New Data from Phase 3 REGAIN Study of Eculizumab (Soliris®) in Patients with
Refractory Generalized Myasthenia Gravis (gMG) Presented at ICNMD Annual Congress
Alexion Pharmaceuticals, Inc. (NASDAQ:ALXN) announced today that researchers presented new results from the REGAIN study, a
global, placebo-controlled Phase 3 registration trial of eculizumab (Soliris®) in patients with refractory generalized
myasthenia gravis (gMG), at the Hot Topics session of the 14th International Congress on Neuromuscular Diseases (ICNMD) in Toronto.
As previously reported, the study’s primary efficacy endpoint of change from baseline in Myasthenia Gravis-Activities of Daily
Living Profile (MG-ADL) total score, a patient-reported assessment, at week 26, did not reach statistical significance (p=0.0698)
as measured by a worst-rank analysis. Results presented at ICNMD showed that 18 of 22 pre-defined endpoints and pre-specified
analyses in the study, based on the primary and five secondary endpoints, achieved p-values <0.05.
New secondary efficacy endpoint data presented included change from baseline in Myasthenia Gravis Composite (MGC) score at week
26, which achieved a p-value of 0.1026, and change from baseline in the 15-item Myasthenia Gravis Quality Of
Life (MG-QOL15) at week 26, which achieved a p-value of 0.0281, both measured by a worst-rank analysis. A pre-specified
sensitivity analysis of the MGC and MG-QOL15 endpoints using repeated measures from baseline to week 26 achieved p-values of 0.0134
and 0.0010, respectively.1 The full presentation can be found on the Investor page of the Alexion website.
“Although the REGAIN study narrowly missed its primary endpoint, the additional data presented today suggest a magnitude of
effect of eculizumab in refractory MG patients across four separate scales of disease severity that is unprecedented in my clinical
investigation experience,” said James F. Howard Jr., M.D., Distinguished Professor of Neuromuscular Disease, Professor of
Neurology, Medicine & Allied Health, and Chief, Neuromuscular Disorders Section, The University of North Carolina School of
Medicine. “These findings are particularly meaningful given the urgent need for a first-ever therapy with the potential to have a
transformative impact on patients with refractory MG, who continue to face disabling limitations in their daily lives, including
difficulty walking, talking, swallowing, and breathing normally.”
|
P-values Less Than 0.05 Achieved in 18 of 22
Pre-specified Analyses |
Outcome
Measure
|
|
|
Primary / Secondary Endpoints |
|
|
Sensitivity Analyses |
|
|
Worst-Rank
ANCOVA
|
|
|
Responder
Analysis
|
|
|
Repeated
Measures
at Week 26
(IST as a Covariate)
|
|
|
Change from
Baseline at Week
26 or
LOCF ANCOVA
|
|
|
Worst-Rank ANCOVA
Sensitivity
|
MG-ADL |
|
|
0.0698 |
|
|
0.0229 |
|
|
0.0058 (0.0077) |
|
|
0.0390 |
|
|
0.0800 |
QMG |
|
|
0.0129 |
|
|
0.0018 |
|
|
0.0006 (0.0007) |
|
|
0.0032 |
|
|
0.0169 |
MGC |
|
|
0.1026 |
|
|
N/A*
|
|
|
0.0134 (0.0168) |
|
|
0.0406 |
|
|
0.1084 |
MG-QOL15 |
|
|
0.0281 |
|
|
N/A*
|
|
|
0.0010 (0.0009) |
|
|
0.0152 |
|
|
0.0328 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
*N/A: Not applicable; not a pre-specified analysis
“The MG Community has been waiting for the full results from the REGAIN trial with great interest,” said Nancy Law, CEO of the
Myasthenia Gravis Foundation of America (MGFA). “There are currently no FDA-approved disease modifying therapies for MG, which
means that doctors and patients must often resort to trial and error with medications approved for other conditions to try to
manage symptoms. For all too many with MG, the currently available treatment approaches are inadequate in efficacy, or have
intolerable side effects. People with MG need more and better treatment options, especially for those with refractory generalized
MG, whose extreme muscle weakness can be devastating and even life-threatening. We look forward to advocating for and supporting
patients with refractory MG who have a tremendous unmet need.”
