CPX-351
CPX-351 is a pharmaceutical drug with 35 clinical trials. Currently 8 active trials ongoing. Historical success rate of 81.0%.
Success Metrics
Based on 17 completed trials
Phase Distribution
Phase Distribution
13
Early Stage
16
Mid Stage
3
Late Stage
Highest Phase Reached
Phase 4Trial Status & Enrollment
68.0%
17 of 25 finished
32.0%
8 ended early
8
trials recruiting
35
all time
Detailed Status
Development Timeline
Analytics
Development Status
Trials by Phase
Trials by Status
Recent Activity
CPX-351 (Vyxeos™) for Transplant Eligible, Higher Risk Patients With Myelodysplastic Syndrome
Phase IB/II of CPX-351 for Relapse Prevention in AML
CPX-351 and Glasdegib for Newly Diagnosed Acute Myelogenous Leukemia With MDS Related Changes or Therapy-related Acute Myeloid Leukemia
Study of CPX-351 (VYXEOS) in Individuals < 22 Years With Secondary Myeloid Neoplasms
Study of Standard Intensive Chemotherapy Versus Intensive Chemotherapy With CPX-351 in Adult Patients With Newly Diagnosed AML and Intermediate- or Adverse Genetics
Clinical Trials (35)
CPX-351 (Vyxeos™) for Transplant Eligible, Higher Risk Patients With Myelodysplastic Syndrome
Phase IB/II of CPX-351 for Relapse Prevention in AML
CPX-351 and Glasdegib for Newly Diagnosed Acute Myelogenous Leukemia With MDS Related Changes or Therapy-related Acute Myeloid Leukemia
Study of CPX-351 (VYXEOS) in Individuals < 22 Years With Secondary Myeloid Neoplasms
Study of Standard Intensive Chemotherapy Versus Intensive Chemotherapy With CPX-351 in Adult Patients With Newly Diagnosed AML and Intermediate- or Adverse Genetics
CPX-351 as a Novel Approach for the Treatment of Older Patients With AML and MDS
Phase I/II Clinical Trial of Proteasome Inhibitor in Combination With CPX-351 for the Treatment of Newly-Diagnosed TP53-mutated Acute Myeloid Leukemia (AML)
Phase I/II Trial of CPX-351 + Palbociclib in Patients With Acute Myeloid Leukemia
Vyxeos(CPX-351) in Adults w R/R Acute Lymphoblastic Leukemia
Evaluation of CPX-351 Monotherapy in Acute Myeloid Leukemia Secondary to Myeloproliferative Neoplasm
Induction Therapy for Patients With FLT3 Mutated Acute Myeloid Leukemia
CPX-351 Therapy for MDS After Hypomethylating Agent Failure
Testing the Use of Combination Therapy in Patients With Persistent Low Level Acute Myeloid Leukemia (AML) Following Initial Treatment
Investigator Initiated Trial of CPX-351 for Untreated Acute Myeloid Leukemia
Magrolimab Plus Intensive Chemotherapy in Newly Diagnosed AML or HR-MDS
A Study of CPX-351 (Vyxeos™) With Quizartinib for the Treatment of FLT3-ITD Mutation-Positive Acute Myeloid Leukemia
A Phase 1b Master Trial to Investigate CPX-351 in Subjects With Previously Untreated Acute Myeloid Leukemia
Comparison of Therapies Before Stem Cell Transplantation in Patients With Higher Risk MDS and Oligoblastic AML
CPX-351+GO in Subjects 55 Years Old, or Older, With AML
CPX-351 Salvage Therapy Followed by Haplo-Cord Transplant for Relapsed/Refractory Leukemia or Myelodysplastic Syndrome
Drug Details
- Intervention Type
- DRUG
- Total Trials
- 35