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Drug

Sutimlimab

Approved medicine
ClassComplement C1s inhibitorResearchOngoing clinical research

Also known as Enjaymo, Humanized IgG4 monoclonal antibody against total complement component 1, subcomponent s.

Complement C1s subcomponent
Primary target
1
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
Sutimlimab
Aliases & brands
EnjaymoHumanized IgG4 monoclonal antibody against total complement component 1, subcomponent s
RxNorm CUI
2591404
ChEMBL ID
CHEMBL4297832
ATC codes
L04AJ04
UNII
GNWE7KJ995
Primary mechanism
Complement C1s inhibitor
Regulatory jurisdictions
ema

Pharmacology & targets

1 target

Known molecular targets and mechanisms supported by curated pharmacology databases.

INHIBITORComplement C1s 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
2022-11-15
Latest approval
2022-11-15
Authorities
EMA
Total events
1
emaEuropean Medicines Agency· 1 event
2022-11-15Approval
Approval: Enjaymo (EMA)

Indication: Enjaymo is indicated for the treatment of haemolytic anaemia in adult patients with cold agglutinin disease (CAD).

Evidence ↗

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

Clinical trials

2 trials

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

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.