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4,414 results for '\"eli lilly\"'

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Articles

Company news

April 23, 2012

Purdue University plans to start construction this summer on two academic buildings in a $79 million project for its newly designated Life and Health Sciences Park, according to the Journal & Courier of Lafayette. The $38 million Lyles-Porter Hall will house health programs, including Purdue's speech and hearing sciences department and the West Lafayette programs of the Indiana University School of Medicine. Purdue also is planning a $25 million Drug Discovery Building that will bring together pharmaceutical researchers from throughout the school. Plans are for the buildings and a new 850-space parking garage to be completed in 2014.

More than 70 workers will lose their jobs at Integra Specialty Hospital in Muncie when it closes in June. Hospital officials notified the Indiana Department of Workforce Development on Thursday that the 32-bed long-term-care facility will shut down on June 17. Renaissance Specialty Hospital of Central Indiana Operations Co. LLC, which operates Integra, did not provide a reason for the closing. The company said it expects that some of the 72 employees will be offered the opportunity to transfer to other long-term-care facilities.

Eli Lilly and Co. could receive up to $100 million from Washington, D.C.,-based Vanda Pharmaceuticals Inc., which licensed an alcohol-dependence drug from the Indianapolis drugmaker last week. The experimental drug, called LY686017, has been shown to reduce alcohol cravings and consumption in alcoholics. If it reaches the market, the drug would compete with Emend, a similar NK-1R antagonist made by New Jersey-based Merck & Co. Inc.

The government-contracting arm of WellPoint Inc. won a renewal of its contract, worth more than $111 million, to support the desktop program used by customer service representatives at the Centers for Medicare & Medicaid Services for the next five years. WellPoint’s National Government Services unit has held the contract since the program’s inception. The program helped Medicare’s call center field 26 million calls last year. NGS, which employs 2,000, also processed 170 million Medicare claims and administered benefits of $75.6 billion from the Medicare Trust Fund in 2011.

An animal rights group wants the federal government to fine a research institute owned by Indiana University Health for what it calls negligence toward animals, according to the Associated Press. The group Stop Animal Exploitation Now says IU Health's Methodist Research Institute had seven violations, including killing one dog and putting another dog in severe pain. According to a March report from the U.S. Department of Agriculture, a dog was fed before surgery, which violated proper protocol. The dog’s heart stopped, and it died. IU Health officials said in a statement that the use of animals in research has contributed significantly to advancements in health care.

Daniels endorses Romney for president

April 18, 2012

Indiana Gov. Mitch Daniels has endorsed presumptive Republican presidential nominee Mitt Romney after declining for months to publicly support any of the Republican candidates.

IPS issues rebuttal to Mind Trust’s reform plan

April 16, 2012

In an hour-long defense of Indianapolis Public Schools, Superintendent Eugene White outlined plans to streamline administrative staff, create more choices for parents, direct more resources to the district’s most challenged schools and give more autonomy to its highest performing schools.

Company news

April 16, 2012

Shares of Endocyte Inc. more than doubled in value Monday morning after the company unveiled an up to $1 billion deal with Merck & Co. Inc. to bring an ovarian cancer drug to market. West Lafayette-based Endocyte’s stock had fallen 60 percent in the past 12 months. New Jersey-based Merck will pay Endocyte $120 million upfront with as much as $880 million in future payments possible based on regulatory approvals and sales of the drug EC145, also known as vitafolide. The agreement gives Merck worldwide commercial rights to EC145, in exchange for double-digit royalty payments to Endocyte. The two companies will split sales revenue and marketing costs in the United States. Endocyte already has begun studying EC145 as a potential lung cancer treatment, and intends to study it in still more applications. Merck also gained the rights to the drug for those other types of cancer. Chris Raymond, an analyst at Robert W. Baird & Co., called the agreement “an amazing deal” for Endocyte.

