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Study identifier: NCT06519266 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

PHP in Combination With IPI1/NIVO3 Compared to IPI3/NIVO1 Only in Patients With Uveal Melanoma Liver Metastases

Condition: Uveal Melanoma · Liver Metastases  ·  Sponsor: Vastra Gotaland Region

PhasePhase 3
Planned participants40
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Uveal melanoma is the most common primary intraocular malignancy in adults. Despite successful control of the primary tumor, metastatic disease will develop in approximately 35%-50% of the patients within 10 years. The liver is the most common site for metastases, and about 50% of the patients will have isolated liver metastases. These metastases are generally refractory to systemic chemotherapy and the median survival for patients with liver metastases is about 6 months. Regardless of treatment, the mortality rate is approximately 90% at 2 years with only about 1% of the patients surviving more than 5 years. The primary objective with this study is to evaluate progression-free survival in patients with uveal melanoma liver metastases randomized to either percutaneous hepatic perfusion (PHP) in combination with ipilimumab and nivolumab or ipilimumab and nivolumab only. Secondary objectives include further efficacy and safety analysis, as well as biomarker discovery.

This description comes directly from the study's public registry record.

Talk to the study team

Roger Olofsson Bagge, Professor  ·  +46313421000  ·  roger.olofsson.bagge@vgregion.se

Always discuss trial participation with your own doctor first.

Locations (6)

Sahlgrenska University HospitalGothenburg, SwedenRecruiting
Linköping University HospitalLinköping, SwedenNot Yet Recruiting
Skåne University HospitalLund, SwedenNot Yet Recruiting
Karolinska University Hospital,Stockholm, SwedenRecruiting
Norrland University HospitalUmeå, SwedenNot Yet Recruiting
Uppsala University HospitalUppsala, SwedenRecruiting

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Source record: clinicaltrials.gov/study/NCT06519266