What is the recommended dose of Inpefa (interferon alfa-2b)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: August 19, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

Recommended Dosage of Inpefa (Interferon Alfa-2b)

The recommended dose of Inpefa (interferon alfa-2b) is 3 million units (MU) administered subcutaneously three times per week for chronic hepatitis C treatment. 1

Dosing Guidelines Based on Treatment Context

Standard Monotherapy Dosing

  • For interferon alfa-2b monotherapy: 3 MU three times weekly by subcutaneous injection 1
  • Treatment duration: 12 months unless there is evidence of failure to respond 1

Weight-Based Dosing for Combination Therapy

When used in combination with ribavirin:

  • Standard dose remains 3 MU three times weekly 1
  • Ribavirin dosing should be weight-adjusted:
    • 1,000 mg/day for patients ≤75 kg
    • 1,200 mg/day for patients >75 kg 1

Special Populations

Pediatric Dosing

  • For patients with body surface area >0.5 m²: 50 mcg/m² three times weekly
  • For patients with body surface area ≤0.5 m²: 1.5 mcg/kg/dose three times weekly 2

Patients with Renal Impairment

  • Normal kidney function: Standard dosing
  • Severe kidney disease (GFR 15-59 mL/min): Reduced dose of 1 μg/kg of peginterferon alfa-2b with careful monitoring
  • Dialysis patients: Consider dose reduction to avoid toxicity 1

Monitoring and Dose Adjustments

Required Monitoring

  • Baseline hematology, blood chemistry, and urinalysis before starting treatment
  • Repeat laboratory tests at 3-month intervals during treatment 2
  • Monitor for virologic response at weeks 12 and 24 to guide treatment decisions 1

Dose Adjustments for Adverse Events

  • If severe reactions occur, reduce dose by 50% or temporarily discontinue therapy until adverse reactions abate 2
  • Treatment should be stopped in patients who fail to achieve an early virologic response (EVR) 1

Important Clinical Considerations

Efficacy Predictors

  • Genotype is the strongest predictor of response to therapy
  • Patients with non-genotype 1 (particularly genotypes 2 and 3) have higher sustained virologic response rates (76-82%) compared to genotype 1 (42-46%) 1
  • CD4+ count >500 × 10⁶/L and baseline HCV viral load <10⁷ copies/mL are associated with better response in HIV co-infected patients 3

Treatment Duration

  • For genotype 1: Standard duration is 48 weeks 1
  • For genotypes 2 and 3: 24 weeks of treatment is generally sufficient 1

Common Pitfalls to Avoid

  1. Failing to screen patients for contraindications before initiating therapy
  2. Not adjusting dose in patients with severe adverse reactions
  3. Continuing treatment in non-responders (those without EVR)
  4. Not considering weight-based dosing when using combination therapy

Interferon alfa-2b is contraindicated in patients with decompensated liver disease, significant cytopenias, severe renal or cardiac disorders, and autoimmune disease 1. Always assess the risk-benefit ratio before initiating treatment, particularly in patients with advanced liver disease.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Interferon alpha for the treatment of chronic hepatitis C in patients infected with human immunodeficiency virus. Hepatitis-HIV Spanish Study Group.

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 1996

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.