Viridian Therapeutics
- Company typePublic
- Founded2016
- HeadquartersWaltham, United States
- Headcount251–500
- GTM typeB2B
- OfferingHardware or Manufacturing
Viridian Therapeutics firmographics
Firmographics- Name
- Viridian Therapeutics
- Legal name
- Viridian Therapeutics, Inc.
- Website
- https://viridiantherapeutics.com
- Company type
- Public
- Founded year
- 2016
- Operating status
- Operating
- Headcount range
- 251–500 employees
- Ownership category
- akta.pro rank
Viridian Therapeutics industry classification
Industry- Product category
- Biopharmaceuticals (Rare Disease / Autoimmune Antibody Therapeutics)
- NAICS
- Biological Product (except Diagnostic) Manufacturing (325414)
- SIC
- Biological Products, (No Disgnostic Substances) (2836)
- akta.pro primary industry
- Rare Immunology, Autoimmune & Autoinflammatory Therapies (HLAIAIAE)
- akta.pro secondary industries
- Immunology & Autoimmune Specialty Pharmaceuticals (HLAIACAB), Monoclonal Antibody Therapeutics (mAbs) (HLAAAAAA)
Keywords
Where Viridian Therapeutics is headquartered
LocationHeadquarters
- HQ city
- Waltham
- HQ country
- United States
- HQ region
- North America
Offices2 records
Markets served
Viridian Therapeutics business model
Business model- GTM type
- B2B
- Offering type
- Hardware or Manufacturing
- Cost components
- Personnel, Technology or R&D, Operations, Marketing or Sales, Supply Chain
Revenue model
- Lumvoa (veligrotug) Product Sales: Viridian's first commercial product following FDA approval on June 26, 2026. Revenue from wholesale acquisition of Lumvoa for thyroid eye disease, priced at approximately $450,000 per five-infusion course for an average 75kg patient. The company is building commercial infrastructure to compete directly with Amgen's Tepezza in the TED market.
Pricing tiers
| Model | Billing | Price |
|---|---|---|
| Unit Pricing | Pay-as-you-go | Lumvoa (veligrotug) wholesale acquisition cost |
Go-to-market motion1 record
Distribution channels3 records
Marketing channels5 records
Viridian Therapeutics product offering
Product offeringCore offering
Viridian Therapeutics develops and commercializes monoclonal antibody therapeutics for autoimmune and rare diseases, with a primary focus on thyroid eye disease (TED). Its lead commercial product, Lumvoa (veligrotug-vvze), is an FDA-approved intravenous anti-IGF-1R antibody administered as five 30–40 minute infusions over 12 weeks. The company's pipeline includes a subcutaneous anti-IGF-1R antibody (elegrobart) for self-administration, anti-FcRn candidates (VRDN-006, VRDN-008) for autoimmune disease, and a preclinical anti-TSHR program for TED and Graves' disease.
Product overview
Viridian Therapeutics is a biotechnology company developing a portfolio of antibody therapeutics for autoimmune and rare diseases, primarily focused on thyroid eye disease (TED). The company has transitioned from a development-stage to a commercial entity following FDA approval of its lead product Lumvoa (veligrotug-vvze), an intravenous IGF-1R antagonist. The pipeline includes Elegrobart (VRDN-003), a subcutaneous IGF-1R antibody for TED with BLA submission expected Q1 2027, an anti-TSHR program for TED and Graves' disease, and an FcRn portfolio (VRDN-006 and VRDN-008) for autoimmune diseases. The company's core strategy leverages antibody discovery and engineering expertise to develop differentiated therapeutic candidates for validated targets.
Differentiator
Problem solved
Functional benefit
Brands
- Lumvoa: Brand name for veligrotug (veligrotug-vvze), an IV treatment for thyroid eye disease
- ViridianCares
- Veligrotug
- Elegrobart
Products and services
- Lumvoa (veligrotug-vvze) An FDA-approved intravenous anti-IGF-1R monoclonal antibody for treating thyroid eye disease (TED) in both active and chronic forms. Administered as five infusions over 12 weeks (30–40 minute infusion time). First approved TED treatment with labeling covering both disease stages, based on THRIVE and THRIVE-2 Phase 3 trials. Priced at approximately $450,000 per five-infusion course for an average 75kg patient.
