A Phase 2 trial of AU-011 via suprachoroidal administration with a dose escalation phase (open-label, ascending single and repeat dose) and a randomized, masked dose expansion phase designed to evaluate the safety and efficacy of AU-011 in subjects with primary indeterminate lesions and small choroidal melanoma
Study of AU-011 in Patients with Melanoma or Lesion in the Eye
Sponsor: Aura Biosciences
Enrolling: Male and Female Patients
IRB Number: AAAT1102
U.S. Govt. ID: NCT04417530
Contact: Research Nurse Navigator: 212-342-5162 / cancerclinicaltrials@cumc.columbia.edu
Additional Study Information: The purpose of this research study is to test the safety and efficacy of AU-011 at different doses and different number of doses of study drug when it is injected into the suprachoroidal space of the eye with one or two laser light applications and to find out what effects, if any, it has on research participants with a choroidal melanoma tumor or indeterminate lesion.
This study is closed
Brian Marr, MD
Do You Qualify?
Are you at least 18 years old? Yes No
Have you had evidence of a metastatic disease confirmed by abdominal and chest imaging? Yes No
You may be eligible for this study

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