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Data updated: Jun 28, 2026

Amgen

AMGN Biotech
OncologyImmunologyMetabolic Execution: Good

Pioneer biotechnology company with strength in oncology and inflammation. Known for biologics innovation including Enbrel, Repatha, and biosimilar portfolio.

$33.4B
Revenue (2024)
$155.0B
Market Cap
-
Trials
3
New Drugs (2yr)
Modality:
3 Small Molecules 11 Biologics

FDA Novel Drug Designations

(2018-2024)
4 Novel 4 First-in-Class 2 Orphan 2 Breakthrough 2 Accelerated 2 Priority Review 1 Fast Track
See 4 novel approvals →
2024 IMDELLTRA (TARLATAMAB-DLLE) First-in-Class · Orphan · Breakthrough · Priority Review · Accelerated
2021 LUMAKRAS (SOTORASIB) First-in-Class · Orphan · Breakthrough · Priority Review · Accelerated · Fast Track
2019 EVENITY (ROMOSOZUMAB-AQQG) First-in-Class
2018 AIMOVIG (ERENUMAB-AOOE) First-in-Class

Amgen at a Glance

  • Leading 15 drug targets across portfolio
  • Fast trial execution (27 months median completion)

Amgen's Therapeutic Areas

Amgen's approved drugs and pipeline span 5 therapeutic areas, led by Oncology and Immunology, across 11 biologic and 3 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 43%
10 drugs Phase 3: 49 Phase 2: 35 Phase 1: 113
Immunology 27%
7 drugs Phase 3: 38 Phase 2: 24 Phase 1: 34
Metabolic 15%
0 drugs Phase 3: 26 Phase 2: 12 Phase 1: 29
Cardiovascular 8%
1 drugs Phase 3: 14 Phase 2: 6 Phase 1: 4
Gastroenterology 7%
5 drugs Phase 3: 4 Phase 2: 6 Phase 1: 13

Amgen Pipeline Snapshot

Amgen has 407 active clinical programs from ClinicalTrials.gov — 131 Phase 3, 83 Phase 2 and 193 Phase 1.

131
Phase 3
83
Phase 2
193
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q3 2026
Apremilast
Plaque Psoriasis
Estimated · aging NCT06088199
Q3 2026
Dazodalibep
Sjogren's Syndrome
Estimated · fresh NCT06104124
Q4 2026
Dazodalibep
Sjögren's Syndrome (SS)
Estimated · fresh NCT06245408
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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

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

Trial Catalysts

  • Oncology 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: 148/214 completed
  • Speed: 27 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