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[放炮] 再乱讲讲明天可以投机的几只股票(6 MAY,2009)

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发表于 2009-5-5 03:56 PM | 显示全部楼层 |阅读模式


首先声明下,俺说的是投机不是投资,投机就是看准就出手,资金流动快,一般2-3天就要换个追踪的目标,涨到了自己的心理价位就走人。
所以对于打算长期捏着股票的人来讲,可以忽略以下俺写的这些。

MNI,这只垃圾俺已经捏了2周了,NYT这只同类但适合投资的股票早于它一周前就开始骚动了,它今天才开骚,让俺对它有了点成见,但俺看好它明天会继续冲,今天是第一天,远远没涨够,明天同志们可以追踪下,俺觉得也该MEDIA 板块涨涨了。
CTIC俺捏了也快2周,俺对BIOTECH的忍耐极限就是2周,再不动俺就抛弃,好在它算争气今天终于也骚了一把,估计明天还会继续骚。另外几只垃圾BIOTECH还没骚,但我想快了,SOMX, HEPH,OSCI有兴趣的也可以追踪下,投机到了就要恭喜你了
HW是只基本面非常不错的个股,俺看好它会很短时间内翻番
BEE,是个狠贱的股票,1个月前和RIV都是8毛的时候它就那么贱,人家RIV1块半的时候它还是8毛,现在人家都2块多了,它才扭扭捏捏的出场,对于BEE捏长期会有更好的收获,对于喜欢资金流动快的人,这只不是特别好的投机选择,不过以它的贱性,俺觉得它肯定会连续跳空高开几天,是在UP TRAEND里,估计2.5-3块是很快实现的,因为它本性狠贱,所以希望它在一天之内速成基本是做梦。
GCFB这个连锁的高档餐馆的股票俺就不说了,1毛8就不属于它的价格,所以昨天开始飙ON NEWS,今天继续前进了一步,明天。。当然。。。
还想再说说VNDA,这只BIOTECH,明天FDA会给RESULTS,俺不看好它,所以没有进它,但如果明天它的结果很差估计会恐慌性抛售,就跟NFLD那天到1毛一样,机会实在难得,所以,如果有兴趣BUY DIP的,明天把它稍上。

就先这么多吧,还有些风险更大回报也许会更高的,俺就不说了,本来是好心怕误导他人让人赔了钱,这个罪过就大了

写这个帖子目的就是希望最近亏了钱的熊熊们换个思维角度,别老盯着大盘走,管它大盘怎么走,跟着个股的UP TRENDS走才是正理。

希望大家都能赚到钱,另外HAPPY TRADING TOMORROW.
发表于 2009-5-5 04:07 PM | 显示全部楼层
研究下。
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发表于 2009-5-5 04:08 PM | 显示全部楼层
  "跟着个股的UP TRENDS走才是正理。"
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发表于 2009-5-5 04:23 PM | 显示全部楼层
谢谢,去研究一下。
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发表于 2009-5-5 04:23 PM | 显示全部楼层
顶,喜欢xxtrader炒股风格!
ctic跟着吃了60%
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发表于 2009-5-5 04:26 PM | 显示全部楼层
谢谢!
CTIC明天续涨的几率超过60%吗? 我是只小蝌蚪。
明天是否会有个asco data presentation, 对CTIC会有什么影响。
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发表于 2009-5-5 04:27 PM | 显示全部楼层
真对俺胃口,俺最喜欢偷鸡
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发表于 2009-5-5 04:37 PM | 显示全部楼层
好,赞,谢
明天看看能不能偷到鸡
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 楼主| 发表于 2009-5-5 04:56 PM | 显示全部楼层
谢谢!
CTIC明天续涨的几率超过60%吗? 我是只小蝌蚪。
明天是否会有个asco data presentation, 对CTIC会有什么影响。
xzanw 发表于 2009-5-5 17:26


