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Genta - der letzte Thread
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www.genta.com/Investor_Relations/Events_Calendar.html
geduld leute, geduld! :D
ray macht dat schon.
ray macht dat schon.
der gewinner hat viele freunde, der verlierer nur gute!
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#7608 
wenn Genta hammernews rausbringen und der Kurs im Amiland pötzlich bei zB 1$ weiter läuft...fast keiner mehr investiert und es macht BUMS....hehehe...
Da hast du recht, erstmals abwarten und ein Tee trinken was meinst du dazu.:)
Frankfurt für 0,058 geordert und für 0,06 bekommen, aber der Kurz bleibt bei 0,058 was ist da los?
mit € 600 auf 0,063
ich glaub die zulassung ist durch
ich glaub die zulassung ist durch
Xetra (Auction) Leitbörse, Teilausführungen möglich 0,064 EUR 3.100
Stück keine 0,06 EUR
03.05.10 13:32eta
Stück keine 0,06 EUR
03.05.10 13:32eta
auch mal eingestiegen. Viell. ergibt sich ja etwas aus der Präsentation heute.
„Das Denken ist zwar allen Menschen erlaubt, aber vielen bleibt es erspart.“
Curt Goetz
Curt Goetz
Mittag mal ein paar größere Order getätig worden:
RT Fra 0,064 EUR +8,47% [+0,005]
13:40:04 bB 0,064 286000
13:21:00 0,063 15000
13:02:54 bB 0,064 27272
13:01:29 bB 0,065 300000
12:59:51 bG 0,063 40000
12:57:53 bB 0,062 70000
12:42:36 bB 0,063 10000
12:42:05 bG 0,06 367300
12:13:06 bG 0,058 46300
RT Fra 0,064 EUR +8,47% [+0,005]
13:40:04 bB 0,064 286000
13:21:00 0,063 15000
13:02:54 bB 0,064 27272
13:01:29 bB 0,065 300000
12:59:51 bG 0,063 40000
12:57:53 bB 0,062 70000
12:42:36 bB 0,063 10000
12:42:05 bG 0,06 367300
12:13:06 bG 0,058 46300
„Das Denken ist zwar allen Menschen erlaubt, aber vielen bleibt es erspart.“
Curt Goetz
Curt Goetz
habe ich noch nicht übersetzt...
www.marketwatch.com/story/...g-2010-05-04?reflink=MW_news_stmp
www.marketwatch.com/story/...g-2010-05-04?reflink=MW_news_stmp
Genta Announces Clinical Presentations on Lead Compounds, Tesetaxel and Genasense®, at 2010 Annual ASCO Meeting
Date : 05/04/2010 @ 8:05AM
Source : Business Wire
Stock : Genta Incorporated (GETA)
Quote : 0.0752 0.0 (0.00%) @ 7:11AM
Genta Announces Clinical Presentations on Lead Compounds, Tesetaxel and Genasense®, at 2010 Annual ASCO Meeting
Genta Incorporated (OTCBB: GETA) announced today that data from clinical trials of the Company's late-stage compounds, tesetaxel and Genasense® (oblimersen sodium) Injection, will be presented at the 2010 American Society of Clinical Oncology (ASCO) Annual Meeting. The meeting will be held from June 4-9, 2010 in Chicago, IL.
Highlights of the presentations include further details on the Phase 3 trials of Genasense in advanced melanoma, including a pooled analysis of early results from the AGENDA trial combined with data from Genta’s previous Phase 3 study, both of which evaluated dacarbazine chemotherapy with or without Genasense. In addition, updated results from a trial in advanced melanoma that combined Genasense plus temozolomide and Abraxane® will be presented, including data from the cohort of patients that received Genasense as a 1-hour, twice-weekly, intravenous (IV) infusion (unlike prior trials that employed a continuous IV infusion for 5-consecutive days every 3 weeks).
Updated clinical and pharmacokinetic (PK) data on tesetaxel, the leading oral taxane in clinical development, will be presented from a dose-ranging study using a once every 3-weeks schedule. The presentation will also include initial clinical and PK data from a dose-ranging study that employs a new schedule whereby the drug is administered weekly for 3 consecutive weeks, followed by 1 week off.
Titles, dates, and times of these presentations appear below.
Results of pooled analyses from two phase III trials of 1,085 patients (pts) with advanced melanoma: Oblimersen (OBL) plus dacarbazine (DTIC) versus DTIC alone. (Abstract #8573). Sunday June 6, 2010. Poster Session: Melanoma/Skin Cancers: 8 AM – 12 PM.
Relation between baseline LDH and tumor burden in advanced melanoma in two phase III trials of oblimersen-dacarbazine (OBL-DTIC) vs. DTIC. (Abstract #8557). Sunday June 6, 2010. Poster Session: Melanoma/Skin Cancers: 8 AM – 12 PM.
Oblimersen 1-hour IV infusion in combination with temozolomide and albumin-bound paclitaxel in patients with advanced melanoma. (Abstract #8561). Sunday June 6, 2010. Poster Session: Melanoma/Skin Cancers: 8 AM – 12 PM.
