Nelson's Story

ITCH study shows reduction in pruritus in Alagille syndrome

ITCH STUDY SHOWS REDUCTION IN PRURITUS IN ALAGILLE SYNDROME
[/fusion_text][fusion_text] WASHINGTON — In a dose-varied study of maralixibat, patients’ caregivers reported trends toward pruritis relief while the drug also demonstrated safety, according to a presenter at The Liver Meeting 2017. “Although the pre-specified primary analyses of ItchRO were not all statistically significant, the data suggest that maralixibat was safe and may reduce pruritus in Alagille Syndrome,” Benjamin L. Shneider, MD, from Texas Children’s Hospital, said during the presidential plenary. Shneider and colleagues used the Itch Reported Outcome (ItchRO) tool, a novel electronic diary in which caretakers report each day’s score from 0 to 4 – with 4 being mutilation of the skin, based upon the child’s itch-related symptoms overnight. This was supported by a clinical provider report as well. Maralixibat delivery was in a dose escalation fashion for 5 weeks with stable dose treatment for an additional 8 weeks, Shneider said. Patients had follow-up with their provider at 4 weeks. Researchers compared the two highest tolerated doses of maralixibat vs. placeboand compared pooled doses to the placebo. Participants received either placebo (n = 12), 70 µg/kg per day (n = 8), 140 µg/kg per day (n = 11) or 280 µg/kg per day (n = 6) and the primary endpoint was change in baseline to week 13 in observer-based ItchRO. The secondary endpoint was serum bile acids. Shneider showed that the 70 µg/kg dose and the 140 µg/kg significantly impacted the ItchRO score (P = .032 and .014, respectively) at week 13 and, additionally, the 70 µg/kg dose significantly lowered serum bile acid (P = .016) at week 13. All other relationships were not significant, but patients often responded to the medication. “Determination of optimal dosing and further assessments of safety and efficacy in children with cholestasis are warranted,” Shneider said. – by Katrina Altersitz Reference: Shneider BL, et al. Abstract 144. Presented at: The Liver Meeting; Oct. 20-24, 2017; Washington, D.C. Disclosure: Shneider reports consulting and holding stocks for Bristol Myers Squibb.

More News

Rare Disease Care

Rare Disease Care

One of the key challenges in rare disease care is the limited understanding of these conditions. Many rare diseases are genetic or congenital, and research into their causes and potential treatments is often underfunded. Patients and their families frequently face diagnostic odysseys, enduring years of uncertainty before receiving a proper diagnosis.

ALGSA Symposium 2024

Come join other ALGS families at a fun and informative event. We have topics to fit every ALGS family from ALGS 101 to deep dives into the genetics of ALGS and current research on the disease.

Virtual Events in October

Virtual Events in October

Read all about the virtual events we have planned for October. There are many opportunities for ALGS families to connect and learn together.