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Drug

Umeclidinium bromide

Approved · EMA
Late-stage development

Also known as Anoro, Trelegy, umeclidinium (as bromide).

2
Regulatory events
Latest activity
beta

Recent clinical, regulatory, research and industry developments relating to this drug.

Profile

Identifiers & mechanism

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

Canonical name
Umeclidinium bromide
Aliases & brands
AnoroTrelegyumeclidinium (as bromide)
RxNorm CUI
1487512
Regulatory jurisdictions
ema

Regulatory timeline

2 events

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
2014-04-28
Latest approval
2017-03-20
Authorities
EMA
Total events
2
emaEuropean Medicines Agency· 2 events
2017-03-20Approval
Approval: Rolufta Ellipta (previously Rolufta) (EMA)

Indication: Rolufta is indicated as a maintenance bronchodilator treatment to relieve symptoms in adult patients with chronic obstructive pulmonary disease (COPD).

Evidence ↗
2014-04-28Approval
Approval: Incruse Ellipta (previously Incruse) (EMA)

Indication: Indicated as a maintenance bronchodilator treatment to relieve symptoms in adult patients with chronic obstructive pulmonary disease (COPD).

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 2017
4
Late-stage (III+)
4
Completed
PHASE DISTRIBUTIONn = 4
Phase 34

Late-stage studies

Phase III+ trials still open or recently active — where late-stage evidence is being generated.

Recent completions

Trials that read out recently, adding to the completed evidence base.

References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • ClinicalTrials.gov — clinical trials
  • Regulatory event sources are credited in the Regulatory Timeline above.