Stock Events

Sarepta Therapeutics 

R$36.27
141
+R$0+0% Monday 23:26

Statistics

Day High
36.27
Day Low
36.27
52W High
45.78
52W Low
18.89
Volume
100
Avg. Volume
821
Mkt Cap
57.06B
P/E Ratio
-
Dividend Yield
-
Dividend
-

Upcoming

Earnings

30OctExpected
Q1 2023
Q2 2023
Q3 2023
Q4 2023
Q1 2024
Q2 2024
Next
-5.86
-3.63
-1.41
0.82
Expected EPS
0.042697
Actual EPS
N/A

People Also Follow

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Competitors

This list is an analysis based on recent market events. It's not an investment recommendation.
Pfizer
PFE
Mkt Cap164.39B
Pfizer is developing gene therapies for Duchenne muscular dystrophy (DMD), directly competing with Sarepta's DMD treatments.
Sangamo Therapeutics
SGMO
Mkt Cap176.57M
Sangamo Therapeutics is working on genomic medicines, including treatments for DMD, which competes with Sarepta's gene therapy portfolio.
Sorrento Therapeutics
SRNE
Mkt Cap3.31M
Sorrento Therapeutics has a diverse pipeline including treatments for diseases that Sarepta also targets, making them competitors in the biotech space.
Biomarin Pharmaceutical
BMRN
Mkt Cap17.36B
BioMarin Pharmaceutical competes with Sarepta in the rare disease space, particularly in treatments for DMD.
PTC Therapeutics
PTCT
Mkt Cap2.72B
PTC Therapeutics offers treatment for DMD, competing directly with Sarepta's DMD therapies.
Solid Biosciences
SLDB
Mkt Cap344.66M
Solid Biosciences is focused on developing therapies for DMD, positioning it as a direct competitor to Sarepta.
Dyadic International DE
DYAI
Mkt Cap39.5M
Dyadic International is working on developing and manufacturing biopharmaceuticals for diseases that Sarepta also targets.
Vertex Pharmaceuticals
VRTX
Mkt Cap127.99B
Vertex Pharmaceuticals is involved in treating cystic fibrosis and other diseases, competing with Sarepta in the broader rare disease market.
Ultragenyx Pharmaceutical
RARE
Mkt Cap5.23B
Ultragenyx Pharmaceutical focuses on rare diseases, including some that overlap with Sarepta's target indications.
Biogen
BIIB
Mkt Cap29.83B
Biogen has a broad portfolio in neurology and rare diseases, competing with Sarepta in areas like gene therapy for neurological disorders.

About

Sarepta Therapeutics, Inc., a commercial-stage biopharmaceutical company, focuses on the discovery and development of RNA-targeted therapeutics, gene therapies, and other genetic therapeutic modalities for the treatment of rare diseases. It offers EXONDYS 51 injection to treat duchenne muscular dystrophy (duchenne) in patients with confirmed mutation of the dystrophin gene that is amenable to exon 51 skipping; and VYONDYS 53 for the treatment of duchenne in patients with confirmed mutation of the dystrophin gene that is amenable to exon 53 skipping. The company is also developing AMONDYS 45, a product candidate that uses phosphorodiamidate morpholino oligomer chemistry and exon-skipping technology to skip exon 45 of the dystrophin gene; SRP-5051, a peptide conjugated PMO that binds exon 51 of dystrophin pre-mRNA; SRP-9001, a DMD micro-dystrophin gene therapy program; and SRP-9003, a limb-girdle muscular dystrophies gene therapy program. It has collaboration agreements with F. Hoffman-La Roche Ltd; Nationwide Children's Hospital; Lysogene; Duke University; Genethon; and StrideBio. The company was incorporated in 1980 and is headquartered in Cambridge, Massachusetts.
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CEO
Mr. Douglas S. Ingram Esq.
Employees
840
Country
United States
ISIN
BRS1RPBDR005

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