First patient dosed in Phase II trial in post-operative patients 

Intestine

Orexa has dosed the first patients in a Phase II clinical trial in the prevention of postoperative ileus. The trial investigates whether patients who undergo major abdominal surgery will develop less gastrointestinal disturbances and will recover more quickly. 

The Dutch life sciences company is developing a new medicine that increases food intake and supports health in patients, and Study 2022-503113-31-00-IN-002 (EudraCT number) is a multi-centre, randomised, double-blind, placebo-controlled study to investigate the efficacy of Orexa’s lead compound ORE-001. It will enroll 100 to 120 female patients who undergo gynaecologic surgery requiring longitudinal laparotomy. The study runs at multiple centres in Germany with lead investigator Professor Alexander Mustae from Universitätsklinikum Bonn (UKB).  

“This is a major milestone for a company like Orexa to start its first clinical Phase II study,” said Professor Ard Peeters, Founder of Orexa. “Finally, we will be able to test our drug in patients. This first study is in a group where we can possibly prevent a so-called postoperative ileus. This is a serious complication, which affects up to 50% of patients in several patient groups and leads to patients being unable to eat and therefore recovering more slowly, resulting in prolonged hospitalisation.” 

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