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Drug

Maraviroc

Approved · EMA
Emerging researchLate-stage developmentRising momentum

Also known as Selzentry, Maravirocum.

3
Research papers
8
Active clinical trials
1
Regulatory events
Latest activity
beta

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

A Novel Anti-inflammation Treatment for Idiopathic Inflammatory Myopathies

Clinical trial2026-06-30Results expected Q3 2029 · ClinicalTrials.gov

Investigating the Feasibility of Repurposing HIV Antivirals in Adults With Long Covid

Clinical trial2026-03-13Results expected Q4 2026 · ClinicalTrials.gov

A Randomized Trial of CCR5 Inhibition as a Complement to Lung Transplant Induction Immunosuppression

Clinical trial2026-01-20Results expected Q2 2028 · ClinicalTrials.gov

Approval: Celsentri (EMA)

Regulatory2007-09-18EMA

Profile

Identifiers & mechanism

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

Canonical name
Maraviroc
Aliases & brands
SelzentryMaravirocum
RxNorm CUI
620216
ChEMBL ID
CHEMBL1201187
UNII
MD6P741W8A
Regulatory jurisdictions
ema

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
2007-09-18
Latest approval
2007-09-18
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
2007-09-18Approval
Approval: Celsentri (EMA)
Indication: Celsentri, in combination with other antiretroviral medicinal products, is indicated for treatment experienced adults, adolescents and children of 2 years of age and older andShow full indication

Celsentri, in combination with other antiretroviral medicinal products, is indicated for treatment experienced adults, adolescents and children of 2 years of age and older and weighing at least 10 kg infected with only CCR5-tropic HIV-1 detectable

Evidence ↗

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

Clinical trials

101 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
101
registered trials across all phases
LATEST COMPLETION 2022
8
Active studies
8
Recruiting
46
Late-stage (III+)
74
Completed
19
Discontinued
PHASE DISTRIBUTIONn = 101
Early Phase 11Phase 125Phase 1 / 24Phase 225Phase 2 / 38Phase 38Phase 425Phase N / A5

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.

Research activity

3 papers

Key research shaping understanding of this drug, combining the latest publications with the most influential evidence.

Publications over time
20122019
Major research themes3
CCR5 Receptor Antagonists1Cognition1Drug Interactions1
Journals, researchers & institutions
Top journals
  • AIDS (London, England)1
  • PloS one1
  • The Journal of antimicrobial chemotherapy1
Leading researchers
  • Allsop JM1
  • Back D1
  • Brew BJ1
  • Cameron DW1
  • Chaganti J1
  • Cysique LA1
  • Dennehy M1
  • Erlwein OW1
Leading institutions
free-text, unnormalised
  • Clinical Epidemiology Program1
  • Clinical Investigation Unit1
  • Imperial College London1
  • Ottawa Hospital Research Institute1
  • Ottawa Methods Centre1
  • St Vincent's Hospital and Peter Duncan Neurosciences Unit1
References & data sources
  • RxNorm (U.S. National Library of Medicine) — drug identity
  • ChEMBL (EMBL-EBI) & UniProt — pharmacology and targets
  • Europe PMC — research literature
  • ClinicalTrials.gov — clinical trials
  • Regulatory event sources are credited in the Regulatory Timeline above.