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TC Biopharm (Holdings) Plc TCBP
$0.80
-$0.03 (-3.64%)
На 18:05, 12 мая 2023
Ключевые показатели
-
Marketcap
2038464.00000000
-
week52high
71.00
-
week52low
0.77
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Revenue
1978659
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P/E TTM
0
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Beta
0.00000000
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EPS
-15.78000000
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Last Dividend
0.00000000
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Next Earnings Date
12 дек 2022 г. в 08:00
Описание компании
TC Biopharm (Holdings) Plc, a clinical-stage biopharmaceutical company, focuses on developing immunotherapy products based on its allogeneic gamma delta T cell platform. Its product pipeline includes OmnImmune, an unmodified cell therapy used in the treatment of acute myeloid leukemia; and ImmuniStim, an unmodified cell therapy to treat COVID-19. The company was founded in 2013 and is headquartered in Motherwell, the United Kingdom.
Рекомендации
аналитиков
Рекомендации аналитиков
Grading company | New grade | Previous grade | Recommendation date |
---|---|---|---|
EF Hutton | Buy | 28 мар 2022 г. | |
HC Wainwright & Co. | Buy | 26 янв 2023 г. |
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Анонимное голосование
Будет ли рост российского рынка к концу года?
-
Да
87% -
Нет
12%
Проголосовал 8 человек
Новостная лента
компании
Insider Summary
Insider Summary
Reporting Name | Acquistion/Disposition | Owned | Transacted | Transaction Date |
---|---|---|---|---|
Randall Kenneth Edward | A | 70000 | 70000 | 30 ноя 2022 г. |
Randall Kenneth Edward | A | 70000 | 70000 | 30 ноя 2022 г. |
Randall Kenneth Edward | A | 136834 | 70000 | 30 ноя 2022 г. |
Randall Mark Edward | A | 70000 | 70000 | 30 ноя 2022 г. |
Randall Mark Edward | A | 70000 | 70000 | 30 ноя 2022 г. |
Randall Mark Edward | A | 136834 | 70000 | 30 ноя 2022 г. |
Randall Diana Elizabeth | A | 70000 | 70000 | 30 ноя 2022 г. |
Randall Diana Elizabeth | A | 70000 | 70000 | 30 ноя 2022 г. |
Randall Diana Elizabeth | A | 70000 | 70000 | 30 ноя 2022 г. |
Randall Mark Edward | A | 382963 | 70000 | 30 ноя 2022 г. |
Новостная лента
Why Are TC Biopharm Shares Trading Higher Today
Benzinga
17 мар 2022 г. в 11:51
The FDA has granted Orphan Drug designation to TC Biopharm Ltd's (NASDAQ: TCBP) lead product OmnImmune for use in Acute Myeloid Leukemia. After reviewing the Phase 1b/2a trial results in relapsed/refractory AML patients, the FDA approved the Company's application.
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