Register for free to join our community of investors and share your ideas. You will also get access to streaming quotes, interactive charts, trades, portfolio, live options flow and more tools.
I also bought into AVEO, I am up to over 30 biotech stock purchases in the past couple of weeks. This is a 4th qtr event for me, Oct thru Jan is always good for the beaten down small cap biotechs....
surf
Buying into some beaten down biotechs over the past couple of weeks, the end year bounce in the sector has begun early this year, in about 30 currently & hopefully can hold until Jan/Feb timeframe....
Could you add IMUC and NWBO please. Thanks
Any way you could add CTIX? Either way, thanks. Interesting page.
VNDA on watch for reversal trade....
RPTP on watch list for purchase...
Biotech still the strongest sector running in the market, hopefully will continue to trend up in the coming weeks/months.
the charts are updating correctly now...............
Got you marked here surf. I'm looking forward to following your board.
Bionovo to Raise $3 Million Through Registered Direct Offering
Press Release Source: Bionovo, Inc. On Friday October 1, 2010, 3:10 pm EDT
EMERYVILLE, Calif., Oct. 1 /PRNewswire-FirstCall/ -- Bionovo, Inc. (Nasdaq:BNVI - News), a drug discovery and development company focused on unmet needs in women's health and oncology, today announced that it has entered into definitive agreements to raise approximately $3.0 million in gross proceeds in a registered direct offering through the sale of common stock and warrants. The Company agreed to sell a total of 2,727,270 shares, at a price of $1.10 per share. In addition, the Company agreed to issue 2,045,451 warrants to purchase shares. The warrants will be exercisable six (6) months after issuance at $1.64 per share and will expire five (5) years from the date of issuance. The shares of common stock and warrants are immediately separable and will be issued separately.
Bionovo estimates that net proceeds from the offering will be approximately $2.8 million, after deducting placement agents' commissions. The Company intends to use the net proceeds from the sale of the securities primarily for general corporate purposes, including clinical trial, research and development, general and administrative and manufacturing expenses.
William Blair & Company, L.L.C. is acting as the exclusive placement agent.
The securities described above are being offered pursuant to a registration statement on Form S-3 previously declared effective by the Securities and Exchange Commission on June 17, 2010. The transaction is expected to close on or about Wednesday, October 6, 2010, subject to customary closing conditions.
A copy of the prospectus supplement relating to the offering and the accompanying base prospectus may be obtained by contacting William Blair & Company, L.L.C. at 222 West Adams, Chicago, Illinois 60606, attention: Equity Capital Markets at 312-236-1600. A copy of the prospectus supplement relating to the offering and the accompanying base prospectus may also be accessed on the SEC website, http://www.sec.gov.
This press release does not constitute an offer to sell or the solicitation of an offer to buy any securities of Bionovo nor shall there be any sale of such securities in any state in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of such state.
8:00AM Sunesis Pharma priced a 44.1 mln unit offering, each unit consisting of one share of its common stock and a warrant to purchase 0.5 of a share of its common stock, at a public offering price of $0.35/unit, for gross proceeds of approximately $15.5 mln (SNSS) 0.42 :
8:31AM Chelsea Therapeutics prices public offering of common stock at $4.90/share (CHTP) 5.36 : Co announces that it has priced a public offering of ~7.14 mln shares of its common stock at a price of $4.90/share which will result in gross proceeds of $35 mln.
Coming Catalysts for Biotech Stocks During October
September was a busy month for the FDA and especially for its advisory committees who met to discuss more than one obesity drug as well as an addiction treatment and an antibiotic. The upcoming month will bring cooler weather and the final decisions on the approvability of some of the drugs discussed by the panels. Biotech investors should keep a close watch on which way the FDA goes with each of these drugs.
October 3
Hospira's (HSP) Dyloject for the treatment of moderate to severe pain, mostly used after operations, will face approval by the FDA. It will be the first non-steroidal anti-inflammatory approved for this purpose in 20 years.
October 4
Human Genome Sciences (HGS) and Novartis (NVS) are expecting a decision on their chronic hepatitis C treatment Zalbin. Don't expect a positive decision on this drug after the FDA expressed concerns about the risk/benefit ratio for the drug at the current dose.
October 11
Alexza Pharmaceuticals (ALXA) is awaiting approval of it schizophrenia drug AZ-004. The drug is an inhaled formulation of the drug loxapine. The Canadian biotech Biovail (BVF) acquired the right to the drug in February and will market it in North America if it gets approved. Analysts believe the drug could have a market of $500 million.
