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Company | Country | Symbol |
---|
Time | Volume | DSGN |
---|---|---|
09:32 ET | 2577 | 6.1 |
10:08 ET | 402 | 6.04 |
10:20 ET | 300 | 6.12 |
10:27 ET | 168 | 6.08 |
10:40 ET | 824 | 6.105 |
10:42 ET | 1200 | 6.12 |
10:44 ET | 100 | 6.105 |
10:45 ET | 736 | 6.12 |
10:56 ET | 200 | 6.135 |
10:58 ET | 378 | 6.17 |
11:05 ET | 100 | 6.16 |
11:07 ET | 100 | 6.17 |
11:09 ET | 100 | 6.17 |
11:12 ET | 2193 | 6.105 |
11:14 ET | 108 | 6.105 |
11:16 ET | 100 | 6.075 |
11:18 ET | 1100 | 6 |
11:20 ET | 700 | 5.96 |
11:23 ET | 813 | 5.945 |
11:25 ET | 200 | 5.945 |
11:27 ET | 100 | 5.945 |
11:30 ET | 1656 | 6.0089 |
11:38 ET | 100 | 5.98 |
11:39 ET | 100 | 5.98 |
11:41 ET | 400 | 5.98 |
11:45 ET | 100 | 6.005 |
11:50 ET | 300 | 6.02 |
11:52 ET | 100 | 5.98 |
11:54 ET | 100 | 5.98 |
11:56 ET | 200 | 5.98 |
11:59 ET | 100 | 5.98 |
12:01 ET | 638 | 6.005 |
12:03 ET | 400 | 6 |
12:06 ET | 800 | 6.02 |
12:10 ET | 400 | 6.04 |
12:12 ET | 100 | 6.03 |
12:14 ET | 1000 | 6.0212 |
12:15 ET | 100 | 6.02 |
12:19 ET | 100 | 6 |
12:21 ET | 100 | 6 |
12:24 ET | 100 | 6 |
12:26 ET | 100 | 6 |
12:28 ET | 100 | 6 |
12:30 ET | 100 | 6 |
12:32 ET | 100 | 6 |
12:33 ET | 920 | 5.96 |
12:35 ET | 100 | 5.96 |
12:39 ET | 100 | 5.96 |
12:42 ET | 100 | 5.95 |
12:44 ET | 409 | 5.9414 |
12:46 ET | 100 | 5.94 |
12:48 ET | 100 | 5.96 |
12:50 ET | 100 | 5.965 |
12:51 ET | 100 | 5.94 |
12:53 ET | 300 | 5.96 |
12:55 ET | 100 | 5.95 |
12:57 ET | 100 | 5.94 |
01:00 ET | 7059 | 5.99 |
Company sortable | Market Cap sortable | P/E Ratio (TTM) sortable | EPS Growth (5yr) sortable |
---|---|---|---|
Design Therapeutics Inc | 348.2M | -7.1x | --- |
Jasper Therapeutics Inc | 348.6M | -4.8x | --- |
Kodiak Sciences Inc | 344.7M | -1.8x | --- |
Q32 Bio Inc | 327.9M | -3.6x | --- |
Northwest Biotherapeutics Inc | 324.5M | -4.5x | --- |
Neurogene Inc | 383.3M | -5.7x | --- |
Design Therapeutics, Inc. is a biotechnology company. It is engaged in the research and development of GeneTACT molecules, which are small-molecule gene targeted chimera therapeutic candidates designed to be disease-modifying by addressing the underlying cause of diseases caused by inherited nucleotide repeat expansion mutations. Its Friedreich ataxia (FA) program is focused on the development of a disease-modifying treatment. Its DT-216 is developed to overcome the FXN transcription impairment that causes FA. DT-216 is in Phase I clinical trial. The Company is also engaged in developing DT-216 to enable higher exposure and chronic administration for treatment of FA, known as DT-216P2, which uses the same drug substance, DT-216. Its FECD program is focused on the development of a potentially disease-modifying medical treatment for FECD, DT-168, which is in Phase I clinical trial. Its HD program is focused on the development of a potentially disease-modifying treatment for HD.
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Market Cap | $348.2M |
---|---|
Revenue (TTM) | $0.00 |
Shares Outstanding | 56.6M |
Dividend Yield | 0.00% |
Annual Dividend Rate | --- |
Ex-Dividend Date | 01-01-01 |
Pay Date | 01-01-01 |
Beta | 1.86 |
EPS | $-0.85 |
Book Value | $4.92 |
P/E Ratio | -7.1x |
Price/Sales (TTM) | --- |
Price/Cash Flow (TTM) | --- |
Operating Margin | --- |
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