December 22, 2024

After Posting Lower Profit, Glaxo to Cut Costs

The company, Britain’s biggest drug maker, said on Wednesday that a new program to restructure European operations, drug manufacturing and research would save at least about $1.6 billion annually by 2016.

After putting a number of major drug patent losses behind it, Glaxo had originally banked on pulling out of its trough in 2012. In the event, sales were held back by larger-than-expected drug price cuts in austerity-hit Europe.

The company reported that its net profit fell 35 percent, to £839 million (about $1.35 billion), from £1.28 billion in the fourth quarter a year earlier. Sales in the quarter fell 3 percent, to £6.80 billion. Excluding onetime items, Glaxo said it earned 32.6 pence a share, up 4 percent.

Analysts had forecast sales of £6.88 billion and earnings of 31.3 pence a share, according to a survey by Thomson Reuters. Glaxo’s chief executive, Andrew P. Witty, hopes to do better this year. He predicted on Wednesday that earnings per share, after stripping out some items, would grow by 3 to 4 percent at constant exchange rates in 2013, with sales rising about 1 percent.

Still, the forecast increase in sales and earnings this year was less than some analysts had hoped. A Deutsche Bank analyst, Mark Clark, also noted Glaxo gave a cautious outlook for profit margins, since these are expected to improve only “over the medium term.”

Europe has been a weak point for many drug makers, but Glaxo’s portfolio has been particularly hard hit by government budget cuts. As a result, Mr. Witty said he was taking action to ”reduce costs, improve efficiencies and reallocate resources.”

Article source: http://www.nytimes.com/2013/02/07/business/after-posting-lower-profit-glaxo-to-cut-costs.html?partner=rss&emc=rss

Glaxo Promises Growth After 2012 Shortfall

Britain’s biggest drugmaker said a new program to restructure European operations, drug manufacturing and research would save at least 1 billion pounds ($1.6 billion) annually by 2016, with related charges of 1.5 billion pounds.

GSK also placed its Lucozade and Ribena drinks brands under strategic review – a process that could see the products repositioned, partnered with another company, or sold off.

After putting a number of major drug patent losses behind it, GSK had originally banked on pulling out of its trough in 2012. In the event, sales were held back by larger than expected drug price cuts in austerity-hit Europe.

Chief Executive Andrew Witty hopes to do better this year.

He predicted on Wednesday that earnings per share, after stripping out some items, would grow by 3 to 4 percent at constant exchange rates in 2013, with sales rising about 1 percent. “2013 should be the first in a series of growth years for GSK,” Witty told reporters.

Still, the forecast 2013 pick-up in sales and earnings was less than some analysts had hoped and Deutsche Bank analyst Mark Clark also noted GSK gave a cautious outlook for profit margins, since these are only expected to improve “over the medium term”.

Europe has been a weak point for many drugmakers but GSK’s portfolio has been particularly hard hit by government budget cuts. As a result, Witty said he was taking action to “reduce costs, improve efficiencies and reallocate resources”.

The action in Europe will involve some job cuts but he declined to go into details.

WAITING FOR SIX NEW DRUGS

GSK is relying on a clutch of new drugs to revive its fortunes in the mid-term, starting with six that have already been submitted for approval in lung disease, melanoma, diabetes and HIV/AIDS.

Keenly awaited final-stage Phase III clinical trial results are also due for two high-risk, high-reward projects in heart disease and cancer.

That makes 2013 a crucial year for GSK’s pipeline, although the main impact on the sales line will be felt during 2014 and beyond – assuming the new medicines live up to expectations.

“Flat sales over the last year highlight the importance to GSK of the potential new product launches in 2013, as it looks to return to growth,” said Mick Cooper, an analyst at Edison Investment Research.

Sales in the final quarter of 2012 fell 3 percent to 6.80 billion pounds, generating core earnings per share (EPS) up 4 percent at 32.6 pence.

Analysts, on average, had forecast sales of 6.88 billion pounds and core EPS, which excludes certain items, of 31.3p, according to Thomson Reuters I/B/E/S.

The results got a muted response from investors, although there was some relief that GSK did not miss earnings forecasts as it did in the four preceding quarters.

The shares were unchanged following the results, in line with a steady European drugs sector.

GSK’s stock has underperformed in the past year, due to disappointment at its lack of growth, and it now languishes second to last among large European drugmakers in terms of sell-side analyst ratings, ahead only of AstraZeneca, according to Thomson Reuters data.

With a busy portfolio of experimental drugs nearing the market, Witty said he had a “low appetite” for acquisitions and would return cash to shareholders if the company did not find compelling deals.

As was the case last year, GSK has set itself a modest target of buying back between 1 billion and 2 billion pounds in stock this year. But Witty said that figure could be increased during 2013, as was the case in 2012.

Although GSK is not champing at the bit for acquisitions, Witty said he was always looking at opportunities in emerging markets and consumer healthcare, two areas where the company sees good growth prospects.

Witty has for several years pushed a diversification strategy designed to cut the drugmaker’s traditional reliance on “white pills in Western markets”.

(Reporting by Ben Hirschler; Editing by Keith Weir and Mark Potter)

Article source: http://www.nytimes.com/reuters/2013/02/06/business/06reuters-glaxosmithkline-earnings.html?partner=rss&emc=rss

F.T.C. Criticizes Agreements That Delay Generic Drugs

Some drug makers are using an indirect method to delay competition from low-cost generic products by promising not to introduce their own generic versions if a potential competitor delays its entry into the market, the Federal Trade Commission said in a report on Wednesday.

Until lately, the so-called pay-for-delay cases have focused mostly on cash payments by drug companies to settle patent litigation with generic competitors in return for concessions on when to enter the market. These new agreements add a twist to the patent settlements.

The industry contends they are legal business decisions.

The F.T.C. says they are illegal sweetheart deals that cost consumers $3.5 billion a year.

“Win-win for the companies, but lose-lose for consumers,” the F.T.C. chairman, Jon Leibowitz, said in an interview on Wednesday after the agency released a 270-page study on so-called brand-name generics.

The Generic Pharmaceutical Association called the study part of a “misguided policy to ban pro-consumer patent litigation settlements.” The system works, the industry trade group said, noting that 17 of 23 expected generic drug introductions this year, like Lipitor and Plavix, will be the result of patent settlements.

The F.T.C. report, based in part on industry documents, found that generic drugs made by the original company, when competing against a truly generic drug in the first 180 days of competition, reduced overall prices by 4 percent to 8 percent.

That was unsurprising, Mr. Leibowitz said. But it was disturbing, he said, how often agreements not to compete have been used to compensate generic firms for delaying entry to the market.

In the 12 months ended Sept. 30, 2010, 15 drug patent settlements combined a promise not to market a brand-name generic drug with a generic company’s agreement to delay its entry to market, the report said.

“Instead of saying, ‘Here’s $200 million, go away,’ they’re saying they could penalize them $200 million, but they won’t, so go away,” Mr. Leibowitz said.

The Pharmaceutical Research and Manufacturers of America, a Washington trade group, said the report proved that brand-name generics help reduce prices.

“However, it is unfortunate that the F.T.C. used this potentially valuable report on the benefits to patients of authorized generics to further its attack on patent settlements,” the group’s senior vice president, Matthew D. Bennett, said in a statement.

Article source: http://feeds.nytimes.com/click.phdo?i=b6c367405b2573840ad851de4b9b595a