TheraRadar
← Back
Data updated: Jun 28, 2026

MIRUM

Pharma

MIRUM is a pharmaceutical company focused on Gastroenterology, Infectious Disease. Key products include CHOLBAM.

2015
Since
3
Drugs
-
Trials
2
New Drugs (2yr)
Modality:
3 Small Molecules

FDA Novel Drug Designations

(2021)
1 Novel 1 Orphan 1 Breakthrough 1 Priority Review
See 1 novel approval →
2021 LIVMARLI (MARALIXIBAT CHLORIDE) Orphan · Breakthrough · Priority Review

MIRUM at a Glance

  • Growing R&D activity with 7 trials in last 2 years
  • Fast trial execution (35 months median completion)

Upcoming FDA Decisions

Full Calendar →
Sep 26, 2026 — Zilurgisertib

MIRUM's Key Drugs

MIRUM's core commercial portfolio centers on CHOLBAM, LIVMARLI, CTEXLI, spanning Gastroenterology and Infectious Disease — its most strategically important drugs approved in the last 15 years.

MIRUM's Recent FDA Approvals

MIRUM secured 2 new FDA approvals for novel drugs (NDA/BLA) in the last two years.

MIRUM's Therapeutic Areas

MIRUM's approved drugs and pipeline span 2 therapeutic areas, led by Gastroenterology and Infectious Disease, across 0 biologic and 3 small-molecule drugs. Weighted by commercial stage — approved drugs count most, then late-stage trials.

Gastroenterology 61%
1 drugs Phase 3: 3 Phase 2: 3 Phase 1: 1
Infectious Disease 39%
0 drugs Phase 3: 2 Phase 2: 3 Phase 1: 2

MIRUM's Top Competitors

MIRUM's closest competitors by therapeutic-area and drug-target overlap include Johnson & Johnson, Bristol-Myers Squibb, and APOTHECON. Ranked by overlap in therapeutic areas and drug targets across approved drugs and pipeline.

MIRUM Pipeline Snapshot

MIRUM has 14 active clinical programs from ClinicalTrials.gov — 5 Phase 3, 6 Phase 2 and 3 Phase 1.

5
Phase 3
6
Phase 2
3
Phase 1

Phase 3 Readout Calendar Pro

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

Full calendar →
Q3 2026
Brelovitug 300 mg
Chronic Hepatitis D Infection
Estimated · fresh NCT07298330
Q4 2026
Maralixibat
Cholestatic Liver Disease (Except ALGS, PFIC, PBC and PSC)
Estimated · fresh NCT06553768
Q2 2027
Brelovitug 300 mg
Chronic Hepatitis D Infection
Estimated · fresh NCT07200908
Unlock 2 more readouts with confidence-graded estimates
Upgrade to Pro

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

  • CHOLBAM leads revenue
  • 3 key drugs tracked

Trial Catalysts

  • Gastroenterology pipeline focus
  • 5 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: 5/9 completed
  • Speed: 35 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