| [November 03, 2017] |
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Alnylam Reports Positive Preliminary Results from Ongoing Phase 1/2 Study of Lumasiran (ALN-GO1) in Patients with Primary Hyperoxaluria Type 1 (PH1)
Alnylam
Pharmaceuticals, Inc. (Nasdaq: ALNY), the leading RNAi therapeutics
company, announced today positive preliminary data from its ongoing
Phase 1/2 study with lumasiran (formerly known as ALN-GO1), an
investigational RNAi therapeutic targeting glycolate oxidase (GO) for
the treatment of Primary Hyperoxaluria Type 1 (PH1). Results were
presented today at the American Society of Nephrology (ASN) Kidney Week
2017 Annual Meeting, being held October 31 to November 5, 2017 in New
Orleans, Louisiana.
At ASN, Alnylam presented initial data from Part B of the Phase 1/2
study in the first two cohorts of patients with PH1 (6-19 years old)
dosed with lumasiran or placebo (N=8). Part B is a randomized (3:1
drug:placebo), single-blind, placebo-controlled study in patients with
PH1. Patients with relatively preserved renal function were enrolled to
allow for measurement of urinary oxalate excretion as a marker for
hepatic oxalate production. The reported data were as of the data
cut-off date of October 3, 2017.
As compared to the one patient receiving placebo, preliminary results
showed that the three patients in the first cohort - who received
monthly subcutaneous doses of lumasiran at 1 mg/kg for three months -
experienced greater than 50 percent decreases in urinary oxalate
excretion relative to baseline. The placebo patient in the first cohort
was subsequently given lumasiran at 1 mg/kg monthly for three months,
and this patient experienced a similar reduction in urinary oxalate. The
mean maximal reduction in urinary oxalate for all four patients in this
initial low dose cohort was 66 percent, and all patients achieved
urinary oxalate levels at or near the normal range. Moreover, lumasiran
lowered urinary oxalate excretion below 1.1 mmol/24hrs/1.73m2
- a threshold associated with reduced progression to end-stage renal
disease in clinical studies* - in all patients with baseline
excretion = 1.6 mmol/24hrs/1.73m2 (N=3). Patients in the
second cohort are receiving monthly doses of lumasiran at 3 mg/kg or
placebo for three months; this cohort is ongoing and remains blinded.
Aggregate data (N=4) from Cohort 2 show a mean reduction of 47 percent
in urinary oxalate output relative to baseline after the first of three
doses. These initial results support the hypothesis that GO inhibition
has the potential to reduce and possibly normalize levels of hepatic
oxalate production, thus potentially halting PH1 disease progression.
"PH1 is a devastating disease, usually manifesting in early childhood,
in which excessive hepatic oxalate production leads to renal failure and
often death. In our initial study results with lumasiran in patients
with PH1, we observed substantial reductions in urinary oxalate, a
biomarker which is directly linked to disease pathology and has been
correlated with both morbidity and disease progression. Accordingly, we
believe these encouraging preliminary results validate our approach of
targeting GO, a key liver enzyme in the pathway leading to excessive
oxalate output in patients with PH1. Further, these results offer hope
that investigational lumasiran may be a potential treatment option for
patients afflicted by this life-threatening disease," said Pushkal Garg,
M.D., Chief Medical Officer at Alnylam. "We now aim to discuss these
data with regulators and advance lumasiran toward Phase 3 clinical
studies, where we also plan to study patients with more severe
manifestations of PH1, such as systemic oxalosis and renal failure.
Indeed, we are working hard to expediently conduct the clinical studies
necessary to gain a more thorough understanding of the full efficacy and
safety profile of lumasiran in patients with PH1."
"Investigational lumasiran has the potential to be a paradigm-shifting
approach in the treatment of patients with PH1, a severely debilitating
and ultra-rare orphan disease that typically presents in early
childhood," said Prof. Georges Deschênes, M.D., Ph.D., Hôpital
Robert-Debré, an investigator in the ongoing lumasiran study. "The
current standard of care for afflicted patients with advanced disease
includes intensive dialysis and, ultimately, a combined liver/kidney
transplant, as there are currently no approved medical interventions.
Although only a small number of patients have been treated to date, the
preliminary results from Part B of the study are very promising, showing
evidence of oxalate reduction, and even normalization, with as few as
three doses of lumasiran. With these promising initial data in patients
who still have relatively healthy kidneys, the PH1 community is now
interested in understanding the safety and efficacy of lumasiran in
patients with more advanced disease, something that Alnylam plans to
test."
