Velmanase Alfa

drug
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Also known as A16ABCHF-LMZYMAA1CHFLMZYMAA1LamazymLamzedeR-h-lamanRecombinant human lamanRhlamanVelmanasa alfaVelmanase alfa-tycv

Summary

Velmanase Alfa (CHEMBL4298010) is an approved enzyme (ATC A16AB15); indicated across 2 conditions including alpha-mannosidosis.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Enzyme
  • ATC class: A16AB15
  • Indications: 2 conditions
  • Clinical trials: 10

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4298010
NameVelmanase Alfa
TypeEnzyme
Max phase4
ATCA16AB15

Also known as: A16AB, CHF-LMZYMAA1, CHFLMZYMAA1, Lamazym, Lamzede, R-h-laman, Recombinant human laman, Rhlaman, Velmanasa alfa, Velmanase alfa, Velmanase alfa-tycv, VELMANASE ALFA

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

1 approved indication. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).

IndicationPhaseMONDOEFO
alpha-mannosidosis4MONDO:0009561MONDO:0009561

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

Clinical trials

Total trials: 10.

Phase distribution

PhaseTrials
PHASE35
PHASE22
Not specified2
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01681953PHASE3COMPLETEDA Placebo-Controlled Phase 3 Trial of Repeated Lamazym Treatment of Subjects With Alpha-Mannosidosis
NCT01908712PHASE3COMPLETEDLamazym Aftercare Study FR Designed to Provide Treatment for French Patients
NCT01908725PHASE3COMPLETEDLamazym Aftercare Study
NCT02478840PHASE3COMPLETEDEvaluation of Long-term Efficacy of Treatment With Lamazym
NCT04031066PHASE3WITHDRAWNInterventional Study to Assess Efficacy and Safety of Velmanase Alfa in Patients With Alpha Mannosidosis
NCT01285700PHASE2UNKNOWNDose Finding Study of Recombinant Human Alpha-mannosidase for the Treatment of Patients With Alpha-mannosidosis
NCT01681940PHASE2COMPLETEDLong-term Efficacy and Safety of Lamazym for the Treatment of Patients With Alpha-Mannosidosis
NCT01268358PHASE1COMPLETEDSafety Study of Recombinant Human Alpha-mannosidase for the Treatment of Patients With Alpha-mannosidosis
NCT04959240Not specifiedAVAILABLEExpanded Access to Velmanase Alfa
NCT06184503Not specifiedRECRUITINGAnalysis of Velmanase Alfa (Lamzede®)’s Effects in the Body of Children With Alpha-Mannosidosis Under the Age 3

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).