Shareholders of Eli Lilly and Co. failed once gain to remove the drugmaker’s tough poison-pill provision against unwanted buyers. The proposal garnered 62.4 percent of the shares voted at Monday’s annual meeting of shareholders, according to preliminary voting results. To pass, the proposal needed support from the owners of 80 percent of Lilly’s shares. That means Lilly’s corporate bylaws still contain an 80-percent approval threshold for hostile takeover bids, even though the company’s board has recommended removing the policy in each of the past three years. The proposal that failed Monday would have required just a bare majority of shareholder votes to approve key moves commonly used in hostile takeovers. In the past two years, the same proposal received 74 percent and 73 percent of all shares, respectively. The supermajority vote requirement dates from the 1980s, the heyday of “corporate raiders” making unsolicited bids to buy public companies. Lilly’s board, which has been fiercely independent during multiple waves of consolidation in the pharmaceutical industry, finally began to support removing the high threshold in 2010. That decision followed three straight years in which a majority of Lilly shareholders expressed support for removing the supermajority voting requirements.

Roche Diagnostics Corp.’s North American sales rose 7 percent in the first quarter, to 615 million Swiss francs, or about $670 million in U.S. dollars, assuming constant exchange rates across the world. The Swiss company’s North American headquarters is in Indianapolis, along with a significant diabetes manufacturing operation. Diabetes sales in North America shrank in the quarter 5 percent, to 119 million Swiss francs, or $130 million. Roche’s sales of lab and testing equipment, and the equipment and chemicals that go with it, all saw double-digit growth in the quarter. Worldwide, Roche’s diagnostic sales grew 4 percent, in constant currencies, to $2.4 billion Swiss francs, or $2.6 billion.

Bloomington-based medical-device maker Cook Group acquired General BioTechnology LLC, an Indianapolis biotech company with about 20 employees. Terms of the deal were not announced. Cook will rename the company Cook General BioTechnology LLC. General BioTechnology was founded in 1997 by former Indiana University School of Medicine researchers. It operates an umbilical-cord blood and tissue bank for families called The Genesis Bank and a reproductive tissue bank called Genome Resources.

Biomet Inc.’s sales rose 5 percent in the three months ended Feb. 29, to nearly $709 million, compared with the same period a year ago. The growth was driven by increased volumes in North America and the Pacific Rim. The Warsaw-based orthopedic-implant maker’s financial results are always closely watched as an early signal for the rest of the industry, which will report first-quarter results later this month. Biomet’s sales of knee implants rose 4 percent and sales of its hip implants rose 6 percent, compared with the same quarter last year. The company’s operating income rose 14 percent, to $108.1 million, primarily due to lower amortization expenses recorded from the company’s 2007 buyout by private equity firms. Biomet has a whopping $5.3 billion in debt, which required interest payments in the quarter of $117 million. That expense and tax payments led Biomet to a loss for the quarter of $16.5 million, up from $11.6 million a year ago.

Poison pills remain as Lilly shareholder vote falls short

April 16, 2012

The proposal garnered support from the owners of 62 percent of Eli Lilly’s outstanding shares. To pass, the proposal needed approval from the owners of 80 percent of Lilly’s shares.

Lilly CEO says cost-cutting won’t solve sales losses

April 13, 2012

Eli Lilly and Co., facing generic competition to two of its top drugs, needs to rely on new medicines rather than cost-cutting to overcome the revenue loss, CEO John Lechleiter said Thursday in Boston at the annual meeting of the Pharmaceutical Research and Manufacturers of America.

RIVERA: Dreaming up charter school possibilities

April 11, 2012

Imagine high school graduates from the Eli Lilly or the Cook Pharma Charter School of Chemistry.

New Lilly drug has small sales potential

April 9, 2012

Eli Lilly and Co.’s newest drug is a boon for Alzheimer’s research but is likely to bring the Indianapolis drugmaker less than $100 million in annual sales—at least initially, according to one of the few analysts to make a forecast.

Lilly wins FDA approval for Alzheimer’s imaging agent

April 9, 2012

The agent, called Amyvid, is not expected to produce high-dollar sales for Lilly, but it could help to identify patients with Alzheimer’s—and those without it—earlier, perhaps improving treatment and focusing research efforts.