其实CTIC今天涨俺猜是因为前天SPPI的INSIDER在买,SPPI跟CTIC的关系说来话长你去GOOGLE一下
SPPI的INSIDER为甚么会买,俺觉得是因为这个
Meeting of the Cellular, Tissue and Gene Therapies Advisory Committee (May 14-15)‏
发件人:  U.S. Food & Drug Administration (FDA) (fda@service.govdelivery.com)  
发送时间: 2009年5月5日 13:06:42
一般来说会议前,凡是CELLULAR, TISSUE,和GENE的股票都会飙一下。
所以俺还看好SOMX,HEPH,OSCI,也该快飙了,特别是SOMX,HEPH,我看它们憋的我都狠难受。。。
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 楼主| 发表于 2009-5-5 05:10 PM | 显示全部楼层
谢谢!
CTIC明天续涨的几率超过60%吗? 我是只小蝌蚪。
明天是否会有个asco data presentation, 对CTIC会有什么影响。
xzanw 发表于 2009-5-5 17:26

还有你说的ASCO会对CTIC,DNDN这类治疗CANCER和肿瘤的药物股票绝对的有影响。
但好象不是明天8,最早的一个MEETING是ASCO’s 45th Annual Meeting will take place as planned May 29 – June 2, 2009 in Orlando, Florida.
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发表于 2009-5-5 05:11 PM | 显示全部楼层
看看
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发表于 2009-5-5 05:22 PM | 显示全部楼层
很有用的信息。
这个asco data presentation只是听说来的, 我自己还没有研究过。 所以日期也不确定。
我比较倾向就盯1个领域的1只领涨股,照你的信息来看, CTIC明天继续涨的可能还是很大是吗。
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 楼主| 发表于 2009-5-5 05:28 PM | 显示全部楼层
很有用的信息。
这个asco data presentation只是听说来的, 我自己还没有研究过。 所以日期也不确定。
我比较倾向就盯1个领域的1只领涨股,照你的信息来看, CTIC明天继续涨的可能还是很大是吗。
xzanw 发表于 2009-5-5 18:22

恩,俺觉得按照它以前飙的高度,这波至少9毛应该到一下的。能不能再高,就要看投机它的M M决心和耐心有多大了
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发表于 2009-5-5 05:36 PM | 显示全部楼层
Thanks for sharing!
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发表于 2009-5-5 06:13 PM | 显示全部楼层
1# xxtrader
多谢多谢!小弟开始研究一下BioTech.
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发表于 2009-5-5 07:18 PM | 显示全部楼层
首先声明下,俺说的是投机不是投资,投机就是看准就出手,资金流动快,一般2-3天就要换个追踪的目标,涨到了自己的心理价位就走人。
所以对于打算长期捏着股票的人来讲,可以忽略以下俺写的这些。

MNI,这只垃圾 ...
xxtrader 发表于 2009-5-5 04:56 PM

好帖!
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发表于 2009-5-5 07:34 PM | 显示全部楼层
看见了好几个熟悉的身影....多谢....
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发表于 2009-5-5 08:12 PM | 显示全部楼层
赞一个!

俺也拿着CTIC 2礼拜了,马马虎虎, 哈哈。
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发表于 2009-5-5 08:30 PM | 显示全部楼层
受益非浅,顶!
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发表于 2009-5-5 09:25 PM | 显示全部楼层
“其实CTIC今天涨俺猜是因为前天SPPI的INSIDER在买,SPPI跟CTIC的关系说来话长你去GOOGLE一下
SPPI的INSIDER为甚么会买,俺觉得是因为这个
Meeting of the Cellular, Tissue and Gene Therapies Advisory Committee (May 14-15)‏
发件人:  U.S. Food & Drug Administration (FDA) (fda@service.govdelivery.com)  
发送时间: 2009年5月5日 13:06:42
一般来说会议前,凡是CELLULAR, TISSUE,和GENE的股票都会飙一下。
所以俺还看好SOMX,HEPH,OSCI,也该快飙了,特别是SOMX,HEPH,我看它们憋的我都狠难受。。。”

俺觉得ctic今天彪的原因不是这个。
早盘就开始彪了,甚至在凌晨4点后就已经5毛几了

Pixantrone Now Available in Europe on a Named-Patient Basis
1:30a ET May 5, 2009 (PR NewsWire)
Cell Therapeutics, Inc. (CTI) (Nasdaq and MTA: CTIC) today announced that pixantrone is now available on a named-patient basis in Europe. Pixantrone will be supplied by IDIS to healthcare professionals for the treatment of individual patients with aggressive non-Hodgkin's lymphoma (NHL) that has either relapsed after standard therapies or is refractory to them. We know of no therapy that has previously been shown to be effective treatment for such patients.

"CTI has worked hard to make pixantrone available in Europe at the prescriber's request as it provides an option for these difficult to treat aggressive NHL patients," noted Craig Philips, President of CTI. "We continue to work toward potential approval of pixantrone at the end of 2009 in the United States and expect to complete the submission of the New Drug Application to the Food & Drug Administration this quarter."

"Our experience with pixantrone has been positive with patients achieving a complete response where such a result was not achievable with other treatments," said Prof. Pier Luigi Zinzani, M.D., Institute of Hematology and Oncology, University of Bologna. "I am pleased that it is now available on a named-patient basis as it has the potential to address a significant unmet need in this heavily pretreated patient population."

A named-patient program is a compassionate use drug supply program under which physicians can legally supply investigational drugs to qualifying patients. Under a named-patient program, investigational drugs can be administered to patients who are suffering from serious illnesses prior to the drug being approved by the European Medicines Evaluation Agency. "Named-patient" distribution refers to the distribution or sale of a product to a specific healthcare professional for the treatment of an individual patient. In Europe, under the named-patient program the drug is most often purchased through the national health system.

Contact Information for Program:

Licensed healthcare professionals in Europe treating individual patients with relapsing or refractory aggressive non-Hodgkin's lymphoma interested in pixantrone should contact:

IDIS Limited Tel: +44 (0) 1932 824 123 Fax: +44 (0) 1932 824 323 Email: internationalsales@idispharma.com Additionally, more information can be found at http://www.celltherapeutics.com/pixantrone_europe   

About Pixantrone

Pixantrone (BBR 2778), is a novel major groove binder with an aza-anthracenedione molecular structure that differentiates it from the anthracyclines and other related chemotherapy agents. Anthracyclines are the cornerstone therapeutic for the treatment of lymphoma, leukemia, and breast cancer. Although they are sufficiently effective to be used as first-line (initial) treatment, they cause cumulative heart damage that may result in congestive heart failure many years later. As a result, there is a lifetime limit of anthracycline doses and most patients who previously have been treated with an anthracycline are not able to receive further anthracycline treatment if their disease returns. Pixantrone has been designed to reduce the potential for these severe cardiotoxicities without sacrificing anti-cancer activity. It also can be administered through a peripheral vein rather than a central implanted catheter as required for other drugs in this class.

About IDIS

IDIS is the world leader in the development and implementation of named-patient programs and has a proven track record of working in strategic partnership with US-based companies to bring new drugs to Europe for the first time. IDIS supports customers in over 100 countries, supplying more than 400 different medicines per month and responding to more than half a million requests on a named-patient basis to medical professionals worldwide. For more information on IDIS please visit their website at http://www.idispharma.com.

About Cell Therapeutics, Inc.

Headquartered in Seattle, CTI is a biopharmaceutical company committed to developing an integrated portfolio of oncology products aimed at making cancer more treatable. For additional information, please visit www.celltherapeutics.com.

This press release includes forward-looking statements that involve a number of risks and uncertainties, the outcome of which could materially and/or adversely affect actual future results. Specifically, the risks and uncertainties that could affect the development of pixantrone include risks associated with preclinical and clinical developments in the biopharmaceutical industry in general and with pixantrone in particular including, without limitation, the results of complete safety information, the failure to receive anticipated number of requests for pixantrone to treat specific patients, the potential failure of pixantrone to prove safe and effective for treatment of relapsed aggressive NHL as determined by the FDA, the possibility that the New Drug Application submission will not be completed in the second quarter of 2009, that priority review will not be granted by the FDA and that a decision by the FDA is not rendered in late 2009, the company's ability to continue to raise capital as needed to fund its operations, competitive factors, technological developments, costs of developing, producing and selling pixantrone, and the risk factors listed or described from time to time in the Company's filings with the Securities and Exchange Commission including, without limitation, the Company's most recent filings on Forms 10-K, 8-K, and 10-Q. Except as may be required by law, CTI does not intend to update or alter its forward-looking statements whether as a result of new information, future events, or otherwise.
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