Merck Writes Off ANOTHER 4% of The Schering-Plough Purchase Price — $1.7 Billion TRA Impairment Charge


UPDATED | 8:40 AM EST | NASDAQ Pre-Market — Shares Now Off Over 3.4% — to $32.65 My overall impression is that the most of the larger stock analysis houses came off as pretty justifiably skeptical — at least about New Merck’s proffered reasons for the withdrawal of its 2012-2013 guidance.

Lowers long term guidance to high-single digits EPS growth; posts a GAAP Q4 2010 loss per share. Vorapaxar is 4 percent; with other 2010 impairments, now nearly 6 percent of Schering-Plough’s $41.5 billion purchase price has been written off, as worthless, in 2010 alone.

More in a moment. . . . from the Merck Year End 2010 press release, here:

. . . .Amounts for the fourth quarter and full year of 2010 reflect $2.2 billion and $2.4 billion, respectively, of in-process research and development impairment charges, including a charge of $1.7 billion to write-down the intangible asset related to vorapaxar recorded in conjunction with the merger. The remaining amounts in 2010 and the amounts in 2009 represent expenses for the amortization of intangible assets and amortization of purchase accounting adjustments to inventories recognized as a result of the merger.

Given industry pressures such as greater E.U. austerity measures and the additional impact of U.S. health care reform, as well as developments in its vorapaxar clinical program, the company has withdrawn its previous long-term target of high single-digit non-GAAP EPS compound annual growth rate from 2009 to 2013. . . .

LIVE-BLOG:

▲ Low to Mid SINGLE DIGIT Sales Growth in 2011 and 2012. Yikes!

▲ And that is ASSUMING Merck wins the J&J aritration.

▲ Venezuela currencies will be a significant drag on sales in 2011.

▲ Gardasil sales down sequentially, worldwide.

Q&A now. . . .

▲ Q: Chris Scott (JP Morgan) — Why is 2013 guidance being withdrawn?

▲ A: CEO Ken Frazier — We are not going to engage in immediate indiscriminate cost cutting; we will make investment in our late stage pipeline — that leads to longer term growth, but it will take down the 2011-2013 guidance.

▲ Q: Catherine Arnold (Credit Suisse) — 2013 guidance? Vorapaxar should have been a 2013 drag on earnings, so why would vorapaxar be to blame for the 2013 down? Why aren’t your people looking for “share the pain” cost cutting?

▲ A: Ken Frazier — These costs are fixed, re vorapaxar — we are decreasing our cardio sales presence. As to sharing the pain — we do need to get our cost structure in line. We did exceed synergy targets in 2010 — we shed 50% of our sales force in the US.

That said, we are trying to be thoughtful about our cost cutting.

▲ Q: Jami Rubin (Goldman, Sachs & Co.) — What about risk mitigation on these large risky trials? And why are you cutting against the approach of Pfizer announced yesterday — i.e., aggressive cost cutting?

▲ A: Ken Frazier — We are trying to assess all programs, from a commercial and science standpoint and then work them by ROI targets. . . . we are still optimistic that some marketa will emerge for vorapaxar.

We also will honor John Horan’s legacy: we have to keep investing in visionary programs, even in a downturn — like the present environment. . . . [Ken Frazier eulogized John Horan a couple of weeks ago at his funeral.]

▲ Q: Tim Anderson (Sanford Bernstein) — I hate to say it, but the explanation for 2013 guidance downturn seems to be about things known for months and months now — at least it sure sounds like it. . .? And when will there be a buyback re-up?

▲ A: Ken Frazier — We knew about EU pricing pressure, but it is increasing; incremental other pipeline set-backs were “tipped” when vorapaxar made a big difference. We have 20 late stage clinical trials underway, we intend to keep funding the vast majority of them. Launch of boceprevir will be a big cost. . . we have decided not to go for short term cost cutting (as Pfizer just did). It is not that we CAN’T get there — we are choosing to keep spending. No update on Remicade or Simponi — won’t comment on whether there are negotiations with J&J.

▲ Q: David Risinger (Morgan Stanley) — Your 2011 sales guidance is above our estimate; EPS is below — so, are you suggesting that you will be reinvesting the synergies in 2011?

▲ A: Ken Frazier — Yes, but recall that Venezuela will be $0.06 off the top in 2011. So we are investing in our portfolio — this is the right time to do this. . . we have no guidance beyond 2011, to be clear. . . .

▲ Q: Seamus Fernandez (Leerink Swann) — So are we supposed to remove Remicade/Simponi from 2011 through 2013 guidance? What has happened to the $15 billion of operating cash flow over 2011 to 2013?

▲ A: CFO Peter Kellog — We expect to keep Remicade; it is in our guidance. We are focused on generating cash in 2011– we are focused on returning to shareholders as well. . . . no other specifics at this point.

[Editor: Call ended at 9:14 AM EST.]

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