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40 clinical studies listed.

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Uveal Melanoma

Tundra lists 40 Uveal Melanoma clinical trials. Each listing includes eligibility criteria, study locations, and direct links to research sites in the Tundra directory.

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RECRUITING

NCT07913412

High-precision Radiosurgery Followed by Minimally Invasive Surgical Approach in Patients With High-prominence Uveal Melanoma: Modern Radiation Techniques and Outcomes

High-precision radiosurgery followed by minimally invasive surgical approach in patients with high-prominence uveal melanomas: modern radiation techniques and outcomes. Evaluation of outcome regarding multiparametric parameters and co-factors

Gender: All

Ages: 18 Years - Any

Updated: 2026-11-03

1 state

Uveal Melanoma
High-risk Uveal Melanoma
Prominent Uveal Melanoma
COMPLETED

NCT03070392

Safety and Efficacy of IMCgp100 Versus Investigator Choice in Advanced Uveal Melanoma

To evaluate the overall survival of HLA-A\*0201 positive adult patients with previously untreated advanced UM receiving IMCgp100 compared to Investigator's Choice of dacarbazine, ipilimumab, or pembrolizumab.

Gender: All

Ages: 18 Years - 99 Years

Updated: 2026-10-29

23 states

Uveal Melanoma
RECRUITING

NCT07364474

Immune Response to Percutaneous Hepatic Perfusion With Melphalan for Ocular Melanoma Metastatic to the Liver

This study seeks to better understand the liver's immune response to receiving chemotherapy agent melphalan through Percutaneous Hepatic Perfusion (PHP) alone or in combination with Ipilimumab and Nivolumab for patients with Uveal Melanoma that has metastasized to the liver.

Gender: All

Ages: 18 Years - Any

Updated: 2026-10-23

1 state

Uveal Melanoma
ACTIVE NOT RECRUITING

NCT07421739

Choroidal Melanoma Patient-Reported Outcome Study (CM-PRO) in a Subset of AU-011-301 (CoMpass) Subjects

To assess subject-centric evidence of QoL outcomes in a subset of subjects enrolled in the global Phase 3 AU-011-301 clinical trial.

Gender: All

Updated: 2026-10-22

1 state

Choroidal Melanoma
Indeterminate Lesions
Uveal Melanoma
+1
RECRUITING

NCT04792463

Frequency and Clinical Phenotype of BAP1 Hereditary Predisposition Syndrome

This research will have a significant impact on the overall management of those cancer patients and their family members who are at risk for hereditary cancer due to germline inactivation of BAP1. Our study will ultimately facilitate the development of novel screening, prevention and treatment strategies for these individuals with the syndrome. Because the vast majority of UM develop in pre-existing nevi, characterization of individuals at high risk for development of UM will allow closer screening and earlier intervention which would improve the treatment outcome not only for retaining vision but also for overall survival. Similarly in patients with germline BAP1 mutation CM develops in premalignant atypical melanocytic lesions and careful follow up of these patients will improve the outcome of their disease. In addition this study could have impact on the management of patients with personal and/or family history of several other cancers reported in patients with germline BAP1 mutation such as mesothelioma, renal cell carcinoma, cholangiocarcinoma, hepatocellular carcinoma, meningioma and basal cell carcinoma.

Gender: All

Updated: 2026-10-16

1 state

Uveal Melanoma
Cutaneous Melanoma
BAP1 Gene Mutation
+5
ACTIVE NOT RECRUITING

NCT06007690

A Phase 3 Randomized, Masked, Controlled Trial to Evaluate Efficacy and Safety of Belzupacap Sarotalocan (AU-011) Treatment Compared to Sham Control in Subjects With Primary Indeterminate Lesions or Small Choroidal Melanoma

The primary objective is to determine the safety and efficacy of belzupacap sarotalocan (bel-sar) compared to sham control in patients with primary indeterminate lesions (IL) or small choroidal melanoma (CM).

