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Biotech / Medical : Biotech Valuation -- Ignore unavailable to you. Want to Upgrade?


To: Biomaven who wrote (6868)8/8/2002 10:05:22 AM
From: aknahow  Read Replies (1) | Respond to of 52153
 
Easy to agree that such actions by "analyst" are despicable. but, real doctors, and real subjects, company insiders and people working on trials are potentially picking up information without having to deceive anyone.

Would it have been o.k. if the trial was being discussed with a real doctor who had a patient with a real problem? Should not a real doctor with a real potential patient just be referred to a trial center?

An if someone claims they are have the condition for which the trial is being run one would hope that a trial being decently run would quickly detect this. The person and the firm involved could be sued, for civil damages.

My point is that we are all indignant about a deceptive attempt to obtain inside information but far more information is being obtained by special groups all the time and not much is said.

The whole issue of release of conference abstracts illustrates this. Is it any wonder that analyst try to level the playing field?



To: Biomaven who wrote (6868)8/8/2002 10:10:39 AM
From: RCMac  Read Replies (2) | Respond to of 52153
 
Maybe RCMac would like to comment?

A quick comment -- I'm pretty tied up today.

I agree that plainly the SEC could go after these guys if it allocated the resources to do so, and that they probably won't in light of other demands (although they're in the process of increasing staff substantially). Since this is a pretty egregious case -- impersonating a doctor is surely a crime as well as enough of a fraud to invoke the securities laws -- it's at least conceivable SEC might get interested. The e-mail address is enforcement@sec.gov. Now, if a Congressional committee could get interested and hold a hearing . . . ?

At first blush, I'd think private actions under 10b-5 would presumably be available, but not likely to do much. Remember that for a private action, the plaintiff must be a "purchaser" or "seller" damaged by the bad conduct of defendant. This probably limits the potential recovery and complicates the fact pattern enough to make a class action unwieldy (in contrast, say, to purchasers while a false/misleading PR of 10-K is outstanding).

SEC has no such obstacles to its enforcement actions. (Some first amendment issues would crop up, however.)

My favorite bit of the article is this:
Mr. Risk's report on the Neurocrine sleep drug was inaccurate, says Mr. Scott, the clinical-trial-center executive. People familiar with the situation say the patient who was hard to rouse from sleep had tested positive for opiates the same day, and doctors blamed those, not the sleep drug. He was kicked out of the trial for violating its protocol. Neurocrine says the trial continues, and the company hopes to apply for marketing approval from the FDA next year. Its stock, meanwhile, has bounced from a high of about $54 in December to a low of $23.25 in June and the current level of $37.14.

Mr. Risk says he didn't know the patient had tested positive for opiates or that doctors weren't blaming the Neurocrine drug. He didn't check with Neurocrine before putting out the report, the 25-year-old analyst says, adding that he doesn't believe it's essential to call companies before attacking or lauding their products. "I'm young and inexperienced and not afraid to be wrong," he says.

'Risky'

Mr. Risk, who calls himself "Risky," basks in the results of his work. "The portfolio managers said we scared the Street," he says. "Creativity knows no bounds with us. We're tracking down the truth."

Steven Kirsch, head of Sterling's research division, says there's no legal obligation to call biotech companies for comment


In other words the little b*****d doesn't care whether he gets the story right, nor does his boss.

--RCM



To: Biomaven who wrote (6868)8/12/2002 11:39:33 AM
From: Vector1  Read Replies (2) | Respond to of 52153
 
Biomaven, CRXA announced a private placement today at what looks like market plus 15% warrant coverage for 12.5c a warrant share. A good deal in this environment. Good group of investors as well. An excerpt from the press release follows:

Under the terms of the agreement, Corixa has agreed to sell approximately 7.3 million shares at a price of $6.13 per share. For an additional $.125 per underlying share, the investors will also purchase approximately 1.2 million five-year warrants for common stock with an exercise price of $6.13. Corixa intends to use the net proceeds from the sale for research and development, working capital and general corporate purposes.

The financing was led by InterWest Partners, and included investments from BankAmerica Ventures, Frazier Healthcare Ventures, Hambrecht & Quist Capital Management, LLC, KBL Healthcare Ventures, Oxford Bioscience Partners, and Sutter Hill Ventures. Pacific Growth Equities, Inc. acted as the placement agency for this transaction.



To: Biomaven who wrote (6868)8/20/2002 2:11:31 AM
From: Doc Bones  Read Replies (1) | Respond to of 52153
 
NASD Probes a Biotech Analyst Who Tried to Get in Drug Trial

Public guardians at NASDAQ embarrassed into investigating "Risky" and "Dr. Rosen." - Doc

By RANDALL SMITH and GEETA ANAND
Staff Reporters of THE WALL STREET JOURNAL

For months, securities regulators have been investigating allegations that bullish Wall Street stock analysts didn't go far enough to find out the true financial picture of companies they followed.

Now, regulators are examining whether one bearish analyst went too far.

The National Association of Securities Dealers has launched an investigation into efforts by a securities analyst at Sterling Financial Investment Group in Florida to enroll himself in a clinical drug trial, in an apparent attempt to glean information about the trial's progress and the drug's side effects, said Sterling executives and the trial's manager.

