Alefacept

drug
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Also known as AmeviveBG-9273BG-9712BG9273BG9712Human lfa-3igg fusion proteinLFA-3CD2LFA-3TIPLFA3TIP

Summary

Alefacept (CHEMBL1201571) is an approved protein (ATC L04AA15) targeting CD2; indicated across 10 conditions including immune system disorder and psoriasis.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Protein
  • ATC class: L04AA15
  • Targets: 1 (CD2)
  • Indications: 10 conditions
  • Clinical trials: 36

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1201571
NameAlefacept
TypeProtein
Max phase4
ATCL04AA15

Also known as: Alefacept, Amevive, BG-9273, BG-9712, BG9273, BG9712, Human lfa-3igg fusion protein, LFA-3CD2, LFA-3TIP, LFA3TIP, ALEFACEPT

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
CD2CD2Inhibition0.2%P06729

Bioactivity

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

Target pathways

Aggregated over 1 target gene(s): CD2.

Top Reactome pathways

2 total, by targets touching each:

PathwayTargetsGenes
Hemostasis1CD2
Cell surface interactions at the vascular wall1CD2

Dominant GO biological processes

GO termTargets
membrane raft polarization1
apoptotic process1
immune response1
cell surface receptor signaling pathway1
natural killer cell activation1
positive regulation of myeloid dendritic cell activation1
positive regulation of type II interferon production1
positive regulation of interleukin-8 production1
positive regulation of tumor necrosis factor production1
heterotypic cell-cell adhesion1
T cell activation1
natural killer cell mediated cytotoxicity1
regulation of T cell differentiation1
cell-cell adhesion1
cell adhesion1

Indications & clinical

Indications

10 indications (1 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
immune system disorder4MONDO:0005046EFO:0000540
psoriasis3MONDO:0005083EFO:0000676
lichen planus2MONDO:0006572EFO:1000726
psoriatic arthritis2MONDO:0011849EFO:0003778
type 1 diabetes mellitus2MONDO:0005147MONDO:0005147
lymphoma1MONDO:0005062EFO:0000574
aplastic anemia1MONDO:0015909HP:0001915
kidney failure1MONDO:0001106EFO:1002048

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

Clinical trials

Total trials: 36.