Gender: All

Ages: 18 Years - Any

Updated: 2026-10-13

23 states

Choroidal Melanoma
Indeterminate Lesions
Uveal Melanoma
+1
RECRUITING

NCT07804186

Study of Adjuvant Darovasertib and Crizotinib in Participants With Primary Non-metastatic Uveal Melanoma

This is a randomized, multi-center, open-label study of adjuvant darovasertib in participants with non-metastatic uveal melanoma (OptimUM-11)

Gender: All

Ages: 18 Years - Any

Updated: 2026-09-15

11 states

Uveal Melanoma
RECRUITING

NCT05607095

A Study of LN-144 or LN-145 in People With Advanced Uveal Melanoma, Undifferentiated Pleomorphic Sarcoma, Dedifferentiated Liposarcoma, or Angiosarcoma

This is an open label study evaluating lifileucel (LN-144) in patients with metastatic uveal melanoma.

Gender: All

Ages: 18 Years - Any

Updated: 2026-09-15

1 state

Uveal Melanoma
Melanoma
Metastatic Uveal Melanoma
+1
ACTIVE NOT RECRUITING

NCT05524935

Olaparib in Combination With Pembrolizumab for Advanced Uveal Melanoma

This is a prospective phase II multi-center trial of the combination of the PARP inhibitor olaparib with the immune checkpoint inhibitor pembrolizumab in advanced uveal melanoma.

Gender: All

Ages: 18 Years - Any

Updated: 2026-09-15

1 state

Uveal Melanoma
Ocular Melanoma
COMPLETED

NCT02678572

Percutaneous Hepatic Perfusion in Patients With Hepatic-dominant Ocular Melanoma

This study will evaluate patients who have ocular melanoma that has spread from the eye to the liver: Patients in the study will be treated with Melphalan/HDS up to 6 total treatments and will be followed until death. This study will evaluate the safety and efficacy of the treatment and how long patients live and how long it takes for the cancer to advance or respond to the treatment.

Gender: All

Ages: 18 Years - Any

Updated: 2026-09-10

11 states

Ocular Melanoma
Uveal Melanoma
NOT YET RECRUITING

NCT05903937

Locoregional Administration of TIL and Lymphodepletion in Patients With Melanoma and Liver Metastases

Evaluate the safety and tolerability of treatment with autologous tumor infiltrating lymphocytes (TIL) administered via hepatic arterial infusion and preconditioning with percutaneous hepatic perfusion in patients with liver metastases (but not restricted to) of malignant melanoma

Gender: All

Ages: 18 Years - Any

Updated: 2026-09-09

Uveal Melanoma
Metastatic Cutaneous Melanoma
RECRUITING

NCT06070012

Tebentafusp in HLA-A*0201 Positive Previously Untreated Metastatic Uveal Melanoma

This is a phase II open-label, single-arm, multi-center study of tebentafusp in HLA- A\*0201 positive previously untreated (1L) untreated metastatic uveal melanoma (mUM) with an integrated circulating tumor DNA (ctDNA) biomarker.

Gender: All

Ages: 18 Years - Any

Updated: 2026-09-09

4 states

Uveal Melanoma
ACTIVE NOT RECRUITING

NCT04588662

A Prospective Natural History Study in Uveal Melanoma

The overall objective of this proposal is to develop and utilize a multicenter UM registry that will, in a longitudinal fashion, capture prospective data in order to characterize the natural history of UM and provide data that will be used to support the development of novel therapies for this disease. The care of patients with UM requires a multi-disciplinary team of physicians that commonly requires the involvement of both radiation oncology and interventional radiology, and is typically directed by an ophthalmologic oncologist at time of initial diagnosis of primary disease. Overall management is transitioned to a medical oncologist when distant recurrence is identified. In the case that a patient presents with metastasis at the time of diagnosis, a medical oncologist typically directs overall management. The management of surveillance for the development of metastasis following the treatment of primary disease is variable and, if performed at all, is managed by either an ophthalmologic oncologist or medical oncologist. Thus, the successful development of a registry that aims to capture the data regarding the full natural history of UM requires a collaborative effort including leaders from both the UM ophthalmologic oncology and medical oncology fields. To this end, the investigators have built an initial consortium of key ophthalmologic oncology and medical oncology leaders from multiple major UM centers in the United States.

