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purine synthesis enzymes Inhibitors

2 drugs
Oncology
Target Attractiveness: Attractive (76%)

About purine synthesis enzymes

Purine synthesis enzymes are essential for creating purines, the building blocks of DNA and RNA, catalyzing reactions crucial for cell growth and proliferation. These enzymes are attractive targets for drug development, particularly in oncology, due to their fundamental role in cell division.

Strategic Insights

ℹ️ How we calculate
  • White space opportunity in Refractory Acute Lymphoblastic Leukemia with only 2 trials.
  • phase2 represents biological uncertainty with 42% completion.
Risk Signals: ℹ️
White Space Available
2
Approved Drugs
2
Companies
1
Indications
1
Therapeutic Areas
Broadest Approval
PURINETHOL
STASON PHARMS
1
approved indications

Top purine synthesis enzymes Drugs

PURINETHOL
STASON PHARMS
1 indications · 1953
PURIXAN
NOVA LABS LTD
1 indications · 2014
🏢

The competitive landscape includes two companies, NOVA LABS LTD and STASON PHARMS, with approved drugs.

purine synthesis enzymes Drug Modality Landscape

Modalities

Small molecule
2
100%

Routes of Administration

💊 Oral
2
100%
💡

purine synthesis enzymes is amenable to small molecule drugs, with oral options available for convenient dosing.

Exploring alternative modalities like antibodies or PROTACs could provide a competitive advantage.

Oral option available Small molecules only

purine synthesis enzymes Clinical Trials 86 trials

86
Total Trials
46
Active
31
Completed
78%
Completion Rate

Completion by Phase

Phase Total Completed Failed Active Completion
Phase 1 15 5 2 8 71%
Phase 2 44 12 7 25 63%
Phase 3 23 10 0 13 100%
Phase 4 4 4 0 0 100%

Top Sponsors

National Cancer Institute (N... 13 80%
Children's Oncology Group 9 100%
St. Jude Children's Research... 9 50%
M.D. Anderson Cancer Center 9 0%
Institute of Hematology & Bl... 5 100%
Alliance for Clinical Trials... 3 100%
University of Chicago 2
Children's Cancer Group, China 2

By Modality

Small molecule
86 78%
Source: ClinicalTrials.gov · Completion rate = completed ÷ (completed + terminated + withdrawn)

Pro Intelligence Preview

Deep insights for drug target analysis

Competitive Landscape

  • 2 companies competing
  • Market share by company

Full Drug Portfolio

  • All 2 approved drugs
  • Approval dates & indications

Genetic Validation

  • Full genetic evidence table
  • Effect sizes & directions

Approval Timeline

  • Full 2-drug timeline
  • First-of-modality markers

Clinical Trials Analysis

  • Competition: High (15 sponsors)
  • White space: 10 underexplored indications
  • Success rates by condition
Unlock Full Intelligence

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 63 clinical trials targeting purine synthesis enzymes.

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