Novartis receives EU approval for Revolade® as first-in-class therapy for children aged 1 year and above with chronic ITP
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Novartis International AG /
Novartis receives EU approval for Revolade® as first-in-class therapy for
children aged 1 year and above with chronic ITP
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* EU approval of Revolade expands treatment options for pediatric patients
aged 1 year and above with chronic ITP who have not responded to other
therapies
* Two formulations approved: once-daily tablet and oral suspension formulation
designed for younger children who may not be able to swallow tablets
* For about one in four children with ITP, a disorder of low blood platelet
count and potential bleeding, the condition becomes chronic[1],[2]
Basel, April 7, 2016 - Novartis announced today that the European Commission
(EC) has approved Revolade(®) (eltrombopag) for the treatment of pediatric (aged
1 year and above) chronic immune (idiopathic) thrombocytopenic purpura (ITP)
patients who are refractory to other treatments (e.g. corticosteroids,
immunoglobulins). The approval includes the use of tablets as well as a new oral
suspension formulation of Revolade, which is designed for younger children who
may not be able to swallow tablets. Revolade was approved by the EC in 2010 for
use in adults with the same condition.
"For the families and caregivers of children affected by a rare disease, having
a new treatment option can be game-changing in managing the disease," said
Alessandro Riva, MD, Global Head, Novartis Oncology Development and Medical
Affairs.
ITP is a rare blood disorder that affects about five in 100,000 children each
year and is characterized by a low platelet count[2],[3]. Because people with
ITP have a low number of platelets, they may bruise easily and experience
bleeding that is hard to stop[2]. Chronic ITP, defined as ongoing disease more
than 12 months after diagnosis[4], occurs in 13-36% of children with ITP[1]. A
small number of pediatric patients with chronic ITP may be at risk of
significant bleeding[5].
The approval is based on data from two double-blind, randomized, placebo-
controlled trials, including the largest Phase III clinical trial in this
patient population. In these studies, patients in the treatment and placebo arms
were permitted to use some stable maintenance ITP therapies, per local treatment
practices. Treatment with Revolade significantly increased and sustained
platelet counts among pediatric patients with chronic ITP who were refractory to
or had relapsed after prior chronic ITP therapies, and some patients taking
concomitant ITP medications were able to reduce or discontinue their use of
these medications, primarily corticosteroids.
The EC approval applies to all 28 EU member states, plus Iceland, Norway and
Liechtenstein.
Revolade is a once-daily oral thrombopoietin (TPO) receptor agonist that works
by inducing stimulation and differentiation of megakaryocytes (large cells,
found especially in bone marrow) from bone marrow stem cells to increase
platelet production[6]. In August 2015, the US Food and Drug Administration
(FDA) approved a new oral suspension formulation, which expanded use of
eltrombopag (marketed as Promacta(®) in the USA) to include children 1 year of
age and older with chronic ITP who have had an insufficient response to
corticosteroids, immunoglobulins or splenectomy.
About the PETIT and PETIT2 clinical trials
PETIT is a Phase II, multi-center, three-part study to investigate the efficacy,
safety and tolerability of Revolade in pediatric patients (ages 1 to 17 years)
with previously treated chronic ITP. The trial included patients living with ITP
for six months or longer who had a platelet count <30 Gi/L. Part one was an open
label, dose finding study; part two was double-blind and placebo-controlled, and
part three was an open-label extension. Patients in the study were permitted to
use some stable maintenance ITP therapies, per local treatment practices. The
primary efficacy outcome, which was percentage of participants who achieved a
platelet count >=50 Gi/L without rescue therapy at least once between weeks one
and six, was met by 62% and 32% of patients in the Revolade arm and the control
arm, respectively (p=0.011). The secondary efficacy endpoint analyses
demonstrated clinically meaningful benefit in terms of decreased need for rescue
treatment (13% of patients on Revolade compared to 50% of patients in the
control arm). Patients received Revolade for a total of six months during the
trial[6],[7].
