Study of IFN-K in Systemic Lupus Erythematosus



Status:Active, not recruiting
Conditions:Lupus
Therapuetic Areas:Immunology / Infectious Diseases
Healthy:No
Age Range:18 - 65
Updated:3/23/2019
Start Date:September 2015
End Date:June 2023

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A Phase IIb, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Neutralization of the Interferon Gene Signature and the Clinical Efficacy of IFNα-Kinoid in Adult Subjects With Systemic Lupus Erythematosus

The safety and immunogenicity of the IFN-Kinoid (IFN-K) have been evaluated in a phase I
clinical study conducted in subjects with SLE. Preliminary results were promising.

The principal aim of the present study is to confirm the neutralization of the interferon
gene signature and the clinical efficacy of IFN-K in subjects with SLE. In addition, the
immune responses and the safety elicited by IFN-K will also be evaluated.


Inclusion Criteria:

- Has had a diagnosis of SLE according to current ACR criteria (4 of 11 ACR criteria)

- Has SLEDAI-2K ≥ 6

- Has at least 1 BILAG A and/or at least 2 BILAG B

- Has a positive IFN gene signature by RT-qPCR

- Has ANA ≥ 1:160 and/or anti-dsDNA antibodies ≥ 7.0 IU/mL

- Currently receiving at least one treatment for SLE

Exclusion Criteria:

- Has active, severe lupus nephritis as defined either by the immediate need for
cyclophosphamide treatment or by renal BILAG A

- Has active, severe, neuropsychiatric SLE, defined as neuropsychiatric BILAG A

- Has been treated with corticosteroids (CS) at a dose of >20 mg of prednisone
equivalent/day for > 7 consecutive days

- Is currently receiving or has received pulse dose CS (≥ 250 mg prednisone
equivalent/day)

- Has received potent immunosuppressive drugs

- Has received abatacept, sifalimumab, rontalizumab, anifrolumab, belimumab, TNF
antagonists or another registered or investigational biological therapy

- Has received anti-B-cell therapy (e.g., rituximab, epratuzumab)

- Has frequent recurrences of oral or genital herpes simplex lesions

- Is at high risk of significant infection and/or has any current signs or symptoms of
infection at entry or has received intravenous antibiotics

- Has received any live vaccine

- Has used any investigational or non-registered product or any investigational or
non-registered vaccine

- Is high-risk human papilloma virus (HPV) positive by rRT-qPCR on a cervical swab

- Has cytological abnormalities ≥ HSIL on a cervical swab
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