HSK21542 in patients with postoperative pain: two phase 3, multicentre, double-blind, randomized, controlled trials

Abstract

HSK21542, a peripherally restricted kappa opioid receptor agonist, was evaluated for efficacy and safety in patients with postoperative pain following abdominal surgery. This was assessed in two phase 3, multicentre, randomized, double-blind, controlled trials (HSK21542-301 [ClinicalTrials.gov identifier, NCT04738357] and HSK21542-303 [ClinicalTrials.gov identifier, NCT05390905]) in China. HSK21542-301 was a dual-arm study comparing HSK21542 1.0 μg/kg with placebo, while HSK21542-303 involved three arms comparing HSK21542 1.0 μg/kg with tramadol 50 mg/dose and placebo. All treatments were administered intravenously. The primary endpoint was the time-weighted summed pain intensity differences over 24 h (SPID_{0-24 h}). Both HSK21542-301 (least squares [LS] mean [± standard error], -39.1 [1.88] vs -27.4 [1.89]; P < 0.001) and HSK21542-303 (-64.0 [2.25] vs -45.9 [2.25]; P < 0.001) demonstrated superiority of HSK21542 over placebo in terms of SPID_{0-24 h}, while HSK21542-303 showed non-inferiority to tramadol (LS mean difference, -1.1; 95% confidence interval, -7.4 to 5.1; P < 0.001). Furthermore, HSK21542 had a comparable safety profile to placebo, inducing fewer gastrointestinal adverse events compared with tramadol. Grade ≥3 treatment-emergent adverse events occurred in eight (5.9%) and three (2.3%) patients in the HSK21542 arm of HSK21542-301 and HSK21542-303, respectively. In conclusion, HSK21542 showed potent analgesic effect and was well tolerated in patients who underwent abdominal surgery and experienced postoperative pain.

Fig. 1. Patient disposition.

Trial profiles of a HSK21542-301 and b HSK21542-303.

Fig. 2. Primary efficacy endpoint.

SPID_0–24 h after the postoperative administration of the first dose in a HSK21542-301 and b HSK21542-303. An ANCOVA model was constructed with the treatment group as a fixed effect and the baseline NRS score as a covariate. The P value of the HSK21542 group and the tramadol group in HSK21542-303 was based on the non-inferiority margin of 11.03. LS least squares, SE standard error, SPID summed pain intensity difference.

Fig. 3. LS mean PID.

Postoperative pain intensity differences at each time point in a HSK21542-301 and b HSK21542-303. The ANCOVA model was constructed with the treatment group as the fixed effect and the baseline NRS score as the covariate. *P < 0.05. **P < 0.01. LS least squares, PID pain intensity difference, SE standard error.