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Data updated: Jul 17, 2026

VIRIDIAN THERAPEUTICS INC

Biotech

VIRIDIAN THERAPEUTICS INC is a biotechnology company focused on Immunology, Metabolic, Ophthalmology.

2026
Since
1
Drugs
-
Trials
1
New Drugs (2yr)

VIRIDIAN THERAPEUTICS INC at a Glance

  • Growing R&D activity with 5 trials in last 2 years
  • Fast trial execution (20 months median completion)

VIRIDIAN THERAPEUTICS INC's Key Drugs

VIRIDIAN THERAPEUTICS INC's core commercial portfolio centers on LUMVOA, spanning Immunology and Metabolic — its most strategically important drugs approved in the last 15 years.

VIRIDIAN THERAPEUTICS INC's Recent FDA Approvals

VIRIDIAN THERAPEUTICS INC secured 1 new FDA approval for novel drugs (NDA/BLA) in the last two years.

VIRIDIAN THERAPEUTICS INC's Therapeutic Areas

VIRIDIAN THERAPEUTICS INC's approved drugs and pipeline span 4 therapeutic areas, led by Immunology and Metabolic. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Immunology 39%
0 drugs Phase 3: 7 Phase 2: 7
Metabolic 30%
0 drugs Phase 3: 8
Ophthalmology 30%
0 drugs Phase 3: 8
Dermatology 2%
0 drugs Phase 2: 1

VIRIDIAN THERAPEUTICS INC's Top Competitors

VIRIDIAN THERAPEUTICS INC's closest competitors by therapeutic-area and drug-target overlap include Eli Lilly, Roche, and BAUSCH. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

VIRIDIAN THERAPEUTICS INC Pipeline Snapshot

VIRIDIAN THERAPEUTICS INC has 31 active clinical programs from ClinicalTrials.gov — 23 Phase 3, 8 Phase 2 and 0 Phase 1.

23
Phase 3
8
Phase 2
0
Phase 1

Phase 3 Readout Calendar Pro

2 Phase 3 trials with confidence-graded primary completion dates.

Full calendar →
Q3 2026
VRDN-003
Thyroid Eye Disease
Estimated · fresh NCT07155668
Q1 2026
VRDN-003
Thyroid Eye Disease
Completed · awaiting NCT06625411

Anchored on CT.gov primary completion date. Topline announcements typically precede this by 3–9 months. Confidence labels combine date type (ACTUAL/ESTIMATED) with last-update freshness.

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • LUMVOA leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Immunology pipeline focus
  • 2 Phase 3 readouts tracked
View readout calendar →

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis

Compare Companies

  • Side-by-side pipeline analysis
  • Revenue & market share comparison

Execution Intelligence

  • Phase 3: 4/8 completed
  • Speed: 20 months avg
Unlock Full Intelligence

Revenue forecasts • Trial milestones • Patent risk modeling

How We Calculate These Metrics

Execution Quality Score

Measures trial completion rates weighted by phase importance. Phase 3 trials count 4x more than Phase 1 because late-stage completion is harder and more valuable.

What counts as "completed": A trial that reached its planned endpoint and reported results. Trials that were terminated early, withdrawn, or suspended are not counted as completed—these often indicate safety issues, lack of efficacy, or strategic pivots.

  • Excellent (80%+): Top-tier execution, most trials reach planned endpoints
  • Good (60-79%): Strong execution with occasional early terminations
  • Fair (40-59%): Average execution, notable rate of terminated/withdrawn trials
  • Needs Improvement (under 40%): High termination rates, execution challenges