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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.

Lancet (London, England)2025-06-26PubMed
Total: 88.5Innovation: 8Impact: 0Rigor: 0Citation: 0

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