Viridian is currently investigating a portfolio of potentially transformative anti-insulin-like growth factor-1 receptor (IGF-1R) and anti-thyroid-stimulating hormone receptor (TSHR) monoclonal antibodies for the potential treatment of thyroid eye disease (TED). IGF-1R, is a transmembrane receptor that plays a role in development, metabolism, and immune regulation, and is a clinically and commercially validated target for the treatment of TED. Based on work in the field, IGF-1R and the co-located TSHR have been found to play a key role in the pathogenesis of TED. Viridian is making meaningful progress advancing potentially improved anti-IGF-1R and anti-TSHR antibodies for people affected by TED and believes its programs have the potential to be transformative treatment options for patients.

Elegrobart

Anti-TSHR

Administration

Self-administered Subcutaneous Injection

Self-administered Subcutaneous Injection

Mechanism

Full Antagonist

Undisclosed

Phase of Development

Phase 3

Preclinical

Treatment Regimen

Dosing every eight or four weeks

Undetermined

Potential Indication

TED

TED & Graves' Disease

TED Program Details

Elegrobart is a subcutaneously delivered, half‑life‑extended, investigational, monoclonal antibody targeting the insulin‑like growth factor‑1 receptor (IGF‑1R). Elegrobart is a full antagonist of IGF-1R and was engineered to have a longer half-life. Elegrobart is designed to be a low volume, infrequently dosed subcutaneous IGF-1R for TED, which we believe has the potential to preserve the efficacy of anti-IGF-1Rs in TED, improve tolerability, and improve convenience for patients with subcutaneous delivery.

We reported positive topline results for elegrobart from two pivotal phase 3 clinical trials, REVEAL-1 and REVEAL-2, for people living with active and chronic TED, respectively.

ElegrobartVRDN-003 is a potential best-in-class subcutaneous monoclonal antibody targeting IGF-1R. VRDN-003 has the same binding domain as its parent molecule, VRDN-001, and was engineered to have a longer half-life. VRDN-003 is designed to maintain the clinical response of VRDN-001 IV while significantly increasing patient convenience and potentially improving safety. Viridian is on track to initiate two phase 3 clinical trials of VRDN-003 in August 2024.

Viridian’s preclinical TSHR inhibitor program includes a potential best-in-class, half-life extended, monoclonal antibody that inhibits TSHR, designed for subcutaneous delivery in an autoinjector with the potential to support extended dosing intervals designed for patient convenience.

Anti-TSHR

 

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