Chiça pra esta GENT(E)A
14 mensagens
|Página 1 de 1
James, nem sempre tudo tem que seguir
a lógica, certo?
Até ao momento, confirma-se nova subida, e mais, ainda hoje deverão surgir novas noticias sobre a GNTA.
Julgo que a aprovação por parte da FDA irá representar muitos milhões de facturação. Quem ficou a ver navios foi a Aventis que desistiu.
Até ao momento, confirma-se nova subida, e mais, ainda hoje deverão surgir novas noticias sobre a GNTA.
Julgo que a aprovação por parte da FDA irá representar muitos milhões de facturação. Quem ficou a ver navios foi a Aventis que desistiu.
-
Inspector
Re: Se apôs a subida dela ontem não corijir..
Anonymous Escreveu:a tendência é de subida clara. Não acham?
Overall Summary: 40%, Bullish
60%, Bearish Trade Quality: Upside: 45%, Poor
Downside: 70%, Good Alerts: None
Price & Volume View the Full Consultant page for GNTA Indicator Intro
Scale: 0 - Neutral, 10 - Extreme
PRICE 2.05, +0.67 pts (+48.6%), Monday, 6 Dec 2004, close
10, excessive up from yesterday's close, expect to pause/stop.
Typical price range from yesterday's close : ± 0.24 pts, ± 11.8%
VOLUME 62.75mil shares, +3184% compared to the typical daily volume over the past 6 months.
High Volume alert! Typical daily volume is 1.91mil shares over the past 6 months.
Overall Summary A summary of bullish and bearish indicators. Summary Help
Should only be used as a general guide. Please look at the indicators for more detailed understanding.
BULLISH Probability - Intermediate trend possibly bullish, Sideways trend near lower support.
Confirmation - Strong bullish 3 day chart pattern with Extreme 3 day accumulation.
BEARISH Probability - 1 Day Price change extreme up, may pause/reverse
Probability - Short term typical rally, rally may start to slow.
Confirmation - Extreme bearish 1 day moneyflow
Confirmation - at resistance
SUMMARY 1 bullish probability indicators. -2,
1 bullish confirmation indicators. Neutral, short term (1-6 wks)
2 bearish probability indicators. 40%, Bullish
2 bearish confirmation indicators. 60%, Bearish
Bom, o after hours deu indicações
de mais subidas. Espero que sim. Como desceu astronómicamente em Maio também pode subir quase da mesma forma com noticias antagónicas a aquelas que provocaram a queda-
-
Inspector
estou dentro já faz algum tempo. era para ter saído mas fui apanhado pela queda de dia 26 e o meu stop não foi accionado. preço medio 1,81. Hoje parece ir fechar com vela negra, após ter fechado o gap e não me agrada nada, apesar das notícias serem encorajadoras ... (mas já são noticias, e deveria vender agora. No entanto, acho que nas farmaceuticas, as notícias têm um efeito diferente).
O q acham?
O q acham?
Rura
__________________________________
Palavras leva-as o vento...
__________________________________
Palavras leva-as o vento...
já agora, encontrei isto:
NEW YORK (CBS.MW) -- Shares of Genta Inc. soared 59 percent in afternoon trading Monday after positive clinical trial results for its cancer drug Genasense were presented this weekend at the annual American Society of Hematology meeting.
Genta (GNTA: news, chart, profile) shares were last trading at $2.20, up 82 cents.
The Berkeley Heights, N.J.-based drugmaker said that two studies of an experimental injection treatment showed synergistic activity with bortezomib, sold under the name Velcade and made by Millennium Pharmaceuticals (MLNM: news, chart, profile), and rituximab, which is sold under the name Rituxan and is made by Genentech (DNA: news, chart, profile) and Biogen Idec (BIIB: news, chart, profile).
Employed individually, Genasense and Rituxan were found to increase the mean survival of mice with non-Hodgkins lymphoma by 130 percent and 170 percent, respectively. A schedule of Rituxan followed by Genasense increased mean survival by 240 percent.
