Taysha Gene Therapies Inc
NASDAQ:TSHA
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Taysha Gene Therapies Inc
Other Operating Expenses
Taysha Gene Therapies Inc
Other Operating Expenses Peer Comparison
Competitors Analysis
Latest Figures & CAGR of Competitors
| Company | Other Operating Expenses | CAGR 3Y | CAGR 5Y | CAGR 10Y | ||
|---|---|---|---|---|---|---|
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Taysha Gene Therapies Inc
NASDAQ:TSHA
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Other Operating Expenses
N/A
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CAGR 3-Years
N/A
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CAGR 5-Years
N/A
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CAGR 10-Years
N/A
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Abbvie Inc
NYSE:ABBV
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Other Operating Expenses
$241m
|
CAGR 3-Years
N/A
|
CAGR 5-Years
N/A
|
CAGR 10-Years
N/A
|
|
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Gilead Sciences Inc
NASDAQ:GILD
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Other Operating Expenses
N/A
|
CAGR 3-Years
N/A
|
CAGR 5-Years
N/A
|
CAGR 10-Years
N/A
|
|
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Amgen Inc
NASDAQ:AMGN
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Other Operating Expenses
-$14m
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CAGR 3-Years
N/A
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CAGR 5-Years
41%
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CAGR 10-Years
N/A
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Vertex Pharmaceuticals Inc
NASDAQ:VRTX
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Other Operating Expenses
-$2.1m
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CAGR 3-Years
N/A
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CAGR 5-Years
31%
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CAGR 10-Years
12%
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Regeneron Pharmaceuticals Inc
NASDAQ:REGN
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Other Operating Expenses
$10m
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CAGR 3-Years
-52%
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CAGR 5-Years
-49%
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CAGR 10-Years
N/A
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Taysha Gene Therapies Inc
Glance View
Taysha Gene Therapies, Inc.is a patient-centric, clinical-stage gene therapy company, which engages in the development and commercialization of adeno-associated viruses (AAV) based gene therapies for the treatment of monogenic diseases of the central nervous system. The company is headquartered in Dallas, Texas and currently employs 178 full-time employees. The company went IPO on 2020-09-24. The firm is focused on developing and commercializing adeno-associated virus (AAV)-based gene therapies for the treatment of monogenic diseases of the central nervous system (CNS). Its portfolio of gene therapy candidates targets a range of neurological indications across three distinct therapeutic categories: neurodegenerative diseases, neurodevelopmental disorders and genetic epilepsies. Its product candidates include TSHA-101, which is being developed for the treatment of giant axonal neuropathy (GAN); TSHA-102, a neurodevelopmental disorder product candidate, which is being developed for the treatment of Rett syndrome; TSHA-118, which is a AAV9 viral vector that expresses human codon-optimized Ceroid Lipofuscinosis Neuronal 1 complementary deoxyribonucleic acid under control of the chicken b-actin hybrid promoter, and TSHA-105, a gene replacement therapy for the treatment of SLC13A5 deficiency.