Solid Tumors Clinical Trial
Official title:
Phase I Trial of Intravenous Recombinant Human TNF-α and Liposomal Doxorubicin in Patients With Advanced Solid Tumors or Lymphomas
Assess the maximum tolerated dose (MTD) and dose limiting toxicity (DLT) of recombinant human tumor necrosis factor-α (rhTNF-α) when given as a single dose intravenously and in combination with liposomal doxorubicin in human subjects
n/a
Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
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Active, not recruiting |
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Phase 1 | |
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Phase 1 | |
Completed |
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Phase 1 | |
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Phase 1 | |
Completed |
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Phase 1 | |
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Phase 1 | |
Active, not recruiting |
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Phase 3 | |
Active, not recruiting |
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Phase 1 | |
Recruiting |
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Phase 1/Phase 2 | |
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Phase 2 | |
Recruiting |
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Phase 1 | |
Active, not recruiting |
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||
Completed |
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Phase 1 | |
Recruiting |
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Phase 1/Phase 2 | |
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Phase 1/Phase 2 | |
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Phase 1 | |
Terminated |
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Phase 1 | |
Withdrawn |
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Pharmacodynamics, Pharmacokinetics, Efficacy and Safety of Balugrastim in Pediatric Patients With Solid Tumors
|
Phase 2 |