Amgen, AstraZeneca announce success of psoriasis drug trial

10 May 2014

Amgen and AstraZeneca have announced a successful Phase III trial of a new drug, `brodalumab' (AMG 827), which can be used for treatment of patients with moderate-to-severe plaque psoriasis.

''The study evaluating novel investigational IL-17 receptor antibody met all primary and secondary endpoints,'' the two said in a joint statement, adding that the study also met all primary and secondary endpoints for both evaluated doses.

Brodalumab is the only investigational treatment in development that binds to the interleukin-17 (IL-17) receptor and inhibits inflammatory signaling by blocking the binding of several IL-17 ligands to the receptor.

Patients achieved at least a 75 per cent improvement from baseline in disease severity and achieved clear or almost clear skin at week 12, according to the assessment of the study.

A significantly higher proportion of patients treated with brodalumab achieved 75 per cent to 100 per cent improvement in 12 weeks.

Results showed that 83.3 per cent of patients in the 210 mg group and 60.3 per cent of patients in the 140 mg group achieved 75 per cent improvement compared to placebo (2.7 per cent). Results also showed that 70.3 per cent of patients in the 210 mg group and 42.5 per cent of patients in the 140 mg group achieved 90 per cent improvement compared to placebo (0.9 per cent).

Further, 41.9 per cent of patients in the 210 mg group and 23.3 per cent of patients in the 140 mg group achieved 100 per cent improvement compared to placebo (0.5 per cent).

Of the 661 patients enrolled in this study, 46 per cent reported prior biologic use and 28.7 per cent weighed more than 100 kg at baseline (mean weight for the study population was 90.8 kg).

The study used the PASI score, which is a measure of psoriatic plaque redness, scaling and thickness and the extent of involvement in each region of the body.

The most common adverse events that occurred during the placebo-controlled period in the brodalumab group (more than 5 per cent of participants) were nasopharyngitis, upper respiratory tract infection and headache. Serious adverse events occurred in 1.8 per cent of patients in the 210 mg group and 2.7 per cent of patients in the 140 mg group compared to 1.4 per cent for placebo during the placebo-controlled period, the two companies said.

''Data from the study suggest that brodalumab may offer a new level of efficacy for patients with moderate-to-severe plaque psoriasis, a disease that affects more than 100 million people globally,'' said Sean E Harper, executive vice president of Research and Development at Amgen. ''This is the first read-out from our Phase III psoriasis clinical programme and we look forward to obtaining additional Phase III data from our two head-to-head studies versus ustekinumab later this year.''

Psoriasis is a non-contagious chronic disease in which the immune system causes skin cells to grow at an accelerated rate. Instead of being shed, skin cells pile up, causing painful and itchy, red, scaly patches.

''Moderate-to-severe plaque psoriasis is a serious disease, and despite available treatments, there is still a significant need for more effective therapies,'' said Briggs Morrison, executive vice president of Global Medicines Development at AstraZeneca. ''We are encouraged by brodalumab's emerging profile and look forward to presenting the full data in the appropriate scientific forum.''

Amagine-1 is one of three Phase III studies designed to assess the efficacy and safety of brodalumab in patients with moderate-to-severe plaque psoriasis. Amagine-2 and Amagine-3 are designed to evaluate the efficacy and safety of induction and maintenance regimens of brodalumab at different dose schedules in patients with moderate-to-severe plaque psoriasis compared to ustekinumab and placebo.