Sunlenca (Lenacapavir) Dosing and Administration for HIV Patients
Sunlenca (lenacapavir) is administered as subcutaneous injections every 6 months (26 weeks) after an initial loading phase, which can be given through two different options. 1
Initial Treatment Options
Option 1:
- Day 1: Two subcutaneous injections of Sunlenca plus two oral Sunlenca tablets 1
- Day 2: Two oral Sunlenca tablets 1
Option 2:
- Day 1: Two oral Sunlenca tablets 1
- Day 2: Two oral Sunlenca tablets 1
- Day 8: One oral Sunlenca tablet 1
- Day 15: Two subcutaneous injections 1
Maintenance Dosing
- After completing either Option 1 or Option 2, patients receive two subcutaneous injections every 6 months (26 weeks) from the date of their last injection 1, 2
- The injections are administered subcutaneously in the abdominal area 1
Special Considerations
Missed Doses
- If a scheduled injection is missed, patients should contact their healthcare provider immediately to discuss treatment options 1
- For patients who plan to miss a scheduled injection, there is an option to temporarily take Sunlenca tablets 1
- In this case, patients take 1 Sunlenca tablet by mouth once every 7 days until injections can resume 1
Medication Interactions
- Sunlenca should not be taken with strong CYP3A inducers 1
- Drug interactions may persist for up to 9 months after the last injection 1
Efficacy and Safety
- In clinical trials, lenacapavir demonstrated high rates of virologic suppression (81-83%) at week 26 in patients with multidrug-resistant HIV-1 3
- The most common side effects include injection site reactions (occurring in 63% of participants) and nausea 4
- Injection site reactions may include swelling, pain, redness, skin hardening, small mass or lump, and itching 1
- Hardened skin or lumps at the injection site may take longer to heal than other reactions 1
Important Clinical Considerations
- Lenacapavir is particularly valuable for patients with multidrug-resistant HIV-1 infection 3
- It is the first in a new class of drugs called capsid inhibitors to receive FDA approval 4
- Recent research is exploring the combination of lenacapavir with other long-acting antiretrovirals such as cabotegravir, with promising results (94% virologic suppression) 5
- The PURPOSE-1 study demonstrated lenacapavir's effectiveness as a prevention option when administered every 6 months 6