Hereditary Periodic Fevers Clinical Trial
Official title:
A Randomized, Double-blind, Placebo Controlled Study of Canakinumab in Patients With Hereditary Periodic Fevers (TRAPS, HIDS, or crFMF), With Subsequent Randomized Withdrawal/Dosing Frequency Reduction and Open-label Long-term Treatment Epochs
This study is to determine whether canakinumab is able to induce and maintain a clinically meaningful reduction of disease activity in participants with Hereditary Periodic Fevers (HPF) compared to placebo.
This study consists of 3 randomized cohorts (one per condition of colchicine
resistant/intolerant Familial Mediterranean Fever (crFMF), Hyper Immunoglobulin D Syndrome
(also known as mevalonate kinase deficiency (HIDS/MKD), and Tumor Necrosis Factor Receptor
Associated Periodic Syndrome (TRAPS), and 4 study epochs:
1. Epoch 1: a screening epoch to assess participant's eligibility;
2. Epoch 2: a randomized treatment epoch of 16 weeks where participants are randomized to
canakinumab 150 mg every 4 weeks (q4w) or to placebo to obtain efficacy and safety data
in a double-blind placebo controlled parallel-arm setting. This epoch contained 2
possible escape options :
1. early blinded escape option for non responders from Day 8 to Day 28 with here an
add-on dose of 150mg canakinumab followed by blinded uptitration at the next
scheduled visit (Day 29)
2. late unblinded escape option for non responders from Day 29 to Day 112; with
open-label uptitration
3. Epoch 3: a randomized withdrawal epoch of 24 weeks where canakinumab responders from the
randomized treatment epoch were re-randomized to canakinumab 150mg q8w or placebo to
assess the potential for canakinumab to maintain clinical efficacy at a reduced dosing
frequency;
4. Epoch 4: an open-label treatment epoch of 72 weeks to collect long-term
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT02334748 -
A Study of Canakinumab in Patients With Systemic Juvenile Idiopathic Arthritis or Hereditary Periodic Fevers Who Participated in the CACZ885G2301E1, CACZ885G2306 or CACZ885N2301 Studies
|
Phase 3 |