Antibody drugs in ophthalmology represent a significant advancement in treating various eye diseases. These biologics target specific proteins involved in pathological processes, such as vascular endothelial growth factor (VEGF), which plays a key role in conditions like age-related macular degeneration (AMD) and diabetic retinopathy. By inhibiting VEGF, drugs like ranibizumab (Lucentis) and bevacizumab (Avastin) reduce abnormal blood vessel growth and leakage, thereby stabilizing and often improving vision. Recent developments have seen the emergence of longer-acting agents like faricimab (Vabysmo) and port delivery systems, which aim to reduce the frequency of injections required. This targeted approach not only enhances efficacy but also minimizes systemic side effects, offering a precise and effective means to manage complex retinal disorders.
Recently, exciting news from the biotech deal space involved a $3 billion USD bid from Merck to acquire EyeBio, in order to diversify their pipeline and add a focus on ophthalmology. Eyebio is a clinical-stage company that develops next-generation therapies to protect, restore and improve vision in patients with sight-threatening eye diseases. Their lead candidate is the tetravalent trispecific antibody Restoret, an agonist of the Wnt signalling pathway and potential treatment of diabetic macular edema (DME) and neovascular age-related macular degeneration (NVAMD).
Meanwhile, a research article published this week by University of Texas Medical Branch assessed a topical solution for retinal delivery of bevacizumab and ranibizumab eye drops. Using a novel anti-aggregation formula (AAF) in rabbits, they demonstrated it to be a potential adjunct to intravitreal injections for the treament of age-related macular degeneration (AMD), a blinding retinal disease. Bevacizumab is a humanized IgG monoclonal antibody that binds to VEGF, and alone, is typically used for cancer treatment. Ranibizumab is a humanized mAb Fab fragment which also targets VEGF-A and used as a blood vessel growth inhibitor.
In the clinical trial space, yesterday Oculis announced positive topline results of a Phase 2b relief trial with licaminlimab (OCS-02), an anti-TNFα eye drop candidate developed with single chain antibody fragment (scFv) technology. The drug is designed to treat ocular inflammatory diseases like Dry Eye Disease (DED). TNF-α inhibition has anti-inflammatory and anti-necrotic effects in inflammatory disorders. Besides licaminlimab, faricimab also holds promise for eye diseases like neovascular age-related macular degeneration and diabetic macular edema. A paper published this week by University of Freiburg reviewed the novel anti-angiopoietin-2 (Ang-2) and anti-VEGF-A bispecific antibody, which demonstrated non-inferior vision gains and improved anatomical outcomes versus aflibercept in patients with DME or nAMD in the phase 3 clinical trial program. Therefore, dual Ang-2/VEGF-A pathway inhibition with faricimab has the potential to provide longer-term improvements in vision over targeting just the VEGF pathway alone in monotherapy.
Ang/Tie2 and VEGF signaling to the regulation of vascular homeostasis.
This report aims to explore the events and trends of the biopharmaceutical industry in Q2 (April, May, June). Besides crovalimab and Vyloy, two more novel antibody drugs have been approved this year
News from the IASLC 2024 World Conference on Lung Cancer (WCLC24) has provided several updates on the clinical trial space for non-small cell lung cancer (NSCLC), with several antibody-based drugs at the forefront. NSCLC is the most common type of lung cancer, accounting for about 85% of all cases.
These past few weeks, several antibody drug startups have progressed from the pre-seed stage to final funding rounds. In the pre-seed stage, the focus is on early research, often funded by founders, grants, or angel investors. As the company progresses to the seed stage, it seeks additional funding to validate its scientific concept and develop initial prototypes, attracting early-stage venture capital.
In August, the US FDA approved Galderma’s Nemluvio (nemolizumab) for adult patients living with prurigo nodularis (PN). Nemluvio is the first approved monoclonal antibody specifically inhibiting the signaling of IL-31, a neuroimmune cytokine that drives multiple disease mechanisms in (PN). Prurigo nodularis is a chronic skin condition that affects approximately 181,000 patients in the United States
