Archive for August, 2009

Oculus Innovative Sciences (OCLS)—Buzz Stock of the Day

Tuesday, August 18th, 2009

Shares of Oculus Innovatie Sciences (NASDAQ: OCLS) were up as much as 21 percent from the previous day’s closing price on Tuesday after the company announced the commercial launch of its wound care product in the United States.

The Petaluma-based company’s Microcyn® wound care gel, which received FDA 510(k) clearance in May of this year, has demonstrated rapid activity against a broad spectrum of infections and has also demonstrated wound healing in chronic and acute wounds in clinical investigational studies. It has been commercialized outside of the United States for the treatment of infected wounds.

“We’re excited to make these products commercially available so quickly after receiving our FDA clearance in May,” said Oculus founder and CEO, Hoji Alimi in a statement. “As well, we are also sampling our new Microcyn hydrogel formulations to U.S. physicians and are preparing to initiate a study of this proprietary hydrogel against other wound gels. We believe this data will provide the evidence necessary for a successful hard launch of the product into the medical community in early 2010.”

The onslaught of the swine flu epidemic in Mexico bolstered first quarter unit sales of the company’s 240-milliliter bottles of the Microcyn hydrogel, which was sold mostly to pharmacies in Mexico.

First quarter unit sales increased 100 percent over the prior year to a monthly average of 57,000 units, up from 35,000 in the fourth quarter of fiscal 2009, and 28,000 in the same quarter last year. Unit sales to hospitals increased 101 percent, partially offset by lower selling prices. Normal unit sales of the 240 mL bottles in the first quarter represent about 38,000 to 40,000 units per month, while the units over that reflect one-time purchases related to the swine flu concerns during the quarter.

Oculus cut its first quarter net loss to $3.5 million, or $0.18 per share, from a net loss of $5.2 million, or $0.33 per share reported in the same period last year. Total revenue for the quarter was $1.8 million, up 52 percent from $1.2 million last year. A 56 percent increase in product revenue, a 37 percent increase in service revenue, and a 40 percent reduction in operating expenses were a few highlights of the quarter over the same period last year.

“In our last earnings call, we provided guidance regarding two objectives to achieve cash breakeven by March 2010 and to achieve annual revenue of $45-to-$60 million by fiscal year 2013 with operating profitability of 20 percent,” said Alimi. “We are reconfirming these targets.”

Oculus is currently sampling the new professional Microcyn Skin & Wound HydroGel formulation to U.S. medical professionals. The OTC version of the HydroGel product will be available to consumers beginning October 2009.

Oculus Innovative Sciences, Inc. was first featured as a Buzz Stock of the Day in late May, when the company received marketing clearance from the FDA for Microcyn. Shares spiked from $1.80 to $4.49 that day..

GreenHunter Energy Inc. (GRH) – Buzz Stock of the Day

Friday, August 14th, 2009

Shares of GreenHunter Energy, Inc.(NYSE amex: GRH) climbed more than 75 percent in morning trading Friday after the company reported improved second quarter results.

Including one-time items, GreenHunter reported earnings of $4.45 million, or $0.13 per-share on revenue of $1.7 million, compared to a net loss of $7.3 million in the same period a year ago. Excluding items, the company’s second quarter

“Our ability to negotiate the final settlement of substantial insurance claims as well as sell and monetize certain non-core assets has to-date provided sufficient working capital to keep our Company viable,” said GreenHunter’s chairman, president and CEO, Gary Evans.

For the six months ended June 30, 2009, GreenHunter reported a net loss of $4.3 million, or $0.20 per share, compared to a net loss of $15.6 million, or $0.79 per share for the six months ended June 30, 2008.

“Our Company has been in survival mode since late last year after the hurricane strike on our largest asset, our Houston biodiesel refinery, and the subsequent collapse of the financial markets,” Evans said in a statement.

The past 12 months have been turbulent for the Texas-based energy company. Last September, Hurricane Ike destroyed the company’s largest biodiesel refinery less than 60-days after it initiated operations. Falling fossil fuel prices have also weighed on the company’s revenue growth from the sales of its biodiesel products.

Despite the difficult market climate and recent setbacks, Evans was optimistic about GreenHunter’s current game plan and market opportunities. “We feel that we are methodically working through our very tight capital issues with a specific game plan that should allow for future opportunities within the renewable space,” he said.

GreenHunter Energy, Inc. works on wind, hydropower, geothermal solar and other renewable energy projects. It has the nation’s largest biodiesel refinery in Houston and a biomass-fired power plant in Brawley, Calif.

Advocat, Inc. (AVCA) – Buzz Stock of the Day

Thursday, August 13th, 2009

Shares of healthcare facilities operator, Advocat, Inc.(NASDAQ: AVCA) surged nearly 17 percent in morning trading Thursday, after the company released second quarter earnings that beat analysts’ estimates.

The Tennessee-based company reported earnings of $937,000, or $0.15 per share, compared to $709,000, or $0.11 per-share for the same period a year ago. Revenue increased 7.3 percent to $76.1 million compared to a year ago.

Analysts had expected per share earnings of $0.14.

Highlights from the quarter included an increase of more than 75 percent in funds provided by operations, from $2.7 million in 2008 to $4.8 million in the second quarter of 2009. Facility also occupancy increased to 76.6 percent, from 74.7 percent in the same quarter last Advocat’s board also approved the payment of a $0.05 per share dividend commencing with the quarter ended June 30, 2009.

