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Data updated: Jun 28, 2026

PARATEK PHARMS

Specialty

PARATEK PHARMS is a specialty pharmaceutical company focused on Infectious Disease, Dermatology. Key products include NUZYRA.

2017
Since
2
Drugs
-
Trials
0
New Drugs (2yr)
Modality:
2 Small Molecules

FDA Novel Drug Designations

(2018)
1 Novel 1 Priority Review 1 Fast Track
See 1 novel approval →
2018 NUZYRA (OMADACYCLINE TOSYLATE) Priority Review · Fast Track

PARATEK PHARMS at a Glance

  • Fast trial execution (15 months median completion)

PARATEK PHARMS's Key Drugs

PARATEK PHARMS's core commercial portfolio centers on NUZYRA, XHANCE, spanning Infectious Disease and Dermatology — its most strategically important drugs approved in the last 15 years.

PARATEK PHARMS's Recent FDA Approvals

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

No recent approvals

PARATEK PHARMS's Therapeutic Areas

PARATEK PHARMS's approved drugs and pipeline span 2 therapeutic areas, led by Infectious Disease and Dermatology, across 0 biologic and 2 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Infectious Disease 50%
1 drugs
Dermatology 50%
1 drugs

PARATEK PHARMS's Top Competitors

PARATEK PHARMS's closest competitors by therapeutic-area and drug-target overlap include Pfizer, Baxter, and B BRAUN. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

PARATEK PHARMS Pipeline Snapshot

Active clinical trials for PARATEK PHARMS across all therapeutic areas, from ClinicalTrials.gov.

No active pipeline data available

Pro Intelligence Preview

Deep insights for investors and analysts

Revenue Insights

  • NUZYRA leads revenue
  • 2 key drugs tracked

Trial Catalysts

  • Infectious Disease pipeline focus
  • Phase 3 readout tracking

Patent Risk

  • Patent expiration timeline
  • Revenue at risk analysis

Compare Companies

  • Side-by-side pipeline analysis
  • Revenue & market share comparison

Execution Intelligence

  • Phase 3: 4/6 completed
  • Speed: 15 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