Indication name: Dravet
syndrome (DS)
Dravet syndrome (DS) – Market
outlook, Epidemiology, Market Forecast and Competitive Landscape Report – 2020
To 2030 (Markets covered: US, Germany, France, Spain, United Kingdom, Italy,
Japan & China)
Dravet syndrome (DS) is a genetic
epilepsy of childhood characterized by a variety of drug-resistant seizures
often induced by fever, presenting in previously healthy children, and which
frequently leads to cognitive and motor impairment. Around 85% of DS cases are
due to a mutation or deletion in the SCN1A gene, encoding a voltage-gated
sodium channel essential for the excitability of neurons. Most mutations are de
novo but in 5-10% they are familial and often part of the generalized epilepsy
with febrile seizures-plus spectrum.
Dravet Syndrome is classified as
a genetic epilepsy syndrome and an epileptic encephalopathy, defined as an
epilepsy syndrome associated with encephalopathic features that present or
worsen after the onset of epilepsy.
According to Thelansis estimates,
Dravet syndrome affects 1:15,700 individuals in the U.S., or 0.0064% of the
population . Approximately 80-90% of those, or 1:20,900 individuals, have both
an SCN1A mutation and a clinical diagnosis of DS. This represents an estimated
0.17% of all epilepsies.
Competitive landscape of Dravet
syndrome (DS) includes country specific approved as well as pipeline therapies.
Any asset/ product specific designation or review and Accelerated Approval are
being tracked and supplemented with analyst commentary.
KOLs insights
of Dravet syndrome (DS) across 8 MM market from center of Excellence/ Public/
Private hospitals participated in the study. Insights around current treatment
landscape, epidemiology, clinical characteristics, future treatment paradigm
and Unmet needs.
Dravet syndrome (DS) Market
Forecast: Patient Based Forecast Model (MS. Excel Based Automated Dashboard)
which Data Inputs with sourcing, Market Event and Product Event, Country
specific Forecast Model, Market uptake and patient share uptake, Attribute
Analysis, Analog Analysis, Disease burden and pricing scenario, Summary and
Insights.
S. No Asset Company Partner Phase
1 Diacomit Laboratoires Biocodex Meiji Seika Pharma Approved
2 Epidiolex GW Pharmaceuticals plc N/A Approved
3 Fintepla Zogenix, Inc. Nippon Shinyaku NDA
4 Onfi H. Lundbeck A/S Daiichi Sankyo; Alfresa Pharma III
5 EPX-200 Epygenix Therapeutics, Inc. N/A II
6 OV935 Ovid Therapeutics, Inc. Takeda II
7 Translarna PTC Therapeutics, Inc. UPenn II
8 Zygel
Zynerba Pharmaceuticals,
Inc. N/A II
9 DiazePen Xeris Pharmaceuticals, Inc. N/A I
10 EPX-100 Epygenix Therapeutics, Inc. N/A I
11 EPX-300 Epygenix Therapeutics, Inc. N/A I
12 XEN901 Xenon Pharmaceuticals, Inc. N/A I
13 Dravet Syndrome Program
(NeuCyte/Trillium) NeuCyte,
Inc. Trillium Therapeutics Preclinical
14 OPK-88001 Opko Health N/A Preclinical
15 SPN-817 Supernus Pharmaceuticals, Inc. Global Drug Development Centre Preclinical
16 STK-001 Stoke Therapeutics, Inc. N/A Preclinical
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