Patients in the first cohort have been monitored for up to seven months
after receiving their first dose of lumasiran with no drug-related
serious adverse events (SAEs) or discontinuations from study. In all
patients, lumasiran was generally well tolerated and the only
drug-related adverse event (AE) reported was a mild and transient
injection site reaction. Five SAEs were reported in three patients,
including two episodes of renal stones and a case of pyelonephritis in a
patient during placebo dosing. The two remaining SAEs were a report of
renal stones and a case of dehydration associated with gastroenteritis,
both of which occurred after dosing with lumasiran but werenot
considered drug-related.
*Zhao F. et al, Clin J Am Soc Nephrol. 2016; 11(1):119-26.
About Lumasiran Phase 1/2 Study
The Phase 1/2 trial of
lumasiran is a randomized, single-blind, placebo-controlled study being
conducted in two parts. Part A, now complete, was a single-dose study
that enrolled 32 healthy adult volunteers in four single ascending dose
cohorts (N=8 per cohort, randomized 3:1 drug:placebo), with subjects
receiving lumasiran at dose ranges of 0.3 to 6 mg/kg. Data previously
reported on Part A of the study showed that a single dose of lumasiran
was generally well tolerated in healthy adult volunteers with
dose-dependent elevations in plasma and urine glycolate, demonstrating
preliminary human proof of concept. Part B is a multi-dose study
designed to enroll up to 24 patients with PH1 (N=4 per cohort; 3:1
randomization of drug:placebo, with delayed lumasiran dosing for
placebo). The primary objective of the study is to evaluate safety and
tolerability of single and multiple subcutaneous doses of lumasiran.
Secondary objectives include evaluation of pharmacokinetics and clinical
activity of lumasiran as measured by its effects on plasma glycolate in
normal healthy volunteers and urinary oxalate levels in patients with
PH1.
About Lumasiran
Formerly known as ALN-GO1, lumasiran
(pronounced "lu-MAH-si-ran") is an investigational RNAi therapeutic
targeting glycolate oxidase (GO) in development for the treatment of
Primary Hyperoxaluria Type 1 (PH1). Lumasiran is designed to reduce the
hepatic levels of the GO enzyme, thereby depleting the substrate
necessary for oxalate production, which directly contributes to the
pathophysiology of PH1. Lumasiran utilizes Alnylam's Enhanced
Stabilization Chemistry (ESC (News - Alert))-GalNAc-conjugate technology, which enables
subcutaneous dosing with increased potency and durability and a wide
therapeutic index. Lumasiran has received both U.S. and EU Orphan Drug
Designations.
The safety and efficacy of lumasiran have not been evaluated by the U.S.
Food and Drug Administration or any other health authority.
About Primary Hyperoxaluria Type 1 (PH1)
PH1 is an inborn
error of metabolism. Specifically, PH1 is an autosomal recessive
disorder of glyoxylate metabolism, where hepatic detoxification of
glyoxylate is impaired due to mutation of the AGXT gene, which encodes
the liver peroxisomal alanine-glyoxylate aminotransferase (AGT) enzyme,
resulting in excessive oxalate production. Excess oxalate in PH1
patients results in the deposition of calcium oxalate crystals in the
kidneys and urinary tract and can lead to the formation of recurrent
kidney stones or nephrocalcinosis. Renal damage is caused by a
combination of tubular toxicity from oxalate, calcium oxalate deposition
in the kidneys, and urinary obstruction by calcium oxalate stones.
Compromised kidney function exacerbates the disease as the excess
oxalate can no longer be effectively excreted, resulting in subsequent
accumulation and crystallization in bones, eyes, skin, and heart,
leading to severe illness and death. About 50 percent of patients will
have kidney failure by age 15, and about 80 percent will have end stage
renal disease by age 30. Current treatment options for advanced disease
are very limited, and include frequent renal dialysis or combined organ
transplantation of liver and kidneys, a procedure with high morbidity
that is limited due to organ availability. Although a small minority of
patients respond to Vitamin B6 supplementation, there are no approved
pharmaceutical therapies for PH1.
Alnylam - Sanofi Genzyme Alliance
In January 2014, Alnylam
and Sanofi Genzyme, the specialty care global business unit of Sanofi,
formed an alliance to accelerate the advancement of RNAi therapeutics as
a potential new class of innovative medicines for patients around the
world with rare genetic diseases. The alliance enables Sanofi Genzyme to
expand its rare disease pipeline with Alnylam's novel RNAi technology
and provides access to Alnylam's R&D engine, while Alnylam benefits from
Sanofi Genzyme's proven global capabilities to advance late-stage
development and, upon commercialization, accelerate market access for
these promising genetic medicine products. Sanofi Genzyme has the right
to opt in to develop and commercialize lumasiran in territories outside
of the United States, Canada and Western Europe and could elect to
exercise its one right to a global license for lumasiran.
