Selective JAK inhibitors (abrocitinib / ritlecitinib)
Pfizer (repurposed agents)
A TrialNet phase-2 study testing two newer oral JAK-pathway drugs - abrocitinib and ritlecitinib - in recent-onset stage-3 T1D. This is distinct from baricitinib: different JAK selectivity, NIH/TrialNet sponsor, and no published T1D efficacy result yet.
The scorecard
No published T1D efficacy result yet; JAKPOT tests C-peptide preservation at new-onset, not presymptomatic onset delay.[1]
Oral delivery is attractive, but JAK-class safety warnings matter strongly for long-term use in young T1D populations.[2]
Both agents are approved for other immune conditions, but T1D use remains investigational.[1]
Editor’s take
Baricitinib made oral JAK inhibition credible in T1D; JAKPOT asks whether more selective JAK-pathway drugs can preserve C-peptide with a better risk-benefit profile. It is promising enough to track, but still pre-result.
The full picture
Why this is separate from baricitinib
Baricitinib is already covered because BANDIT published a positive new-onset phase-2 result. JAKPOT is a separate TrialNet test of abrocitinib and ritlecitinib, two different oral JAK-pathway drugs, in the same broad idea: preserve residual beta-cell function after diagnosis.1
No T1D efficacy result is published yet. This is pipeline coverage, not a positive-result record.
References
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National Library of Medicine. JAK inhibitors to preserve C-peptide production in new-onset T1D. ClinicalTrials.gov NCT05743244. https://clinicaltrials.gov/study/NCT05743244 ↩
Coming soon
ETA · Phase 2 active not recruiting; completion estimated 2027
- →JAKPOT T1D phase-2 results · completion estimated 2027
Sources
- [1]Janus Kinase (JAK) Inhibitors to Preserve C-Peptide Production in New Onset Type 1 Diabetes · registry · 2026-05-29 — TrialNet / NIDDK phase 2; active not recruiting; estimated n=78; ages 12-35; abrocitinib vs ritlecitinib vs placebo.
- [2]CIBINQO (abrocitinib) prescribing information · regulatory · 2022-01-14 — FDA label for atopic dermatitis; no T1D indication.