PETIT2 is a Phase III, multi-center, two-part study to investigate the efficacy,
safety and tolerability of Revolade in pediatric patients (ages 1 to 17 years)
with previously treated chronic ITP. The trial included patients living with
chronic ITP for 12 months or longer who also had a platelet count <30 Gi/L. Part
one was randomized, double-blind and placebo-controlled and part two was an
open-label extension. Patients in the study were permitted to use some stable
maintenance ITP therapies, per local treatment practices. The primary efficacy
outcome, which was percentage of participants who achieved a platelet count >=50
Gi/L without rescue therapy for at least six out of eight weeks between weeks
five and 12 of part one of the study, was met by 40% of patients treated with
Revolade and 3% of patients in the control arm (p<0.001). This result was
consistent across the age cohorts. The secondary efficacy endpoint analyses
demonstrated clinically meaningful benefit in terms of decreased need for rescue
treatment (19% of patients on Revolade compared to 24% of patients in the
control arm) during the randomized, double-blind period. Patients were permitted
to reduce or discontinue baseline ITP therapy only during the open-label phase
of the trial. In the open label eltrombopag-only period, 15 of 87 patients were
taking concomitant ITP medications at baseline. Of these 15 patients, eight
(53%) had a sustained reduction or permanent discontinuation of at least one
baseline ITP medication (seven patients permanently discontinued and one patient
had sustained reduction for >=18 weeks). Patients received Revolade for a total
of nine months during the trial[6],[8].
In both studies, safety was consistent with the known safety profile of Revolade
in chronic ITP in adults and the population under study. No new safety signals
were detected. The most common adverse reactions in pediatric chronic ITP
patients 1 year and older (greater than or equal to 10% and greater than
placebo) were upper respiratory tract infection and nasopharyngitis[6],[7],[8].
About chronic ITP
ITP is a blood disorder characterized by blood that does not clot as it should
due to a low number of platelets. People who have ITP often have purple bruises
or tiny red or purple dots on the skin. They also may have nosebleeds, bleeding
from the gums during dental work, or other bleeding that's hard to stop. In most
cases, an autoimmune response is thought to cause ITP in which a person's immune
system attacks and destroys its own platelets[2].
The two types of ITP are acute (temporary or short-term) and chronic (long-
lasting). Acute ITP mainly occurs in children, often after a viral infection,
and generally lasts less than six months. The platelet count returns to normal
within six to 12 months and treatment may not be needed[2]. Chronic ITP, defined
as ongoing disease more than 12 months after diagnosis[4], occurs in 13-36% of
children with ITP[1]. A small number of pediatric patients with chronic ITP may
be at risk of significant bleeding[5].
The goal of treatment in chronic ITP for children is to maintain a safe platelet
count that reduces the risk of bleeding[2]. The most commonly available and used
therapies-corticosteroids and intravenous immunoglobulin (IVIG)-are associated
with side effects that are often difficult to tolerate in a pediatric
setting[5],[9],[10].
About Revolade(®) (eltrombopag)
Revolade is approved in more than 100 countries worldwide for the treatment of
thrombocytopenia in adult patients with chronic immune (idiopathic)
thrombocytopenic purpura (ITP) who have had an inadequate response or are
intolerant to other treatments. Eltrombopag (marketed as Promacta(®) in the
USA), is approved by the US Food and Drug Administration for once-daily use in
pediatric patients 1 year and older with chronic ITP who have had an
insufficient response to corticosteroids, immunoglobulins or splenectomy.
Revolade is also approved in over 45 countries worldwide for the treatment of
thrombocytopenia (low blood platelet counts) in patients with chronic hepatitis
C to allow them to initiate and maintain interferon-based therapy. In September
2015, the European Commission approved Revolade for the treatment of adults with
severe aplastic anemia (SAA) who were either refractory to prior
immunosuppressive therapy or heavily pretreated and are unsuitable for
hematopoietic stem cell transplant.
