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ImClone Systems

 
Hoover's Profile: ImClone Systems Incorporated
Contact Information
ImClone Systems Incorporated
180 Varick St.
New York, NY 10014
NY Tel. 212-645-1405
Fax 212-645-2054

Type: Subsidiary
On the web: http://www.imclone.com

ImClone Systems has one drug and it is making the most of it. The drug development company's only product on the market, Erbitux, is approved for treatment of colorectal cancer, as well as head and neck cancers. ImClone Systems co-promotes the drug with Bristol-Myers Squibb in North America and with Merck KGaA elsewhere. ImClone is continuing to develop Erbitux as a possible treatment for other kinds of cancer, including lung cancer. The company is also working on additional oncology-related antibody therapies. In 2008 ImClone was acquired by Eli Lilly for $6.5 billion, after rejecting bids from Bristol-Myers Squibb.

Officers:
CEO: John H. Johnson
Media Relations: Tracy Henrikson
VP Commercial Operations: Joseph I. DePinto

Competitors:
Amgen
Genentech
OSI Pharmaceuticals

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Company History: ImClone Systems Inc.
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Incorporated: 1984
NAIC: 325414 Biological Product (Except Diagnostic Manufacturing)

ImClone Systems Inc., a biotech company based in New York City, is best known for a highly publicized stock scandal that involved its founder and longtime CEO, Samuel Waksal, and his celebrity friend Martha Stewart. The company has never produced a profit and for many years continually shifted the focus of its research before turning in the 1990s to the development of a drug called Erbitux, a genetically engineered protein used to slow the spread of cancer. Difficulty winning approval from the Federal Drug Administration (FDA) triggered the scandal that brought to light many of the past dealings of Waksal and his younger brother Harlan, ultimately forcing them to resign from ImClone. The company has enjoyed greater success in Europe in its attempts to gain approval to sell Erbitux.

Samuel and Harlan Waksal emigrated with their parents from Europe to Dayton, Ohio, in the early 1950s. Their mother had survived the horrors of the Auschwitz concentration camp while their father had fought for the Polish underground. The elder Waksal supported his family in the United States by going into the scrap metal business. Both of the sons were drawn to study science, with Samuel attending the Ohio State University, where in 1969 he earned an undergraduate degree, then in 1974 a Ph.D. in immunology. Harlan became a pathologist, receiving a medical degree from Tufts University School of Medicine in 1979. In the years preceding the founding of ImClone, Samuel Waksal achieved an academic reputation that took on a different character after his life received greater scrutiny during the media frenzy surrounding the company's 2002 stock scandal.

Following a postdoctoral fellowship in Israel, Samuel Waksal was able to secure a prestigious position at Stanford University, championed by Dr. Irv Weissman, a Stanford professor who had met Waksal during a visit to the Ohio State laboratory. Although impressing his new colleagues with both his brilliance and charm, Waksal was soon asked to leave the Stanford lab after its head, Dr. Leonard Herzenberg, became convinced that the young researcher had repeatedly lied about acquiring prized antibodies from the Sloan-Kettering Institute. According to the Wall Street Journal, Waksal later called to apologize and said "he was seeking psychiatric help and had changed."

Waksal then went to work at the National Cancer Institute under a temporary research position, one that would not be renewed. "The reason was a disturbing pattern in Dr. Waksal's research," according to the Wall Street Journal. "Dr. Waksal was involved in a large number of projects with other scientists, recalls Dr. Terry [in charge of NCI hiring]. 'When the critical time came to deliver his part of the collaboration, there would be a catastrophe of some sort--a tissue culture would become contaminated or the mice would develop an infection and have to be killed.'" Despite NCI's decision not to offer him a permanent position, Waksal was able to secure employment at Tufts. As had been the case at his previous stops, the effects of the charismatic Waksal soon wore off and his superiors grew suspicious about his work: some experiments were not conducted on time and, more troubling, others appeared to be purely fictional. It was at this point, in February 1981, that Harlan Waksal, a medical resident at Tufts, was arrested in the Fort Lauderdale International Airport with more than two pounds of cocaine stashed in his underwear and carry-on bag. According to rumors reported by the press, Sam Waksal attempted to cover for Harlan by impersonating his brother and making his rounds at the New England Medical Center. According to Sam Waksal, as told to Barron's, "There was a patient of Harlan's who was a very nice lady who spoke only Yiddish. And Harlan, when he wasn't in town at one point, wanted me to go talk to her because she loved him. So I went and talked to her. That was the scope of it." Whatever the truth of the situation, this story would periodically crop up, along with questions about Sam Waksal's academic background, causing some investors to shy away from ImClone. There was no ambiguity about what happened to Harlan Waksal, however. In April 1982 he was found guilty of possession of cocaine with intent to distribute and sentenced to a nine-year prison term. A year later, however, the conviction was overturned on a technicality. The search that led to the discovery of the drugs was deemed illegal because it lacked valid consent.

