TheraRadar
← All Targets

RNA methyltransferases Inhibitors

1 drugs
Oncology
Target Attractiveness: Attractive (76%)

About RNA methyltransferases

RNA methyltransferases catalyze the addition of methyl groups to RNA, regulating splicing, stability, and translation. These enzymes are emerging as drug targets due to their role in critical cellular processes.

Strategic Insights

ℹ️ How we calculate
  • phase1 represents biological uncertainty with 42% completion.
1
Approved Drugs
1
Companies
1
Indications
1
Therapeutic Areas
Broadest Approval
ONUREG
Bristol-Myers Squibb
1
approved indications

Top RNA methyltransferases Drugs

ONUREG
Bristol-Myers Squibb
1 indications · 2020
🏢

Bristol-Myers Squibb is the only company with an approved drug targeting RNA methyltransferases.

RNA methyltransferases Drug Modality Landscape

Modalities

Small molecule
1
100%

Routes of Administration

💊 Oral
1
100%
💡

Only one approved drug targets RNA methyltransferases, using small molecule modality.

Explore alternative modalities like oligonucleotides or PROTACs to differentiate from existing approaches and expand therapeutic potential.

Oral option available Small molecules only

RNA methyltransferases Clinical Trials 523 trials

523
Total Trials
230
Active
162
Completed
57%
Completion Rate

Completion by Phase

Phase Total Completed Failed Active Completion
Phase 1 244 78 72 86 52%
Phase 2 217 68 36 108 65%
Phase 3 56 15 13 27 54%
Phase 4 6 1 1 4 50%

Top Sponsors

M.D. Anderson Cancer Center 49 59%
National Cancer Institute (N... 29 67%
Celgene 21 90%
The First Affiliated Hospita... 16 100%
AbbVie 13 50%
Institute of Hematology & Bl... 12 0%
Novartis Pharmaceuticals 11 20%
Groupe Francophone des Myelo... 10 75%

By Modality

Small molecule
523 57%
Source: ClinicalTrials.gov · Completion rate = completed ÷ (completed + terminated + withdrawn)

Phase 3 Readout Calendar Pro

2 Phase 3 trials testing approved RNA methyltransferases drugs across all sponsors.

Full calendar →
Q4 2027
Azacitidine
Taiho Oncology, Inc. · Myelodysplastic Syndromes
Estimated · fresh NCT04256317
Q4 2027
BL-M11D1
Sichuan Baili Pharmaceutical Co., Ltd. · Acute Myeloid Leukemia
Estimated · fresh NCT07255872

Coverage: trials whose intervention is an approved drug targeting RNA methyltransferases. Pre-approval candidates with development codes (e.g. AZD0901, MK-7240) are not yet linked. Anchored on CT.gov primary completion date.

Pro Intelligence Preview

Deep insights for drug target analysis

Competitive Landscape

  • 1 companies competing
  • Market share by company

Full Drug Portfolio

  • All 1 approved drugs
  • Approval dates & indications

Genetic Validation

  • Full genetic evidence table
  • Effect sizes & directions

Approval Timeline

  • Full 1-drug timeline
  • First-of-modality markers

Clinical Trials Analysis

  • Competition: High (15 sponsors)
  • 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 405 clinical trials targeting RNA methyltransferases.

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