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Data updated: Jun 28, 2026

MEDIWOUND, LTD

Biotech
GastroenterologyOncology Execution: Good

MEDIWOUND, LTD is a biotechnology company focused on Gastroenterology, Oncology.

2022
Since
1
Drugs
-
Trials
0
New Drugs (2yr)

FDA Novel Drug Designations

(2022)
1 Novel
See 1 novel approval →
2022 NEXOBRID (ANACAULASE-BCDB)

MEDIWOUND, LTD's Key Drugs

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

MEDIWOUND, LTD's Recent FDA Approvals

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

No recent approvals

MEDIWOUND, LTD's Therapeutic Areas

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

Gastroenterology 92%
0 drugs Phase 3: 1 Phase 2: 4
Oncology 8%
0 drugs Phase 1: 1

MEDIWOUND, LTD's Top Competitors

MEDIWOUND, LTD'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.

MEDIWOUND, LTD Pipeline Snapshot

MEDIWOUND, LTD has 6 active clinical programs from ClinicalTrials.gov — 1 Phase 3, 4 Phase 2 and 1 Phase 1.

1
Phase 3
4
Phase 2
1
Phase 1

Phase 3 Readout Calendar Pro

1 Phase 3 trial with confidence-graded primary completion dates.

Full calendar →
Q4 2026
EscharEx (EX-03)
Venous Leg Ulcer (VLU)
Estimated · fresh NCT06568627

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

  • NEXOBRID leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Gastroenterology pipeline focus
  • 1 Phase 3 readout 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: 2/3 completed
  • Speed: 47 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