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Data updated: Jun 28, 2026

Iovance Biotherapeutics, Inc.

Biotech
OncologyDermatologyOphthalmology Execution: Needs Improvement

Iovance Biotherapeutics, Inc. is a biotechnology company focused on Oncology, Dermatology, Ophthalmology. Key products include AMTAGVI.

2024
Since
1
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
1 Biologics

Iovance Biotherapeutics, Inc.'s Key Drugs

Iovance Biotherapeutics, Inc.'s core commercial portfolio centers on AMTAGVI, spanning Oncology and Dermatology — its most strategically important drugs approved in the last 15 years.

Iovance Biotherapeutics, Inc.'s Recent FDA Approvals

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

No recent approvals

Iovance Biotherapeutics, Inc.'s Therapeutic Areas

Iovance Biotherapeutics, Inc.'s approved drugs and pipeline span 3 therapeutic areas, led by Oncology and Dermatology, across 1 biologic and 0 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 89%
0 drugs Phase 3: 1 Phase 2: 8 Phase 1: 4
Dermatology 7%
0 drugs Phase 2: 1
Ophthalmology 4%
0 drugs Phase 1: 1

Iovance Biotherapeutics, Inc.'s Top Competitors

Iovance Biotherapeutics, Inc.'s closest competitors by therapeutic-area and drug-target overlap include Bayer, FOUGERA PHARMS, and Pfizer. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

Iovance Biotherapeutics, Inc. Pipeline Snapshot

Iovance Biotherapeutics, Inc. has 15 active clinical programs from ClinicalTrials.gov — 1 Phase 3, 9 Phase 2 and 5 Phase 1.

1
Phase 3
9
Phase 2
5
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q1 2028
Lifileucel plus Pembrolizumab
Metastatic Melanoma
Estimated · fresh NCT05727904

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

  • AMTAGVI leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Oncology 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: 0/1 completed
  • Speed: 84 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