NEOVACS ANNOUNCES THE COMPLETION OF PATIENT ENROLLMENT IN PHASE IIB CLINICAL STUDY OF IFNalpha KINOID IN LUPUS
Company Expects the Availability of Results from the Study in Q2 2018
the completion of patient enrollment for its phase IIb clinical study, IFN-K-002, evaluating IFNalpha Kinoid for the treatment of lupus.
Study IFN-K-002 includes 178 patients who have moderate to severe systemic lupus erythematosus (SLE). This worldwide, randomized, multicentre international phase IIb study is evaluating IFNalpha Kinoid versus placebo and is being conducted under IND in Europe, Asia, North Africa, South America, and the United States. All the patients are being treated and followed up for 9 months for the main study.
Neovacs designed this Phase IIb clinical trial to obtain relevant and meaningful data on:
- Biological efficacy: by measuring the decrease of interferon gene signature, one of the primary markers of disease activity.
- Clinical efficacy: by using the BICLA response score at Month 9. This score is one of the end-points validated by health authorities to evaluate the clinical response in lupus clinical studies.
The company has chosen a successful strategy which promotes the recruitment of eligible patients in this phase IIb clinical trial in lupus, a rare and complex disease, with a number of patients worldwide estimated to 5 million.
In order to ensure the validity of the clinical results of this study, Neovacs is taking advice from three expert committees: 1) the independent Data Safety Monitoring Board "iDSMB", whose mission is related to assessing safety, 2) an independent "Adjudication Committee" to evaluate the consistency of the clinical response data to the vaccine-(BICLA), and 3) an internal "Steering Committee" to oversee the conduct of the clinical trial.
About Neovacs Technology
Neovacs targets pathologies associated with an overproduction of endogenous cytokines. This technology is based on active immunotherapy to generate an immune response through the administration of an immunogenic complex involving the targeted cytokine to a carrier protein. The intramuscular injection of this Kinoid induces an immune response and stimulates the production of polyclonal antibodies against the targeted cytokines. It is thus possible to block cytokine overproduction and its pharmacological effects. Several autoimmune and inflammatory diseases (lupus, dermatomyositis, Type 1 diabetes ...) are characterized by a disorder of cytokines that are found produced in excess. As an example, the overproduction of IFNalpha will promote inflammation and dysregulation of the immune system.
Systemic lupus erythematosus (SLE) or lupus erythematosus is a debilitating, chronic autoimmune disease whose etiology remains unknown. SLE is characterized by a loss of tolerance of self-antigens, with the production of autoantibodies, especially antinuclear antibodies that attack healthy tissues and cause inflammatory reactions in different parts of the body. The disease can affect multiple organs (skin, kidneys, joints, heart, lungs, central nervous system, etc.) and is characterized by heterogeneous clinical signs (skin rashes, arthritis, photosensitivity, nephritis, neurological disorders, anemia, thrombocytopenia, etc.), which vary from one person to another and change as the disease progresses. Systemic lupus erythematosus affects mostly women.
Listed on Alternext Paris since 2010, Neovacs is today a leading biotechnology company focused on an active immunotherapy technology platform (Kinoids) with applications in autoimmune and/or inflammatory diseases. On the basis of the company's proprietary technology for inducing a polyclonal immune response (covered by five patent families that potentially run until 2032) Neovacs is focusing its clinical development efforts on IFNalpha-Kinoid, an immunotherapy being developed for the indication of lupus and dermatomyositis. Neovacs is also conducting preclinical development works on other therapeutic vaccines in the fields of auto-immune diseases, oncology, allergies and Type 1 diabetes. The goal of the Kinoid approach is to enable patients to have access to safe treatments with efficacy that is sustained in these life-long diseases. www.neovacs.fr
NEOVACS - Corporate Communication & Investor Relations
+33 (0)1 53 10 93 14
NEWCAP- Press relations
+33 1 44 71 00 12 / + 33 6 88 20 35 59
+33 1 44 71 20 41 / +33 6 58 14 84 66
LIFESCI ADVISORS- Investor Relations / Financial Communications
+41 79 367 6254
 Neovacs obtains FDA approval to extend its Phase IIb clinical trial in Lupus to United States
 The BILAG-Based Composite Lupus Assessment- BICLA score : Wallace D. Ann Rheum Dis 2014;73:183-190
 The lupus foundation of America : http://www.lupus.org/
The issuer of this announcement warrants that they are solely responsible for the content, accuracy and originality of the information contained therein.
Source: NEOVACS via Globenewswire