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I6T-MC-AMAJ

A Multicenter Randomized Double-Blind Placebo-Controlled Study Comparing the Efficacy and Safety of Mirikizumab to Secukinumab and Placebo in Patients with Moderate-to-Severe Plaque Psoriasis OASIS-2

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080224006
Enrollment
120
Registered
2018-08-15
Start date
2018-08-22
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psoriasis valgaris, Generalized pustular psoriasis, Erythrodermic psoriasis

Interventions

Sponsors

Eli Lilly Japan K.K.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: -Participant must have chronic plaque psoriasis for at least 6 months.

Exclusion criteria

Exclusion criteria: -Participant must not be breastfeeding or nursing woman. -Participant must not have had serious, opportunistic, or chronic/recurring infection within 3 months. -Participant must not have received a Bacillus Calmette-Guerin (BCG) vaccination within 12 months or received live vaccine(s) (including attenuated live vaccines) within 12 weeks of baseline or intend to receive either during the study. -Participant must not have any other skin conditions (excluding psoriasis). -Participant must not have previous exposure to Cosentyx and any other biologic therapy targeting IL-17 (including Taltz). -Participant must not have received anti-tumor necrosis factor (TNF) biologics within 8 weeks. -Participant must not have previous exposure to any biologic therapy targeting IL-23 (including Stelara).

Design outcomes

Primary

MeasureTime frame
efficacy sPGA and PASI

Secondary

MeasureTime frame
efficacy pharmacokinetics PASI etc., PK parameters

Countries

Asia except Japan, Europe, Japan, North America, Oceania, South America

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026