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JAK Inhibition in PReclinical Arthritis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-514026-23-00
Enrollment
20
Registered
2024-05-17
Start date
2023-09-06
Completion date
Unknown
Last updated
2024-05-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

preclinical phase of rheumatoid arthritis

Brief summary

Number of patients with development of arthritis at week 48

Detailed description

Number of patients with development of arthritis at week 24, Fulfillment of the ACR/EULAR 2010 RA classification criteria, Ultrasound: number of patients without signs of PD synovitis or PD tenosynovitis at week 24 and week 48 compared to baseline and compared within both groups, Safety: (S)AE, Subjective (SACRAH, sMHQ) and objective (moberg pick up test (MPUT)) hand function, Change in anti CCP2 antibody levels (RE/ml)

Interventions

DRUGBaricitinib-Placebo ident appearance
DRUGBARICITINIB

Sponsors

Universitaetsklinikum Erlangen AöR
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Number of patients with development of arthritis at week 48

Secondary

MeasureTime frame
Number of patients with development of arthritis at week 24, Fulfillment of the ACR/EULAR 2010 RA classification criteria, Ultrasound: number of patients without signs of PD synovitis or PD tenosynovitis at week 24 and week 48 compared to baseline and compared within both groups, Safety: (S)AE, Subjective (SACRAH, sMHQ) and objective (moberg pick up test (MPUT)) hand function, Change in anti CCP2 antibody levels (RE/ml)

Countries

Germany

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026