Sam Waksal's difficulties at Tufts led to his departure in 1982, but he was soon hired by New York's Mount Sinai School of Medicine to run an immunology lab. According to the Wall Street Journal, Waksal's supervisor at Tufts said "that he didn't warn anyone at Mount Sinai about Dr. Waksal because no one called to ask his opinion." As had been the case with his previous positions since graduating from Ohio State, Waksal's stay at Mount Sinai was brief and ended in controversy. The Wall Street Journal interviewed Alexandra Bona who worked for Waksal: "'One day in 1985, the Waksal lab imploded,' she recalls. Returning from lunch, Dr. Bona found 'everyone crying and Sam was out of his mind.' He and a few technicians had been asked to leave immediately, she says. ... His file is legally sealed under a confidentiality agreement he reached with Mount Sinai. But a person familiar with the situation says Mount Sinai asked Dr. Waksal to leave because of evidence he had falsified data." A 1993 Barron's profile cites two former colleagues at Mount Sinai who maintained that "Waksal departed under a cloud of dispute over his division's financial condition and ownership of some molecular modeling technology that ImClone later pursued."

As the situation at Mount Sinai soured for Waksal, he took a leave of absence in 1984 to establish ImClone, an endeavor to which he would devote all his energy after exiting Mount Sinai. Harlan Waksal told Business Week in 2001, some months before ImClone became engulfed in controversy, that he and his brother "started kicking around some fun ideas about how to start a company. We thought we'd focus on infectious diseases, cancer, and diagnostics, make some products, get rich, and retire early." To launch the business, the Waksal brothers secured $4 million in venture capital. It was during a flight to Denver to meet with venture capitalists that they coined the ImClone name by fusing the types of the businesses they planned to pursue: immunology, DNA cloning, and medical information systems. Investor Tom Rosse was a key early backer, supplying an initial $250,000 needed to complete a business plan, then providing entry to other major investors. Also of significant importance to landing investors was Sam Waksal's resume, which listed a number of prestigious institutions and appeared impressive, at least on the surface.

At first, ImClone operated essentially as a holding company for the scientists whose work they funded, focusing initially on immunology-based diagnostics and infectious disease vaccines. The hope was that the company had the potential to develop vaccines for the Hepatitis B virus and AIDS. ImClone soon introduced a product that brought in some revenue, a battery of tests to detect Hepatitis B, but the company's ambitions and need for cash far exceeded the expectations for this diagnostic business. In 1986 ImClone opened its own laboratories, located in Manhattan's SoHo district on the site of a bankrupt shoe factory. A year later the company prepared to go public, but was forced to pull the offering in the wake of the October 1987 stock crash. According to Business Week, "Over the next few years, Sam engineered several funding deals to keep ImClone alive until the company went through with its IPO in 1991. ImClone still had not decided on a lead product, however, and its research was unfocused." The company went public at $14 a share and despite little demonstrable success in its research efforts grew in value, reaching a high of $27 before the biotech category fell out of favor with investors.

While ImClone may have struggled to succeed and was in constant need of fresh cash to fund its research, Sam Waksal, now divorced from his high school sweetheart, was becoming a fixture of the social scene in New York and the Hamptons, often mentioned in the gossip columns of the New York tabloids. "By all external appearances, Dr. Waksal had made it big," wrote the Wall Street Journal. "He counted among his friends and business partners Ms. [Martha] Stewart and financier Carl Icahn, both of whom invested in ImClone. He became chairman of the New York Council for the Humanities and hosted monthly soirees in his swank Soho loft, where guests were invited to discuss current issues of intellectual interest. ... While living a lavish lifestyle, Dr. Waksal was borrowing heavily from his companies. In the early 1990s he borrowed about $300,000 from ImClone." Waksal played at being a film producer as well as a restaurateur, co-producing two movies and co-owning a pair of eateries, one of them with Alexis Stewart, Martha Stewart's daughter and Waksal's girlfriend of four years. He also had occasional difficulties meeting his debts. According to a 2002 New York Times profile, "Dr. Waksal has been sued several times for not paying his bills. An auction house got a judgment against him in 1994 after a check for nearly $58,000 bounced. Charles Antrell, an ImClone investor, sued Dr. Waksal in 1993 for failure to pay back $100,000 he had borrowed. ... The Internal Revenue Service and New York State have both filed tax liens against Mr. Waksal several times, in some cases for more than $100,000."

