TheraRadar
← Back
Data updated: Jun 28, 2026

SYNDAX

Pharma
OncologyRespiratory Execution: Fair

SYNDAX is a pharmaceutical company focused on Oncology, Respiratory. Key products include REVUFORJ.

2024
Since
1
Drugs
-
Trials
1
New Drugs (2yr)
Modality:
1 Small Molecules

FDA Novel Drug Designations

(2024)
1 Novel 1 First-in-Class 1 Orphan 1 Breakthrough 1 Priority Review 1 Fast Track
See 1 novel approval →
2024 REVUFORJ (REVUMENIB CITRATE) First-in-Class · Orphan · Breakthrough · Priority Review · Fast Track

SYNDAX at a Glance

  • Fast trial execution (28 months median completion)

SYNDAX's Key Drugs

SYNDAX's core commercial portfolio centers on REVUFORJ, spanning Oncology and Respiratory — its most strategically important drugs approved in the last 15 years.

SYNDAX's Recent FDA Approvals

SYNDAX secured 1 new FDA approval for novel drugs (NDA/BLA) in the last two years.

SYNDAX's Therapeutic Areas

SYNDAX's approved drugs and pipeline span 2 therapeutic areas, led by Oncology and Respiratory, across 0 biologic and 1 small-molecule drug. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Oncology 95%
1 drugs Phase 3: 1 Phase 2: 5 Phase 1: 15
Respiratory 5%
0 drugs Phase 2: 1

SYNDAX's Top Competitors

SYNDAX's closest competitors by therapeutic-area and drug-target overlap include Novartis, Merck, and GSK. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

SYNDAX Pipeline Snapshot

SYNDAX has 22 active clinical programs from ClinicalTrials.gov — 1 Phase 3, 6 Phase 2 and 15 Phase 1.

1
Phase 3
6
Phase 2
15
Phase 1

Phase 3 Readout Calendar Pro

1 Phase 3 trial with confidence-graded primary completion dates.

Full calendar →
Q2 2029
Revumenib
Acute Myeloid Leukemias
Estimated · fresh NCT07211958

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

  • REVUFORJ leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Oncology pipeline focus
  • 1 Phase 3 readout 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: 0/1 completed
  • Speed: 28 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