Vera Therapeutics Reports Positive Interim Phase 2 Data Showing MAU868 Has Significant BK Antiviral Activity in Kidney Transplant Patients
04 Giugno 2022 - 8:30PM
Vera Therapeutics, Inc. (Nasdaq: VERA), a late-stage biotechnology
company focused on developing and commercializing transformative
treatments for patients with serious immunological disease, today
announced that interim data from the Phase 2 trial of MAU868 versus
placebo to treat BK Virus (BKV) in kidney transplant patients
showed that MAU868 was well tolerated and demonstrated significant
BK antiviral activity in kidney transplant recipients with BK
viremia. These data were delivered today as a late-breaking oral
presentation by Daniel C. Brennan, M.D., medical director,
Comprehensive Transplant Center, professor of medicine, The Johns
Hopkins University School of Medicine, and study investigator, at
the American Transplant Congress (ATC) 2022 in Boston,
Massachusetts.
“BKV infections represent significant morbidity and mortality
factors in kidney transplant recipients. Patients are
typically given drugs to suppress their immune systems, which
increases their risk of BKV nephropathy, which is strongly
correlated with allograft loss and organ rejection. The current
immunosuppressive protocols that we have in kidney transplantation
can lead to reactivation of BKV. There is a need for a BKV
treatment option that could address escalating BKV infections early
without risking allograft rejection,” said Stanley C. Jordan, M.D.,
FASN, FAST, director of nephrology & transplant immunology,
Cedars-Sinai Medical Center, professor of pediatrics and medicine
at the David Geffen School of Medicine at University of California,
Los Angeles, and study lead investigator. “These interim results
from the Phase 2 clinical trial showed that MAU868 was well
tolerated and demonstrated significant BK antiviral activity in
kidney transplant recipients with BK viremia. These data support
the further development of MAU868 as a therapy for BK viremia.”
“MAU868 is a first-in-class targeted therapy specifically
designed to neutralize BKV. Data presented at ATC showed that
MAU868 has a clinically meaningful virologic effect in kidney
transplant patients with BK viremia,” said Celia Lin, M.D., chief
medical officer at Vera Therapeutics. “These results demonstrate
the transformative potential of MAU868, which may prevent
devastating downstream consequences caused by BKV. We are working
diligently on advancing our clinical program for MAU868 so that we
can bring this important potential treatment option to kidney
transplant patients who currently have no effective treatment
options.”
Details of the oral late-breaking
presentation are as follows: |
|
|
|
Title: |
|
A Randomized Study of MAU868 vs. Placebo to Treat BK Viremia in
Kidney Transplant Recipients |
Presenter: |
|
Daniel C. Brennan, M.D. |
Abstract Number: |
|
7056 |
Presentation Number: |
|
9004 |
This Phase 2, randomized, double-blind, placebo-controlled
clinical trial is evaluating the safety and efficacy of MAU868 in
patients who received a kidney transplant within one year of
enrollment and, within 10 days of enrollment, had BK viremia.
Patients received MAU868 or placebo intravenously (IV) every 28
days for 12 weeks, with 24 weeks follow-up. In this
clinical trial, 20 patients received MAU868 and eight patients
received placebo; all patients completed 12 weeks of treatment.
This interim analysis reported results at 12 weeks for two cohorts:
MAU868 1350 mg IV x4 doses, and MAU868 6750 mg IV followed by
MAU868 1350 mg IV x3 doses. The primary endpoint was safety and
tolerability; antiviral activity was assessed in secondary and
post-hoc analyses.
Results showed that the antiviral effect was higher in the
MAU868 group than the placebo group (see Table). Further, MAU868
was well tolerated, with a comparable frequency of adverse events
and serious adverse events between groups.
