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Suprachoroidal Administration in Subjects With Metastases to the Choroid

RecruitingPhase 2

A Phase 2, Open-Label, Dose Escalation Trial Assessing the Safety, Tolerability, and Treatment Effect of Belzupacap Sarotalocan (AU-011) With Suprachoroidal Administration in Subjects With Metastases to the Choroid

Who can join

Ages 18 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Have a clinical diagnosis of Metastases to the Choroid, from a histopathologically or cytologically confirmed tumor.
* Have at least one Metastases to the Choroid in the study eye

Exclusion Criteria:

* Active ocular infection or disease.
* Must not have evidence of a primary tumor or metastatic lesion in the brain requiring treatment with radiation therapy per the primary treating oncologist's assessment.
* Must not be planning or expecting to switch/add systemic antineoplastic therapies during treatment

About the study

The primary objective is to assess the safety and tolerability of bel-sar treatment in subjects with metastases to the choroid from any primary solid tumor.

What is being tested

Sponsor: Aura Biosciences · Participants: 24 · Started: Dec 16, 2024

Contact the study team

Official record on ClinicalTrials.gov — NCT06643884

Locations in the U.S.

CaliforniaByers Eye Institute at Stanford University, Palo Alto
FloridaBascom Palmer Eye Institute, Miami
MassachusettsMassachusetts Eye and Ear, Boston
MichiganKellogg Eye Center, Ann Arbor
MinnesotaMayo Clinic, Rochester (Not yet recruiting)
OhioCleveland Clinic, Cole Eye Institute, Cleveland (Not yet recruiting)
PennsylvaniaShields and Shields, PC, Philadelphia (Not yet recruiting)
TennesseeTennessee Retina, PC, Nashville
TexasRetina Consultants of Texas, Bellaire
WashingtonUniversity of Washington, Seattle

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.