- Elegrobart (VRDN-003) A subcutaneously delivered, half-life-extended monoclonal antibody targeting IGF-1R for thyroid eye disease. Designed for self-administration via subcutaneous autoinjector with dosing every four or eight weeks. If approved, would be the first subcutaneous autoinjector treatment for TED. BLA submission targeted Q1 2027.
- VRDN-006 An anti-neonatal Fc receptor (FcRn)-targeting Fc fragment designed for convenient, self-administered subcutaneous delivery. Non-human primate studies demonstrated specificity for blocking FcRn-IgG interactions with comparable potency to efgartigimod. Currently in Phase 1 study.
- VRDN-008 A novel, first-in-class FcRn inhibitor designed for subcutaneous self-administration. Aims to pair IgG suppression with extended half-life technology, potentially enabling deeper and more durable suppression than existing anti-FcRn therapies. IND submitted.
- Anti-TSHR program A preclinical program developing a half-life extended monoclonal antibody that inhibits TSHR, designed for subcutaneous delivery in an autoinjector. Being developed for potential treatment of thyroid eye disease (TED) and Graves' disease.
- ViridianCares patient support program A comprehensive patient support program launched alongside Lumvoa to assist patients with access, reimbursement, co-pay support, and navigation services for the thyroid eye disease treatment.
Quantifiable outcome
- 48% placebo-adjusted proptosis responder rate in THRIVE Phase 3 trial
- +2 more outcomes
Companies that use Viridian Therapeutics
Customer profileSegments1 record
Ideal customer profiles1 record
Viridian Therapeutics technology and API
TechnologyTechnology focussed Yes
API detail
- Has API
- No
- API docs
- API detail
Core technology
AI maturity
App detail
Feature5 records
Viridian Therapeutics partnerships and signals
Strategic signalPartnerships
One partnership is on record.
- WuXi BiologicscoreNon-exclusive commercial supply agreement for veligrotug with commercial supply to begin upon FDA approval. The 5-year pact includes binding volume commitments and volume-based pricing. While WuXi Biologics was originally targeted by the Biosecure Act, the final legislation did not name the company, reducing regulatory risk for this supply arrangement.
Scale indicators8 records
Recent moves6 records
Expansion highlights6 records
Viridian Therapeutics competitors and assessment
Company assessmentDirect peers
- Amgen: Amgen markets Tepezza (teprotumumab), the incumbent anti-IGF-1R therapy for thyroid eye disease and Viridian's primary competitor. Tepezza generates ~$1.9-2B in annualized revenue, making Amgen the most directly comparable competitive threat to Viridian's Lumvoa franchise.
- argenx: argenx markets efgartigimod (Vyvgart), an FcRn inhibitor for autoimmune IgG-mediated diseases including myasthenia gravis. Viridian's VRDN-006 and VRDN-008 programs target the same FcRn pathway, making argenx a direct competitor in the broader autoimmune pipeline.
- Horizon Therapeutics: Horizon originally developed and commercialized Tepezza before being acquired by Amgen. While now part of Amgen, Horizon's rare disease commercial model and Tepezza launch playbook provide a directly relevant template for Viridian's rare autoimmune disease strategy.
Emerging players
- Immunovant: Immunovant is developing anti-FcRn therapies (batoclimab, IMVT-1402) for multiple autoimmune indications. Competes with Viridian's VRDN-006/008 FcRn portfolio in the same mechanism class, with overlapping target indications.
- Krystal Biotech: Krystal Biotech is a commercial-stage rare disease biotech that successfully transitioned from development-stage to commercial entity with a focused launch. Comparable size, stage, and rare disease commercial infrastructure make it a relevant operational peer.