Jazz Pharmaceuticals (JAZZ) will also face an FDA decision on this day for its fibromyalgia drug JZP-6. The drug, with the proposed brand name Rekinla, was scrutinized by the Arthritis and Drug Safety and Risk Management Advisory Committees on August 20 which decided that it was safe and effective. The drug is already approved for the treatment of narcolepsy under the brand name Xyrem. Concerns were raised about the abuse potential for Rekinla because of its close chemical relationship to the date rape drug GHB. (See Jazzing Up a Date Rape Drug)
October 12
Alkermes (ALKS) expects an approval decision for its opioid addiction treatment Vivitrol on this date. The drug is already approved as an injectable treatment for alcohol dependence. In November, the biotech announced positive results of a phase 3 study that showed Vivitrol helped patients stay off opioids. A recent panel of experts recommended approval of the drug for the new indication in mid-September.
October 18
The Cardiovascular and Renal Drugs Advisory Committee will meet to discuss the risks and benefits of erythropoeisis-stimulating agents, which are drugs that stimulate production of red blood cells. The drugs that will be scrutinized include Amgen's (AMGN) Aranesp and Epogen, and Johnson & Johnson's (JNJ) Procrit.
October 21 and October 22
The Anesthetic and Life Support Drugs Advisory and the Drug Safety and Risk Management Advisory Committees will meet to discuss Purdue Pharma's OxyContin pain tablets and King Pharmaceuticals (KG) Embeda, an extended release pain medication.
October 22
Later in the month, Alkermes will face the FDA again, along with Eli Lilly (LLY) and Amylin Pharmaceuticals (AMLN). The companies will be looking for the approval of Bydureon -- the long-acting formulation of their diabetes drug Byetta. The once-weekly injectible was passed over once by the regulatory agency, which wanted more information on the risks of the drug. It will face stiff competition from Novo Nordisk's (NVO) Victoza if it finally gets to market. Victoza has gained 27% of the GLP-1 market since it was approved in January.
Arena's obesity drug will face approval on this day as well. Lorqess, also known as lorcaserin, was panned by an advisory committee in mid-September. The panel was concerned with the moderate efficacy of the drug and had worries over tumors that appeared in rats. Shareholders have brought suit against the company for not properly disclosing this information. The stock has lost 80% of its value since hitting its 52-week high in July.
October 28
The FDA will make its decision on Vivus' Qnexa. An advisory panel to the FDA voted against approval in July. The panel thought that risks surrounding pregnancy and cardiovascular issues were too great to allow the drug to reach the market without more testing. Newer data from a two-year study may help the company gain approval at a later date. Expect the FDA to issue a Complete Response Letter or extend the date of approval.
October 29
Forest Laboratories (FRX) is hoping to gain approval of its antibiotic for the treatment of skin infections (cSSSI) and community-acquired pneumonia (CABP). A panel voted 21 to 0 in favor of approval in early September. The panel decided that the drug looked efficacious without presenting any further safety risks than products already on the market.
The FDA will make an approvable call on Avanir Pharmaceuticals' (AVNR) Zenvia, meant for the treatment of involuntary emotional outbursts related to brain disease. Four years ago, the FDA asked for more information on the drug. The company has since conducted another late-stage trial with a lower dose of the drug. Analysts expect an 80% chance of approval.
October 30
Biodel's (BIOD) injectable diabetes drug Linjeta, formerly known as VIAject, has many investors believing that it can't make it past the FDA this time around, but will likely get approval at a later date. The company can't afford more clinical trials or to commercialize the drug on its own. Eli Lilly and Sanofi-Aventis (SNY) are likely to go after a partnership on the drug. (See Sanofi and Lilly Likely Suitors for Biodel).
http://www.minyanville.com/businessmarkets/articles/lorcaserin-qnexa-linjeta-embeda-oxycontin-diabetes/9/30/2010/id/30332?camp=syndication&medium=portals&from=yahoo
4:01PM Achillion Pharma announces dosing of first patient in Phase II trial of ACH-1625 for the treatment of Hepatitis C (ACHN) 3.02 -0.03 : Co announces that it has initiated patient dosing in a Phase II clinical trial of ACH-1625 for the treatment of hepatitis C virus infection.
Allos Therapeutics ALTH Brean Murray Buy $9
Please no posting to this board, this will be used for a quick reference for charts on a 100 biotech stocks that I follow.
Followers
|
5
|
Posters
|
|
Posts (Today)
|
0
|
Posts (Total)
|
22
|
Created
|
09/23/10
|
Type
|
Free
|
Moderators |
Volume | |
Day Range: | |
Bid Price | |
Ask Price | |
Last Trade Time: |