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Data updated: Jun 28, 2026

ACACIA

Pharma
Oncology Execution: Excellent

ACACIA is a pharmaceutical company focused on Oncology. Key products include BARHEMSYS.

2020
Since
2
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
2 Small Molecules

FDA Novel Drug Designations

(2020)
2 Novel
See 2 novel approvals →
2020 BARHEMSYS (AMISULPRIDE)
2020 BYFAVO (REMIMAZOLAM BESYLATE)

ACACIA at a Glance

  • Strong track record with 95% execution quality across 17 trials
  • Fast trial execution (7 months median completion)

ACACIA's Key Drugs

ACACIA's core commercial portfolio centers on BARHEMSYS, BYFAVO, spanning Oncology — its most strategically important drugs approved in the last 15 years.

ACACIA's Recent FDA Approvals

New NDA/BLA approvals for ACACIA over the last two years — novel drugs only, excluding generics and label supplements.

No recent approvals

ACACIA's Therapeutic Areas

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

Oncology 100%
0 drugs Phase 2: 2

ACACIA's Top Competitors

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

ACACIA Pipeline Snapshot

ACACIA has 2 active clinical programs from ClinicalTrials.gov — 0 Phase 3, 2 Phase 2 and 0 Phase 1.

0
Phase 3
2
Phase 2
0
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q4 2027
Remimazolam
Pediatric ALL
Estimated · aging NCT04851717

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

  • BARHEMSYS leads revenue
  • 2 key drugs tracked

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: 5/5 completed
  • Speed: 7 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