Cue Biopharma (NASDAQ:CUE) on Sunday shared topline results from a Phase 2 trial of CUE-221 in patients with moderate to severe chronic spontaneous urticaria.
The study met its primary and secondary endpoints, demonstrating sustained efficacy and a favorable safety profile.
Cue Biopharma shares initially traded higher Monday before pulling back and turning negative.
Genesis Life Sciences conducted the trial in China, enrolling 145 patients whose chronic hives were inadequately controlled by H1 antihistamines.
The study evaluated subcutaneous CUE-221 at doses of 4 mg/kg, 2 mg/kg, and 1 mg/kg administered every four weeks against placebo and active comparator omalizumab.
At Week 12, CUE-221 met its primary endpoint of complete hive resolution across all dose levels.
Specifically, 54% of patients receiving the 4 mg/kg dose attained complete resolution compared to 11% for placebo.
The 4 mg/kg group also met the key secondary endpoint, achieving a statistically significant 46% complete response rate at Week 12.
Peak effect occurred at Week 22, with 69% of patients in the 4 mg/kg group exhibiting complete resolution.
Following final dosing at Week 16, benefits lasted through Week 28.
At Week 28, 12 weeks off drug, CUE-221 demonstrated a statistically significant 36% efficacy advantage over omalizumab.
Shao-Lee Lin, President and CEO of Cue Biopharma, highlighted that CUE-221 represents a potential best therapeutic option.
Lin stated the company is preparing to initiate a Phase 2b/3 trial in chronic hives while advancing a Phase 2 study in food allergy.
The candidate demonstrated a favorable safety profile with no treatment-related serious adverse events or anaphylaxis.
CUE Price Action: Cue Biopharma shares were down 28.53% to $26.48 at the time of publication on Monday, according to Benzinga Pro data.
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