Gender: All

Ages: 18 Years - Any

Updated: 2026-08-11

4 states

Uveal Melanoma
NOT YET RECRUITING

NCT07747935

Study of Neoadjuvant RBP-01 In Patients With Primary Uveal Melanoma

Neoadjuvant RBP-01 in patients with primary uveal melanoma.

Gender: All

Ages: 18 Years - Any

Updated: 2026-08-05

Uveal Melanoma
TERMINATED

NCT03417739

A Phase II Study of BVD-523 in Metastatic Uveal Melanoma

This research study is studying a targeted therapy called BVD-523 as a possible treatment for advanced uveal melanoma.

Gender: All

Ages: 18 Years - Any

Updated: 2026-07-27

1 state

Uveal Melanoma
ACTIVE NOT RECRUITING

NCT04328844

A Study to Assess a PI3Kδ Inhibitor (IOA-244) in Patients With Metastatic Cancers

The objective of study IOA-244-101 is to determine whether IOA-244 is safe and tolerable in cancer patients (Part A). In addition, the study will assess whether IOA-244 can increase the anti-tumour immune response in patients both as monotherapy and in combination pemetrexed/cisplatin/avelumab (Part B Mesothelioma and NSCLC 1st line), in combination with avelumab (Part B Cutaneous Melanoma and NSCLC 2nd/3rd line) and ruxolitinib (Part B Primary Myelofibrosis)

Gender: All

Ages: 18 Years - Any

Updated: 2026-07-08

1 state

Solid Tumor, Adult
Non-Hodgkin Lymphoma, Adult
NSCLC
+2
ACTIVE NOT RECRUITING

NCT03635632

C7R-GD2.CART Cells for Patients With Relapsed or Refractory Neuroblastoma and Other GD2 Positive Cancers (GAIL-N)

This study is for patients with neuroblastoma, sarcoma, uveal melanoma, breast cancer, or another cancer that expresses a substance on the cancer cells called GD2. The cancer has either come back after treatment or did not respond to treatment. Because there is no standard treatment at this time, patients are asked to volunteer in a gene transfer research study using special immune cells called T cells. T cells are a type of white blood cell that helps the body fight infection. The body has different ways of fighting infection and disease. No single way seems perfect for fighting cancers. This research study combines two different ways of fighting cancer: antibodies and T cells. Both antibodies and T cells have been used to treat patients with cancers. They have shown promise but have not been strong enough to cure most patients. We have found from previous research that we can put a new gene into T cells that will make them recognize cancer cells and kill them. In our last clinical trial we made a gene called a chimeric antigen receptor (CAR) from an antibody that recognizes GD2, a substance found on almost all neuroblastoma cells (GD2-CAR). We put this gene into the patients' own T cells and gave them back to 11 neuroblastoma patients. We saw that the cells did grow for a while, but started to disappear from the blood after 2 weeks. We think that if T cells are able to last longer they may have a better chance of killing GD2 positive tumor cells. Therefore, in this study we will add a new gene to the GD2 T cells that can cause the cells to live longer. T cells need substances called cytokines to survive and the cells may not get enough cytokines after infusion. We have added the gene C7R that gives the cells a constant supply of cytokine and helps them to survive for a longer period of time. In other studies using T cells, investigators found that giving chemotherapy before the T cell infusion can improve the amount of time the T cells stay in the body and therefore the effect the T cells can have. This is called lymphodepletion and we think that it will allow the T cells to expand and stay longer in the body, and potentially kill cancer cells more effectively. The GD2-C7R T cells are an investigational product not approved by the Food and Drug Administration. The purpose of this study is to find the largest safe dose of GD2-C7R T cells, and also to evaluate how long they can be detected in the blood and what affect they have on cancer.

