
Optipeg-A135 mcg/0.
Incepta Pharmaceuticals Ltd.
Peginterferon alfa-2a [Pegylated Interferon alfa-2a] is a pegylated (long-acting) form of interferon alfa-2a used for the following established indications: FDA-approved / established uses Chronic…
Peginterferon alfa-2a [Pegylated Interferon alfa-2a] is a pegylated (long-acting) form of interferon alfa-2a used for the following established indications:
In most settings, interferon-based regimens for hepatitis C have been largely superseded by direct-acting antiviral (DAA) regimens, which are better tolerated and more effective. Peginterferon alfa-2a [Pegylated Interferon alfa-2a] for hepatitis C is now generally reserved for specific situations where DAAs are unavailable, not tolerated, or not indicated. Use for hepatitis B remains an option alongside nucleos(t)ide analogues, chosen based on patient-specific factors.
Peginterferon alfa-2a [Pegylated Interferon alfa-2a] should only be prescribed and monitored by a physician experienced in the management of viral hepatitis.
| Regimen/Genotype | Dose | Duration |
|---|---|---|
| Combination therapy (with other antivirals), genotype 1/4 | 180 mcg subcutaneously once weekly | Typically 48 weeks |
| Combination therapy, genotype 2/3 | 180 mcg subcutaneously once weekly | Typically 24 weeks |
180 mcg/1.73 m² body surface area (BSA) subcutaneously once weekly, up to a maximum of 180 mcg, in combination with ribavirin, for a duration determined by genotype (24-48 weeks).
180 mcg subcutaneously once weekly for 48 weeks as monotherapy.
180 mcg/1.73 m² BSA subcutaneously once weekly (maximum 180 mcg) for 48 weeks.
| Creatinine Clearance | Recommended Dose |
|---|---|
| 30-50 mL/min | 180 mcg once weekly (use with caution) |
| Less than 30 mL/min, including hemodialysis | Reduce to 135 mcg once weekly |
Not recommended in patients with decompensated liver disease (see Contraindications). Monitor closely in cirrhotic patients.
Dose modification: Dose reduction or temporary/permanent discontinuation of Peginterferon alfa-2a [Pegylated Interferon alfa-2a] may be required for severe adverse reactions such as significant depression, severe cytopenias, or other serious toxicities, based on physician assessment.
Side effects of Peginterferon alfa-2a [Pegylated Interferon alfa-2a] range from very common, mild flu-like symptoms to rare but serious reactions.
Patients should seek prompt medical attention for mood changes, unusual bleeding/bruising, vision changes, chest pain, or signs of infection while on Peginterferon alfa-2a [Pegylated Interferon alfa-2a]. See Precautions and Warnings for monitoring recommendations related to the boxed warning.
Peginterferon alfa-2a [Pegylated Interferon alfa-2a] is contraindicated in patients with:
When Peginterferon alfa-2a [Pegylated Interferon alfa-2a] is used in combination with ribavirin, the combination is additionally contraindicated in pregnant women and in men whose female partners are pregnant, due to ribavirin's teratogenic and embryocidal effects (see Pregnancy and Lactation).
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