Uveal Melanoma, Recurrent

2

Review clinical trials related to Uveal Melanoma, Recurrent. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

A Dose Escalation and Dose Expansion Study of Intratumoral ONM-501 Alone and in Combination With Cemiplimab in Patients With Advanced Solid Tumors and Lymphomas.

A phase 1, multicenter, open label, non-randomized dose escalation and dose expansion study to examine the maximum tolerated dose, (MTD), minimum effective dose (MED) and/or recommended dose for expansion (RDE) of intratumoral ONM-501 as monotherapy and in combination with a PD-1 checkpoint inhibitor in patients with advanced solid tumors and lymphomas.

Participants needed: 168
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: OncoNano Medicine, Inc.Updated: Dec 24, 2025Locations: 16
Eligibility criteria

Ability to understand and willingness to sign written informed consent before pe... [+6]

Other malignancy active within the previous 2 years except for basal or squamous... [+12]

Status: Recruiting

Evaluation of the Safety, Efficacy, and Pharmacokinetics of NBM-BMX in Patients With Metastatic Uveal Melanoma

This study is being done to find the best dose of an investigational drug called NBM-BMX for people with metastatic uveal melanoma, a type of eye cancer that has spread to other parts of the body. The study will help doctors learn about the side effects of NBM-BMX, how the drug is processed in the body, and whether it may slow down or shrink tumors. Participants will take NBM-BMX as a capsule by mouth twice daily on an empty stomach with at least six ounces (180 mL) of water. No food or drink (other than water) should be consumed for at least two hours after each dose. Participants will visit the clinic about once every week or two for exams and blood tests while taking NBM-BMX. After stopping treatment, a follow-up visit will occur about 30 days later. Treatment may continue as long as the cancer does not get worse and side effects remain manageable.

Participants needed: 36
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Novelwise Pharmaceutical CorporationUpdated: Nov 28, 2025Locations: 3
Eligibility criteria

Signed, written IRB-approved informed consent. [+20]

Pregnant or nursing women. NOTE: Women of child-bearing potential and men must a... [+10]