Such activity could be considered insider trading if the research analyst misappropriated clinical-trial information or obtained it under false pretenses, then traded on it or passed it along to someone who did, securities lawyers say. The information would have to be material, meaning substantial enough to influence the stock price, they add. Sterling has denied wrongdoing, but said it will take action as appropriate; the NASD declined to comment on the probe.

On Monday, Sterling suspended the analyst, David Risk, for 90 days and fined him $25,000, after learning that he had signed additional forms to participate in the trial that he hadn't told Sterling about previously. Mr. Risk couldn't be reached to comment.

In a separate development, another stock analyst, Jonathan Aschoff, was let go by Friedman, Billings, Ramsey Group Inc., an Arlington, Va., securities firm, after posing as a doctor in his own effort to glean information about a different trial. In a statement, the firm attributed the action to Mr. Aschoff's "failure to follow firm policy related to the conduct of research analysts." Mr. Aschoff couldn't be reached to comment.

In the Sterling inquiry, being conducted by the NASD's regulatory arm, investigators interviewed David Scott, vice president of the Palm Beach Research Center, and other employees of the center over a two-day period last week, according to Mr. Scott. NASD regulatory officials also told Sterling executives of the probe last week, said Sterling Chief Executive Charles P. Garcia.

As reported in a page-one article Aug. 8 in The Wall Street Journal, Sterling's Mr. Risk signed up as an insomnia sufferer in February as a first step to enrolling in a trial of a sleep drug being conducted for Neurocrine Biosciences Inc. Although Mr. Risk never actually took the drug, he did publish a research report five days later recommending the sale of Neurocrine stock, citing a side effect he learned of during the registration process. The stock later fell about 34%.

Sterling said Mr. Risk wasn't available to comment. In an interview in the spring, Mr. Risk defended his actions and said he did nothing wrong. The 25-year-old analyst said at the time that he didn't check with Neurocrine before putting out the report, adding that he didn't believe it was essential to call companies before attacking or lauding their products. "I'm young and inexperienced and not afraid to be wrong," he said.

The NASD probe shows the eagerness of regulators these days to crack down on possible instances of analyst misconduct in a broader effort to restore investor confidence. In the past year, a series of scandals -- involving misleading accounting, analysts' rosy research that was conflicted by investment-banking considerations, and misconduct in handing out hot IPOs -- has roiled the markets. Just last month, the NASD unveiled a series of measures aimed at securities firms that improperly hand out hot initial public offerings of stock in exchange for kickbacks from investors in the form of oversize commissions or promises of future business from corporate clients.

"In today's climate, regulators are going to be much quicker on the draw to respond to this type of behavior," said Michael McAlevey, a former deputy director of corporate finance at the Securities and Exchange Commission who now practices law at the firm of Alston & Bird LLP in Washington.


Regulators generally want to balance the need for analysts to behave ethically with the importance of "creating incentives for analysts to be industrious and inquisitive in trying to root out information," Mr. McAlevey added. In the current environment, he said, regulators may give priority to "the perception of unethical behavior."

In an interview Monday, Mr. Garcia said NASD officials "told us they are conducting a very narrow investigation to find out if some of the allegations are true or not." He defended Mr. Risk's actions, saying that although he does suffer from insomnia, he didn't actually intend to enter the trial, but was merely "getting as much information on the drug" as possible. Sterling, he added, prides itself on offering no-nonsense research without the kind of investment-banking conflicts prevalent among major firms that also serve as securities underwriters.

However, Mr. Scott, the clinical-trials executive, asserted that Mr. Risk signed a separate agreement promising "not to divulge any and all treatment information concerning patients or families participating" in trials being conducted by the Palm Beach Research Center. What's more, he said, Mr. Risk gave his occupation as "student" in a patient data form.

Asked for comment on Mr. Scott's allegations, Sterling said Mr. Risk had been suspended after he acknowledged signing additional agreements, which he hadn't previously disclosed to Sterling executives. A Sterling spokesman said the firm was cooperating with the NASD probe.

Meanwhile, Friedman Billings's Mr. Aschoff posed as a "Doctor Rosen" in calling Casey Cunningham, who runs clinical trials of a cancer drug for Genta Inc. Mr. Aschoff said he had a leukemia patient interested in enrolling in the Genta drug trial, but when Dr. Cunningham realized the purported subterfuge, he chastised the analyst for what he considered unethical behavior.

In a July interview, Mr. Aschoff defended his actions. "Companies are saying to investors, 'Give me your money.' Are you going to give it to idiots who go off unchecked? I'm trying to bring the truth to investors." He acknowledged at the time lying about being a doctor, but said it was for the greater good of unearthing the truth.

In explaining Mr. Aschoff's termination, Friedman Billings said the firm "holds its employees to the highest standards of ethical and professional conduct. Deviations from these standards will not be tolerated. Improper behavior will be met with prompt disciplinary action." The firm's disclosure reflecting Mr. Aschoff's termination indicated there wasn't any regulatory probe of his actions.

Write to Randall Smith at randall.smith@wsj.com and Geeta Anand at geeta.anand@wsj.com

Updated August 20, 2002

online.wsj.com