Characterization of Corneal Epithelial Changes in Participants Treated With Belantamab Mafodotin
Summary
Third Opinion Trial Synopsis:
If you have been getting belantamab mafodotin treatment for relapsed/refractory multiple myeloma, you can join a study about corneal events. You don't need to still be getting the treatment. Doctors will take a small piece of tissue from your eye to study it. The study will last about four months, and around 25 people will be in it.
If you have been getting belantamab mafodotin treatment for relapsed/refractory multiple myeloma, you can join a study about corneal events. You don't need to still be getting the treatment. Doctors will take a small piece of tissue from your eye to study it. The study will last about four months, and around 25 people will be in it.
*Third Opinion AI Generated Synopsis
Trial Summary
This study will be available to any participant who has received or is currently receiving belantamab mafodotin treatment through either a clinical trial, an access program, or a physician prescription. Participants do not need to be on active treatment. The purpose of this study is to gain a more complete understanding of the pathophysiology of the corneal events seen in some participants with relapsed/refractory multiple myeloma (RRMM) treated with belantamab mafodotin. A superficial corneal epithelial tissue specimen will be obtained by performing impression cytology (IC) or superficial keratectomy (SK) procedure in participants treated with belantamab mafodotin. The procedure will only be performed in one eye, most affected by the corneal epithelial changes. This specimen will undergo pathologic examination and composition analysis. Study duration will be approximately 4 months. Approximately 25 participants will be enrolled in the study.
This study will be available to any participant who has received or is currently receiving belantamab mafodotin treatment through either a clinical trial, an access program, or a physician prescription. Participants do not need to be on active treatment. The purpose of this study is to gain a more complete understanding of the pathophysiology of the corneal events seen in some participants with relapsed/refractory multiple myeloma (RRMM) treated with belantamab mafodotin. A superficial corneal epithelial tissue specimen will be obtained by performing impression cytology (IC) or superficial keratectomy (SK) procedure in participants treated with belantamab mafodotin. The procedure will only be performed in one eye, most affected by the corneal epithelial changes. This specimen will undergo pathologic examination and composition analysis. Study duration will be approximately 4 months. Approximately 25 participants will be enrolled in the study.
Locations & Contact
Fill out the form and "Notify Multiple Myeloma Research Foundation" to let the Multiple Myeloma Research Foundation know you are interested in this trial.
Contacts: