MARKET

BNTC

BNTC

Benitec Biopharm
NASDAQ
9.13
-0.14
-1.51%
Closed 16:00 07/25 EDT
OPEN
9.36
PREV CLOSE
9.27
HIGH
9.46
LOW
9.00
VOLUME
9.04K
TURNOVER
0
52 WEEK HIGH
10.88
52 WEEK LOW
1.860
MARKET CAP
85.53M
P/E (TTM)
-0.9252
1D
5D
1M
3M
1Y
5Y
1D
Weekly Report: what happened at BNTC last week (0715-0719)?
Weekly Report · 4d ago
Benitec Biopharma Price Target Announced at $13.00/Share by Leerink Partners
Dow Jones · 4d ago
Benitec Biopharma Initiated at Outperform by Leerink Partners
Dow Jones · 4d ago
Buy Rating on Benitec Biopharma: Anticipating BB-301’s Impact on OPMD Treatment and Stock Value
TipRanks · 4d ago
Leerink Partners Initiates Coverage On Benitec Biopharma with Outperform Rating, Announces Price Target of $13
Benzinga · 4d ago
U.S. RESEARCH ROUNDUP-Align Technology, McKesson, Schneider National
Wall Street analysts revise their ratings and price targets on several U.S.-listed companies. Align Technology, McKesson, and Schneider National have lower targets. Abercrombie & Fitch, American Airlines and Amazon.com among the companies with new targets cut.
Reuters · 4d ago
Benitec Biopharma (BNTC) Receives a Buy from Piper Sandler
TipRanks · 07/17 16:12
Analysts Are Bullish on These Healthcare Stocks: Madrigal Pharmaceuticals (MDGL), Benitec Biopharma (BNTC)
TipRanks · 07/16 05:41
More
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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