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Clinical Trial Active — Not Recruiting Phase II NCT06980805

A Study to Assess the Safety, Tolerability, and Efficacy of IMVT-1402 in Participants With Cutaneous Lupus Erythematosus (CLE)

A Study to Assess the Safety, Tolerability, and Efficacy of IMVT-1402 in Participants With Cutaneous Lupus Erythematosus (CLE) — Active Not Recruiting • Phase II • Rheumatology •…

📅 17 Jun 2026 ⏱ 1 min read
Active — Not Recruiting
Check the registry for current status and eligibility criteria.
Status
Active — Not Recruiting
Phase
Phase II
NCT ID
NCT06980805
Start
2025-02-19
Completion
2026-10
ClinicaliQ Trial Snapshot
  • A Study to Assess the Safety, Tolerability, and Efficacy of IMVT-1402 in Participants With Cutaneous Lupus Erythematosus (CLE) — Active Not Recruiting • Phase II • Rheumatology • NCT06980805.
  • Trial testing IMVT-1402 injection versus placebo for skin lupus, measuring safety and effectiveness over 52 weeks.

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What This Trial Is Studying

The primary purpose of this study is to evaluate the efficacy, safety, and tolerability of IMVT-1402 in participants with Cutaneous Lupus Erythematosus. The study will consist of 3 periods: Period 1: eligible participants will be randomized 1:1 to IMVT-1402 Dose 1 or placebo SC QW for 12 weeks. Period 2: participants who completed Period 1 will receive IMVT-1402 Dose 1 SC QW for 14 weeks. Period 3: after completion of Period 2, participants will be re-randomized 1:1 to blinded IMVT-1402 Dose 1 or Dose 2 SC QW for 26 weeks.…

Full Trial Details
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Eligibility criteria, protocol, and results when available
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Related Clinical Intelligence

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Guideline
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