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CD274 Inhibitors

5 drugs
Oncology
Target Attractiveness: Attractive (77%)

About CD274

CD274, also known as PD-L1, is a transmembrane protein that suppresses the immune system by binding to PD-1 on T cells, inhibiting their activation and effector functions. This mechanism is often exploited by cancer cells to evade immune surveillance.

Strategic Insights

ℹ️ How we calculate
  • phase1 represents biological uncertainty with 58% completion.
5
Approved Drugs
4
Companies
9
Indications
1
Therapeutic Areas
Broadest Approval
BAVENCIO
EMD SERONO INC
5
approved indications

Human Genetic Evidence Strong

Genetic Verdict
✅ STRONG SUPPORT
Clinical Translation
~1.8x
vs baseline success
Direction
❓ Unknown
Confidence
Low (0% consistent)

Top Drugs

BAVENCIO
EMD SERONO INC
5 indications · 2017
IMFINZI
AstraZeneca
3 indications · 2017
TECENTRIQ
Roche
2 indications · 2016
🏢

Four companies have approved drugs targeting CD274, including EMD SERONO INC, Roche and AstraZeneca.

Drug Modality Landscape

Modalities

Antibody
3
60%
Biologic (other)
2
40%

Routes of Administration

💉 Injection
4
80%
💉 IV
1
20%
💡

CD274 is exclusively targeted by antibodies, suggesting it may be a cell-surface or secreted protein.

The presence of biologic drugs suggests opportunities for novel small molecule inhibitors to enter the market.

Biologics only

📈 Modality Evolution

2016 Antibody (TECENTRIQ)
2024 Biologic (other) (TECENTRIQ HYBREZA)

Antibodies pioneered CD274 targeting (2016), with other biologics entering more recently (2024).

5 drugs since 2015

Clinical Trials 1,543 trials

1,543
Total Trials
718
Active
504
Completed
62%
Completion Rate

Completion by Phase

Phase Total Completed Failed Active Completion
Phase 1 544 211 138 191 60%
Phase 2 775 218 156 398 58%
Phase 3 210 70 19 120 79%
Phase 4 14 5 2 7 71%

Top Sponsors

Hoffmann-La Roche 156 76%
AstraZeneca 95 92%
National Cancer Institute (N... 83 67%
M.D. Anderson Cancer Center 52 57%
Genentech, Inc. 27 83%
Memorial Sloan Kettering Can... 27 64%
ImmunityBio, Inc. 24 0%
Pfizer 22 30%

By Modality

Antibody
967 61%
Small molecule
576 62%
Source: ClinicalTrials.gov · Completion rate = completed ÷ (completed + terminated + withdrawn)

Phase 3 Readout Calendar Pro

8 Phase 3 trials testing approved CD274 drugs across all sponsors.

Full calendar →
Q2 2026
Durvalumab
AstraZeneca · Hepatocellular Carcinoma
Estimated · fresh NCT03847428
Q2 2026
XL092
Exelixis · Colorectal Cancer
Estimated · aging NCT05425940
Q2 2026
Durvalumab
AstraZeneca · Esophageal Squamous Cell Carcinoma
Estimated · fresh NCT04550260
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Coverage: trials whose intervention is an approved drug targeting CD274. Pre-approval candidates with development codes (e.g. AZD0901, MK-7240) are not yet linked. Anchored on CT.gov primary completion date.

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Competitive Landscape

  • 4 companies competing
  • Market share by company

Full Drug Portfolio

  • All 5 approved drugs
  • Approval dates & indications

Genetic Validation

  • Full genetic evidence table
  • Effect sizes & directions

Approval Timeline

  • Full 5-drug timeline
  • First-of-modality markers

Clinical Trials Analysis

  • Competition: High (15 sponsors)
  • Success rates by condition
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Full summary • All drugs • Genetic evidence • Trials • Timeline

How We Calculate These Metrics

Target Attractiveness Score

A 0-100 score based on trial activity, sponsor diversity, and completion rates. Calculated from 1477 clinical trials targeting CD274.

Completion rate: Percentage of trials that reached their planned endpoint. Trials terminated early, withdrawn, or suspended are not counted—these often indicate safety issues, lack of efficacy, or strategic pivots.

  • Highly Attractive (80+): High trial activity, many sponsors, strong completion rates
  • Attractive (60-79): Good trial activity and validation
  • Moderate (40-59): Moderate interest from sponsors
  • Low (under 40): Limited trial activity or validation concerns

Strategic Insights

Auto-generated insights based on trial analytics including competition intensity, white space opportunities, modality shifts, and failure patterns. We analyze trial sponsors, phases, indications, and outcomes.

Risk Signals

  • High Competition: Many sponsors competing for this target (may reduce market opportunity)
  • High Failure Risk: Low trial completion rates suggest development challenges
  • Low Validation: Limited trial activity or poor outcomes indicate uncertain viability
  • White Space Available: Underexplored indications present opportunities