An inter-subject dose-escalation study of tesetaxel administered orally once every 3 weeks and once weekly for 3 consecutive weeks in patients with advanced or metastatic solid tumors. (Abstract #TPS159). Monday June 7, 2010. Poster Session: Clinical Trials, Special Session: 8 AM – 12 PM.
Phase I dose-ranging, pharmacokinetic (PK) study of tesetaxel, a novel orally active tubulin-binding agent. (Publication only).
About Genta
Genta Incorporated is a biopharmaceutical company with a diversified product portfolio that is focused on delivering innovative products for the treatment of patients with cancer. Two major programs anchor the Company’s research platform: DNA/RNA-based Medicines and Small Molecules. Genasense® (oblimersen sodium) Injection is the Company's lead compound from its DNA/RNA Medicines program. Genasense® is being developed as an agent that may enhance the effectiveness of anticancer therapy. The Company is currently collecting long-term followup data on durable response and overall survival from the recently completed randomized Phase 3 study of Genasense® in patients with advanced melanoma (the AGENDA trial). The Company is also developing tesetaxel, a novel, orally absorbed, semi-synthetic taxane that is in the same class of drugs as paclitaxel and docetaxel. Genta has initiated a broad clinical program to evaluate the safety and efficacy of tesetaxel in patients with solid tumors. In the U.S., Genta is exclusively marketing Ganite® (gallium nitrate injection), which is indicated for treatment of symptomatic patients with cancer-related hypercalcemia that is resistant to hydration. The Company has developed proprietary oral formulations of the active ingredient in Ganite® that are being evaluated as potential treatments for diseases associated with accelerated bone loss. Ganite® and Genasense® are available on a “named-patient” basis in countries outside the United States. For more information about Genta, please visit our website at: www.genta.com.
Safe Harbor
This press release may contain forward-looking statements with respect to business conducted by Genta Incorporated. By their nature, forward-looking statements and forecasts involve risks and uncertainties because they relate to events and depend on circumstances that will occur in the future. Such forward-looking statements include those that express plan, anticipation, intent, contingency, goals, targets, or future developments and/or otherwise are not statements of historical fact. The words “potentially”, “anticipate”, “could”, “calls for”, and similar expressions also identify forward-looking statements. The Company does not undertake to update any forward-looking statements. Factors that could affect actual results include, without limitation, risks associated with:
the Company’s ability to obtain necessary regulatory approval for its product candidates from regulatory agencies, such as the U.S. Food and Drug Administration and the European Medicines Agency;
the safety and efficacy of the Company’s products or product candidates;
the commencement and completion of any clinical trials;
the Company’s assessment of its clinical trials;
the Company’s ability to develop, manufacture, license, or sell its products or product candidates;
the Company’s ability to enter into and successfully execute any license and collaborative agreements;
the adequacy of the Company’s capital resources and cash flow projections, or the Company’s ability to obtain sufficient financing to maintain the Company’s planned operations;
the adequacy of the Company’s patents and proprietary rights;
the impact of litigation that has been brought against the Company; and
the other risks described under Certain Risks and Uncertainties Related to the Company’s Business, as contained in the Company’s Annual Report on Form 10-K and Quarterly Report on Form 10-Q.
There are a number of factors that could cause actual results and developments to differ materially. For a discussion of those risks and uncertainties, please see the Company's Annual Report on Form 10-K for 2009 and its most recent quarterly report on Form 10-Q.
ih.advfn.com/...mona&article=42647604&symbol=NB%5EGETA
Date : 05/04/2010 @ 8:05AM
Source : Business Wire
Stock : Genta Incorporated (GETA)
Quote : 0.0752 0.0 (0.00%) @ 7:11AM
Genta Announces Clinical Presentations on Lead Compounds, Tesetaxel and Genasense®, at 2010 Annual ASCO Meeting
Genta Incorporated (OTCBB: GETA) announced today that data from clinical trials of the Company's late-stage compounds, tesetaxel and Genasense® (oblimersen sodium) Injection, will be presented at the 2010 American Society of Clinical Oncology (ASCO) Annual Meeting. The meeting will be held from June 4-9, 2010 in Chicago, IL.
Highlights of the presentations include further details on the Phase 3 trials of Genasense in advanced melanoma, including a pooled analysis of early results from the AGENDA trial combined with data from Genta’s previous Phase 3 study, both of which evaluated dacarbazine chemotherapy with or without Genasense. In addition, updated results from a trial in advanced melanoma that combined Genasense plus temozolomide and Abraxane® will be presented, including data from the cohort of patients that received Genasense as a 1-hour, twice-weekly, intravenous (IV) infusion (unlike prior trials that employed a continuous IV infusion for 5-consecutive days every 3 weeks).
Updated clinical and pharmacokinetic (PK) data on tesetaxel, the leading oral taxane in clinical development, will be presented from a dose-ranging study using a once every 3-weeks schedule. The presentation will also include initial clinical and PK data from a dose-ranging study that employs a new schedule whereby the drug is administered weekly for 3 consecutive weeks, followed by 1 week off.
Titles, dates, and times of these presentations appear below.
