Efficacy and safety of maribavir in Japanese patients with post-transplant cytomegalovirus infections: a phase III study.

Int J HematolJun 12, 2026 (epub)
Clinical ResearchInfectious DiseasesHematologyOpen access

Yoshinobu Kanda, Katsuto Takenaka, Tatsu Tanabe et al.

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In 30 seconds

This phase III, multicenter study evaluated the efficacy and safety of maribavir in Japanese patients aged ≥16 years with cytomegalovirus (CMV) infections post-transplant. Among 41 patients treated, 68.3% achieved confirmed CMV viremia clearance at week 8, indicating maribavir's effectiveness in this population.

Key findings

  • 68.3% of patients achieved confirmed CMV viremia clearance at week 8.
  • 87.8% of patients experienced at least one treatment-emergent adverse event.
  • The most common adverse events included nausea (24.2%) and anemia (17.1%).

Why it matters

The study highlights maribavir as a potential treatment option for CMV infections in transplant recipients, particularly for those resistant to standard therapies, addressing a significant clinical challenge in post-transplant care.

Source

Published in Int J Hematol. This summary was written by xxcode from the publication's abstract and metadata. It is not peer reviewed and is not a substitute for the original article. For clinical decisions, review the original publication.

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AI-generated summaries may contain errors or omissions. Verify clinically important information with the original publication.

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