Detailed Study Results1
At ICNMD, Dr. Howard reported that 18 of the study’s 22 pre-specified analyses achieved p-values <0.05. As previously
reported, these included the first three secondary efficacy endpoints of change from baseline to week 26 in Quantitative Myasthenia
Gravis (QMG) total score, a physician-administered assessment of MG clinical severity (p=0.0129), as measured by a worst-rank
analysis; the proportion of patients with at least a 3-point reduction in MG-ADL total score and no rescue therapy from baseline to
week 26 (p=0.0229); and the proportion of patients with at least a 5-point reduction in QMG total score and no rescue therapy from
baseline to week 26 (p=0.0018). The primary efficacy endpoint of change from baseline in MG-ADL total score at week 26 did not
reach statistical significance (p=0.0698) as measured by a worst-rank analysis.
Several prospectively defined sensitivity analyses were conducted to validate results for the primary and secondary endpoints,
including sensitivity analyses for change from baseline in MG-ADL, QMG, MGC, and MG-QOL15 using repeated measures, all of which
achieved p-values <0.05. As previously reported, the pre-specified sensitivity analyses of the primary and first secondary
endpoints of MG-ADL and QMG using repeated measures had p-values of 0.0058 and 0.0006, respectively. The pre-specified sensitivity
analyses of MGC and MG-QOL15 using repeated measures at week 26 showed a mean change from baseline in MGC with eculizumab treatment
at week 26 of -8.1 versus a mean change with placebo of -4.8 (p=0.0134), and a mean change from baseline in MG-QOL15 with
eculizumab treatment at week 26 of -12.6 versus a mean change with placebo of -5.4 (p=0.0010).
Additional results from the study, including detailed outcomes from the MG-ADL and QMG responder analyses, were presented at
ICNMD.
“While the REGAIN study narrowly missed statistical significance on the primary endpoint, the totality of data from this
landmark trial supports the potential of eculizumab to provide an early, sustained, and substantial response in patients with
refractory gMG. Notably, 18 out of 22 pre-specified endpoints and analyses achieved p-values less than 0.05 for patients treated
with eculizumab compared to placebo, underscoring the pivotal role of complement inhibition in addressing the underlying cause of
disease,” said Martin Mackay, Ph.D., Executive Vice President and Global Head of R&D at Alexion. “Today, there are no
effective treatments for the ultra-rare segment of patients with gMG who are refractory to conventional therapies and continue to
suffer from profound, complement-mediated muscle weakness. Alexion is committed to addressing the urgent needs of this patient
population, and we look forward to discussing study results with U.S. and EU regulators.”
The safety of eculizumab in this study was consistent with the Soliris labels. The most common adverse events in patients
receiving eculizumab and placebo, respectively, were: headache (16.1%, 19.0%), upper respiratory tract infection (16.1%, 19.0%),
nasopharyngitis (14.5%, 15.9%), nausea (12.9%, 14.3%), and myasthenia gravis (9.7%, 17.5%). Serious adverse events were reported in
14.5% of eculizumab patients and 28.6% of placebo patients. Four patients receiving eculizumab (6.5%) discontinued treatment due to
an adverse event. There were no discontinuations due to adverse events in the placebo arm. Half as many patients treated with
eculizumab received rescue therapy compared with placebo (9.7%, 19.0%).
Ninety-four percent of patients (117 of 125) from the REGAIN study continued into a Phase 3 open-label extension study
evaluating the safety and efficacy of eculizumab in the treatment of patients with refractory gMG. Eculizumab has received Orphan
Drug Designation (ODD) for the treatment of patients with MG in the U.S., EU, and Japan. Eculizumab is not approved in any country
for the treatment of patients with gMG.
REGAIN Study Design
The REGAIN study is a randomized, double-blind, placebo-controlled, multicenter trial evaluating the safety and efficacy of
eculizumab in patients with refractory gMG. The study enrolled and treated 125 adult patients across North America, South America,
Europe, and Asia. Patients had a confirmed MG diagnosis with positive serologic test for anti-AChR antibodies. All patients were
required to have previously failed treatment with at least two immunosuppressive agents or failed treatment with at least one
immunosuppressive agent and required chronic plasma exchange or IVIg, and had an MG-ADL total score ≥6 at study entry.
Patients were randomized 1:1 to receive eculizumab or placebo for a total of 26 weeks. Patients initially received 900 mg of
eculizumab or placebo weekly for 4 weeks followed by 1200 mg of eculizumab or placebo one week later, and then 1200 mg of
eculizumab or placebo every two weeks. Patients were able to continue to receive stable dose and type of supportive
immunosuppressive therapy (IST), but no new ISTs and no increase in IST dosage were permitted during the trial, unless patient
required rescue therapy for disease worsening.
