ASN's Mission

To create a world without kidney diseases, the ASN Alliance for Kidney Health elevates care by educating and informing, driving breakthroughs and innovation, and advocating for policies that create transformative changes in kidney medicine throughout the world.

learn more

Contact ASN

1401 H St, NW, Ste 900, Washington, DC 20005

email@asn-online.org

202-640-4660

The Latest on X

Kidney Week

Please note that you are viewing an archived section from 2022 and some content may be unavailable. To unlock all content for 2022, please visit the archives.

Abstract: SA-PO288

Impact of Difelikefalin on 5D-Itch Domains in Patients With CKD-Associated Pruritus

Session Information

Category: Dialysis

  • 701 Dialysis: Hemodialysis and Frequent Dialysis

Authors

  • Rastogi, Anjay, David Geffen School of Medicine, Los Angeles, California, United States
  • Topf, Joel M., Oakland University, William Beaumont School of Medicine, Rochester, Michigan, United States
  • Schaufler, Thilo, Vifor Pharma Ltd, Glattbrugg, Zurich, Switzerland
  • Morin, Isabelle, Vifor Pharma Ltd, Glattbrugg, Zurich, Switzerland
  • Menzaghi, Frederique, Cara Therapeutics Inc, Stamford, Connecticut, United States
  • Wen, Warren, Cara Therapeutics Inc, Stamford, Connecticut, United States
  • Mccafferty, Kieran, Barts Health NHS Trust, London, London, United Kingdom
Background

Chronic kidney disease-associated pruritus (CKD-aP) is common in hemodialysis (HD) patients, impacting quality of life (QoL). In the Phase 3 KALM studies, difelikefalin (DFK), a selective kappa opioid receptor agonist approved in the United States and Europe for the treatment of moderate–severe pruritus in adults undergoing HD, improved itch intensity and QoL. The impact of DFK treatment on the subdomains of the 5D-itch scale (a multidimensional questionnaire validated in patients with chronic pruritus) were explored.

Methods

In this pooled KALM-1 and KALM-2 analysis (n=712), HD patients with moderate–severe CKD-aP were randomized 1:1 to receive intravenous DFK 0.5 µg/kg or placebo (PBO) 3 times/week (Wk) for 12 Wks (double-blind [DB], PBO-controlled phase), followed by an up to 52-Wk open-label extension ([OLE] all patients receiving DFK). The change from DB baseline (BL) in 5D-itch scale domains was assessed including duration, degree, direction, and body distribution of itch and disability (sleep and daily activities) with a 2-Wk recall period.

Results

In the DB phase, patients on DFK reported greater improvements than PBO in all domains. Throughout the OLE, patients reported ongoing improvements: Duration of itch (~6 h/day at OLE Wk 52 vs ~12–18 h/day at BL); Degree (“mild-moderate” vs “moderate-severe” at BL); Direction (“a little/much better” vs “unchanged” at BL); Disability, (“rarely” affected daily activities [including sleep] vs “frequently/occasionally” affected at BL); and Distribution (3–5 body parts affected vs 6-10 at BL).

Conclusion

In the 12-wk DB period patient-reported improvements in 5D-itch scale domains were greater with DFK than PBO. In the OLE, with all patients receiving DFK up to 52 wks, further improvements were observed across all domains.

Funding

  • Commercial Support –