Published in Pipeline

RevOpsis raises $16.5M to advance nAMD tri-specific therapy

This is editorially independent content
5 min read

RevOpsis Therapeutics has closed on its first seed funding round of $16.5 million to promote the continued clinical development of its investigational lead candidate for neovascular (wet) age-related macular degeneration (nAMD).

Give me a refresh on the company.

Launched in 2018, RevOpsis is a privately-held, next-generation biopharmaceutical company developing multispecific antibody biologics to target multiple dominant biologic pathways in complex multifactorial ophthalmic diseases.

Chief among these:

  • nAMD
  • Dry AMD
  • Diabetic macular edema (DME)
  • Retinal vein occlusion (RVO)
  • Uveitic macular edema
  • Thyroid eye disease (TED)

Key to this: the company’s fully human, multispecific, proprietary Rev-Mod Platform

Explain what this platform is.

The Rev-Mod Platform utilizes a modular “plug-and-play” method to streamlining and expediting the “efficient discovery and development of multispecific biologics targeting a wide spectrum of chronic, prevalent, large diseases,” according to RevOpsis.

The technology features nearly 30 billion fully human antibody components in a structured phage display system of a library.

And its purpose?

Essentially, it’s designed to enable a rapid identification and assembly process of multispecific products.

How: by being compatibility so as to allow for the development of multispecific biologics that address unmet needs in major therapeutic areas:

  • Ophthalmology
  • Oncology
  • Immune-mediated diseases

Gotcha. Now talk about this investigational candidate.

The company’s lead asset, RO-104 is a first-in-class, fully human modular tri-specific biologic that’s designed to address the three dominant angiogenic pathways that may cause retinal vascular disease (RVD) progression:

  • Vascular endothelial growth factor (VEGF)-A
    • Protein that can promote angiogenesis, vascular permeability, cell migration, and gene expression
  • VEGF-C
    • Protein considered essential to the potential development of lymphatic vessels
  • Angiopoietin (Ang)-2
    • Protein expressed in endothelial cells for remodeling blood vessels and regulating  blood vessel stability

And how is it unique from other anti-VEGF therapies?

Per RevOpsis, by the very fact that RO-104 is designed to target these three angiogenic pathways—unlike standard therapies that typically require repeat monthly injections and primarily only target the VEGF-A pathway to treat nAMD.

So why not just stick with targeting VEGF-A?

Based on prior research, when the VEG-A pathway is treated for nAMD (as with current therapies), both the VEG-C and Ang-2 become more active in RVDs, which then results in the possible need for either more frequent treatment or the efficacy of the therapy to diminish, according to the company.

Plus: only a reported less than 30% of patients with nAMD respond optimally to VEGF-A therapy.

Which means: RevOpsis hypothesized that “most patients with nAMD might benefit from a treatment that simultaneously targets” all three angiogenic pathways.

And the intended purpose of RO-104?

The candidate, which was developed using the Rev-Mod Platform, is designed to target and neutralize

all three of these pathways in order to provide “improved outcomes and extended disease remission” for nAMD patients.

  • How: by binding to each pathway with a high, matched affinity, per RevOpsis.
    • Note: The asset has reportedly demonstrated its intended efficacy via animal models.

Alrighty, so what exactly will this funding go toward?

The seed funding (which includes $7.5 million in non-dilutive capital) will be used to fund the company’s completion of its investigational new drug (IND)-enabling studies for RO-104.

Plus: “The funds will be used to strengthen RevOpsis’ research capabilities to further develop a pipeline of first and best-in-class retinal treatments,” stated Interim CEO Ram Bhandrai, MD.

The ultimate goal: to secure FDA authorization and conduct the first-in-human (FIH) clinical trials on RO-104 for nAMD by 2025

And the significance of this asset?

RO-104 has the potential to be the first monotherapy for treating nAMD, representing a new therapeutic standard for RVDs.

How would you rate the quality of this content?