Drugs / BI 3000202
last change 5 days ago re-read 9 days ago

BI 3000202

Developed for
systemic lupus erythematosus · type 1 interferonopathy
Investigated by
Boehringer Ingelheim

Trials 8

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 17 trials
Phase 1 NCT07774325 Sep → Oct 2026 expected — Boehringer Ingelheim Recruiting No outcome recorded
Phase 1 NCT07486102 May 2026 → Feb 2027 expected — Boehringer Ingelheim Recruiting No outcome recorded
Phase 1 NCT07273474 Dec 2025 → Mar 2026 — Boehringer Ingelheim Completed No outcome recorded
Phase 1 NCT07215260 Nov → Dec 2025 — Boehringer Ingelheim Completed No outcome recorded
Phase 1 NCT06878365 Jul 2025 → Dec 2026 expected type 1 interferonopathy Boehringer Ingelheim Active not recruiting No outcome recorded
Phase 1 NCT06327256 Apr → Sep 2024 — Boehringer Ingelheim Completed No outcome recorded
Phase 1 NCT05945888 Jul → Nov 2023 — Boehringer Ingelheim Completed No outcome recorded
Phase 21 trial
Phase 2 NCT07409181 Apr 2026 → Feb 2029 expected systemic lupus erythematosus Boehringer Ingelheim Recruiting No outcome recorded

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 8 sources stand behind the page.

FieldValueCited text
Known as BI 3000202 ClinicalTrials.gov intervention name — accepted as the source's own label NCT05945888 ↗
7

NCT06878365 ↗

NCT07409181 ↗

NCT07486102 ↗

NCT07215260 ↗

NCT06327256 ↗

NCT07774325 ↗

NCT07273474 ↗

Route Oral “was administered orally with 240 mL of water” NCT05945888 ↗