Table: Antiviral Effect of MAU868 vs. Placebo at Week
12
|
MAU868(N=20) |
Placebo(N=8) |
P-value |
Proportion of patients with a prespecified reduction of BK plasma
viral load - n (%) |
|
|
|
- by ≥1 log |
11 (55%) |
1 (13%) |
0.040 |
- to <lower limit of quantification (LLOQ) |
4 (20%) |
0 |
0.172 |
- of <104 DNA copies/mL |
15 (75%) |
3 (38%) |
0.061 |
Log reduction in BK viremia - median (interquartile range [IQR])
DNA copies/mL |
-1.14 (-1.88, -0.50) |
0.37 (-0.72, 0.04) |
0.051 |
Change in estimated glomerular filtration rate (eGFR) - median
(IQR) mL/min/1.73 m2 |
2.0 (-5.0, 4.0) |
-6.0 (-8.5, -0.5) |
0.217 |
About BK Virus (BKV)BK Virus (BKV) is a polyoma
virus that can be reactivated in settings of immunosuppression,
such as in kidney transplant. It is a leading cause of kidney
transplant loss and transplant-associated morbidity; there are
currently no approved treatments for BKV.
About MAU868MAU868 has the potential to
neutralize infection by blocking BKV virions from binding to host
cells. MAU868 is currently undergoing a randomized, double-blind,
placebo-controlled Phase 2 clinical trial to assess the safety,
pharmacokinetics, and efficacy for the treatment of BKV in kidney
transplant patients. Vera holds an exclusive worldwide license for
the development and commercialization of MAU868 in all indications
acquired from Amplyx Pharmaceuticals, Inc., a wholly owned
subsidiary of Pfizer Inc.
About Vera Vera Therapeutics is a late-stage
biotechnology company focused on developing treatments for serious
immunological diseases. Vera’s mission is to advance treatments
that target the source of immunologic diseases in order to change
the standard of care for patients. Vera’s lead product candidate is
atacicept, a fusion protein self-administered as a subcutaneous
injection once weekly that blocks both B lymphocyte stimulator
(BLyS) and a proliferation inducing ligand (APRIL), which stimulate
B cells and plasma cells to produce autoantibodies contributing to
certain autoimmune diseases, including IgA nephropathy (IgAN), also
known as Berger’s disease, and lupus nephritis. In addition, Vera
is evaluating additional diseases where the reduction of
autoantibodies by atacicept may prove medically useful. Vera is
also developing MAU868, a monoclonal antibody designed to
neutralize infection with BK Virus, a polyomavirus that can have
devastating consequences in certain settings such as kidney
transplant. For more information, please visit www.veratx.com.
Forward-looking Statements Statements contained
in this press release regarding matters, events or results that may
occur in the future are “forward-looking statements” within the
meaning of the Private Securities Litigation Reform Act of 1995.
Such forward-looking statements include statements regarding, among
other things, the potential for MAU868 to be a first-in-class
targeted therapy specifically designed to neutralize BKV and Vera’s
strategy and regulatory matters. Because such statements are
subject to risks and uncertainties, actual results may differ
materially from those expressed or implied by such forward-looking
statements. Words such as “plans,” “will,” “may,” “expects,”
“potential,” and similar expressions are intended to identify
forward-looking statements. These forward-looking statements are
based upon Vera’s current expectations and involve assumptions that
may never materialize or may prove to be incorrect. Actual results
could differ materially from those anticipated in such
forward-looking statements as a result of various risks and
uncertainties, which include, without limitation, risks related to
the regulatory approval process, results of earlier clinical trials
may not be obtained in later clinical trials, risks and
uncertainties associated with Vera’s business in general, the
impact of the COVID-19 pandemic, and the other risks described in
Vera’s filings with the Securities and Exchange Commission. All
forward-looking statements contained in this press release speak
only as of the date on which they were made and are based on
management’s assumptions and estimates as of such date. Vera
undertakes no obligation to update such statements to reflect
events that occur or circumstances that exist after the date on
which they were made, except as required by law.
For more information, please contact:
Investor Contact:IR@veratx.com
Media Contact:Kathy VincentGreig
Communications, Inc.kathy@greigcommunications.com
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