Percutaneous Hepatic Perfusion in Patients With Hepatic-dominant Ocular Melanoma
Trial details
- Registry ID
- NCT02678572
- Phase
- Phase 3
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Research sample: selected versions from May 2023 onward plus a preceding baseline where available. Only selected fields were retained; endpoint measures were truncated to 300 characters. This is not complete trial or sponsor history. Daily snapshots begin when collection starts.
| Trial | Sponsor | Phase | Status | Primary completion |
|---|---|---|---|---|
| Percutaneous Hepatic Perfusion in Patients With Hepatic-dominant Ocular MelanomaNCT02678572 | DCTH | Phase 3 | Completed | 2023-05-18Actual |
| An Open-Label Expanded Access Study of the Melphalan/Hepatic Delivery System (HDS) in Patients With Hepatic Dominant Ocular MelanomaNCT05022901 | DCTH | Phase 3 | Active not recruiting | 2024-03-01Estimated |
| Evaluation of the Safety and Efficacy of Treatment w/High Dose Melphalan Given Directly Into the Liver Followed by Treatment w/Approved Cancer Treatment or Approved Cancer Treatment Alone in Patients w/ Metastatic Colorectal Cancer w/Liver Dominant DiseaseNCT06607458 | DCTH | Phase 2 | Recruiting | 2026-12Estimated |
| Evaluation of the Safety and Efficacy of Treatment w/High Dose Melphalan Given Directly Into the Liver Followed by Treatment w/Approved Cancer Treatment or Approved Cancer Treatment Alone in Patients w/ Metastatic Breast Cancer w/Liver Dominant DiseaseNCT06875128 | DCTH | Phase 2 | Recruiting | 2029-05Estimated |
NCT02678572 · Delcath Systems Inc.
Text changed; whether the study measures changed has not been verified. Saved text may be shortened.
Measure: Objective Response Rate (ORR) as determined by Independent Central Review Committee
Measure: Objective Response Rate (ORR) as Determined by Independent Central Review Committee.
NCT06875128 · Delcath Systems Inc.
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