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Randomised clinical trial: safety, pharmacokinetics and pharmacodynamics of trazpiroben (TAK‐906), a dopamine D 2 /D 3 receptor antagonist, in patients with gastroparesis
Author(s) -
Kuo Braden,
Scimia Cecilia,
Dukes George,
Zhang Wenwen,
Gupta Saurabh,
Chen Chunlin,
Chuang Emil,
Camilleri Michael
Publication year - 2021
Publication title -
alimentary pharmacology and therapeutics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.308
H-Index - 177
eISSN - 1365-2036
pISSN - 0269-2813
DOI - 10.1111/apt.16451
Subject(s) - metoclopramide , medicine , gastroparesis , gastric emptying , domperidone , tolerability , gastroenterology , pharmacodynamics , receptor antagonist , adverse effect , endocrinology , dopamine , anesthesia , pharmacology , pharmacokinetics , antagonist , stomach , vomiting , receptor
Summary Background Gastroparesis is a chronic gastric motility disorder. Dopamine D 2 /D 3 receptor antagonists metoclopramide and domperidone are current treatment options but are associated with central nervous system and cardiovascular safety concerns, respectively, precluding chronic use. Trazpiroben (TAK‐906), a dopamine D 2 /D 3 receptor antagonist, is under development for chronic treatment of moderate‐to‐severe gastroparesis. Nonclinical data suggest trazpiroben will have D 2 /D 3 receptor antagonism comparable with metoclopramide or domperidone. Aims To evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics (effect on prolactin and gastric function) of twice‐daily trazpiroben (5, 25 and 100 mg) in participants with gastroparesis. Methods This phase 2a pilot study evaluated gastric emptying using the gastric emptying breath test, with metoclopramide as an internal control. Gastric accommodation and gastroparesis symptoms were assessed using the nutrient drink test and American Neurogastroenterology and Motility Society Gastroparesis Cardinal Symptom Index‐Daily Diary, respectively. Results Overall, 51 participants were enrolled. Trazpiroben was well tolerated, demonstrating a favourable safety profile without cardiovascular or central nervous system adverse events. All trazpiroben doses were rapidly absorbed and eliminated (t 1/2z 4‐5 hours), and D 2 /D 3 receptor target engagement confirmed by increased serum prolactin (peaking at trazpiroben 25 mg). No effect on gastric emptying was demonstrated with trazpiroben or metoclopramide ( P > 0.05), although benefits in volume‐to‐fullness were seen at trazpiroben 5 mg ( P > 0.05) and 25 mg (88.5 vs −26.3 mL; P = 0.019), and nonsignificant numerical aggregate symptom score improvements were observed with trazpiroben 25 mg vs placebo ( P = 0.182). Conclusions Trazpiroben was well tolerated with a favourable safety profile, supporting its further development for the treatment of gastroparesis. ClinicalTrials.gov identifier: NCT03268941.