A Study of Baricitinib (LY3009104) in Adult and Pediatric Japanese Participants With NNS/CANDLE, SAVI, and AGS
- Sponsor
- Eli Lilly and Company
- Study ID
- NCT04517253
- Phase
- PHASE2/PHASE3
- Status
- Terminated
Conditions
- Aicardi Goutieres Syndrome
- Chronic Atypical Neutrophilic Dermatosis With Lipodystrophy and Elevated Temperature Syndrome
- Nakajo-Nishimura Syndrome
- STING-Associated Vasculopathy With Onset in Infancy
Eligibility Criteria
- Sex
- ALL
- Age
- 6 Months - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Baricitinib — DRUGAdministered orally
Study Details
The main purpose of this study is to evaluate the efficacy and safety of baricitinib in adult and pediatric Japanese participants with Nakajo-Nishimura Syndrome/chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (NNS/CANDLE), STING-associated vasculopathy with onset during infancy (SAVI), and Aicardi-Goutières Syndrome (AGS).
Key Dates
- Start date
- Oct 27, 2020
- Status verified
- Jun 2025
- Primary completion
- Apr 4, 2023
- Completion
- Nov 28, 2024
Study Design
- Enrollment
- 10 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: CANDLEParticipants with chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) were administered an optimized final dosage of baricitinib, ranging from 8 mg to 12 mg daily (initially 8 mg, with gradual escalation to 10 mg and 12 mg), either as tablets or oral suspension, for 12 weeks. This dosage was determined during a prior 8-week dose-adjustment period, tailored to each participant's weight and estimated glomerular filtration rate (eGFR). Participants then continued receiving baricitinib at their optimized dosage for 191.1 weeks.
- Experimental: SAVIParticipants with stimulator of interferon genes (STING)-associated vasculopathy with onset during infancy (SAVI) were administered an optimized final dosage of baricitinib, ranging from 6 mg to 12 mg daily (initially 6 mg, with gradual escalation to 8 mg, 10 mg, and 12 mg), either as tablets or oral suspension, for 24 weeks. This dosage was determined during a prior 8-week dose-adjustment period, tailored to each participant's weight and eGFR. Participants then continued receiving baricitinib at their optimized dosage for 202.9 weeks.
- Experimental: Aicardi-Goutières Syndrome (AGS)Participants with Aicardi-Goutières Syndrome (AGS) were administered an optimized final dosage of baricitinib, ranging from 6 mg to 8 mg daily (initially 6 mg, with gradual escalation to 8 mg), either as tablets or oral suspension, for 24 weeks. This dosage was determined during a prior 8-week dose-adjustment period, tailored to each participant's weight and eGFR. Participants then continued receiving baricitinib at their optimized dosage for 206.1 weeks.
Primary Outcome Measure
Change From Baseline in Mean Daily Diary Scores in Participants With CANDLE (Primary Treatment Period) [ Time Frame: Baseline, 20 weeks ]
Related Studies
- The Myelin Disorders Biorepository ProjectRecruiting · Children's Hospital of Philadelphia · Los Angeles, California