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Data updated: Jun 28, 2026

PHARMAESSENTIA CORP

Biotech

PHARMAESSENTIA CORP is a biotechnology company focused on Infectious Disease, Oncology, Immunology.

2021
Since
1
Drugs
-
Trials
0
New Drugs (2yr)

FDA Novel Drug Designations

(2021)
1 Novel 1 First-in-Class 1 Orphan
See 1 novel approval →
2021 BESREMI (ROPEGINTERFERON ALFA-2B-NJFT) First-in-Class · Orphan

PHARMAESSENTIA CORP at a Glance

  • Fast trial execution (23 months median completion)

Upcoming FDA Decisions

Full Calendar →
Aug 30, 2026 — BESREMi (ropeginterferon alfa-2b-njft)

PHARMAESSENTIA CORP's Key Drugs

PHARMAESSENTIA CORP's core commercial portfolio centers on BESREMI, spanning Infectious Disease and Oncology — its most strategically important drugs approved in the last 15 years.

PHARMAESSENTIA CORP's Recent FDA Approvals

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

No recent approvals

PHARMAESSENTIA CORP's Therapeutic Areas

PHARMAESSENTIA CORP's approved drugs and pipeline span 3 therapeutic areas, led by Infectious Disease and Oncology. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Infectious Disease 53%
0 drugs Phase 3: 1 Phase 2: 1 Phase 1: 2
Oncology 40%
0 drugs Phase 3: 1 Phase 1: 2
Immunology 7%
0 drugs Phase 1: 1

PHARMAESSENTIA CORP's Top Competitors

PHARMAESSENTIA CORP's closest competitors by therapeutic-area and drug-target overlap include Pfizer, AbbVie, and Johnson & Johnson. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

PHARMAESSENTIA CORP Pipeline Snapshot

PHARMAESSENTIA CORP has 8 active clinical programs from ClinicalTrials.gov — 2 Phase 3, 1 Phase 2 and 5 Phase 1.

2
Phase 3
1
Phase 2
5
Phase 1

Phase 3 Readout Calendar Pro

2 Phase 3 trials with confidence-graded primary completion dates.

Full calendar →
Q3 2027
Ropeginterferon alfa-2b
Primary Myelofibrosis
Estimated · aging NCT06468033
Q2 2025
P1101 (Ropeginterferon alfa-2b-njft)
Polycythemia Vera
Completed · awaiting NCT05481151

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

  • BESREMI leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Infectious Disease pipeline focus
  • 2 Phase 3 readouts 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: 2/5 completed
  • Speed: 23 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