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Drug

Tirbanibulin

Approved medicine
ClassTyrosine-protein kinase SRC inhibitorResearchOngoing clinical research

Also known as Klisyri.

1
Active clinical trials
SRC
Primary target
1
Regulatory events

Profile

Identifiers & mechanism

Canonical identifiers, marketed brand names and mechanism, resolved across RxNorm, ChEMBL and ATC.

Canonical name
Tirbanibulin
Aliases & brands
Klisyri
RxNorm CUI
2471078
ChEMBL ID
CHEMBL571546
ATC codes
D06BX03
UNII
4V9848RS5G
Primary mechanism
Tyrosine-protein kinase SRC inhibitor
Regulatory jurisdictions
ema

Pharmacology & targets

1 target

Known molecular targets and mechanisms supported by curated pharmacology databases.

INHIBITORTyrosine-protein kinase SRC inhibitor

Regulatory timeline

1 event

The complete regulatory record, grouped by authority — approvals, safety advisories and label changes. Each authority shows its most recent events; expand one to read its full history.

Earliest approval
2021-07-16
Latest approval
2021-07-16
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
2021-07-16Approval
Approval: Klisyri (EMA)

Indication: Klisyri is indicated for the field treatment of non-hyperkeratotic, non-hypertrophic actinic keratosis (Olsen grade 1) of the face or scalp in adults.

Evidence ↗

Contains information from the European Medicines Agency (European Medicines Agency), © EMA, reused under CC BY 4.0.

Clinical trials

4 trials

The current development programme across all trial phases — status mix, phase distribution and the late-stage studies shaping the evidence base.

Development programme
CLINICALTRIALS.GOV · LIVE REGISTRY
4
registered trials across all phases
LATEST COMPLETION 2025
1
Active studies
1
Recruiting
3
Late-stage (III+)
2
Completed
1
Discontinued
PHASE DISTRIBUTIONn = 4
Phase 21Phase 31Phase 42
References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
  • ClinicalTrials.gov — clinical trials
  • Regulatory event sources are credited in the Regulatory Timeline above.