Co-crystal of Tramadol-Celecoxib Versus Tramadol or Placebo for Acute Moderate-to-Severe Pain After Oral Surgery: Randomized, Double-Blind, Phase 3 Trial (STARDOM1)

被引:7
作者
Langford, Richard [1 ]
Pogatzki-Zahn, Esther M. [2 ]
Morte, Adelaida [3 ]
Sust, Mariano [3 ]
Cebrecos, Jesus [3 ]
Vaque, Anna [3 ]
Ortiz, Esther [3 ]
Fettiplace, James [4 ]
Adeyemi, Shola [4 ]
Lopez-Cedrun, Jose Luis [5 ]
Bescos, Socorro [6 ]
Gascon, Neus [3 ]
Plata-Salaman, Carlos [3 ]
机构
[1] London Clin, London W1G 6BW, England
[2] Univ Hosp Munster, Munster, Germany
[3] ESTEVE Pharmaceut, Barcelona, Spain
[4] Mundipharma Res Ltd, Cambridge, England
[5] Complexo Hosp Univ A Coruna, La Coruna, Spain
[6] Hosp Univ Vall dHebron, Barcelona, Spain
关键词
Acute pain; Celecoxib; Co-crystal; CTC; Efficacy; SPID0-4; Tramadol; PATIENT NONADHERENCE; MULTIMODAL ANALGESIA; POSTOPERATIVE PAIN; ENHANCED RECOVERY; MANAGEMENT; PREVALENCE; PHARMACOKINETICS; CONSEQUENCES; ANESTHESIA; GUIDELINE;
D O I
10.1007/s12325-023-02744-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Introduction: Co-crystal of tramadol-celecoxib (CTC) is the first analgesic co-crystal for acute pain. This completed phase 3 multicenter, double-blind trial assessed the efficacy and safety/tolerability of CTC in comparison with that of tramadol in the setting of moderate-to-severe pain up to 72 h after elective third molar extraction requiring bone removal.Methods: Adults (n = 726) were assigned randomly to five groups (2:2:2:2:1): orally administered twice-daily CTC 100 mg (44 mg rac-tramadol hydrochloride/56 mg celecoxib; n = 164), 150 mg (66/84 mg; n = 160) or 200 mg (88/112 mg; n = 160); tramadol 100 mg four times daily (n = 159); or placebo four times daily (n = 83). Participants in CTC groups also received twice-daily placebo. The full analysis set included all participants who underwent randomization. The primary endpoint was the sum of pain intensity differences over 0 to 4 h (SPID0-4; visual analog scale). Key secondary endpoints included 4-h 50% responder and rescue medication use rates. Safety endpoints included adverse events (AEs), laboratory measures, and Opioid-Related Symptom Distress Scale (OR-SDS) score.Results: All CTC doses were superior to placebo (P < 0.001) for primary and key secondary endpoints. All were superior to tramadol for SPID0-4 (analysis of covariance least squares mean differences [95% confidence interval]: - 37.1 [- 56.5, - 17.6], - 40.2 [- 59.7, - 20.6], and - 41.7 [- 61.2, - 22.2] for 100, 150, and 200 mg CTC, respectively; P < 0.001) and 4-h 50% responder rate. Four-hour 50% responder rates were 32.9% (CTC 100 mg), 33.8% (CTC 150 mg), 40.6% (CTC 200 mg), 20.1% (tramadol), and 7.2% (placebo). Rescue medication use was lower in the 100-mg (P = 0.013) and 200-mg (P = 0.003) CTC groups versus tramadol group. AE incidence and OR-SDS scores were highest for tramadol alone.Conclusions: CTC demonstrated superior pain relief compared with tramadol or placebo, as well as an improved benefit/risk profile versus tramadol.
引用
收藏
页码:1025 / 1045
页数:21
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