Results of pooled analyses from two phase III trials of 1,085 patients (pts) with advanced melanoma: Oblimersen (OBL) plus dacarbazine (DTIC) versus DTIC alone. (Abstract #8573). Sunday June 6, 2010. Poster Session: Melanoma/Skin Cancers: 8 AM – 12 PM.
Relation between baseline LDH and tumor burden in advanced melanoma in two phase III trials of oblimersen-dacarbazine (OBL-DTIC) vs. DTIC. (Abstract #8557). Sunday June 6, 2010. Poster Session: Melanoma/Skin Cancers: 8 AM – 12 PM.
Oblimersen 1-hour IV infusion in combination with temozolomide and albumin-bound paclitaxel in patients with advanced melanoma. (Abstract #8561). Sunday June 6, 2010. Poster Session: Melanoma/Skin Cancers: 8 AM – 12 PM.
An inter-subject dose-escalation study of tesetaxel administered orally once every 3 weeks and once weekly for 3 consecutive weeks in patients with advanced or metastatic solid tumors. (Abstract #TPS159). Monday June 7, 2010. Poster Session: Clinical Trials, Special Session: 8 AM – 12 PM.
Phase I dose-ranging, pharmacokinetic (PK) study of tesetaxel, a novel orally active tubulin-binding agent. (Publication only).
About Genta
Genta Incorporated is a biopharmaceutical company with a diversified product portfolio that is focused on delivering innovative products for the treatment of patients with cancer. Two major programs anchor the Company’s research platform: DNA/RNA-based Medicines and Small Molecules. Genasense® (oblimersen sodium) Injection is the Company's lead compound from its DNA/RNA Medicines program. Genasense® is being developed as an agent that may enhance the effectiveness of anticancer therapy. The Company is currently collecting long-term followup data on durable response and overall survival from the recently completed randomized Phase 3 study of Genasense® in patients with advanced melanoma (the AGENDA trial). The Company is also developing tesetaxel, a novel, orally absorbed, semi-synthetic taxane that is in the same class of drugs as paclitaxel and docetaxel. Genta has initiated a broad clinical program to evaluate the safety and efficacy of tesetaxel in patients with solid tumors. In the U.S., Genta is exclusively marketing Ganite® (gallium nitrate injection), which is indicated for treatment of symptomatic patients with cancer-related hypercalcemia that is resistant to hydration. The Company has developed proprietary oral formulations of the active ingredient in Ganite® that are being evaluated as potential treatments for diseases associated with accelerated bone loss. Ganite® and Genasense® are available on a “named-patient” basis in countries outside the United States. For more information about Genta, please visit our website at: www.genta.com.
Safe Harbor
This press release may contain forward-looking statements with respect to business conducted by Genta Incorporated. By their nature, forward-looking statements and forecasts involve risks and uncertainties because they relate to events and depend on circumstances that will occur in the future. Such forward-looking statements include those that express plan, anticipation, intent, contingency, goals, targets, or future developments and/or otherwise are not statements of historical fact. The words “potentially”, “anticipate”, “could”, “calls for”, and similar expressions also identify forward-looking statements. The Company does not undertake to update any forward-looking statements. Factors that could affect actual results include, without limitation, risks associated with:
the Company’s ability to obtain necessary regulatory approval for its product candidates from regulatory agencies, such as the U.S. Food and Drug Administration and the European Medicines Agency;
the safety and efficacy of the Company’s products or product candidates;
the commencement and completion of any clinical trials;
the Company’s assessment of its clinical trials;
the Company’s ability to develop, manufacture, license, or sell its products or product candidates;
the Company’s ability to enter into and successfully execute any license and collaborative agreements;
the adequacy of the Company’s capital resources and cash flow projections, or the Company’s ability to obtain sufficient financing to maintain the Company’s planned operations;
the adequacy of the Company’s patents and proprietary rights;
the impact of litigation that has been brought against the Company; and
the other risks described under Certain Risks and Uncertainties Related to the Company’s Business, as contained in the Company’s Annual Report on Form 10-K and Quarterly Report on Form 10-Q.
There are a number of factors that could cause actual results and developments to differ materially. For a discussion of those risks and uncertainties, please see the Company's Annual Report on Form 10-K for 2009 and its most recent quarterly report on Form 10-Q.
ih.advfn.com/...mona&article=42647604&symbol=NB%5EGETA
|
Neueste Beiträge aus dem Genta Forum
| Wertung | Antworten | Thema | Verfasser | letzter Verfasser | letzter Beitrag | |
2 | 302 | Gensense ist Tod es lebe Tesetaxel! | raurunter | raurunter | 25.04.21 13:15 | |
| 10 | 2.653 | Die 1000% Chance noch dieses Jahr.... | Happydepot | steven-bln | 25.04.21 13:13 | |
| 13 | 2.456 | Analyse. GENTA Kursexplosionsgefahr!! | brunneta | steven-bln | 25.04.21 02:54 | |
| 4 | 1.447 | was mit der Aktie passiert, etc.. | Lucky2020 | Lucky2020 | 25.04.21 02:10 | |
| 622 | Hoffnung stirbt zum Schluss...! | raurunter | raurunter | 25.04.21 00:48 |