- Kiniksa Pharmaceuticals: Kiniksa is a commercial-stage biotech focused on autoimmune and rare diseases. Multiple Viridian executives (CEO Steve Mahoney, COO Tom Beetham, CHRO Melissa Manno) previously held senior roles at Kiniksa, making it a directly relevant operational and strategic peer.
- Caballeta Bio: Cabaletta Bio is a clinical-stage biotechnology company developing cell therapies for autoimmune diseases. While focused on a different modality, it competes for autoimmune disease pipeline assets and has overlap with Viridian's broader autoimmune strategy.
- Prothena: Prothena is a clinical-stage biotech developing therapies for proteinopathies and autoimmune diseases. Viridian CMO Radhika Tripuraneni previously served as Prothena's Chief Development Officer, and the company represents a relevant peer in autoimmune pipeline development.
Broad incumbents
- Regeneron Pharmaceuticals: Regeneron is a major biotechnology company with leading franchises in ophthalmology (Eylea) and immunology (Dupixent via Sanofi partnership). The Eylea franchise and broader ophthalmology infrastructure make Regeneron a strategic adjacent comparator for TED market dynamics.
- Sanofi: Sanofi has a major immunology franchise (Dupixent via Regeneron partnership) and rare disease presence (Genzyme legacy, where multiple Viridian executives worked). As a broad incumbent in autoimmune disease therapeutics, Sanofi represents both competitive and partnership dynamics relevant to Viridian's positioning.
Market position
Strengths5 records
Weaknesses5 records
Competitive moat4 records
Key risks6 records
Key highlights7 records
Customer concentration
Viridian Therapeutics social profiles
Digital presenceViridian Therapeutics financial estimates
Financial estimateRevenue estimate
Valuation estimate
Viridian Therapeutics leadership team
Management profileNumber of profiles
Profiles12 records
Viridian Therapeutics funding detail
Funding detailFunding overview
Funding rounds34 records
Investors13 records
Funding detail is available on the Subscription and Enterprise plan.Contact sales →
Viridian Therapeutics M&A and investment
M&A and investmentM&A2 records
Investments
M&A and investment is available on the Subscription and Enterprise plan.Contact sales →
Frequently asked questions about Viridian Therapeutics
What does Viridian Therapeutics do?
Viridian Therapeutics develops and commercializes monoclonal antibody therapeutics for autoimmune and rare diseases, with a primary focus on thyroid eye disease (TED). Its lead commercial product, Lumvoa (veligrotug-vvze), is an FDA-approved intravenous anti-IGF-1R antibody administered as five 30–40 minute infusions over 12 weeks. The company's pipeline includes a subcutaneous anti-IGF-1R antibody (elegrobart) for self-administration, anti-FcRn candidates (VRDN-006, VRDN-008) for autoimmune disease, and a preclinical anti-TSHR program for TED and Graves' disease.
Is Viridian Therapeutics a public or private company?
Viridian Therapeutics is a public company. It is classified as public and is currently operating.
When was Viridian Therapeutics founded?
Viridian Therapeutics was founded in 2016. It employs 251 to 500 people.
Where is Viridian Therapeutics based?
Viridian Therapeutics is headquartered in Waltham, United States, in the North America region.
How does Viridian Therapeutics make money?
One revenue line is on record: lumvoa (veligrotug) Product Sales.
Who are Viridian Therapeutics's main competitors?
Direct peers on record are Amgen, argenx and Horizon Therapeutics. Emerging players are Immunovant, Krystal Biotech, Kiniksa Pharmaceuticals, Caballeta Bio and Prothena. Broad incumbents are Regeneron Pharmaceuticals and Sanofi.
Does Viridian Therapeutics have an API?
No public API is recorded for Viridian Therapeutics.
What industry is Viridian Therapeutics in?
Viridian Therapeutics's product category is Biopharmaceuticals (Rare Disease / Autoimmune Antibody Therapeutics). Its primary akta.pro industry code is HLAIAIAE, Rare Immunology, Autoimmune & Autoinflammatory Therapies, with a secondary code of HLAIACAB, Immunology & Autoimmune Specialty Pharmaceuticals. Its NAICS code is 325414 and its SIC code is 2836.