TheraRadar
← Back
Data updated: May 24, 2026

EXELIXIS

Pharma
OncologyMetabolicGastroenterology Execution: Needs Improvement

EXELIXIS is a pharmaceutical company focused on Oncology, Metabolic, Gastroenterology. Key products include CABOMETYX.

2012
Since
2
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
2 Small Molecules

EXELIXIS at a Glance

  • Growing R&D activity with 8 trials in last 2 years

Upcoming FDA Decisions

Full Calendar →
Dec 3, 2026 — Zanzalintinib (XL-092) + atezolizumab
Dec 3, 2026 — zanzalintinib
Jan 20, 2027 — Foundayo (orforglipron)

Key Drugs

Top revenue-generating and strategically important drugs approved in the last 15 years. These represent the company's core commercial portfolio.

Recent FDA Approvals

New drug approvals (NDA/BLA) in the last 2 years. Shows novel drugs only, excluding generics and label supplements.

No recent approvals

Therapeutic Areas

Disease areas where this company has approved drugs and active pipeline. Weighted by commercial stage: approved drugs count most, followed by late-stage trials.

Oncology 77%
2 drugs Phase 3: 11 Phase 2: 5 Phase 1: 19
Metabolic 21%
2 drugs Phase 3: 2 Phase 1: 3
Gastroenterology 3%
0 drugs Phase 1: 3

Pipeline Snapshot

Active clinical trials across all therapeutic areas. Data from ClinicalTrials.gov.

13
Phase 3
5
Phase 2
25
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q2 2026
XL092
Colorectal Cancer
Estimated · aging NCT05425940
Q3 2028
Zanzalintinib
Head and Neck Squamous Cell Carcinoma
Estimated · aging NCT06082167
Q2 2029
Zanzalintinib
Pancreatic Neuroendocrine Tumor (pNET)
Estimated · fresh NCT06943755

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

  • CABOMETYX leads revenue
  • 2 key drugs tracked
View revenue breakdown →

Trial Catalysts

  • Oncology pipeline focus
  • 3 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
Compare with competitor →

Execution Intelligence

  • Phase 3: 4/11 completed
  • Speed: 41 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