ImClone was in desperate need of a lead product in the early 1990s when it became involved with the targeted cancer drug Erbitux, originally dubbed IMC-C225, the result of research first conducted by Dr. John Mendelsohn at the University of California at San Diego in 1980. Mendelsohn struggled for years to find someone willing to back his efforts to see the drug reach the market. While others hesitated, Sam Waksal believed in the potential of the drug and convinced Mendelsohn to strike a deal with ImClone. To move into clinical trials as soon as possible the Waksals bought a former New Jersey computer-chip factory and retrofitted it to produce the drug, which began to be tested on human patients in 1994, the same year that the biotech stocks suffered another crash. The company was pushed to the brink of bankruptcy, with a third of its employees laid off. Rather than license Erbitux to a giant pharmaceutical for a nominal amount of money, the Waksals decided to scrape by in hopes that positive Phase I results would lead to fresh investments. In the spring of 1995 ImClone reached a major turning point when two patients with head and neck cancer showed some tumor shrinkage while using Erbitux. As a result, the price of ImClone stock rebounded and the Waksals received licensing offers as well as takeover bids. The only deal they decided to accept was a co-marketing agreement with the German drug maker Merck KgaA for European rights.

Still working with limited funds, ImClone opted to focus on head and neck cancer patients. That emphasis would shift in 1999 when Erbitux was used on a patient named Shannon Kellum, who had colon cancer that spread to her liver and abdomen. By chance her doctor had earlier worked with Mendelsohn, studying the effects of C225 on colon cancer, and was able to convince ImClone to supply the substance for her use. Erbitux was used in conjunction with another round of chemotherapy and Kellum's tumors shrank so much that they could be removed surgically. Due to this case, ImClone now decided to test Erbitux on colon cancer. The initial 125-patient study launched in 1999 was another gamble for the company, limited to patients who had already failed irinotecan treatment. They were now given another round of chemotherapy, but this time with Erbitux. Failure could have scuttled the entire project, but in November 2000 the early results were strong enough for ImClone to gain fast-track status from the FDA for the drug to be used as an advanced treatment of colon cancer. Good results continued to be announced in 2001, with Erbitux showing promise not only with colon cancer and head and neck cancer, but also pancreatic cancer, which was particularly resistant to treatment and usually killed patients in a short period of time. In the end, the trial produced a 22.5 percent favorable response rate among patients, a very high number for a cancer treatment.

Strong Phase 2 results for Erbitux caused management to file for drug approval from the FDA, which generally required a three-stage trial. It also translated into an escalating stock price for ImClone in 2001. While Erbitux continued in the next phase of its clinical trials, the high-flying company was in a position to now cut a lucrative deal with a major pharmaceutical. In September 2001 Bristol-Myers Squibb Co. agreed to pay up to $2 billion for a 40 percent share of the profits in Erbitux. The terms of the transaction called for $1 billion in upfront payments, $200 million immediately, followed by two payments of $300 million and $500 million, triggered by steps in the FDA approval process. In addition, Bristol-Myers agreed to pay purchase and copromotion fees and share some of ImClone's research expenses and, more important, buy 19.9 percent of ImClone's stock for another $1 billion. In return, Bristol-Myers received two seats on the ImClone board, exclusive rights to market Erbitux in the United States and Canada, an equal share of selling rights in Japan, and first rights to the products in ImClone's pipeline for the next five years. It was a rich deal for ImClone, one that would soon be the cause of buyer's remorse among the upper tier of Bristol-Myers management.

In November and December 2001 communications from the FDA about the Erbitux application grew negative in tone, prompting some concern at ImClone. Then on December 20 ImClone and Bristol-Myers were informed that the FDA had made its decision, which would be communicated on December 28. According to the Wall Street Journal, "On Christmas Day, a Bristol-Myers official reached Harlan Waksal on vacation in Colorado to tell him the application looked doomed, based on a conversation with an FDA official. Harlan Waksal began calling his brother on the morning of Dec. 26, and they attempted to stave off the FDA action. ... According to the SEC complaint [that would ultimately be filed], Samuel Waksal began relaying the information to family members. On the night of Dec. 26 and early the next morning, it says, he telephoned family members to alert them that ImClone would be receiving this bad news. Within hours of learning about the impending FDA action, the criminal complaint charges, Dr. Waksal directed that 79,797 of his own ImClone shares, valued at about $4.9 million, be transferred to a person the complaint didn't name but was later identified as his daughter Aliza, calling the transfer 'urgent' and 'imperative.' After transferring the shares, Dr. Waksal directed that they be sold. ... Federal authorities say several Waksal family members were able to sell a total of $10 million of ImClone stock on Dec. 27 and Dec. 28."

