LENZ Therapeutics, Inc. LENZ 深 滬
等待開盤 06-25 09:30:00 美东时间
5.58
-0.170
-2.96%
華盛通- 最 高6.1827
- 今 開5.94
- 成交量 77.38万股
- 最 低 5.56
- 昨 收 5.75
- 總市值 1.75亿
- 52周最高 50.40
- 市盈率 靜 --
- 換手率 2.47%
- 52周最低 5.56
- 委 比 74.06%
- 總股本 3135.44万
- 歷史最高 230.79
- 量 比 0.94
- 振 幅 10.83%
- 歷史最低 3.92
- 每 手 1
- 風險率 12.51%
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更多LENZ Therapeutics Eye Drug Profile Supports Blockbuster Opportunity: Analyst
LENZ Therapeutics, Inc. (NASDAQ:LENZ) on Wednesday announced an exclusive licensing and commercialization agreement with Arrotex Pharmaceuticals Pty Ltd. The agreement marks LENZ’s latest effort to expand the commercial reach of its recently approved eye drop therapy beyond the U.S. market. Read Als...
今天 01:41
LENZ Therapeutics And Arrotex Pharma Announce Exclusive License And Commercialization Agreement For Arrotex To Register And Commercialize VIZZ For Treatment Of Presbyopia In Australia And New Zealand
LENZ Therapeutics, Inc. (NASDAQ:LENZ) and Arrotex Pharmaceuticals Pty Ltd. ("Arrotex") today announced an exclusive license and commercialization agreement for Arrotex to register and commercialize VIZZ™ for the treatment of presbyopia in Australia and New Zealand. LENZ Therapeutics is a pharmaceuti...
06-24 20:32
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05-13 11:46
Piper Sandler Downgrades LENZ Therapeutics to Neutral, Lowers Price Target to $12
Piper Sandler analyst Biren Amin downgrades LENZ Therapeutics (NASDAQ:LENZ) from Overweight to Neutral and lowers the price target from $39 to $12.
05-12 18:23
LENZ Therapeutics Q1 EPS $(1.32) Misses $(1.05) Estimate, Sales $1.901M Beat $1.759M Estimate
LENZ Therapeutics (NASDAQ:LENZ) reported quarterly losses of $(1.32) per share which missed the analyst consensus estimate of $(1.05) by 25.71 percent. This is a 149.06 percent decrease over losses of $(0.53) per share
05-12 04:07
Earnings Scheduled For May 11, 2026
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04-22 12:41
LENZ Therapeutics Files Marketing Authorization Application Review, Approval Of VIZZ To Medicines And Healthcare products Regulatory Agency To Treat Presbyopia In Adults
LENZ Therapeutics, Inc. (NASDAQ:LENZ) today announced that it has submitted a Marketing Authorization Application (MAA) to the United Kingdom's Medicines and Healthcare products Regulatory Agency (MHRA) for the review
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