TheraRadar
← Back
Data updated: Jun 28, 2026

Krystal Biotech, Inc.

Biotech

Krystal Biotech, Inc. is a biotechnology company focused on Respiratory, Oncology, Dermatology.

2023
Since
1
Drugs
-
Trials
0
New Drugs (2yr)

Krystal Biotech, Inc. at a Glance

  • Fast trial execution (18 months median completion)

Krystal Biotech, Inc.'s Key Drugs

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

Krystal Biotech, Inc.'s Recent FDA Approvals

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

No recent approvals

Krystal Biotech, Inc.'s Therapeutic Areas

Krystal Biotech, Inc.'s approved drugs and pipeline span 3 therapeutic areas, led by Respiratory and Oncology. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Respiratory 40%
0 drugs Phase 1: 2
Oncology 40%
0 drugs Phase 1: 2
Dermatology 20%
0 drugs Phase 1: 1

Krystal Biotech, Inc.'s Top Competitors

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

Krystal Biotech, Inc. Pipeline Snapshot

Krystal Biotech, Inc. has 5 active clinical programs from ClinicalTrials.gov — 0 Phase 3, 0 Phase 2 and 5 Phase 1.

0
Phase 3
0
Phase 2
5
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q4 2026
KB803
Dystrophic Epidermolysis Bullosa
Estimated · fresh NCT07016750

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

  • VYJUVEK leads revenue
  • Drug-level revenue analysis

Trial Catalysts

  • Respiratory 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: 2/3 completed
  • Speed: 18 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