Tags : Skyrizi

Clinical Trials

AbbVie Reports Results of Skyrizi (risankizumab) in P-III Induction Studies

Shots: The P-III ADVANCE & MOTIVATE studies involves assessing of Risankizumab (600/1200mg) vs PBO in adult patients with mod. to sev. CD who had an inadequate response/ were intolerant to conventional and/or biologic therapy & patients who had responded inadequately or were intolerant to biologic therapy respectively Results: @12wks. clinical remission as per CDAI (45%/42% […]Read More

Clinical Trials

AbbVie Reports Results of SKYRIZI (risankizumab) in P-III LIMMitless Study

Shots: The P-III LIMMitless study is designed to evaluate the long-term safety & efficacy assessing risankizumab (150 mg q12wks.) continuous risankizumab with a loading dose in adults with moderate to severe plaque psoriasis. The analysis includes integrated data from five P-II & III studies (ultIMMa-1, ultIMMa-2, SustaIMM, IMMvent and NCT03255382) and the LIMMitless study Results: […]Read More


AbbVie’s Skyrizi (risankizumab) Receives Japanese Ministry of Health, Labour and

Shots: The approval is based on P-II & P-III sustaIMM, ultIMMa-1 and IMMspire study results assessing Skyrizi in Japanese patients with plaque psoriasis, generalized pustular psoriasis and erythrodermic psoriasis & active psoriatic arthritis The study resulted in safe and effective results and has capabilities to improve the signs of these chronic immune-mediated diseases Skyrizi (risankizumab) […]Read More