BEL512 (CM512 in Greater China), an investigational bispecific antibody targeting thymic stromal lymphopoietin (TSLP) and interleukin-13 (IL-13), met its primary endpoint and all secondary endpoints in a phase 2 trial in adults with inadequately controlled chronic rhinosinusitis with nasal polyps (CRSwNP), according to Belenos Biosciences.1
The double-blind, placebo-controlled trial (NCT06930612) was conducted in China by Belenos' partner, Keymed Biosciences, and enrolled 120 patients with a Nasal Polyp Score (NPS) of 5 or higher, at least 2 polyps per nostril, and a Nasal Congestion Score of 2 to 3 at baseline.1 Patients were randomized to subcutaneous BEL512 300 mg every 12 weeks, 300 mg every 24 weeks, 600 mg every 24 weeks, or placebo, each added to daily intranasal mometasone furoate 200 μg, over 24 weeks of treatment followed by a 12-week safety follow-up.1
“These results provide important clinical validation for simultaneously targeting TSLP and IL-13 in treating CRSwNP,” said Donnie McGrath, MD, chief executive officer of Belenos Biosciences. “The magnitude, speed of onset and durability of improvement across objective measures of nasal polyp disease and the symptoms that matter most to patients, in conjunction with infrequent dosing indicate that BEL512 may offer patients an attractive treatment option.”1
What were the trial’s end points?
The primary endpoint, change from baseline in NPS at week 24, was met with statistically significant improvement across all BEL512 dosing groups versus placebo.1 All secondary endpoints were also met, including Nasal Congestion Score, Loss of Smell Score, Total Symptom Score, sinus CT Lund-Mackay score, and the 22-item Sino-Nasal Outcome Test (SNOT-22).1 Improvements were observed as early as week 4 and remained durable through the treatment and follow-up periods, including in the every-24-week dosing groups.1