Archive for the ‘Health Care Stocks’ Category

Akorn, Inc. (AKRX) – Buzz Stock of the Day

Tuesday, May 4th, 2010

Shares of generic drug developer, Akorn, Inc. (Nasdaq: AKRX) began their climb in after-hours trading yesterday after the company announced it swung to a profit in the first quarter.

The Buffalo Grove, Ill.-based company reported a net income of $3.5 million, or 4 cents a share, compared with a net loss of $10.7 million, or 12 cents a share a year ago. Consolidated revenue for the quarter dipped 7 percent to $20.5 million, due to winding down of the company’s vaccine business segment. Revenue from its core business, consisting of ophthalmic, hospital drugs & injectables and contract services, rose 36 percent to $15.4 million.
[–quote–]
Other highlights in the quarter included operating income of $1.8 million, EBITDA of $3.9 million, improved gross margins to 41 percent, and positive cash flow of $2 million.

“We are off to a solid start for the year,” said Interim CEO, Raj Rai in a statement. “Our strategy to focus on the core business and on operating efficiencies has translated into favorable results. In addition, we are experiencing strong demand for Akorn products as well as for our third-party contract manufacturing business.”

Raptor Pharmaceutical Corp (RPTP) — Buzz Stock of the Day

Monday, May 3rd, 2010

Shares of drug developer, Raptor Pharmaceutical Corp. (Nasdaq: RPTP) were up as much as 58 percent from Friday’s close, in morning trading today after the company announced that a mid-stage study of its liver disease drug met its main goal.


The mid-stage study had 11 adolescent patients with non-alcoholic steatohepatitis, who were given oral doses of up to 1,000 mg of Raptor’s drug twice daily for six months, followed by a six-month post-treatment monitoring period.

The patients had at least twice normal levels of two liver enzymes that are often associated with a presence of liver problems. The patients showed a decline in the level of one enzyme — alanine transaminase (ALT) — during the treatment period, with seven of 11 patients achieving a greater than 50 percent reduction, and in six of 11, the enzyme reduced to within normal range.

Levels of the second enzyme, aspartate aminotransferase (AST), also saw significant improvements with patients seeing 41 percent reduction by the end of the treatment phase.

Raptor is also developing its drug, DR Cysteamine, for genetic disorders like cystinosis and Huntington’s disease.

C.K. Cooper and Co’s Jeffrey Cohen, who is the sole analyst covering Raptor, said Monday’s news does not change his “hold” rating on the stock.

“The net-present value of the pipeline is about $2.88,” Cohen said.

Synergetics USA (SURG) – Buzz Stock of the Day

Wednesday, April 28th, 2010

Shares of medical device maker Synergetics USA, Inc. (Nasdaq: SURG) were up as much as 72 percent today after the company said Alcon Laboratories Inc (ACL.N) agreed to pay $32 million for the right to sell some of Synergetics’ products worldwide and to settle all pending litigation between the two companies.


Earlier this month, Synergetics announced a strategic agreement with Stryker Corporation. The agreement includes the sale of Synergetics’ accounts receivable, open sales orders, inventory and certain intellectual property related to the Omni® product line. In addition, the agreement provides for Synergetics to supply disposable ultrasonic instrument tips and certain other consumable products used in conjunction with the Sonopet/Omni® ultrasonic aspirator console and handpieces; and pursue certain development projects for new products associated with Stryker’s intraoperative ultrasound products.

Synergetics will receive between $2.5 million and $3.0 million in proceeds from the transactions once all inventory transfers are completed.

For the quarter ended Jan. 31, Synergetics profit more than doubled to $877,000, or 4 cents per share, from $389,000, or 2 cents per share, in the same period a year earlier. Second quarter revenue slipped to $13 million from $13.7 million due to lower sales neurosurgical products

The company reduced its sales and marketing costs by about $900,000, and trimmed its general and administrative and research and development spending.

Shares of Synergetics have been up as much as 139 percent over the past three months.



Cardiovascular Systems, Inc. (Nasdaq: CSII) Buzz Stock of the Day

Tuesday, November 10th, 2009


Shares of Cardiovascular Systems, Inc (CSI) have been steadily rising in the week following the Company’s announcement of promising financials for the first quarter fiscal 2010 ended September 30, 2009.

CSI increased revenue 30 percent in the first quarter of fiscal 2010, to $15.2 million compared to revenue of $11.6 million for the same quarter of the previous year. Likewise, CSI’s net loss improved 55 percent to $(6.2) million, or $(0.43) per basic and diluted share, in the first quarter of fiscal 2010, from $(13.7) million, or $(2.75) per basic and diluted share, for the same quarter 2009.

