Extension Study of Semapimod 60 mg IV x 3 Days

Completed · Phase 2

Conditions studied: Crohn's Disease

In brief

Study CNI-1493-CD06 is an open, single-arm extension studies to CD03 and CD05. CDAI is the only efficacy measure assessed in this study. The safety of multiple courses of semapimod is to be determined by the incidence of clinical and laboratory adverse events.

Key facts

Study ID

NCT00741910

Run by

Ferring Pharmaceuticals

People needed

15

Starts

2003-07-01

Expected to finish

2006-06-01

Last updated by the study team

2023-11-18

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• The study was open to patients who had satisfactorily completed either study CNI-1493-CD-03 or CNI-1493-CD-05. Initial entry criteria were:
• Patients who satisfactorily completed either study CNI-1493-CD-03 or CD-05 were eligible for participation in this study. Satisfactory completion was defined as follows:
• The patient completed 5 treatment courses in the previous trial.
• The patient had responded to treatment, as defined by a decrease in CDAI of at least 70 points from original baseline (prior to treatment on study CD-02 or CD-04) at the last assessment for study CD-03 or CD-05, respectively. The decrease had to be attributable to semapimod treatment. Thus, patients whose response was attributable to other anti-Crohn's disease therapy are not to be included.
• The patient had no adverse event >grade 2 felt to be probably or definitely related to study medication.
• The patient did not meet any discontinuation criterion in previous trial.
• Patients had to sign informed consent specifically for this study, in addition to the consents for the previous studies, CNI-1493-CD-02 or CD-03, and CNI-1493-CD-04 or CD-05.
• Patients could not take any other investigational therapies during the course of this study.
• Men and women of childbearing potential had to be using a barrier method (diaphragm or condom) of contraception and continue doing so for at least 3 months after last study medication. It was strongly recommended that two forms be used.
• Patients had to be able to adhere to the study visit schedule and/or protocol requirements.

You may not qualify if…

• Could not have met any of the exclusion criteria for the CD02, 03, 04 or 05 studies.

Where it is running

• Northwestern University — Chicago, Illinois, United States
• Long Island Clinical Research Associates — Great Neck, New York, United States
• Asher Kornbluth, MD — New York, New York, United States
• Benjamin Franklin University — Berlin, Germany
• Rambam Medical Center — Haifa, Israel
• Shaare Zedek Hospital — Jerusalem, Israel
• Tel Aviv Sourasky Medical Center — Tel Aviv, Israel
• Erasmus Medical Center — Rotterdam, Netherlands

Full record on ClinicalTrials.gov

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