Gender: All

Ages: 1 Year - 74 Years

Updated: 2026-07-06

1 state

Relapsed Neuroblastoma
Refractory Neuroblastoma
Relapsed Osteosarcoma
+4
RECRUITING

NCT07501117

Neoadjuvant Immunotherapy for Patients With High-risk Eye Melanoma

The goal of this clinical trial is to investigate the safety and feasibility of neoadjuvant immunotherapy for patients with high-risk uveal melanoma. The main question is: \- Is neoadjuvant treatment with nivolumab and ipilimumab safe and feasible for patientt with high-riks uveal melanoma? In addition pathological response, distant metastases-free survival, overall survival and immunological changes in the tumor microenviroenment after therapy will be assesed.

Gender: All

Ages: 18 Years - 80 Years

Updated: 2026-07-01

1 state

Uveal Melanoma
RECRUITING

NCT06246149

Adjuvant Tebentafusp in High Risk Ocular Melanoma

At least 50% of patients with high-risk primary uveal melanoma will develop a recurrence following treatment of the primary tumour. Observation is currently the standard of care in the non-metastatic setting. Tebentafusp is the first agent proven to improve overall survival in patients with metastatic uveal melanoma in a randomized trial. Based on the results in the advanced setting, it is hypothesized that treatment with tebentafusp may reduce the risk of development of disease recurrence.

Gender: All

Ages: 18 Years - Any

Updated: 2026-06-30

1 state

Uveal Melanoma
RECRUITING

NCT06932757

Adjuvant Quisinostat in High-Risk Uveal Melanoma

The purpose of this study is to see if giving participants quisinostat will prevent participants' uveal melanoma tumor from spreading. The researchers want to find out the effects that quisinostat has on participants' condition.

Gender: All

Ages: 19 Years - Any

Updated: 2026-06-18

1 state

Uveal Melanoma
RECRUITING

NCT07015190

Neoadjuvant Darovasertib in Primary Uveal Melanoma

This is a Phase 3, randomized, multi-center, open-label study of neoadjuvant darovasertib in subjects with primary non-metastatic uveal melanoma (OptimUM-10)

Gender: All

Ages: 18 Years - Any

Updated: 2026-05-06

55 states

Uveal Melanoma
ACTIVE NOT RECRUITING

NCT05377957

Prospective Registration Of Patient Data and Quality of Life in Eye Melanoma Patients

PROQEM is a prospective cohort study among patients diagnosed with uveal melanoma to assess quality of life before and in the first five years after treatment.

Gender: All

Ages: 18 Years - Any

Updated: 2026-04-15

1 state

Uveal Melanoma
ACTIVE NOT RECRUITING

NCT05496686

Targeted Alpha Particle Radiotherapy for Metastatic Uveal Melanoma

The primary aim of the study is to establish the maximum-tolerated dose (MTD) of 225Ac-MTI-201 in participants with metastatic uveal melanoma. The secondary aims are to describe the pharmacokinetics of 225Ac-MTI-201 and the toxic effects of 225Ac-MTI-201 in participants with metastatic uveal melanoma.

Gender: All

Ages: 18 Years - Any

Updated: 2026-04-03

1 state

Uveal Melanoma
Metastatic
ACTIVE NOT RECRUITING

NCT06075589

Psychoeducation for Uveal Melanoma

This clinical trial evaluates a video-based psychoeducational intervention for patients with uveal melanoma. Uveal melanoma (UM) is a rare intraocular cancer. UM patients face an uncertain course of survivorship in terms of their visual acuity, treatment-related side effects, and risk for eventual metastasis of the cancer. Learning about patients' thoughts and reactions to informational resources may better support patients during ocular melanoma survivorship.

Gender: All

Ages: 18 Years - Any

Updated: 2026-03-19

1 state

Uveal Melanoma