“Based on strong scientific rationale, BION-1301 is currently being evaluated in a Phase 1/2 clinical study for the treatment of multiple myeloma. The preclinical data presented today further indicate BION-1301’s potential in the treatment of IgAN,” stated
The abstract, “BION-1301: A Novel Fully Blocking APRIL Antibody for the Treatment of IgA Nephropathy,” was presented in a poster session titled “Molecular Mechanisms of CKD - II” and is available online at the ASN Kidney Week 2018 website.
IgAN, commonly referred to as Berger’s disease, is a progressive kidney disease characterized by an autoimmune antibody response against endogenous IgA. This results in local inflammation impeding kidney function, which may eventually lead to end-stage renal disease and the need for renal transplant. While IgAN has unclear causality and lacks approved disease-modifying options for therapy, preclinical data indicate that suppressing serum IgA and the anti-IgA autoimmune response by a neutralizing APRIL antibody, such as BION-1301, may reduce the progression and severity of proteinuria and other symptoms.
APRIL (a proliferation-inducing ligand) is a member of the tumor necrosis factor superfamily and is primarily secreted by bone marrow and/or myeloid cells. APRIL is overproduced in patients with multiple myeloma (MM) and binds to B cell maturation antigen (BCMA) and transmembrane activator and cyclophilin ligand interactor (TACI) to stimulate a wide variety of responses that promote MM growth and survival and suppress the immune system so that the tumor cells are protected and sustained in the bone marrow.
Aduro is currently evaluating BION-1301, its most advanced proprietary B-select monoclonal antibody, as a novel therapy for MM. Despite new treatments recently approved in MM, this disease remains incurable as patients relapse, or become resistant to, currently-available therapies. In preclinical studies, Aduro has established that APRIL plays a crucial part in the protective bone marrow tumor microenvironment. In these studies, APRIL, through BCMA, was shown to be critically involved in the survival, proliferation and chemoresistance of MM, and upregulates mechanisms of immunoresistance, including PD-L1 upregulation. BION-1301, a humanized antibody that blocks APRIL from binding to its receptors, has been shown in preclinical studies to halt tumor growth and overcome drug resistance. In addition, BION-1301 also demonstrated the ability to inhibit immune suppressive effects of regulatory T cells via TACI but not BCMA in MM blood and bone marrow. BION-1301 is currently being evaluated in a Phase 1/2 clinical study in patients with relapsed or refractory MM.
Cautionary Note on Forward-Looking Statements
This press release contains forward-looking statements for purposes of the safe harbor provisions of the Private Securities Litigation Reform Act of 1995. Forward-looking statements include statements regarding our intentions or current expectations concerning, among other things, the potential for BION-1301 for the treatment of IgAN or MM, the timing of clinical data, and our ability to advance our drug development programs on our own or with our collaborators. In some cases you can identify these statements by forward-looking words such as “may,” “will,” “continue,” “anticipate,” “intend,” “could,” “project,” “expect” or the negative or plural of these words or similar expressions. Forward-looking statements are not guarantees of future performance and are subject to risks and uncertainties that could cause actual results and events to differ materially from those anticipated, including, but not limited to, our history of net operating losses and uncertainty regarding our ability to achieve profitability, our ability to develop and commercialize our product candidates, our ability to use and expand our technology platforms to build a pipeline of product candidates, our ability to obtain and maintain regulatory approval of our product candidates, our ability to operate in a competitive industry and compete successfully against competitors that have greater resources than we do, our reliance on third parties, and our ability to obtain and adequately protect intellectual property rights for our product candidates. We discuss many of these risks in greater detail under the heading “Risk Factors” contained in our quarterly report on Form 10-Q for the quarter ended
|Noopur Liffick||Aljanae Reynolds|
|Investor Relations & Corporate Affairs||510-809-2452|