“We continue to record excellent comparable and sequential quarterly results in a difficult economy,” said Chief Executive Officer, William Council. “One of our most important measurements is funds provided from operations which were $4.8 million, a 75 percent increase over the 2008 comparable quarter.”

Seven of the company’s long-term nursing facilities recently received national recognition at the 2009 National Quality Awards by the American Healthcare Association (AHCA). AHCA looks at facilities that demonstrate at least a three-year track record of quality care, staff and residents’ satisfaction, and regulatory compliance.
With these awards, 37 of our 50 facilities have won National Quality Awards, with three winning Step II awards,” said Council. “We are very proud of the employees of these facilities for their commitment to quality performance.”

Advocat provides long term care services to patients in 50 skilled nursing centers, primarily in the Southeast and Southwest. It offers various non-institutional and institutional services, which include skilled nursing, ancillary health care services, and assisted living to the elderly, as well as rehabilitative, nutritional, respiratory, and other specialized ancillary services.

ADC Telecommunications (ADCT) – Buzz Stock of the Day

Wednesday, August 12th, 2009

Shares of network equipment maker ADC Telecommunications (NASDAQ: ADCT) jumped nearly 25 percent in morning trading on Wednesday after the company raised its earnings forecast for the July quarter and said it plans to cut more costs by expanding its global restructuring.

ADC said it expects third-quarter per-share earnings of between $0.05 and $0.10 on revenue of around $280 million, which is higher than the company’s previously forecasted range of a loss of $0.04 per share and earnings of $0.04 cents a share, on revenue in the range of $265 million and $290 million.

“Today’s announcement is a reflection of our ongoing strategic commitment to managing through the global recession, taking actions to transform our business and strengthening our competitive position,” Chief Executive Robert E. Switz said in a statement.

The better-than-previously expected projections were largely due to reducing the company’s workforce by 400 jobs, compared to the 100-130 layoffs originally stated. In June, ADC announced plans to cut jobs in Europe, the Middle East and Africa. On Wednesday, the company said it has increased the downsizing to include the United States, Latin America and Asia.

The new total represents about 4 percent of ADC’s total workforce, and is part of a company-wide restructuring plan that will cost the company between $24 million and $34 million.

The company, which has been hit hard by the recession, suffered a loss of $0.11 per share for the quarter ending May 1, compared to earnings of $0.14 per share for the same quarter last year.

ADC said in a statement that the efforts made over the past year to realign business operations are expected to continue improving the Minnesota-based company’s near term financial performance as well as increase long-term earnings potential.

Avanir Pharmaceuticals, Inc. (AVNR) – Buzz Stock of the Day

Tuesday, August 11th, 2009

Shares of Avanir Pharmaceuticals, Inc. (NASDAQ: AVNR) were up nearly 80 percent on Tuesday morning, after the drug maker announced positive results from a late-stage clinical trial of the company’s neurological disorder drug, Zenvia.

Zenvia reduced emotional outbursts by 47.2 percent, compared with placebo in the study. That topped the study’s goal, of demonstrating a 36 percent reduction. Both Zenvia 30/10 mg and 20/10 mg provided a statistically significant reduction in the number of emotional outbursts when compared to placebo. Further analysis of the initial endpoint, at week twelve, patients in the Zenvia 30/10 mg group reported a statistically significant mean reduction of 88% from baseline in PBA episode rates. Additionally, patients involved with the study found Zenvia generally safe and well tolerated.

Zenvia is used to treat pseudobulbar affect (PBA), which is categorized by uncontrollable emotional outbursts including laughing or crying. PBA is also known as involuntary emotional expression disorder (IEED), and often occurs alongside brain injuries or neurologic diseases such multiple sclerosis, Lou Gehrig’s disease, or Parkinson’s disease. PBA is estimated to affect approximately 2 million Americans.

“It was all that we had hoped for and more,” said Avanir Chief Executive Officer Keith Katkin in an interview. “It really exceeded our expectations from an efficacy perspective.”

The drug could bring in $500 million in annual U.S. sales by 2015, according to Summer Street Research analyst Carol Werther. “They’ve got a much safer drug that looks efficacious in a condition that has basically nothing,” he said. “It bodes very well for approval.”

Shares of the Southern California-based Avanir traded as high as $3.86 in the first half hour of trading, up $1.67 from Monday’s closing price of $2.19. In early morning trading, the volume of shares changing hands increased three and a half times, from the previous daily average of 850,000 to over 3 million, and the company’s market value rose to about $310 million.

The results are especially encouraging after Avanir was forced to restart the STAR clinical trial in 2007 after the U.S. Food and Drug Administration expressed safety concerns about the heart rhythm impact of quindine, a component of Zanvia after receiving data from the initial 2006 testing of the drug.

The FDA’s main objection was concerning the heart rhythm impact of quinidine, used to increase the amount of the active ingredient, dextromethorphan, in the body. The agency asked Avanir to go back and perform new trials with only one-third as much quinidine — 10 milligrams instead of 30 milligrams.

“We are very encouraged by the top-line results and we believe that the STAR data should be sufficient to address the issues outlined in the FDA approvable letter,” said Katkin. “We hope to have a full presentation of the STAR trial results at a scientific meeting later this year and plan to submit our complete response to the FDA in the first half of 2010.”