Kinetic Concepts, Inc. (KCI)
Q2 2010 Earnings Call
July 27, 2010 8:30 am ET
Research Recap submits:
J&J (JNJ) estimated in its second-quarter earnings release that ongoing manufacturing problems within its McNeil Consumer Products unit will result in a $600 million hit to 2010 revenue. The revenue loss results from the May 2010 voluntary shut-down of McNeil’s Fort Washington, Pennsylvania, plant. Separately, on Wednesday, the US Food and Drug Administration (FDA) cited new manufacturing deficiencies at a different McNeil plant in Lancaster, Pennsylvania.
These events are negative for J&J’s credit profile not only because of lost earnings and cash flow, but also because of increasing reputational risk as the deficiencies continue to escalate.
Zacks.com submits:
WellPoint Inc. (WLP) is scheduled to report its second quarter results before the market opens on Wednesday, July 28. The Zacks Consensus Estimate for the second quarter is $1.55 per share, representing a growth of about 8.6% over the year-ago quarter.
The company has concerns over the impact of the health reform bill and continued high unemployment, which are expected to overshadow the stock. Further, Wellpoint is expected to report in-line results based on its improving fundamentals.
Zacks.com submits:
Second Quarter Revisited
Medical devices giant Stryker Corp. (SYK) produced a mixed bag in the second quarter, matching earnings expectations while missing on the revenue front. Earnings of 80 cents per share came in line with the Zacks Consensus Estimate and net income leapt 9.5% year-over-year, led by healthy growth at the MedSurg Equipment division.
Zacks.com submits:
Thermo Fisher Scientific (TMO) is expected to report its second-quarter fiscal 2010 results before the market opens on Tuesday, July 27, 2010. Following first quarter results, the company had raised its revenue and adjusted EPS guidance for fiscal 2010 to $10.65-$10.80 billion and $3.40-$3.50, respectively.
Rockford Coscia submits:
This December, Afrezza, MannKind’s (MNKD) inhalable insulin therapy for prandial (meal-time) management of blood glucose in diabetics, faces FDA decision. Afrezza’s path to approval is well worn and bloodied, most notably by an approval and subsequent market withdrawal of Pfizer’s (PFE) Exubera. Other inhalable therapies have also been attempted by such high-powered partnerships as Alkermes/Eli Lilly (LLY) and Aradigm/Novo Nordisk (NVGN); all abandoned in the wake of Exubera’s withdrawal. Currently Afrezza is the only form of inhaled insulin still under FDA review.
With the market failure of Pfizer’s Exubera, potential investors in MannKind’s endeavor must address why Afrezza will not suffer the same market setbacks assuming a favorable decision by the FDA in December. MannKind has, of course, amassed a number of reasons to convince investors that Afrezza will become a market blockbuster with varying degrees of substance.
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