Key Takeaways
- Linaclotide has proven effective in treating various subtypes of chronic constipation in both adult and pediatric patients.
- Patients who received linaclotide reported a significant mean reduction in spontaneous bowel movements (2.22 per week) compared to those receiving the placebo (1.05 per week) at the end of the 12-week treatment period.
- Patients treated with linaclotide also showed a significant improvement in mean BSFS scores (1.11) compared to those on placebo (0.69) at the 12-week mark.
A once-daily dose of 72 mg linaclotide (Linzess) was associated with significant reduction to the frequency of spontaneous bowel movements and improved stool consistency in patients with functional constipation, according to new late-stage data.
Pivotal phase 3 trial data presented in an abstract at the North American Society for Pediatric Gastroenterology, Hepatology and Nutrition (NASPGHAN) 2023 Annual Meeting in San Diego this week, showed pediatric patients receiving the constipation-indicated therapy reported significantly improved disease management and a safety profile consistent with that of previously treated adult patients.
The findings add to the robust portfolio for linaclotide in the treatment of differing subtypes of chronic constipation across both adult and pediatric patients.
Investigators led by Carlo Di Lorenzo, MD, chief of the division of pediatric gastroenterology, hepatology and nutrition at the Nationwide Children’s Hospital, conducted the randomized, controlled phase 3 trial to observe the efficacy and safety of linaclotide versus placebo in patients with functional constipation aged 6 - 17 years old. The guanylate cyclase-C agonist therapy was approved by the US Food and Drug Administration (FDA) for the indication in June2; it was additionally approved to treat irritable bowel syndrome with constipation in 2021.3
The trial included pediatric participants who met modified Rome III criteria for functional constipation. Patients were stratified by younger (6 - 11 years) and older (12 - 17 years) age cohorts and randomized 1:1 to receive either the daily 72 mg oral linaclotide dose or placebo for 12 weeks. Di Lorenzo and colleagues sought a primary efficacy endpoint of change from baseline in weekly spontaneous bowel movements; the key secondary endpoint was change from baseline in stool consistency per the Bristol Stool Form Scale (BSFS).
The team used the age groups as fixed factors and participants’ baseline values as covariate. They additionally assessed for adverse events, laboratory values, and electrocardiograms.