malignancies
Status: Enrolling
Updated: 3/21/2017
Bendamustine Hydrochloride, Clofarabine, and Etoposide in Treating Younger Patients With Relapsed or Refractory Hematologic Malignancies
Updated: 3/21/2017
A Phase I Trial of Bendamustine in Combination With Clofarabine and Etoposide in Pediatric Patients With Relapsed or Refractory Hematologic Malignancies
Status: Enrolling
Updated: 3/21/2017
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Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
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Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
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Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
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Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
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Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
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Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
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Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
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Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
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Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
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Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
Safety Study of Mocetinostat in Combination With Azacitidine in Subjects With MDS
Updated: 3/21/2017
A Phase I/II, Multi-Center Study of Mocetinostat (MGCD0103) in Combination With Azacitidine in Subjects With Intermediate or High Risk Myelodysplastic Syndrome (MDS)
Status: Enrolling
Updated: 3/21/2017
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A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
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A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
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A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
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A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
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A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
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A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
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A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
Click here to add this to my saved trials
A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
Click here to add this to my saved trials
A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
A Trial In Patients With Advanced Cancer And Leukemia
Updated: 4/3/2017
A Phase I Trial Of Pf-03084014 In Patients With Advanced Solid Tumor Malignancy And T-cell Acute Lymphoblastic Leukemia/Lymphoblastic Lymphoma
Status: Enrolling
Updated: 4/3/2017
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Delayed Effects of Treatment in Cancer Survivors (DETECS)
Updated: 4/3/2017
Delayed Effects of Treatment in Cancer Survivors (DETECS)
Status: Enrolling
Updated: 4/3/2017
Delayed Effects of Treatment in Cancer Survivors (DETECS)
Updated: 4/3/2017
Delayed Effects of Treatment in Cancer Survivors (DETECS)
Status: Enrolling
Updated: 4/3/2017
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Cognitive-Behavioral Intervention for Worry, Uncertainty, and Insomnia for Cancer Survivors
Updated: 4/4/2017
Worry, Uncertainty and Insomnia: A Cognitive-behavioral Intervention for Cancer Survivors
Status: Enrolling
Updated: 4/4/2017
Cognitive-Behavioral Intervention for Worry, Uncertainty, and Insomnia for Cancer Survivors
Updated: 4/4/2017
Worry, Uncertainty and Insomnia: A Cognitive-behavioral Intervention for Cancer Survivors
Status: Enrolling
Updated: 4/4/2017
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Tipifarnib in Treating Patients With Anemia or Neutropenia and Large Granular Lymphocyte Leukemia
Updated: 4/4/2017
A Phase 2 Study of Tipifarnib in Large Granular Lymphocyte (LGL) Leukemia
Status: Enrolling
Updated: 4/4/2017
Tipifarnib in Treating Patients With Anemia or Neutropenia and Large Granular Lymphocyte Leukemia
Updated: 4/4/2017
A Phase 2 Study of Tipifarnib in Large Granular Lymphocyte (LGL) Leukemia
Status: Enrolling
Updated: 4/4/2017
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Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma
Updated: 4/5/2017
A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 4/5/2017
Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma
Updated: 4/5/2017
A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 4/5/2017
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Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma
Updated: 4/5/2017
A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 4/5/2017
Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma
Updated: 4/5/2017
A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 4/5/2017
Click here to add this to my saved trials
Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma
Updated: 4/5/2017
A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 4/5/2017
Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma
Updated: 4/5/2017
A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 4/5/2017
Click here to add this to my saved trials
Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma
Updated: 4/5/2017
A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 4/5/2017
Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma
Updated: 4/5/2017
A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 4/5/2017
Click here to add this to my saved trials
Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma
Updated: 4/5/2017
A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 4/5/2017
Study of ACY-1215 Alone and in Combination With Bortezomib and Dexamethasone in Multiple Myeloma
Updated: 4/5/2017
A Phase 1/2, Open-Label, Multicenter Study of ACY-1215 Administered Orally as Monotherapy and in Combination With Bortezomib and Dexamethasone for the Treatment of Relapsed or Relapsed/Refractory Multiple Myeloma
Status: Enrolling
Updated: 4/5/2017
Click here to add this to my saved trials