Egrifta WR · tesamorelin
EGRIFTA WR stimulates GH production and increases serum IGF-1. The effects of prolonged elevations in IGF-1 levels are unknown. Monitor IGF-1 levels during EGRIFTA WR therapy.
- Role of the marker
- Monitoring instruction
- Formulation
- For injection, 11.6 mg/vial kit
- Jurisdiction
- United States (FDA-approved labeling on DailyMed)
- Population in the source
- HIV-infected adult patients with lipodystrophy
- Indication and status
- Reduction of excess abdominal fat in HIV-infected adult patients with lipodystrophy. The label states it is not indicated for weight loss management and that long-term cardiovascular safety has not been established.
- What this does not establish
- The label addresses IGF-1 as a safety consideration because treatment raises it. It does not say that IGF-1 shows whether the treatment is working, and this page does not repeat the label's discontinuation language as a threshold for anyone.
Question to bring: “Why are we following IGF-1 in my case, and what change would prompt discussion about the treatment plan?”