Understanding the Relationship Between Infliximab Levels to Clinical Response of Remicade in Crohn's Disease

NATerminatedINTERVENTIONAL
Enrollment

11

Participants

Timeline

Start Date

December 31, 2011

Primary Completion Date

December 31, 2013

Study Completion Date

December 31, 2013

Conditions
Crohn's Disease
Interventions
DRUG

Remicade

The first potential for dose augmentation will be at infusion #3 (visit 1 and 2 patients will receive 5 mg/kg). Patients will be assessed at each infusion visit for response defined as a reduction in HBI score by 2 or more points from prior visit (unless in remission; HBI score of 4 or less). Patients with a response will be maintained at the dose where response was achieved. If there is no response to treatment, or flare at any visit (beginning at visit #3), infliximab dose or dosing frequency will be increased in a gradual fashion, up to a maximum of 15 mg/kg every 6 weeks, until response is achieved.

Trial Locations (1)

10029

Icahn School of Medicine at Mount Sinai, New York

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Prometheus Laboratories

INDUSTRY

lead

Shradha Agarwal

OTHER

NCT01438151 - Understanding the Relationship Between Infliximab Levels to Clinical Response of Remicade in Crohn's Disease | Biotech Hunter | Biotech Hunter