The primary efficacy endpoint of change from baseline in MG-ADL total score at week 26, as well as the three secondary endpoints
that involved changes from baseline—QMG, MGC, and MG-QOL15—were assessed using a worst-rank analysis.
About Refractory Generalized Myasthenia Gravis
Refractory generalized myasthenia gravis (gMG) is an ultra-rare segment of MG—a debilitating, complement-mediated neuromuscular
disease—in which patients experience severe morbidities despite currently available MG therapies.2,3,4
MG typically begins with weakness in the ocular muscles and often progresses to the more severe and generalized form, known as
gMG, to include weakness of the head, neck, trunk, limb and respiratory muscles.5 While most gMG patients are managed
with conventional therapies, 10% to 15% of patients are considered refractory—meaning they have largely exhausted conventional
therapy and continue to suffer profound muscle weakness throughout the body, resulting in slurred speech, impaired swallowing and
choking, double vision, upper and lower extremity weakness, disabling fatigue, shortness of breath due to respiratory muscle
weakness, and episodes of respiratory failure.6,7,8 Patients with refractory gMG frequently require hospitalization,
often involving intensive care unit stays.9
Today, there are no therapies that are effective in this ultra-rare population of patients suffering from refractory gMG.
About Soliris® (eculizumab)
Soliris is a first-in-class terminal complement inhibitor developed from the laboratory through regulatory approval and
commercialization by Alexion. Soliris is approved in the U.S. (2007), European Union (2007), Japan (2010) and other countries as
the first and only treatment for patients with paroxysmal nocturnal hemoglobinuria (PNH) to reduce hemolysis. PNH is a
debilitating, ultra-rare and life-threatening blood disorder, characterized by complement-mediated hemolysis (destruction of red
blood cells). Soliris is also approved in the U.S. (2011), European Union (2011), Japan (2013) and other countries as the first and
only treatment for patients with atypical hemolytic uremic syndrome (aHUS) to inhibit complement-mediated thrombotic
microangiopathy, or TMA (blood clots in small vessels). aHUS is a debilitating, ultra-rare and life-threatening genetic disorder
characterized by complement-mediated TMA. Soliris is not indicated for the treatment of patients with Shiga-toxin E.
coli-related hemolytic uremic syndrome (STEC-HUS). For the breakthrough medical innovation in complement inhibition, Alexion
and Soliris have received some of the pharmaceutical industry's highest honors: the Prix Galien USA (2008, Best Biotechnology
Product) and France (2009, Rare Disease Treatment).
More information on Soliris, including the full U.S. prescribing information, is available at www.soliris.net.
Important Safety Information
The U.S. product label for Soliris includes a boxed warning: “Life-threatening and fatal meningococcal infections have occurred
in patients treated with Soliris. Meningococcal infection may become rapidly life-threatening or fatal if not recognized and
treated early [see Warnings and Precautions (5.1)]. Comply with the most current Advisory Committee on Immunization Practices
(ACIP) recommendations for meningococcal vaccination in patients with complement deficiencies. Immunize patients with a
meningococcal vaccine at least two weeks prior to administering the first dose of Soliris, unless the risks of delaying Soliris
therapy outweigh the risk of developing a meningococcal infection. [See Warnings and Precautions (5.1) for additional guidance on
the management of the risk of meningococcal infection]. Monitor patients for early signs of meningococcal infections and evaluate
immediately if infection is suspected. Soliris is available only through a restricted program under a Risk Evaluation and
Mitigation Strategy (REMS). Under the Soliris REMS, prescribers must enroll in the program [see Warnings and Precautions (5.2)].
Enrollment in the Soliris REMS program and additional information are available by telephone: 1-888-SOLIRIS (1-888-765-4747).”
In patients with PNH, the most frequently reported adverse events observed with Soliris treatment in clinical studies were
headache, nasopharyngitis (runny nose), back pain and nausea. Soliris treatment of patients with PNH should not alter anticoagulant
management because the effect of withdrawal of anticoagulant therapy during Soliris treatment has not been established. In patients
with aHUS, the most frequently reported adverse events observed with Soliris treatment in clinical studies were headache, diarrhea,
hypertension, upper respiratory infection, abdominal pain, vomiting, nasopharyngitis, anemia, cough, peripheral edema, nausea,
urinary tract infections, and pyrexia. Soliris is not indicated for the treatment of patients with Shiga-toxin E.
coli-related hemolytic uremic syndrome (STEC-HUS). Please see full prescribing information for Soliris, including BOXED WARNING
regarding risk of serious meningococcal infection.
