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Data updated: Jun 28, 2026

TG THERAPEUTICS, INC

Biotech
ImmunologyOncologyNeurology Execution: Fair

TG THERAPEUTICS, INC is a biotechnology company focused on Immunology, Oncology, Neurology.

2022
Since
1
Drugs
-
Trials
0
New Drugs (2yr)

FDA Novel Drug Designations

(2022)
1 Novel 1 Orphan
See 1 novel approval →
2022 BRIUMVI (UBLITUXIMAB-XIIY) Orphan

TG THERAPEUTICS, INC's Key Drugs

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

TG THERAPEUTICS, INC's Recent FDA Approvals

New NDA/BLA approvals for TG THERAPEUTICS, INC over the last two years — novel drugs only, excluding generics and label supplements.

No recent approvals

TG THERAPEUTICS, INC's Therapeutic Areas

TG THERAPEUTICS, INC's approved drugs and pipeline span 5 therapeutic areas, led by Immunology and Oncology. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Immunology 36%
0 drugs Phase 3: 7 Phase 2: 7 Phase 1: 1
Oncology 32%
0 drugs Phase 3: 2 Phase 2: 8 Phase 1: 14
Neurology 29%
1 drugs Phase 3: 5 Phase 2: 4
Dermatology 2%
0 drugs Phase 2: 1
Gastroenterology 1%
0 drugs Phase 1: 1

TG THERAPEUTICS, INC's Top Competitors

TG THERAPEUTICS, INC's closest competitors by therapeutic-area and drug-target overlap include Pfizer, Eli Lilly, and Bristol-Myers Squibb. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

TG THERAPEUTICS, INC Pipeline Snapshot

TG THERAPEUTICS, INC has 50 active clinical programs from ClinicalTrials.gov — 14 Phase 3, 20 Phase 2 and 16 Phase 1.

14
Phase 3
20
Phase 2
16
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q4 2026
Ublituximab
Relapsing Multiple Sclerosis
Estimated · fresh NCT07211633
Q4 2027
Ublituximab
Relapsing Multiple Sclerosis
Estimated · fresh NCT05877963
Q1 2030
Ublituximab
Relapsing Multiple Sclerosis
Estimated · fresh NCT07220252

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

  • BRIUMVI leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Immunology pipeline focus
  • 3 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: 3/7 completed
  • Speed: 48 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