Summary

Eligibility
for people ages 18-74 (full criteria)
Location
at San Francisco, California and other locations
Dates
study started
completion around

Description

Summary

This study is open to adults with selected type 1 interferonopathies. People can join the study if they have Aicardi-Goutières syndrome (AGS), Coatomer subunit alpha (COPA) syndrome, Familial chilblain lupus (FCL), or another type 1 interferonopathy with a specific gene mutation.

The purpose of this study is to find out how BI 3000202 is tolerated in people with selected type 1 interferonopathies. Participants take a lower dose of BI 3000202 as tablets for 4 weeks. Afterwards, they take a higher dose of BI 3000202 as tablets for 8 weeks. The participants may continue their regular treatment for their condition during the study.

Participants are in the study for about 6 months. During this time, they visit the study site 9 times. The doctors check the health of the participants and note any health problems that could have been caused by BI 3000202.

Official Title

Single-arm Open-label Trial to Assess Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BI 3000202 in Adult Patients With Selected Type 1 Interferonopathies

Keywords

Type 1 Interferonopathies, BI 3000202_low dose, BI 3000202_high dose

Eligibility

You can join if…

Open to people ages 18-74

  • Male and female adult patients from ≥18 years (or alternative age for adults based on local regulations) to <75 years.
  • Genetic diagnosis with mutations in the following affected genes: three prime repair exonuclease 1 (TREX1), ribonuclease H2 subunit A, B or C (RNASEH2B, RNASEH2C, RNASEH2A), SAM And HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 (SAMHD1), U7 Small Nuclear RNA Associated sm-like protein (LSM11), RNA component of the U7 snRNP (RNU7-1) for AGS; Coatomer subunit alpha (COPA) for COPA syndrome; TREX1, SAM And HD domain containing deoxynucleoside triphosphate triphosphohydrolase 1 (SAMHD1) for Familial chilblain lupus (FCL); DNA nuclease 2 (DNASE2), Adenosine triphosphate synthase family AAA domain containing 3A (ATAD3A) for other type 1 interferonopathies. Genotype documented in medical history is sufficient for eligibility determination and does not require confirmation. Variant identification as "pathogenic" or "likely pathogenic" is preferred according to a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. In the absence of such identification, clinical assessment of pathogenicity is required to be documented in the medical records.
  • Patients may be either:
    • On standard of care, provided it is on stable doses
    • Not on standard of care
  • If women of childbearing potential (WOCBP): must be ready and able to use highly effective methods of birth control.

You CAN'T join if...

  • Major chronic inflammatory or connective tissue disease other than selected type 1 interferonopathies, as assessed by the investigator.
  • Increased risk of infectious complications based on investigator's judgement.
  • Evidence of potential moderate to severe loss of kidney function.
  • Evidence of hepatic impairment.
  • If diagnosed with Aicardi-Goutières syndrome (AGS) or other interferonopathy with neurological involvement, AGS Severity Scale >3.
  • Further exclusion criteria apply.

Locations

  • UCSF
    San Francisco California 94121 United States
  • Children's Hospital Los Angeles
    Los Angeles California 90027 United States

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
Boehringer Ingelheim
Links
Related Info
ID
NCT06878365
Phase
Phase 1 Type 1 Interferonopathies Research Study
Study Type
Interventional
Participants
Expecting 18 study participants
Last Updated