When the two were used together mean survival increased by 400 percent.
Genasense used in combination with bortezomib and the chemotherapy agent cyclophosphamide was also found to be curative, but only when Genasense was taken before cyclophosphamide and followed by bortezomib.
The preclinical trial findings "could bode well for some interesting clinical work that is currently ongoing," Janney Montgomery Scott analyst Brian Rye wrote in a morning note to clients.
Rye also said that all eyes would be on results from a Phase III study evaluating the addition of Genasense to cyclophosphamide and the chemotherapy agent fludarabine in patients with relapsed or refractory chronic lymphocytic leukemia. The results were due to be released by Genta on Monday afternoon.
"The company has already announced that the primary endpoint of a statistically significant difference in complete or nodular partial remission was achieved," he wrote, "and we look forward to learning the exact magnitude of this difference in order to further assess its clinical relevance and gain additional clarity on the likelihood of a near-term NDA submission."
In another study whose results were released over the weekend, of 30 patients with relapsed myeloma who were given Genasense plus thalidomide and high-dose dexamethasone, 60 percent achieved a major response.
On Nov. 26, Genta said a Phase III trial of its Genasense for patients with advanced multiple myeloma failed to meet its primary endpoint. The trial was set up to evaluate whether adding Genasense to standard therapy would increase the time to development of progressive disease in patients who had previously received extensive therapy.
The data for this study was also released over the weekend.
NEW YORK (CBS.MW) -- Shares of Genta Inc. soared 59 percent in afternoon trading Monday after positive clinical trial results for its cancer drug Genasense were presented this weekend at the annual American Society of Hematology meeting.
Genta (GNTA: news, chart, profile) shares were last trading at $2.20, up 82 cents.
The Berkeley Heights, N.J.-based drugmaker said that two studies of an experimental injection treatment showed synergistic activity with bortezomib, sold under the name Velcade and made by Millennium Pharmaceuticals (MLNM: news, chart, profile), and rituximab, which is sold under the name Rituxan and is made by Genentech (DNA: news, chart, profile) and Biogen Idec (BIIB: news, chart, profile).
Employed individually, Genasense and Rituxan were found to increase the mean survival of mice with non-Hodgkins lymphoma by 130 percent and 170 percent, respectively. A schedule of Rituxan followed by Genasense increased mean survival by 240 percent.
When the two were used together mean survival increased by 400 percent.
Genasense used in combination with bortezomib and the chemotherapy agent cyclophosphamide was also found to be curative, but only when Genasense was taken before cyclophosphamide and followed by bortezomib.
The preclinical trial findings "could bode well for some interesting clinical work that is currently ongoing," Janney Montgomery Scott analyst Brian Rye wrote in a morning note to clients.
Rye also said that all eyes would be on results from a Phase III study evaluating the addition of Genasense to cyclophosphamide and the chemotherapy agent fludarabine in patients with relapsed or refractory chronic lymphocytic leukemia. The results were due to be released by Genta on Monday afternoon.
"The company has already announced that the primary endpoint of a statistically significant difference in complete or nodular partial remission was achieved," he wrote, "and we look forward to learning the exact magnitude of this difference in order to further assess its clinical relevance and gain additional clarity on the likelihood of a near-term NDA submission."
In another study whose results were released over the weekend, of 30 patients with relapsed myeloma who were given Genasense plus thalidomide and high-dose dexamethasone, 60 percent achieved a major response.
On Nov. 26, Genta said a Phase III trial of its Genasense for patients with advanced multiple myeloma failed to meet its primary endpoint. The trial was set up to evaluate whether adding Genasense to standard therapy would increase the time to development of progressive disease in patients who had previously received extensive therapy.
The data for this study was also released over the weekend.
-
Visitante
Re: O medicamento julgo que...
