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Data updated: Jun 28, 2026

Boehringer Ingelheim

Big Pharma
RespiratoryMetabolicOncology Execution: Excellent

Boehringer Ingelheim is a major pharmaceutical company focused on Respiratory, Metabolic, Oncology. Key products include PRAXBIND.

1961
Since
43
Drugs
-
Trials
3
New Drugs (2yr)
Modality:
21 Small Molecules 1 Biologics

FDA Novel Drug Designations

(2022-2025)
3 Novel 2 First-in-Class 2 Orphan 3 Breakthrough 1 Accelerated 3 Priority Review 2 Fast Track
See 3 novel approvals →
2025 JASCAYD (NERANDOMILAST) First-in-Class · Orphan · Breakthrough · Priority Review · Fast Track
2025 HERNEXEOS (ZONGERTINIB) Breakthrough · Priority Review · Accelerated · Fast Track
2022 SPEVIGO (SPESOLIMAB-SBZO) First-in-Class · Orphan · Breakthrough · Priority Review

Boehringer Ingelheim at a Glance

  • Strong track record with 83% execution quality across 1171 trials
  • Leading 14 drug targets across portfolio

Boehringer Ingelheim's Recent FDA Approvals

Boehringer Ingelheim secured 3 new FDA approvals for novel drugs (NDA/BLA) in the last two years.

Boehringer Ingelheim's Therapeutic Areas

Boehringer Ingelheim's approved drugs and pipeline span 5 therapeutic areas, led by Respiratory and Metabolic, across 1 biologic and 21 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Respiratory 30%
8 drugs Phase 3: 52 Phase 2: 40 Phase 1: 40
Metabolic 28%
8 drugs Phase 3: 57 Phase 2: 20 Phase 1: 33
Oncology 24%
2 drugs Phase 3: 29 Phase 2: 33 Phase 1: 110
Cardiovascular 10%
4 drugs Phase 3: 23 Phase 2: 6 Phase 1: 2
Immunology 8%
2 drugs Phase 3: 10 Phase 2: 21 Phase 1: 9

Boehringer Ingelheim's Top Competitors

Boehringer Ingelheim's closest competitors by therapeutic-area and drug-target overlap include Novartis, AstraZeneca, and Merck. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

Boehringer Ingelheim Pipeline Snapshot

Boehringer Ingelheim has 485 active clinical programs from ClinicalTrials.gov — 171 Phase 3, 120 Phase 2 and 194 Phase 1.

171
Phase 3
120
Phase 2
194
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q3 2026
zongertinib
Lung Cancer, Non-squamous, Non-small Cell
Estimated · fresh NCT06151574
Q2 2027
Spesolimab
Pyoderma Gangrenosum
Estimated · fresh NCT06624670
Q2 2027
Nerandomilast
Idiopathic Pulmonary Fibrosis
Estimated · fresh NCT06238622
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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

  • JARDIANCE leads revenue
  • 5 key drugs tracked
View revenue breakdown →

Trial Catalysts

  • Respiratory pipeline focus
  • 8 Phase 3 readouts tracked
View readout calendar →

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis
View patent timeline →

Compare Companies

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

  • Phase 3: 195/231 completed
  • Speed: 12 months avg
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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