Comparing The Efficacy Of An Anti-Human VEGF-A Neutralizing Antibody Versus Bevacizumab On A Laser-Induced Choroidal Neovascularization (CNV) Rhesus Monkey Model.

Abstract

PURPOSE:

To evaluate the efficacy of a therapy on improving characteristics of laser-induced choroidal neovascularization (CNV) via single intravitreal injection of a humanized anti-human VEGF monoclonal antibody (PRO-169) versus bevacizumab in a rhesus monkey model.

METHODS:

To induce experimental CNV, small high-energy laser spots were used to treat several areas, around the macula in the retinas of monkeys at Day -21. Eighteen rhesus monkeys were used for CNV induction. The efficacy endpoints were fluorescein leakage by FFA and retinal thickness by OCT. FFA examinations were performed 19 days after induction. Appropriate animals were enrolled for treatment and randomly divided into 3 groups: bevacizumab (n=5, 7 eyes), PRO-169 (n=5, 7 eyes), and vehicle controls (n=4, 7 eyes).

RESULTS:

In 25 of 36 (69.4%) eyes, CNV lesions were identified. The average percent change of retinal thickness in the eyes of bevacizumab group was -159.3±62.2% and -154.0±45.1% (p<0.01 vs Vehicle) at Day 14 and Day 28, respectively; in the eyes of PRO-169 group it was -131.6±68.7% and -131.5±63.8% (p<0.01 vs Vehicle), respectively. The average percent change of leakage area in the eyes of bevacizumab group was -75.3±49.4% and -78.0±42.6% (p<0.01 vs Vehicle) at Day 14 and Day 28, respectively; in the eyes of PRO-169 group it was -82.0±19.3% and -81.4±21.0% (p<0.01 vs Vehicle), respectively. There were no abnormalities found in behavior, skin and hair, excretion and overall eye appearance before and after treatment in all groups.

CONCLUSION:

After photocoagulation, the eyes enrolled in this studio showed CNV related characteristics including increased retinal thickness, and fluorescein leakage at laser spots. PRO-169 (1.25 mg per eye) can reduce the retinal thickness and fluorescein leakage area after treatment for 14 and 28 days in this rhesus monkeys model, without toxic effect or adverse events. These findings suggested that PRO-169 can inhibit CNV.

• Authors: Oscar Olvera-Montaño, Leopoldo Baiza-Duran, Juan D Quintana-Hau, Mayra G Quiñonez-Alvarado, Wen Zeng, Li Gong, Patricia Muñoz-Villegas
• Journal: Drug design, development and therapy (Drug Des Devel Ther) Vol. 13 Pg. 3813-3821 ( 2019) ISSN: 1177-8881 [Electronic] New Zealand
• PMID: 31806932 (Publication Type: Comparative Study, Journal Article)
• Copyright: © 2019 Olvera-Montaño et al.

Chemical References

• Angiogenesis Inhibitors
• Antibodies, Neutralizing
• VEGFA protein, human
• Vascular Endothelial Growth Factor A
• Bevacizumab

Topics

• Angiogenesis Inhibitors (pharmacology)
• Animals
• Antibodies, Neutralizing (pharmacology)
• Bevacizumab (pharmacology)
• Choroidal Neovascularization (drug therapy, metabolism)
• Disease Models, Animal
• Dose-Response Relationship, Drug
• Drug Delivery Systems
• Fluorescein Angiography
• Lasers
• Macaca mulatta
• Molecular Structure
• Structure-Activity Relationship
• Vascular Endothelial Growth Factor A (antagonists & inhibitors, metabolism)