Once-weekly insulin efsitora alfa versus once-daily insulin degludec in adults with type 2 diabetes currently treated with basal insulin (QWINT-3): a phase 3, randomised, non-inferiority trial.
Summary
In this 78-week, multicenter, phase 3, treat-to-target non-inferiority RCT, once-weekly efsitora achieved non-inferior glycemic control to daily degludec in adults with type 2 diabetes on basal insulin. Efsitora was well tolerated and offers a marked reduction in injection frequency.
Key Findings
- Once-weekly efsitora was non-inferior to once-daily degludec for HbA1c control over 78 weeks.
- The study supports efsitora as a well-tolerated weekly basal insulin option.
- Injection frequency is substantially reduced with weekly dosing, potentially improving adherence.
Clinical Implications
Efsitora can be considered for adults with T2D requiring basal insulin, especially those struggling with daily injections; real-world studies should assess adherence, quality-of-life, and long‑term safety.
Why It Matters
This trial introduces a once-weekly basal insulin as a viable alternative to daily regimens, potentially improving adherence and patient experience without sacrificing glycemic outcomes.
Limitations
- Open-label design may introduce performance and detection bias
- Generalizability limited to adults on basal insulin without prandial insulin
Future Directions
Evaluate real-world effectiveness, adherence, quality-of-life, hypoglycemia profiles, and outcomes in special populations (older adults, CKD, hepatic impairment).
Study Information
- Study Type
- RCT
- Research Domain
- Treatment
- Evidence Level
- I - Phase 3 randomized controlled non-inferiority trial
- Study Design
- OTHER