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Data updated: Jun 17, 2026

GSK

GSK Big Pharma

GSK is a major pharmaceutical company focused on Respiratory, Infectious Disease, Oncology. Key products include NUCALA.

$38.4B
Revenue (2024)
$85.0B
Market Cap
-
Trials
4
New Drugs (2yr)
Modality:
31 Small Molecules 17 Biologics

FDA Novel Drug Designations

(2017-2025)
9 Novel 4 First-in-Class 4 Orphan 4 Breakthrough 2 Accelerated 6 Priority Review 2 Fast Track
See 9 novel approvals →
2025 BLUJEPA (GEPOTIDACIN MESYLATE) First-in-Class · Priority Review
2025 BLENREP (BELANTAMAB MAFODOTIN-BLMF) First-in-Class · Orphan · Breakthrough · Priority Review · Accelerated
2025 EXDENSUR (DEPEMOKIMAB-ULAA)
2023 JESDUVROQ (DAPRODUSTAT) First-in-Class
2023 OJJAARA (MOMELOTINIB DIHYDROCHLORIDE) Orphan
2021 JEMPERLI (DOSTARLIMAB-GXLY) Breakthrough · Priority Review · Accelerated
2021 BREXAFEMME (IBREXAFUNGERP CITRATE) First-in-Class · Priority Review · Fast Track
2018 KRINTAFEL (TAFENOQUINE SUCCINATE) Orphan · Breakthrough · Priority Review
2017 ZEJULA (NIRAPARIB TOSYLATE) Orphan · Breakthrough · Priority Review · Fast Track

GSK at a Glance

  • Fast trial execution (8 months median completion)

GSK's Therapeutic Areas

GSK's approved drugs and pipeline span 5 therapeutic areas, led by Respiratory and Infectious Disease, across 17 biologic and 31 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Respiratory 34%
11 drugs Phase 3: 109 Phase 2: 76 Phase 1: 163
Infectious Disease 34%
2 drugs Phase 3: 128 Phase 2: 67 Phase 1: 146
Oncology 16%
3 drugs Phase 3: 28 Phase 2: 63 Phase 1: 128
Immunology 10%
2 drugs Phase 3: 23 Phase 2: 27 Phase 1: 70
Metabolic 7%
0 drugs Phase 3: 18 Phase 2: 17 Phase 1: 50

GSK Pipeline Snapshot

GSK has 1113 active clinical programs from ClinicalTrials.gov — 306 Phase 3, 250 Phase 2 and 557 Phase 1.

306
Phase 3
250
Phase 2
557
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q3 2026
Investigational varicella vaccine
Chickenpox
Estimated · stale NCT06693895
Q3 2026
RSVPreF3 OA vaccine
Respiratory Syncytial Virus Infections
Estimated · fresh NCT07220109
Q3 2026
Candidate varicella vaccine
Chickenpox
Estimated · aging NCT06855160
Unlock 5 more readouts with confidence-graded estimates
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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

  • NUCALA leads revenue
  • 5 key drugs tracked
View revenue breakdown →

Trial Catalysts

  • Respiratory pipeline focus
  • 8 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: 0/2 completed
  • Speed: 8 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