About RNAi
RNAi (RNA interference) is a natural cellular
process of gene silencing that represents one of the most promising and
rapidly advancing frontiers in biology and drug development today. Its
discovery has been heralded as "a major scientific breakthrough that
happens once every decade or so," and was recognized with the award of
the 2006 Nobel (News - Alert) Prize for Physiology or Medicine. By harnessing the
natural biological process of RNAi occurring in our cells, a major new
class of medicines, known as RNAi therapeutics, is on the horizon. Small
interfering RNA (siRNA), the molecules that mediate RNAi and comprise
Alnylam's RNAi therapeutic platform, function upstream of today's
medicines by potently silencing messenger RNA (mRNA) - the genetic
precursors - that encode for disease-causing proteins, thus preventing
them from being made. This is a revolutionary approach with the
potential to transform the care of patients with genetic and other
diseases.
About Alnylam Pharmaceuticals
Alnylam (Nasdaq: ALNY) is
leading the translation of RNA interference (RNAi) into a whole new
class of innovative medicines with the potential to transform the lives
of people afflicted with rare genetic, cardio-metabolic, and hepatic
infectious diseases. Based on Nobel Prize-winning science, RNAi
therapeutics represent a powerful, clinically validated approach for the
treatment of a wide range of severe and debilitating diseases. Founded
in 2002, Alnylam is delivering on a bold vision to turn scientific
possibility into reality, with a robust discovery platform and deep
pipeline of investigational medicines, including four product candidates
that are in late-stage development. Looking forward, Alnylam will
continue to execute on its "Alnylam 2020" strategy of building a
multi-product, commercial-stage biopharmaceutical company with a
sustainable pipeline of RNAi-based medicines to address the needs of
patients who have limited or inadequate treatment options. Alnylam
employs over 600 people in the U.S. and Europe and is headquartered in
Cambridge, MA. For more information about our people, science and
pipeline, please visit www.alnylam.com
and engage with us on Twitter (News - Alert) at @Alnylam
or on LinkedIn.
Forward-Looking Statements
Various statements in this
release concerning Alnylam's future expectations, plans and prospects,
including without limitation, Alnylam's views with respect to the
potential for investigational RNAi therapeutics, including lumasiran,
its expectations regarding the future development of lumasiran and its
planned interactions with regulatory authorities to discuss the Phase
1/2 data and advance lumasiran into Phase 3 development, and
expectations regarding its "Alnylam 2020" guidance for the advancement
and commercialization of RNAi therapeutics, constitute forward-looking
statements for the purposes of the safe harbor provisions under The
Private Securities Litigation Reform Act of 1995. Actual results and
future plans may differ materially from those indicated by these
forward-looking statements as a result of various important risks,
uncertainties and other factors, including, without limitation,
Alnylam's ability to discover and develop novel drug candidates and
delivery approaches, successfully demonstrate the efficacy and safety of
its product candidates, the pre-clinical and clinical results for its
product candidates, which may not be replicated or continue to occur in
other subjects or in additional studies or otherwise support further
development of product candidates for a specified indication or at all,
actions or advice of regulatory agencies, which may affect the design,
initiation, timing, continuation and/or progress of clinical trials or
result in the need for additional pre-clinical and/or clinical testing,
delays, interruptions or failures in the manufacture and supply of our
product candidates, obtaining, maintaining and protecting intellectual
property, Alnylam's ability to enforce its intellectual property rights
against third parties and defend its patent portfolio against challenges
from third parties, obtaining and maintaining regulatory approval,
pricing and reimbursement for products, progress in establishing a
commercial and ex-United States infrastructure, competition from others
using technology similar to Alnylam's and others developing products for
similar uses, Alnylam's ability to manage its growth and operating
expenses, obtain additional funding to support its business activities,
and establish and maintain strategic business alliances and new business
initiatives, Alnylam's dependence on third parties for development,
manufacture and distribution of products, the outcome of litigation, the
risk of government investigations, and unexpected expenditures, as well
as those risks more fully discussed in the "Risk Factors" filed with
Alnylam's most recent Quarterly Report on Form 10-Q filed with
the Securities and Exchange Commission (SEC (News - Alert)) and in other filings that
Alnylam makes with the SEC. In addition, any forward-looking statements
represent Alnylam's views only as of today and should not be relied upon
as representing its views as of any subsequent date. Alnylam explicitly
disclaims any obligation, except to the extent required by law, to
update any forward-looking statements.
The scientific information discussed in this news release relating to
Alnylam's investigational therapeutic, lumasiran, is preliminary and
investigative. Lumasiran has not been approved by the U.S. Food and Drug
Administration, European Medicines Agency, or any other regulatory
authority and no conclusions can or should be drawn regarding the safety
or effectiveness of lumasiran.
View source version on businesswire.com: http://www.businesswire.com/news/home/20171103005482/en/
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