Revolade Important Safety Information
Revolade may cause serious side effects, such as liver problems, high platelet
counts and a higher chance for blood clots, bleeding after stopping treatment,
and bone marrow problems.
Revolade may damage the liver and cause serious, even life threatening, illness.
Blood tests to check the liver are needed before taking Revolade and during
treatment. When certain antiviral treatments are given together with Revolade
for the treatment of thrombocytopenia due to hepatitis C virus (HCV) infections,
some liver problems can get worse.
A doctor will order the blood tests and any other tests required. In some cases
Revolade treatment may need to be stopped. Patients should tell a doctor right
away if they have any of these signs and symptoms of liver problems: yellowing
of the skin or the whites of the eyes (jaundice), unusual darkening of the
urine, unusual tiredness, right upper stomach area pain.
Patients have a higher chance of getting a blood clot if their platelet count is
too high during treatment with Revolade, but blood clots can occur with normal
or even low platelet counts. Patients who have cirrhosis of the liver are at
risk of a blood clot in a blood vessel that feeds the liver. Patients may have
severe complications from some forms of blood clots, such as clots that travel
to the lungs or that cause heart attacks or strokes. A doctor will check the
patient's blood platelet counts, and change the dose or stop Revolade if
platelet counts get too high. Patients should tell their doctor right away if
they have signs and symptoms of a blood clot in the leg, such as swelling or
pain/tenderness of one leg.
When patients with chronic ITP stop taking Revolade, their blood platelet count
will drop back down to what it was before they started taking Revolade. These
effects are most likely to happen within 4 weeks after patients stop taking
Revolade. The lower platelet counts may increase risk of bleeding. A doctor will
check platelet counts for at least 4 weeks after patients stop taking Revolade.
Patients should tell their doctor or pharmacist if they have any bruising or
bleeding after they stop taking Revolade.
Patients being treated for the disease may have problems with their bone marrow.
Medicines like Revolade could make this problem worse. Signs of bone marrow
changes may show up as abnormal results in blood tests. A doctor may also carry
out tests to directly check the bone marrow during treatment with Revolade.
The most common side effects of Revolade when used to treat adult patients with
chronic ITP include headache, anemia, decreased appetite, insomnia, cough,
nausea, diarrhea, alopecia, pruritus, myalgia, pyrexia, fatigue, influenza-like
illness, asthenia, chills and peripheral edema.
The most common side effects of Revolade when used to treat pediatric patients
with chronic ITP include upper respiratory tract infection, nasopharyngitis,
cough, diarrhea, pyrexia, rhinitis, abdominal pain, oropharyngeal pain,
toothache, rash, increased AST and rhinorrhea.
The most common side effects of Revolade when used to treat patients with
chronic HCV and antiviral agents include headache, anemia, decreased appetite,
insomnia, cough, nausea, diarrhea, alopecia, pruritus, myalgia, pyrexia,
fatigue, influenza-like illness, asthenia, chills and peripheral edema.
The most common side effects of Revolade when used to treat patients with severe
aplastic anemia (SAA) include headache, dizziness, insomnia, cough, dyspnea,
oropharyngeal pain, rhinorrhea, nausea, diarrhea, abdominal pain, transaminases
increased, ecchymosis, arthralgia, muscle spasms, pain in extremity, fatigue,
febrile neutropenia, and pyrexia. Common side effects that may show up in blood
tests include increase in some liver enzymes and laboratory tests that may show
abnormal changes to the cells in the bone marrow.
Please see full EU Summary of Product Characteristics for Revolade
(eltrombopag).
