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Clinical Trial ● Currently Recruiting Phase II NCT07409181

A Study to Test Whether Different Doses of BI 3000202 Help People With Systemic Lupus Erythematosus (SLE)

A Study to Test Whether Different Doses of BI 3000202 Help People With Systemic Lupus Erythematosus (SLE) — Recruiting • Phase II • Rheumatology • NCT07409181.

📅 29 May 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase II
NCT ID
NCT07409181
Start
2026-04-20
Completion
2029-02-04
ClinicaliQ Trial Snapshot
  • A Study to Test Whether Different Doses of BI 3000202 Help People With Systemic Lupus Erythematosus (SLE) — Recruiting • Phase II • Rheumatology • NCT07409181.
  • Trial testing whether new drug BI 3000202 at different doses improves lupus symptoms in adults over one year.

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What This Trial Is Studying

This study is open to adults with systemic lupus erythematosus (SLE). The purpose of this study is to find out whether a medicine called BI 3000202 helps people with SLE. The study tests different doses of BI 3000202 and aims to find the best dose for people with this condition. Participants are put into 5 groups randomly, which means by chance. 4 groups get different doses of BI 3000202, and 1 group gets a placebo. Placebo tablets look like BI 3000202 tablets but do not contain any medicine. Participants take…

Full Trial Details
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Eligibility criteria, protocol, and results when available
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Guideline
Systemic Lupus Erythematosus (BSR Guidelines)
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Guideline
2023 EULAR Recommendations for Systemic Lupus Erythematosus
Rheumatology · 30 Mar 2026
This EULAR guideline addresses 2023 EULAR Recommendations for Systemic Lupus Erythematosus in Rheumatology. Use it to review current recommendation wording, eligibility criteria,…
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Experimental immune reset treatment has induced drug-free remission in lupus patients during clinical trials, representing a significant advancement in disease management Patients…
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JAK Inhibitors: Updated Safety Signals, Patient Selection and Post-ORAL Surveillance
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