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Data updated: Jun 28, 2026

ADC Therapeutics SA

Biotech
OncologyGastroenterology Execution: Needs Improvement

ADC Therapeutics SA is a biotechnology company focused on Oncology, Gastroenterology.

2021
Since
1
Drugs
-
Trials
0
New Drugs (2yr)

FDA Novel Drug Designations

(2021)
1 Novel 1 First-in-Class 1 Orphan 1 Accelerated 1 Priority Review
See 1 novel approval →
2021 ZYNLONTA (LONCASTUXIMAB TESIRINE-LPYL) First-in-Class · Orphan · Priority Review · Accelerated

ADC Therapeutics SA at a Glance

  • Fast trial execution (34 months median completion)

ADC Therapeutics SA's Key Drugs

ADC Therapeutics SA's core commercial portfolio centers on ZYNLONTA, spanning Oncology and Gastroenterology — its most strategically important drugs approved in the last 15 years.

ADC Therapeutics SA's Recent FDA Approvals

New NDA/BLA approvals for ADC Therapeutics SA over the last two years — novel drugs only, excluding generics and label supplements.

No recent approvals

ADC Therapeutics SA's Therapeutic Areas

ADC Therapeutics SA's approved drugs and pipeline span 2 therapeutic areas, led by Oncology and Gastroenterology. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 97%
1 drugs Phase 3: 1 Phase 2: 4 Phase 1: 14
Gastroenterology 3%
0 drugs Phase 1: 1

ADC Therapeutics SA's Top Competitors

ADC Therapeutics SA's closest competitors by therapeutic-area and drug-target overlap include Johnson & Johnson, Bristol-Myers Squibb, and Takeda. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

ADC Therapeutics SA Pipeline Snapshot

ADC Therapeutics SA has 20 active clinical programs from ClinicalTrials.gov — 1 Phase 3, 4 Phase 2 and 15 Phase 1.

1
Phase 3
4
Phase 2
15
Phase 1

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • ZYNLONTA leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Oncology pipeline focus
  • Phase 3 readout tracking

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis

Compare Companies

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

Execution Intelligence

  • Phase 3: 0/1 completed
  • Speed: 34 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