Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06119490

Evaluation of the Efficacy and Safety of Methylprednisolone Combined With the JAK Inhibitors in the Treatment of Toxic Epidermal Necrolysis

Evaluation of the Efficacy and Safety of Methylprednisolone Combined With the JAK Inhibitors in the Treatment of Toxic Epidermal Necrolysis: Two-arm, Open, Single-center Study

Status
Recruiting
Phase
EARLY_Phase 1
Study type
Interventional
Enrollment
30 (estimated)
Sponsor
Peng Zhang · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

To evaluate the efficacy and safety of methylprednisolone combined with the JAK inhibitor abxitinib and tofacitinib in the treatment of toxic epidermal necrolysis

Conditions

Interventions

TypeNameDescription
DRUGAbrocitinibSolu-Medrol® 1 mg/kg body weight intravenous infusion per day in combination with Arocitinib tablets 200 mg per day for 2 weeks
DRUGTofacitinibSolu-Medrol® 1 mg/kg body weight intravenous infusion per day in combination with Tofacitinib tablets 10 mg per day for 2 weeks

Timeline

Start date
2023-07-05
Primary completion
2026-07-01
Completion
2026-09-01
First posted
2023-11-07
Last updated
2023-11-28

Locations

1 site across 1 country: China

Regulatory

Source: ClinicalTrials.gov record NCT06119490. Inclusion in this directory is not an endorsement.