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Data updated: Jun 28, 2026

LIB THERAPEUTICS, INC.

Biotech

LIB THERAPEUTICS, INC. is a biotechnology company focused on Immunology, Cardiovascular, Dermatology.

2025
Since
1
Drugs
-
Trials
1
New Drugs (2yr)

FDA Novel Drug Designations

(2025)
1 Novel
See 1 novel approval →
2025 LEROCHOL (LERODALCIBEP-LIGA)

LIB THERAPEUTICS, INC. at a Glance

  • Fast trial execution (20 months median completion)

LIB THERAPEUTICS, INC.'s Key Drugs

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

LIB THERAPEUTICS, INC.'s Recent FDA Approvals

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

LIB THERAPEUTICS, INC.'s Therapeutic Areas

LIB THERAPEUTICS, INC.'s approved drugs and pipeline span 3 therapeutic areas, led by Immunology and Cardiovascular. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Immunology 84%
0 drugs Phase 3: 7 Phase 2: 7
Cardiovascular 12%
1 drugs
Dermatology 4%
0 drugs Phase 2: 1

LIB THERAPEUTICS, INC.'s Top Competitors

LIB THERAPEUTICS, INC.'s closest competitors by therapeutic-area and drug-target overlap include BAUSCH, BAUSCH AND LOMB INC, and Pfizer. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

LIB THERAPEUTICS, INC. Pipeline Snapshot

LIB THERAPEUTICS, INC. has 15 active clinical programs from ClinicalTrials.gov — 7 Phase 3, 8 Phase 2 and 0 Phase 1.

7
Phase 3
8
Phase 2
0
Phase 1

Phase 3 Readout Calendar Pro

1 Phase 3 trial with confidence-graded primary completion dates.

Full calendar →
Q4 2026
lerodalcibep 300 mg Monthly SC
Familial Hypercholesterolemia - Heterozygous
Estimated · aging NCT07102511

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

  • LEROCHOL leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Immunology pipeline focus
  • 1 Phase 3 readout 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: 5/7 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