New data brightens Indy area’s jobs picture

April 5, 2012

Bureau of Labor Statistics revises numbers, but region is still 30,000 jobs short of pre-recession peak.

Purchase of city water utility lifts Citizens Energy’s profits

April 5, 2012

The $1.9 billion sale of the city’s water and sewer utilities was a profit gusher last year for buyer Citizens Energy Group—at least on paper. Dwarfing the returns of its gas, thermal and other divisions, the newly renamed Citizens Water turned a profit of $53.4 million.

People in the news – April 9, 2012

April 5, 2012

People listings are free.

Promised tariff cuts could spur Indiana exports to China

March 27, 2012

Indiana logistics firms and their manufacturing clients could gain new export opportunities to China if the country follows through on plans to reduce taxes on imported goods.

Company news

March 26, 2012

Researchers at the Indiana University School of Medicine may have found a way to predict who will develop Type 1 diabetes, according to a study published March 22 in the journal Diabetes. Dr. Raghu Mirmira and Sarah Tersey, both professors in the pediatric department of the IU medical school, reported that they had been able to identify problems in insulin-producing cells in mice before the mice actually developed symptoms of diabetes. They were also able to identify a protein in the mice that rises in level as insulin-producing cells become dysfunctional. Screening for that protein in blood tests could identify patients in the process of developing diabetes. Type 1 diabetes, also known as juvenile diabetes, occurs when the body’s immune system attacks insulin-producing cells in the pancreas.

Purdue University’s Emerging Innovations Fund invested $80,000 in Spensa Technologies Inc. and another $20,000 in Tymora Analytical Operations LLC. Both companies are based in the Purdue Research Park in West Lafayette. Spensa Technologies is commercializing the Z-Trap, which detects target insects captured by the trap and sends the data wirelessly to a farmer’s mobile phone or computer. Knowing the types of pests can help farmers select the correct pesticide and the right amount to apply. Tymora Analytical incorporates nanotechnology in laboratory products designed to make cancer research and drug discovery more efficient and effective.

European regulators approved an expanded use for the diabetes treatment Byetta developed by drugmakers Amylin Pharmaceuticals Inc. and Eli Lilly and Co., according to the Associated Press. The companies said Friday they received approval for Byetta to be used with or without common treatments like metformin and Actos to treat adult Type 2 diabetes patients who have not been able to control their blood sugar levels with just insulin. The U.S. Food and Drug Administration approved the same expanded use last fall. Byetta, or exenatide, is a twice-a-day injection. It was first approved in Europe in 2006. Amylin and Lilly announced in November that they are ending their collaboration on Byetta and its successor, Bydureon, which is designed to be taken once per week. The two companies have already ended their partnership in the United States, and Amylin will take over marketing of Byetta outside the U.S. by the end of 2013.

40-foot molecule sculpture going up along I-70

March 26, 2012

An Interstate 70 ramp in downtown Indianapolis is expected to be shut down for several days so that a 40-foot metal sculpture of a molecule can be built.

Lilly receives Europe’s OK for new Byetta use

March 23, 2012

European regulators have approved an expanded use for the diabetes treatment Byetta, developed by Eli Lilly and Co. and Amylin Pharmaceuticals Inc. The FDA approved the same expanded use last fall.

People in the news – March 26, 2012

March 22, 2012

People listings are free.

Lilly to focus on cancer, diabetes in China, CEO says

March 20, 2012

Indianapolis-based Eli Lilly and Co. will introduce “over a dozen” new products in China in the next five years, focusing on “unmet needs” such as cancer and diabetes, CEO John Lechleiter said this week.

Lilly gets good news on insulin

March 19, 2012

Decision by industry giant Pfizer Inc. to abandon its generic insulin project is good news for Eli Lilly and Co.

PROXY CORNER: Eli Lilly and Co.

March 15, 2012

Indianapolis-based Eli Lilly and Co discovers, develops, manufactures and sells pharmaceutical products for humans and animals.

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