MedPath

Aldesleukin

Generic Name
Aldesleukin
Brand Names
Proleukin
Drug Type
Biotech
CAS Number
110942-02-4
Unique Ingredient Identifier
M89N0Q7EQR

Overview

Aldesleukin, a lymphokine, is produced by recombinant DNA technology using a genetically engineered E. coli strain containing an analog of the human interleukin-2 gene. Genetic engineering techniques were used to modify the human IL-2 gene, and the resulting expression clone encodes a modified human interleukin-2. This recombinant form differs from native interleukin-2 in the following ways: a) Aldesleukin is not glycosylated because it is derived from E. coli; b) the molecule has no N-terminal alanine; the codon for this amino acid was deleted during the genetic engineering procedure; c) the molecule has serine substituted for cysteine at amino acid position 125.

Background

Aldesleukin, a lymphokine, is produced by recombinant DNA technology using a genetically engineered E. coli strain containing an analog of the human interleukin-2 gene. Genetic engineering techniques were used to modify the human IL-2 gene, and the resulting expression clone encodes a modified human interleukin-2. This recombinant form differs from native interleukin-2 in the following ways: a) Aldesleukin is not glycosylated because it is derived from E. coli; b) the molecule has no N-terminal alanine; the codon for this amino acid was deleted during the genetic engineering procedure; c) the molecule has serine substituted for cysteine at amino acid position 125.

Indication

For treatment of adults with metastatic renal cell carcinoma.

Associated Conditions

  • Metastatic Melanoma
  • Metastatic Renal Cell Carcinoma ( mRCC)

FDA Approved Products

Proleukin
Manufacturer:Clinigen Limited
Route:INTRAVENOUS
Strength:1.1 mg in 1 mL
Approved: 2019/09/19
NDC:76310-022
Proleukin
Manufacturer:Prometheus Laboratories Inc.
Route:INTRAVENOUS
Strength:1.1 mg in 1 mL
Approved: 2018/08/31
NDC:65483-116
PROLEUKIN
Manufacturer:Iovance Biotherapeutics, Inc
Route:INTRAVENOUS
Strength:1.1 mg in 1 mL
Approved: 2024/01/31
NDC:73776-022

Singapore Approved Products

No Singapore products found for this drug

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