CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 10 enrolled
Drug / intervention
Infliximab [infliximab biosimilar 3]drug
Likely dose
5 mg/kg intravenous infusion; initial dose at Week 0, then Week 2 and Week 6, then every 8 weeksAI-extracted
Key inclusion· 2
  • Diagnosed with psoriasis vulgaris, psoriasis arthropathica, pustular psoriasis, or erythrodermic psoriasis
  • Starting infliximab treatment for the first time at this medical institution after drug launch
Key exclusion· 0

None specified.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03885089
NCT03885089N/ACompleted

Infliximab BS for Intravenous Drip Infusion 100 mg "Pfizer" General Investigation (Psoriasis Vulgaris, Psoriasis Arthropathica, Pustular Psoriasis, or Erythrodermic Psoriasis)

Pfizer·observational·Posted Mar 21, 2019·Updated Jun 19, 2025

In Brief

An observational study evaluating Infliximab [infliximab biosimilar 3] for Psoriasis Vulgaris and 3 related conditions. Completed, enrolled 10 participants across 1 site.

Detailed Summary

To collect information on the safety and effectiveness of Infliximab BS for Intravenous Drip Infusion 100 mg "Pfizer" against psoriasis vulgaris, psoriasis arthropathica, pustular psoriasis, or erythrodermic psoriasis under actual status of use.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesJapan
Collaborators--

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedMar 21, 2019
Enrollment StartOct 21, 2019
Primary CompletionMar 8, 2024
TodayJul 2, 2026
Enrollment to primary: 4.4 yearsPosted 7.3 years ago

Interventions

Infliximab [infliximab biosimilar 3]drug

\<Psoriasis\> The usual dose is 5 mg as Infliximab (Genetical Recombination) \[Infliximab Biosimilar 3\] for every kg of body weight given as an intravenous infusion. After an initial dose is given, the subsequent doses are given at Weeks 2 and 6, and every 8 weeks thereafter. After a dose at Week 6 is given, the dose may be increased or the dosing interval may be reduced for patients who have an incomplete response or reduced effects. These adjustments should be made in a stepwise manner according to condition of patients. The maximum dose is 10 mg for every kg of body weight at the dosing interval of 8 weeks and 6 mg for every kg of body weight at a reduced dosing interval. The minimum dosing interval is 4 weeks.