Tardive Dyskinesia – Market outlook, Epidemiology, Competitive Landscape and Market Forecast Report – 2020 To 2030
Tardive dyskinesia (TD) is an involuntary neurological movement disorder caused by the use of dopamine receptor blocking drugs that are prescribed to treat certain psychiatric or gastrointestinal conditions.
Etiology-
Tardive dyskinesia is caused by the
long-term use of a class of drugs known as neuroleptics. These drugs are also
called antipsychotics or major tranquillizers.
Medicines that most commonly cause this
disorder are older antipsychotics, including Chlorpromazine, Fluphenazine,
Haloperidol, Perphenazine, Prochlorperazine, Thioridazine, Trifluoperazine Other
drugs that can cause TD to include Metoclopramide, Antidepressant drugs such as
amitriptyline, fluoxetine, phenelzine, sertraline, trazodone, Antiparkinson
drugs such as levodopa, Antiseizure drugs such as phenobarbital and phenytoin.
Epidemiology-
The occurrence of TD is estimated to be 2%-5%
annually, and the condition occurs in 15%-30% of those who receive long-term
treatment with APDs. The occurrence of TD can also depend on whether the APD is
typical (also known as first-generation) or atypical (also known as
second-generation), with a 32.4% occurrence with typical APDs and a 13.1%
occurrence with atypical APDs. A 2015 study of 293 patients showed a 2.5%
incidence of TD in those receiving olanzapine for treatment compared to 5.5% of
those taking typical APDs.
The competitive landscape of Tardive Dyskinesia 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 Tardive
Dyskinesia across 8 MM market from the centre of Excellence/ Public/ Private
hospitals participated in the study. Insights around current treatment
landscape, epidemiology, clinical characteristics, future treatment paradigm,
and Unmet needs.
Tardive
Dyskinesia 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 Stage
1 Mavorixafor X4
Pharmaceuticals Phase 1
2 HSP-130 Hospira,
now a wholly-owned subsidiary of Pfizer Phase
1
3 EC-18 Enzychem Lifesciences
Corporation Phase 2
4 Eflapegrastim Spectrum
Pharmaceuticals, Inc Phase 1
5 pegfilgrastim Kyowa
Kirin Co., Ltd. Phase 2
6 rHSA-GCSF 2.4mg Tianjin
SinoBiotech Ltd. Phase 2
7 Myelo001 Myelo
Therapeutics GmbH Phase 2
8 Lozanoc Mayne
Pharma International Pty Ltd Phase 2
9 Pegfilgrastim Eurofarma
Laboratorios S.A. Phase 1
10 TXA127 Tarix
Pharmaceuticals Phase 2
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