Anonymous Escreveu:está a ser exprementado em doente com lucemia e com uma taxa de secesso de 60%.
Bem hajam por dois motivos, o primeiro dos quias pelos milhões em todo o Mundo que padecem dessa terrivel doença.
Eu não acompanho o titulo daí que estas observações sejam superficiais:
penso que a Genta apenas tem uma droga em desenvolvimento, o Genesense, que não obteve aprovação pela FDA para o tratamento de melanoma (Maio 2004), desde então têm testado o Genesense no tratamento de leucemia (chronic lymphocytic leukemia - CLL), segundo eles com bons resultados, no entanto, a Aventis recentemente terminou a parceria que tinha com a Genta no desenvolvimento do Genasense...ora a Aventis estava a par dos resultados no combate á leucemia quando terminou a parceria, daí que se pergunte se os resultados fossem positivos pq que terminou a parceria?
como referi no incio, não acompanho a Genta pelo que posso não estar em posse de todos os factos, este post apenas é para alertar para o carácter especulativo desde titulo, pelo que os investidores devem ter consciência dos possiveis riscos em que incorrem em investir num titulo como a Genta
-
Visitante
O medicamento julgo que...
está a ser exprementado em doente com lucemia e com uma taxa de secesso de 60%.
Bem hajam por dois motivos, o primeiro dos quias pelos milhões em todo o Mundo que padecem dessa terrivel doença.
Bem hajam por dois motivos, o primeiro dos quias pelos milhões em todo o Mundo que padecem dessa terrivel doença.
-
Visitante
Re: Chiça pra esta GENT(E)A
u2u Escreveu:A Genta deve ser um dos títulos mais malucos que, por acaso, tenho acompanhado (sempre sem entrar) nas últimas semanas. Primeiro, uma queda há duas semanas de 50% num só dia para o mínimo de 1,28. Três dias depois recupera atingindo quase os 2,00.
Segue-se-lhe uma correcção rápida que a leva de novo aos mínimos. Hoje no pré-market está a subir já 61%.
Caramba!
u2u
No Millennium BCP, não tenho acesso a essa cotação.
Pode indicar-me, onde segui-la?
-
Visitante
Re: Se amnhã a FDA...
Anonymous Escreveu:aprovar na reunião o novo medicamento . vão apnhar-la lá pros 7 ou 8 Dolares.
Reforçei mais 2.500 a 2.15
Qual é o novo medicamento ?
Genasense no tratamento de chronic lymphocytic leukemia (CLL) ?
-
Visitante
Se amnhã a FDA...
aprovar na reunião o novo medicamento . vão apnhar-la lá pros 7 ou 8 Dolares.
Reforçei mais 2.500 a 2.15
Reforçei mais 2.500 a 2.15
-
Visitante
UUIIIIII!!!
ainda bem, grande cabeçudo que eu sou, foi reforçar a 1.84 na CNXT com 1.500, e não reforçei as 1.600 que tenho na GNTA a 1.30.
-
Visitante
Chiça pra esta GENT(E)A
A Genta deve ser um dos títulos mais malucos que, por acaso, tenho acompanhado (sempre sem entrar) nas últimas semanas. Primeiro, uma queda há duas semanas de 50% num só dia para o mínimo de 1,28. Três dias depois recupera atingindo quase os 2,00.
Segue-se-lhe uma correcção rápida que a leva de novo aos mínimos. Hoje no pré-market está a subir já 61%.
Caramba!
u2u
Segue-se-lhe uma correcção rápida que a leva de novo aos mínimos. Hoje no pré-market está a subir já 61%.
Caramba!
u2u
- Mensagens: 251
- Registado: 4/11/2002 22:17
- Localização: Lisboa
14 mensagens
|Página 1 de 1
Quem está ligado:
Utilizadores a ver este Fórum: cali010201, Ferreiratrade, Kiko_463, Opcard33, PAULOJOAO, Phil2014 e 120 visitantes