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Data updated: Jun 28, 2026

SHANGHAI HENLIUS BIOTECH

Biotech
OncologyImmunologyOphthalmology Execution: Needs Improvement

SHANGHAI HENLIUS BIOTECH is a biotechnology company focused on Oncology, Immunology, Ophthalmology.

2025
Since
3
Drugs
-
Trials
3
New Drugs (2yr)

SHANGHAI HENLIUS BIOTECH at a Glance

  • Growing R&D activity with 41 trials in last 2 years
  • Fast trial execution (20 months median completion)

SHANGHAI HENLIUS BIOTECH's Key Drugs

SHANGHAI HENLIUS BIOTECH's core commercial portfolio centers on BILPREVDA, spanning Oncology and Immunology — its most strategically important drugs approved in the last 15 years.

SHANGHAI HENLIUS BIOTECH's Recent FDA Approvals

SHANGHAI HENLIUS BIOTECH secured 3 new FDA approvals for novel drugs (NDA/BLA) in the last two years.

SHANGHAI HENLIUS BIOTECH's Therapeutic Areas

SHANGHAI HENLIUS BIOTECH's approved drugs and pipeline span 4 therapeutic areas, led by Oncology and Immunology. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 84%
2 drugs Phase 3: 15 Phase 2: 22 Phase 1: 24
Immunology 7%
0 drugs Phase 3: 2 Phase 2: 1 Phase 1: 1
Ophthalmology 5%
0 drugs Phase 3: 2 Phase 1: 1
Gastroenterology 4%
0 drugs Phase 3: 1 Phase 2: 1

SHANGHAI HENLIUS BIOTECH's Top Competitors

SHANGHAI HENLIUS BIOTECH's closest competitors by therapeutic-area and drug-target overlap include Novartis, AbbVie, and Johnson & Johnson. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

SHANGHAI HENLIUS BIOTECH Pipeline Snapshot

SHANGHAI HENLIUS BIOTECH has 70 active clinical programs from ClinicalTrials.gov — 20 Phase 3, 24 Phase 2 and 26 Phase 1.

20
Phase 3
24
Phase 2
26
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q2 2027
HLX17
Non-Squamous Non-Small Cell Lung Cancer
Estimated · stale NCT06847334
Q2 2027
HLX22
Gastroesophageal-junction Cancer
Estimated · fresh NCT06532006
Q2 2027
HLX13
Hepatocellular Carcinoma (HCC)
Estimated · stale NCT06841185
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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

  • BILPREVDA leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Oncology pipeline focus
  • 7 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: 9/20 completed
  • Speed: 20 months avg
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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