MedPath

Interferon alfa-2a

Generic Name
Interferon alfa-2a
Drug Type
Biotech
CAS Number
76543-88-9
Unique Ingredient Identifier
47RRR83SK7

Overview

Interferon a (human leukocyte protein moiety reduced). A type I interferon consisting of 165 amino acid residues with lysine in position 23. This protein is produced by recombinant DNA technology and resembles interferon secreted by leukocytes. It is used extensively as an antiviral or antineoplastic agent. An oral form is being developed by Amarillo Biosciences.

Indication

For the treatment of chronic hepatitis C, hairy cell leukemia, AIDS-related Kaposi's sarcoma, and chronic myelogenous leukemia. Also for the treatment of oral warts arising from HIV infection.

Associated Conditions

  • Chronic Hepatitis B Infection
  • Chronic Hepatitis C Virus (HCV) Infection
  • Chronic Myelogenous Leukemia (CML)
  • Cutaneous T-Cell Lymphoma (CTCL)
  • Hairy Cell Leukemia (HCL)
  • Kaposi's Sarcoma
  • Multiple Myeloma (MM)
  • Non-Hodgkin's Lymphoma (NHL)
  • Thrombocytosis

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2018/12/11
Not Applicable
Recruiting
Sun Yat-sen University
2017/07/06
Phase 3
Completed
2015/12/10
N/A
Completed
2015/04/30
Phase 2
Completed
Eiger BioPharmaceuticals
2015/01/19
Phase 2
Completed
2014/06/10
Phase 2
Terminated
2008/11/24
Phase 2
Completed
2008/07/21
Phase 2
Completed
2008/02/20
Phase 2
Completed
2007/08/24
Phase 2
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
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Effective Date
No FDA approvals found for this drug.

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
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Approval Number
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Approval Date
No HSA approvals found for this drug.

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

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Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA approvals found for this drug.

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