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Data updated: Sep 20, 2026

DIZAL

Pharma
OncologyGastroenterology Execution: Needs Improvement

DIZAL is a pharmaceutical company focused on Oncology, Gastroenterology. Key products include ZEGFROVY.

2025
Since
1
Drugs
-
Trials
1
New Drugs (2yr)
Modality:
1 Small Molecules

FDA Novel Drug Designations

(2025)
1 Novel 1 Breakthrough 1 Accelerated 1 Priority Review
See 1 novel approval →
2025 ZEGFROVY (SUNVOZERTINIB) Breakthrough · Priority Review · Accelerated

DIZAL at a Glance

  • Fast trial execution (13 months median completion)

DIZAL's Key Drugs

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

DIZAL's Recent FDA Approvals

DIZAL secured 1 new FDA approval for novel drugs (NDA/BLA) in the last two years.

DIZAL's Therapeutic Areas

DIZAL's approved drugs and pipeline span 2 therapeutic areas, led by Oncology and Gastroenterology, across 0 biologic and 1 small-molecule drug. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 98%
0 drugs Phase 3: 4 Phase 2: 9 Phase 1: 18
Gastroenterology 2%
0 drugs Phase 1: 1

DIZAL's Top Competitors

DIZAL'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.

DIZAL Pipeline Snapshot

DIZAL has 32 active clinical programs from ClinicalTrials.gov — 4 Phase 3, 9 Phase 2 and 19 Phase 1.

4
Phase 3
9
Phase 2
19
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q4 2027
Golidocitinib
Peripheral T-cell Lymphoma
Estimated · aging NCT07234162
Q1 2029
DZD8586
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Estimated · fresh NCT07139873
Q1 2026
sunvozertinib
Non-small Cell Lung Cancer
Completed · awaiting NCT05668988

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

  • ZEGFROVY leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Oncology 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: 0/2 completed
  • Speed: 13 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