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Sugemalimab

ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS

Also known as: cejemly, CS1001, WBP3155

EMA approvedATC L01FF11

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Sugemalimab is a drug catalogued in DrugCentral. It was first approved by the EMA in 2024. DrugCentral lists 1 molecular target, including CD274. Recorded indications include Non-small cell lung cancer.

  • Molecular targets: CD274 (1 listed in DrugCentral).
  • Indications: Non-small cell lung cancer.
  • ATC code: L01FF11 (PD-1/PD-L1 (Programmed cell death protein 1/death ligand 1) inhibitors).

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (1)

  • Non-small cell lung cancer

Mechanism & targets

Molecular targets (1)

TargetGeneActionActivity
Programmed cell death 1 ligand 1CD274otherKd 8.86

Regulatory approvals (1)

DateAgencyMarketed asApplicantOrphan
2024-07-24EMA—Cstone Pharmaceuticals Ireland Limited

ATC classification

ATC codeTherapeutic hierarchy
L01FF11ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS › ANTINEOPLASTIC AGENTS › MONOCLONAL ANTIBODIES AND ANTIBODY DRUG CONJUGATES › PD-1/PD-L1 (Programmed cell death protein 1/death ligand 1) inhibitors

Chemical structure

Molecular formula—
Molecular weight—
CAS number—
InChIKey—
PubChem CID13444038

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Sugemalimab used for?

DrugCentral lists the following indications for Sugemalimab: Non-small cell lung cancer.

How does Sugemalimab work?

Its molecular targets in DrugCentral include CD274.

When was Sugemalimab first approved?

Sugemalimab was first approved by the EMA in 2024.

Browse: all drugs starting with S · drug guides by category · protein targets A–Z.

Sources

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For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

Status—
First approval2024-07-24
AgencyEMA
Targets1
Indications1
Formula—
DrugCentral ID5849
Interactive profile