MARKET

BNTC

BNTC

Benitec Biopharm
NASDAQ
9.48
-0.33
-3.36%
After Hours: 9.47 -0.01 -0.11% 16:00 10/04 EDT
OPEN
9.90
PREV CLOSE
9.81
HIGH
10.26
LOW
8.49
VOLUME
51.56K
TURNOVER
--
52 WEEK HIGH
12.89
52 WEEK LOW
2.690
MARKET CAP
100.07M
P/E (TTM)
-1.7206
1D
5D
1M
3M
1Y
5Y
1D
Benitec Biopharma (BNTC) Stock Surges on Potentially Groundbreaking OPMD Treatment
TipRanks · 4d ago
12 Health Care Stocks Moving In Tuesday's Intraday Session
Benzinga · 6d ago
Benitec Biopharma Price Target Maintained With a $16.00/Share by JMP Securities
Dow Jones · 09/30 13:44
JMP Securities Reiterates Market Outperform on Benitec Biopharma, Maintains $16 Price Target
Benzinga · 09/30 13:35
Weekly Report: what happened at BNTC last week (0923-0927)?
Weekly Report · 09/30 12:02
Buy Rating Affirmed for Benitec Biopharma on Strong Clinical Progress and Solid Financials
TipRanks · 09/30 04:35
I'm happy to help! However, I don't see any article text provided. The text you provided appears to be the table of contents for a 10-K financial report, which is a lengthy document that publicly traded companies are required to file with the Securities and Exchange Commission (SEC). If you could provide the actual article text, I'd be happy to help you generate a title for the article.
Press release · 09/26 23:10
Benitec Biopharma reports FY24 EPS ( $5.51) vs ($14.12) in FY23
TipRanks · 09/26 20:40
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About BNTC
Benitec Biopharma Inc. is a clinical-stage biotechnology company focused on the advancement of novel genetic medicines with headquarters in Hayward, California. The Company’s platform, DNA-directed RNA interference (ddRNAi), combines ribonucleic acid (RNA) interference with gene therapy to create medicines that facilitate sustained silencing of disease-causing genes following a single administration. The Company is also engaged in developing a silence and replace-based therapeutic (BB-301) for the treatment of Oculopharyngeal Muscular Dystrophy (OPMD), a chronic, life-threatening genetic disorder. The Company's BB-301 is an adeno-associated viral vector (AAV)-based gene therapy designed to permanently silence the expression of the disease-causing gene (to slow, or halt, the biological mechanisms underlying disease progression in OPMD) and to simultaneously replace the mutant gene with a wildtype gene (to drive restoration of function in diseased cells).

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