Sugemalimab

drug
On this page

Also known as CejemlyCS-1001Cs1001WBP-315WBP315

Summary

Sugemalimab (CHEMBL4594535) is an approved antibody (ATC L01FF11); indicated across 11 conditions including neoplasm and non-small cell lung carcinoma.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Antibody
  • ATC class: L01FF11
  • Indications: 11 conditions
  • Clinical trials: 18

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4594535
NameSugemalimab
TypeAntibody
Max phase4
ATCL01FF11

Also known as: Cejemly, CS-1001, Cs1001, CS1001, Sugemalimab, WBP-315, WBP315, SUGEMALIMAB

Targets

Targets

No target linkage available.

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

11 indications (3 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
neoplasm4MONDO:0005070EFO:0000616
non-small cell lung carcinoma4MONDO:0005233EFO:0003060
gastric adenocarcinoma3MONDO:0005036EFO:0000503
nasal cavity and paranasal sinus lethal midline granuloma3MONDO:0006828MONDO:0019472
esophageal squamous cell carcinoma3MONDO:0005580EFO:0005922
adenocarcinoma3MONDO:0004970MONDO:0003219
Hodgkins lymphoma2MONDO:0004952EFO:0000183
lymphoma2MONDO:0005062EFO:0000574
small cell lung carcinoma2MONDO:0008433EFO:0000702
hepatocellular carcinoma1MONDO:0007256EFO:0000182

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 18.

Phase distribution

PhaseTrials
PHASE36
PHASE14
PHASE23
PHASE1/PHASE22
Not specified2
PHASE2/PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03789604PHASE3ACTIVE_NOT_RECRUITINGA Study of CS1001 in Subjects With Stage IV Non-Small Cell Lung Cancer
NCT05623267PHASE2/PHASE3RECRUITINGSugemalimab as Consolidation Therapy in Patients With LS-SCLC Following cCRT or sCRT
NCT05700448PHASE3NOT_YET_RECRUITINGStudy of Sugemalimab (or Placebo) Plus PGemOx Regimen in Participants With Extranodal NK/T-Cell Lymphoma
NCT06617416PHASE3RECRUITINGA Study of AK104 in Subjects With Unresectable Locally Advanced NSCLC
NCT03728556PHASE3COMPLETEDA Study of CS1001 in Subjects With Stage III Non-Small Cell Lung Cancer
NCT03802591PHASE3COMPLETEDA Study of CS1001 in Subjects With Gastric Adenocarcinoma or Gastro-Esophageal Junction Adenocarcinoma
NCT04187352PHASE3COMPLETEDA Study of CS1001 in Subjects With Esophageal Squamous Cell Carcinoma
NCT05940532PHASE2RECRUITINGA Trial of Sugemalimab and Chemotherapy in Unresectable Stage III NSCLC
NCT06217757PHASE1/PHASE2RECRUITINGSafety and Tolerability of LDRT+Sugemalimab+Chemotherapy+Olaparib for First-Line Treatment of SLFN-11 Positive ES-SCLC
NCT03505996PHASE2COMPLETEDA Study of CS1001 in Subjects With Relapsed or Refractory Classical Hodgkin Lymphoma
NCT03595657PHASE2COMPLETEDA Study of CS1001 in Subjects With Relapsed or Refractory Extranodal Natural Killer/ T Cell Lymphoma(ENKTL)
NCT04200404PHASE1/PHASE2COMPLETEDA Study of CS1001 in Combination With Regorafenib in Patients With Advanced or Refractory Solid Tumors
NCT03312842PHASE1COMPLETEDA Phase Ia/Ib Study of CS1001 in Subjects With Advanced Solid Tumors
NCT03744403PHASE1COMPLETEDA Study of CS1001 in Subjects with Advanced Solid Tumors
NCT04421352PHASE1COMPLETEDSafety and Tolerability Evaluation of Low-dose Radiation in Combination With CS1001 in Relapsed SCLC Patients
NCT04472858PHASE1UNKNOWNA Study of CS1001 in Combination With Donafenib in Subjects With Advanced Solid Tumors
NCT07247227Not specifiedRECRUITINGReal-world First-line Sugemalimab-Chemotherapy in Advanced NSCLC
NCT05131438Not specifiedNO_LONGER_AVAILABLEAn Expanded Access Program to Provide Sugemalimab for the Treatment of Relapsed or Refractory Extranodal Natural Killer/T-Cell Lymphoma (R/R ENKTL)

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).