Phase distribution

PhaseTrials
PHASE29
Not specified9
PHASE48
PHASE35
PHASE14
PHASE1/PHASE21

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00168753PHASE4COMPLETEDCommunity Based Trial for AMEVIVE®
NCT00493324PHASE4COMPLETEDStudy to Evaluate the Immune Response to Pneumococcal Vaccine in Alefacept-treated Adults With Chronic Plaque Psoriasis
NCT00655564PHASE4COMPLETEDLong-Term One Year Use of Alefacept (Amevive®) in Moderate to Severe Chronic Plaque Type Psoriasis
NCT00658606PHASE4COMPLETEDAssess the Efficacy and Safety of Alefacept With Narrow Band Ultraviolet B Phototherapy (nbUVB) vs. Alefacept Alone in Chronic Plaque Psoriasis Subjects
NCT00794807PHASE4COMPLETEDSafety and Tolerability of Repeat Courses of IM Alefacept
NCT00815633PHASE4TERMINATEDA Pilot Study of Alefacept for the Treatment of Pityriasis Rubra Pilaris
NCT00832585PHASE4COMPLETEDStudy to Evaluate the Safety and Efficacy of Alefacept (Amevive) in Subjects With Moderate to Severe Atopic Dermatitis
NCT00953329PHASE4TERMINATEDAlefacept in Subjects With Chronic Plaque Psoriasis Who Failed to Respond to Anti-TNF Therapy
NCT00233662PHASE3COMPLETEDSafety and Tolerability of Repeat Courses of IM Alefacept
NCT00361413PHASE3TERMINATEDAlefacept for Prevention of Graft Versus Host Disease (GVHD)
NCT00673556PHASE3COMPLETEDA Study to Assess the Efficacy and Safety of Alefacept in Psoriasis Patients for Whom Conventional Treatment is Ineffective or Inappropriate
NCT00674063PHASE3COMPLETEDA Study to Assess the Efficacy and Safety of Two Dosing Regimens of Alefacept in Subjects Weighing Between 100kg and 150kg With Moderate to Severe Chronic Plaque Psoriasis
NCT00692172PHASE3COMPLETEDOpen-label Study to Evaluate Safety of Multiple Courses of IM Alefacept During Treatment of Chronic Plaque Psoriasis
NCT00135733PHASE2TERMINATEDA Safety and Efficacy Study of Alefacept in the Treatment of Moderate to Severe Erosive Mucosal Lichen Planus
NCT00301002PHASE2COMPLETEDStudy to Evaluate the Efficacy of Alefacept to Treat Palmar Plantar Pustulosis
NCT00376129PHASE2COMPLETEDOpen-Label,Singel Center Study of Alefacept in Patients With Atopic Dermatitis
NCT00397332PHASE1/PHASE2COMPLETEDAlefacept for Chronic Graft Versus Host Disease
NCT00543569PHASE2COMPLETEDA Study to Assess the Safety and Efficacy of Alefacept in Kidney Transplant Recipients
NCT00617604PHASE2COMPLETEDA Study to Assess the Efficacy and Safety of Alefacept in Kidney Transplant Recipients
NCT00659412PHASE2COMPLETEDA Placebo-controlled Study With an Extension Examining the Safety and Efficacy of Alefacept in Psoriatic Arthritis
NCT00808223PHASE2COMPLETEDSafety and Pharmacokinetics (PK) of Alefacept in Adolescent Subjects With Moderate to Severe Psoriasis
NCT00965458PHASE2TERMINATEDInducing Remission in Type 1 Diabetes With Alefacept
NCT01226420PHASE2TERMINATEDAlefacept in Subjects With Steroid-Refractory Chronic Graft-versus-Host Disease
NCT00438802PHASE1COMPLETEDAlefacept in Treating Patients With Relapsed or Refractory Cutaneous T-Cell Lymphoma or Peripheral T-Cell Non-Hodgkin’s Lymphoma
NCT00653822PHASE1COMPLETEDA Study of Pharmacokinetics and Safety of Alefacept in Caucasian and Japanese Healthy Volunteers
NCT01163799PHASE1TERMINATEDA Pilot Study to Assess the Safety and Efficacy of Alefacept in de Novo Kidney Transplant Recipients
NCT01267643PHASE1TERMINATEDAlefacept in Patients With Relapsed/Refractory Aplastic Anemia
NCT00167102Not specifiedCOMPLETEDAlefacept in Patients With Severe Scalp Alopecia Areata
NCT00342862Not specifiedTERMINATEDAMEVIVE® Pregnancy Registry
NCT00407342Not specifiedCOMPLETEDAlefacept (Amevive) With or Without Narrowband UVB Treatment in Patients With Psoriasis.
NCT00422617Not specifiedCOMPLETEDEvaluate the Efficacy and Safety of One Course of Amevive in Taiwan Patients
NCT00454701Not specifiedTERMINATEDAssessment and Tracking of Long-term Alefacept Safety
NCT00678470Not specifiedCOMPLETEDOpen Label Study of Alefacept Injections to Patients With Moderate to Severe Psoriasis
NCT00795353Not specifiedTERMINATEDAssess the Long-term Effectiveness and Safety of Amevive (Alefacept) in Subjects With Moderate to Severe Chronic Plaque Psoriasis
NCT01319851Not specifiedTERMINATEDAlefacept and Allogeneic Hematopoietic Stem Cell Transplantation
NCT01433770Not specifiedWITHDRAWNAlefacept in Kidney Transplant Recipients

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).