· This disease modifying therapy is the
first and only approved treatment available in India for SMA patients across
all types.
·
Evrysdi® is being studied as part of the broadest and largest
global clinical trial program in SMA - from newborn infants to adults aged 60
years, with varying symptoms and motor function.
About SMA
SMA is a severe, progressive rare neuromuscular disease that can be fatal. It affects approximately one in 10,000 live births globally1 and one in 7744 live births in India2 and is the leading genetic cause of infant mortality. SMA is caused by a mutation of the survival motor neuron 1 (SMN1) gene, which leads to a deficiency of SMN protein. This protein is found throughout the body and is essential to the function of nerves that control muscles and movement. Without it, nerve cells cannot function correctly, leading to muscle weakness over time. Depending on the type of SMA, an individual’s physical strength and their ability to walk, eat or breathe can be significantly diminished or lost.
About Evrysdi® and global clinical
trials
Evrysdi® is administered daily
at home orally (it is supplied as powder which is constituted into a
liquid solution and taken once daily by mouth or feeding tube if required) and
is designed to treat SMA by increasing production of the Survival Motor Neuron
(SMN) protein. It is approved for the treatment of spinal muscular
atrophy (SMA) in adults and children 2 months of age and older.
Evrysdi® is being studied in
more than 450 people as part of the broadest, large and robust clinical trial
program in SMA. The program included newborn infants to adults aged 60 years
with varying symptoms and motor function, and is the only program that has
included those that were previously treated for SMA with another
medication.
Evrysdi® was
approved by Indian Health Authorities after reviewing its efficacy and safety
data from three global clinical studies designed to represent a broad spectrum
of people living with SMA:
1. FIREFISH3 in symptomatic infants aged 1 to 7 months with
Type 1 SMA
2. SUNFISH3 in children and adults aged 2 to 25 years.
SUNFISH is the first and only placebo-controlled trial to include adults with
Types 2 and 3 SMA.
Evrysdi® showed clinically-meaningful improvements in motor function across these two clinical trials in people with varying ages and levels of disease severity, including Types 1, 2, and 3 SMA. Infants achieved the ability to sit without support for at least 5 seconds, a key motor milestone not
normally seen in the natural course of the
disease. Evrysdi® also improved survival without permanent
ventilation at 12 and 23 months, compared to natural history. Evrysdi
maintained the ability to swallow and feed orally in the majority of the
infants after 2 years of therapy. This is a unique characteristic of Evrysdi
that was not observed with other medications for SMA.
3. JEWELFISH3 (interim data) is a study assessing people with any SMA type and disease severity who have previously been treated with other SMA targeted therapies between 6 months and 60 years. This study enrolled the broadest patient population ever studied in an SMA trial. Data from the JEWELFISH study, which included a diverse patient population with a high degree of motor impairment, show that Evrysdi® has a favorable safety profile in patients previously treated with other SMA targeting therapies. Evrysdi also showed to improve SMN protein levels to 2 fold and above in all the patients who have received a previous therapy.
Evrysdi’s clinical
development program also includes:
RAINBOWFISH3 is a study assessing pre-symptomatic infants with Type 1 SMA from birth to 6 weeks old. Preliminary efficacy data from RAINBOWFISH showed that infants treated for 12 months achieved age appropriate motor milestones within the WHO windows for healthy children, including sitting, standing and walking, and improvements in motor function.
V Simpson Emmanuel, CEO
and Managing Director, Roche Pharma India says, “The launch of Evrysdi® in India is a fine
example of Roche living its purpose of ‘Doing now what patients need next’. We are betting big on
solving complex challenges related to rare diseases as we believe no patient
should be deprived an opportunity to live a healthy life, however complex or
rare the disease is. Today heralds a new journey of hope as we are all coming together
to add color into the lives of SMA patients in India with the launch of
Evrysdi®, the first and only
approved treatment in India for patients living with SMA. This also marks our
foray into rare disease treatment in India, he added.”
Patient Support
Program (PSP) to drive access
To ensure every patient
gets access to this disease modifying therapy, Roche is announcing its Patient
Support program (PSP) for Evrysdi®. Through this program:
·
In the first two years of treatment, Roche
provides three bottles free for every two bottles bought by the patient
·
From the third year onwards, Roche
provides two bottles free for every one bottle bought by the patient
To provide a holistic
solution to SMA patients and caregivers, we identified the most important
challenges they face throughout their journey and have designed solutions to
support them to mitigate those challenges. Through our PSP program, Roche will
provide services like: Physiotherapy,Financial counselling, Psychosocial and Nutritional
counselling to SMA patients.Patients and
caregivers can reach out to us at 1800-202-4755
for information on the PSP program.
Home delivery of Evrysdi®: SMA patients have weak pulmonary health and find it difficult to visit a hospital to receive therapy, especially in COVID times. Moreover, motor disability adds to this burden and makes it very difficult for these patients and caregivers to travel to receive the drug. To solve this challenge, Roche will provide free home delivery of Evrysdi® to each and every patient following consent
from the patient/ caregiver and their HCPs. Being the only oral medication for SMA that can be administered in a home setting, this facility will add tremendous convenience to both patients and their caregivers, especially the added challenge Covid-19 poses. Patients, caregivers and HCPs can reach out to us at 1800-202-4755 to know more about Evrysdi’s availability and free home delivery.
“Given the majority of people with SMA in India
remain untreated, we believe Evrysdi, with its highly efficacious clinical
profile and oral administration advantage, will offer meaningful benefits for
many living with this rare neurological disease,” said Dr. Bruno Jolain,
Chief Medical Officer, Roche Pharma India. “Administration of Evrysdi
requires no hospitalization, no anesthesia, no specialized care center, no
complex administration and no steroids. A simple oral administration gives SMA
patients, treating physicians and caregivers more control over their daily
lives.”
“Throughout their lives,
many people with SMA may lose their ability to perform critical movements,
which can impact the ability to independently participate in different aspects
of daily life and even be life altering. SMA patients in India have long lived
without a viable treatment option. We are today encouraged by the availability
of an approved solution in India,” said Alpana Sharma, Co-Founder &
Director Patient Advocacy at CureSMA Foundation of India.
“The launch of Evrysdi in India is an eagerly awaited milestone for our community. We appreciate Roche’s commitment in making this drug available in India soon after its global launch and in developing a treatment that can be administered at home,” said Archana Vashist Panda, Co-Founder & Director Patient Advocacy, CureSMA Foundation of India.
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