AU-011-301 (Primary Indeterminate Lesions or Small Choroidal Melanoma) - Clinical Trial

¿Cuál es el Propósito de este estudio?

We are doing this study to find out if a study drug called belzupacap sarotalocan (bel-sar) is a safe and effective option when it is combined with laser light therapy for people who have a type of eye cancer called an indeterminate lesion (a growth in your eye that is suspected to be melanoma) or choroidal melanoma, which is also known as eye melanoma.

¿Cuál es la Condición que se está estudiando?

Melanoma of the Eye

¿Quién puede participar en el Estudio?

Adults ages 18+ who:

  • Have no evidence of metastatic disease
  • Have not received any previous treatment for eye melanoma

For more information, contact the study team at ethel.garcia@duke.edu.

¿Qué Implica?

If you choose to join this study, you will get a random assignment to 1 of 3 groups:

  • Group 1: If you are in this group, you will receive a high dose of the study drug and will then get the laser application.
  • Group 2: If you are in this group, you will receive a lower dose of the study drug and will then get the laser application.
  • Group 3: If you are in this group, you will receive a sham dose (inactive dosing that doesn't have drug) and will then get a sham laser application.

The sham procedure will be the same as for the study drug and laser light application, except that no study drug will be injected in the eye (only firm pressure to the eyeball will be applied with a needleless syringe) and no laser light will be applied during the sham laser procedure.

Your chance of being assigned to any of the 3 groups are as follows:

  • Group 1: 40%
  • Group 2: 20%
  • Group 3: 40%

Detalles del Estudio

Título Completo
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
Investigador Principal
Especialista en oncología ocular
Número de Protocolo
IRB: PRO00115154
NCT: NCT06007690
Fase
Phase III
ClinicalTrials.gov
Estado de inscripción
Abierto para inscripción