About Alexion
Alexion is a global biopharmaceutical company focused on developing and delivering life-transforming therapies for patients with
devastating and rare disorders. Alexion is the global leader in complement inhibition and has developed and commercializes the
first and only approved complement inhibitor to treat patients with paroxysmal nocturnal hemoglobinuria (PNH) and atypical
hemolytic uremic syndrome (aHUS), two life-threatening ultra-rare disorders. In addition, Alexion’s metabolic franchise includes
two highly innovative enzyme replacement therapies for patients with life-threatening and ultra-rare disorders, hypophosphatasia
(HPP) and lysosomal acid lipase deficiency (LAL-D). Alexion is advancing the most robust rare disease pipeline in the biotech
industry with highly innovative product candidates in multiple therapeutic areas. This press release and further information about
Alexion can be found at: www.alexion.com.
[ALXN-G]
Forward-Looking Statements
This news release contains forward-looking statements, including statements related to the potential medical benefits of
eculizumab (Soliris®) for the treatment of myasthenia gravis, and Alexion's future clinical,
regulatory and commercial plans for Soliris for the treatment of myasthenia gravis. Forward-looking statements are subject to
factors that may cause Alexion's results and plans to differ from those expected, including for example, decisions of regulatory
authorities regarding marketing approval or material limitations on the marketing of our products, delays, interruptions or
failures in the manufacture and supply of our products and our product candidates, progress in establishing and developing
commercial infrastructure, failure to satisfactorily address matters raised by the FDA and other regulatory agencies, the
possibility that results of clinical trials are not predictive of safety and efficacy results of our products in broader patient
populations in the disease studied or other diseases, the possibility that clinical trials of our product candidates could be
delayed or that additional research and testing is required by regulatory agencies, the adequacy of our pharmacovigilance and drug
safety reporting processes, the risk that third party payors (including governmental agencies) will not reimburse or continue to
reimburse for the use of our products at acceptable rates or at all, risks regarding government investigations, including the SEC
and DOJ investigations, the risk that estimates regarding the number of patients with the diseases that our products treat are
inaccurate, the risks of shifting foreign exchange rates, and a variety of other risks set forth from time to time in Alexion's
filings with the U.S. Securities and Exchange Commission, including but not limited to the risks discussed in Alexion's Quarterly
Report on Form 10-Q for the period ended March 31, 2016 and in our other filings with the U.S. Securities and Exchange Commission.
Alexion does not intend to update any of these forward-looking statements to reflect events or circumstances after the date hereof,
except when a duty arises under law.
References
1 Howard JF. REGAIN: A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Multi-Center Study to Evaluate the
Safety and Efficacy of Eculizumab in Subjects With Refractory Generalized Myasthenia Gravis (gMG). Presented at the 14th
International Congress on Neuromuscular Diseases (ICNMD), Toronto, July 7, 2016.
2Suh J, Goldstein JM, Nowak RJ. Clinical characteristics of refractory myasthenia gravis patients. Yale J Biol
Med. 2013; 86:255-60.
3Gilhus NE, Verschuuren JJ. Myasthenia gravis: subgroup classification and therapeutic strategies. Lancet
Neurol. 2015;14:1023-36.
4Drachman D, Adams R, Hu R, Jones R, Brodsky R. Rebooting the immune system with high-dose cyclophosphamide for
treatment of refractory myasthenia gravis. Ann NY Acad Sci. 2008;1132:305-314.
5Melzer N, Ruck T, Fuhr P, et al. Clinical features, pathogenesis, and treatment of myasthenia gravis: a supplement
to the Guidelines of the German Neurological Society. J Neurol. 2016 Feb 17. [Epub ahead of print]
6Sathasivam S. Diagnosis and management of myasthenia gravis. Prog Neurol Psychiatry. 2014;18(1):6-14.
7Howard JF, ed. Myasthenia Gravis: A Manual for the Health Care Provider. St. Paul, MN: Myasthenia Gravis
Foundation of America, Inc.; 2008.
8Targeting the Complement System in Refractory Myasthenia Gravis. Supplement to Neurology Reviews. February
2016.
9Safety and efficacy of eculizumab in refractory generalized myasthenia gravis (REGAIN study). Clinicaltrials.gov
identifier NCT01997229.
Alexion Pharmaceuticals, Inc.
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