David L. Martin, CSI president and chief executive officer, said, “Balancing revenue growth with effective expense management helped drive a substantial reduction in our loss from the fiscal 2009 first quarter, moving CSI toward our goal of profitability.”

The number of weighted average common shares outstanding increased to 14.5 million from 5.0 million in the first quarter of fiscal 2009, primarily due to new shares issued in conjunction with the February 2009 reverse merger with Replidyne, Inc., including the conversion of all preferred stock of the company to common stock.

Additionally, the fiscal first-quarter 2010 gross margin increased to 77 percent from 67 percent in the same period last year, driven by higher disposable volumes, manufacturing efficiencies, product cost reductions and shipment of fewer controller units. Operating expenses decreased 18 percent, due to effective expense management, the year-earlier write-off of $1.7 million in IPO costs, and completion and timing of development projects and clinical studies.

Adjusted EBITDA, calculated as loss from operations, less depreciation and amortization and stock-based compensation expense, improved by 70 percent to a loss of $(3.6) million versus a loss of $(11.8) million in the year-ago period. Cash and cash equivalents remained strong at $30.8 million and included $3.0 million of net funding received in conjunction with signing an agreement to establish a second production facility in Pearland, Texas.

Martin continued, “During the quarter, we focused on driving adoption in existing accounts, including re-educating physicians on proper clinical protocols for using the Diamondback 360° to change lesion compliance in vessels above the knee. As a result, we are seeing greater product usage in many accounts. These improvements were offset by seasonal weakness in endovascular procedures, resulting in revenue slightly below our expected range.”

The number of hospitals using the Diamondback 360® PAD System rose to 611 by the end of the fiscal 2010 first quarter, a nearly 90-percent increase over a year ago and 55 more than the end of the fourth quarter of fiscal 2009. Sales of disposable device units totaled 4,541 units in the first quarter of fiscal 2010 versus 3,636 units in the first quarter of last fiscal year, a 25-percent increase. Revenue generated from customer reorders continued to grow, increasing to 92 percent of total revenue for the fiscal 2010 first quarter from 72 percent in last year’s first quarter.

Human Genome Sciences, Inc. (Nasdaq: HGSI) Buzz Stock of the Day

Monday, November 2nd, 2009

Human Genome Sciences, Inc. (Nasdaq: HGSI) shares rallied to a 52-week high of $26.21, and added $1 billion to its market value after the company announced favorable results from the second phase of clinical trials for its lupus treatment, Benlysta on Monday.

Rockville, Maryland-based Human Genome said it expects to file its marketing application for Benlysta, early next year, and could have the drug on the market by the end of 2010. If approved, Benlysta will be the first new lupus treatment on the market in more than 50 years.

“The lupus community has waited for decades for one, positive phase III trial of an investigative drug developed for lupus,” said Dr. Joan T. Merrill, a lupus expert at the Oklahoma Medical Research Foundation and an investigator in the trial, in a statement issued by Human Genome Sciences and its development partner, GlaxoSmithKline. “Now we have two.”

Data from a composite of three measures in the latest trial showed that after 52 weeks, 43.2 percent of patients taking 10 milligrams of Benlysta in combination with standard therapies achieved an improvement in symptoms, with no significant worsening of the disease in individual organs.

Only 33.8 percent of patients receiving the placebo and standard care had noticeable improvement. Serious side effects were reported in 26.8 percent of patients taking Benlysta, compared with 24 percent of patients taking a placebo.

Lupus, which affects approximately 5 million people worldwide, is an autoimmune disorder in which the body’s own defense system against pathogens turns on the body and begins attacking healthy tissues. The symptoms can include, but are not limited to, rashes, arthritis, mouth sores, and kidney damage. Historically, it has been difficult to demonstrate in clinical trials the effectiveness of potential lupus drug candidates as the symptoms vary greatly from one individual to another.

Benlysta, which is known generically as belimumab is given once a month by IV infusion, and works by blocking a protein that stimulates B cells that are produced by the immune system. Human Genome, a trailblazer in studying genomics, first discovered the gene for that protein. The discovery would make Benlysta one of the first drugs to arise from genomics, if the drug is approved.

The company has not yet nailed down a price for the drug, but biologic drugs that treat rheumatoid arthritis and multiple sclerosis, which are also autoimmune disorders, range between $15,000 and $30,000 per patient per year, according to Barry Labinger, Human Genome’s chief commercial officer.

Shares of Human Genome Sciences, which traded at $3.32 the day before the positive first trial data was announced in July, closed the following day at $18.69 per share.

Analysts expect the drug to generate annual sales of at least $1 billion and potentially much more. Human Genome will split profits from the drug with its larger partner, GlaxoSmithKline Plc (NYSE: GSK).