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Pharmacokinetics and Pharmacodynamic Biomarkers of Janus Kinase Inhibitor Therapy in Patients With Ulcerative Colitis (PROPHETIC Study)

Pharmacokinetics and Pharmacodynamic Biomarkers of Janus Kinase Inhibitor Therapy in Patients With Ulcerative Colitis (PROPHETIC Study) - PROPHETIC Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON54935
Enrollment
13
Registered
2020-02-21
Start date
2020-08-25
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

inflammatory bowel disease Ulcerative colitis

Interventions

None listed

Sponsors

Alimentiv B.V.
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. 18 years of age or older. 2. Male or nonpregnant, nonlactating females. 3. Diagnosis of UC for at least 3 months prior to screening. 4. Moderately to severely active UC (total MCS * 6), with objective evidence of inflammation defined by a Mayo endoscopic subscore (MES) * 2 and disease extending > 15 cm from the anal verge. 5. Physician plans to administer JAKi for at least 8 weeks of induction therapy as part of SOC. 6. Documentation of a negative test result for latent tuberculosis within the last 12 months, or according to routine clinical practice. 7. Able to participate fully in all aspects of this clinical trial, including collection of tissue biopsies. 8. Written informed consent must be obtained and documented.

Exclusion criteria

Exclusion criteria: 1. Diagnosis of CD or indeterminate colitis. 2. An active, serious infection, including localized infections. 3. Concomitant administration of biological therapies for UC or potent immunosuppressants, such as azathioprine and cyclosporine. Subjects with previous exposure to these treatments should undergo an appropriate washout period according to local practice prior to starting JAKi, in keeping with routine clinical practice. 4. Hematology laboratory results (e.g., absolute lymphocyte count, absolute neutrophil count, and hemoglobin levels) that contraindicate the product label. 5. Interval between live vaccinations and initiation of JAKi therapy should be in accordance with current vaccination guidelines regarding immunosuppressive agents. 6. Serious underlying disease other than UC that in the opinion of the investigator may interfere with the subject*s ability to participate fully in the study.

Design outcomes

Primary

MeasureTime frame
See objectives

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)