Disclaimer
The foregoing release contains forward-looking statements that can be identified
by words such as "can," "may," "goal," "will," or similar terms, or by express
or implied discussions regarding potential new indications or labeling for
Revolade (eltrombopag), new formulations of Revolade, or regarding potential
future revenues from Revolade. You should not place undue reliance on these
statements. Such forward-looking statements are based on the current beliefs and
expectations of management regarding future events, and are subject to
significant known and unknown risks and uncertainties. Should one or more of
these risks or uncertainties materialize, or should underlying assumptions prove
incorrect, actual results may vary materially from those set forth in the
forward-looking statements. There can be no guarantee that Revolade will be
submitted or approved for any additional indications, labeling or formulations
in any market, or at any particular time. Nor can there be any guarantee that
Revolade will be commercially successful in the future. In particular,
management's expectations regarding Revolade could be affected by, among other
things, the uncertainties inherent in research and development, including
unexpected clinical trial results and additional analysis of existing clinical
data; unexpected regulatory actions or delays or government regulation
generally; the company's ability to obtain or maintain proprietary intellectual
property protection; general economic and industry conditions; global trends
toward health care cost containment, including ongoing pricing pressures;
unexpected safety issues; unexpected quality or manufacturing issues, and other
risks and factors referred to in Novartis AG's current Form 20-F on file with
the US Securities and Exchange Commission. Novartis is providing the information
in this press release as of this date and does not undertake any obligation to
update any forward-looking statements contained in this press release as a
result of new information, future events or otherwise.
About Novartis
Novartis provides innovative healthcare solutions that address the evolving
needs of patients and societies. Headquartered in Basel, Switzerland, Novartis
offers a diversified portfolio to best meet these needs: innovative medicines,
eye care and cost-saving generic pharmaceuticals. Novartis is the only global
company with leading positions in these areas. In 2015, the Group achieved net
sales of USD 49.4 billion, while R&D throughout the Group amounted to
approximately USD 8.9 billion (USD 8.7 billion excluding impairment and
amortization charges). Novartis Group companies employ approximately 119,000
full-time-equivalent associates. Novartis products are available in more than
180 countries around the world. For more information, please visit
http://www.novartis.com.
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References
[1] George JN, Woolf SH, Raskob GE. Idiopathic thrombocytopenic purpura: a
practice guideline developed by explicit methods for the American Society of
Hematology. Blood. 1996;88(1):3-40.
[2] Immune Thrombocytopenia. US National Institutes of Health website.
http://www.nhlbi.nih.gov/book/export/html/4917. Accessed February 1, 2016.
[3] Fogarty PF, Segal JB. The epidemiology of immune thrombocytopenic purpura.
Curr Opin Hematol. 2007;14(5):515-519.
[4] Rodeghiero F, Stasi R, Gernsheimer T, et al. Standardization of terminology,
definitions and outcome criteria in immune thrombocytopenic purpura of adults
and children: report from an international working group. Blood.
2009;113(11):2386-2393.
[5] Neunert C, Lim W, Crowther M, et al. The American Society of Hematology
2011 evidence-based practice guideline for immune thrombocytopenia. Blood.
2011;117(16):4190-4207.
[6] Revolade Summary of Product Characteristics.
[7] Bussel JB, Garcia de Miguel P, Despotovic JM, et al. Eltrombopag for the
treatment of children with persistent and chronic immune thrombocytopenia
(PETIT): a randomised, multicentre, placebo-controlled study. Lancet Haematol.
2015; published online July 29, 2015.
[8] Grainger JD, Locatelli F, Chotsampancharoen T, et al. Eltrombopag for
children with chronic immune thrombocytopenia (PETIT2): a randomised,
multicentre, placebo-controlled trial. Lancet. 2015; published online July
29, 2015.
[9] Provan D, Stasi R, Newland AC, et al. International consensus report on the
investigation and management of primary immune thrombocytopenia. Blood.
2010;115(2):168-186.
[10] Cines DB, Blanchette VS. Immune thrombocytopenic purpura. N Engl J Med.
2002;346(13):995-1008.
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