ImClone stock plunged on word that the FDA had refused the Erbitux application. Sam Waksal initially maintained that the FDA's concerns were simply a matter of documentation and that the marketing of the drug would be delayed until the third quarter of 2002. The Cancer Letters, a Washington newsletter, obtained a copy of the FDA letter, however, and it became clear that problems with the study went much deeper. The price of ImClone stock continued to slide, causing great concern at Bristol-Myers, which watched its $1 billion investment in ImClone decrease in value by about two-thirds.

In light of the Enron scandal and other prominent examples of corporate malfeasance, a great deal of scrutiny was paid to the affairs of ImClone, and the questionable backgrounds of the Waksal brothers were recounted in the media. In January 2002 the House Energy and Commerce Committee called for hearings into the matter. Moreover, the SEC began to investigate charges of possible insider trading activity involving the Waksal family and friends, which resulted in Martha Stewart becoming swept up into the controversy and even more media coverage of the ImClone story.

Sam Waksal attempted to hang tough but in May he resigned as ImClone's CEO, replaced by his brother Harlan. In the early morning hours of June 12, 2002, four FBI agents visited Sam Waksal's Soho loft, arrested him, and led him away in handcuffs. Facing a string of insider trading and other charges he began negotiating with authorities on a plea bargain. He finally pleaded guilty to six of the 13 counts against him in the apparent hope that the prosecutors would drop the remaining charges and cease to pursue cases against his elderly father and daughter. In May 2003 he settled with the SEC on civil charges, agreeing to pay some $800,000. In June 2003 he was sentenced to 87 months in prison and ordered to pay $3 million in fines. A short time later Martha Stewart was indicted on charges of obstructing justice.

Following the arrest of Sam Waksal, the fallout continued at ImClone. The company's general counsel, John B. Landes, resigned in October 2002. In 2003 it came to light that Harlan Waksal and other company officials, including Chairman Robert Goldhammer, had attempted to obtain a legal opinion that they did not owe taxes on some stock warrants and options they exercised. According to the Wall Street Journal, they were unsuccessful yet "decided they didn't owe the money, and ImClone didn't withhold it." As a result of this revelation, both Harlan Waksal and Goldhammer resigned, although Harlan stayed on as chief scientist overseeing the ongoing development of Erbitux.

Despite all the controversy surrounding the company, ImClone's fortunes, as well as the price of its stock, began to rebound in 2003, mostly on the strength of continuing efforts by Merck KgaA to gain approval for Erbitux in Europe. In June 2003 the results of a European study were released, mirroring those found in the trials sponsored by ImClone in the United States. More important, the new study was more thorough and appeared to answer the concerns raised by the FDA. Merck was encouraged enough by the results to announce that it would seek European approval for the drug and might have it on the market by the end of the year. ImClone also planned to seek the FDA's opinion on the study in hopes of rekindling the company's plan to gain domestic approval for Erbitux.

Principal Subsidiaries

EndoClone Inc.

Principal Competitors

Genentech, Inc.; Medarex, Inc.; OSI Pharmaceuticals, Inc.

Further Reading

Anand, Geeta, "In Waksal's Past: Repeated Ousters," Wall Street Journal, September 27, 2002, p. A1.

Anand, Geeta, Jerry Markon, and Chris Adams, "Biotech Bust: ImClone's Ex-CEO Arrested, Charged with Insider Trading," Wall Street Journal, June 13, 2002, p. A1.

Arnst, Catherine, "The Birth of a Cancer Drug," Business Week, July 9, 2001, pp. 94-102.

Arnst, Catherine, John Carey, and Jack Ewing, "Where ImClone Went Wrong," Business Week, February 18, 2002, pp. 68-71.

Pollack, Andrew, "For ImClone Drug Entrepreneur, A Past of Celebrity and Notoriety," New York Times, January 24, 2002, p. C1.

Wyatt, Edward A., "Outside the Lab: Biotech CEO's Lifestyle Raises Investor Eyebrows," Barron's, June 28, 1993, p. 14.

— Ed Dinger


Wikipedia: ImClone Systems
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ImClone Systems Incorporated is a biopharmaceutical company dedicated to developing biologic medicines in the area of oncology. It was founded in 1984 and is headquartered in New York City. On October 6, 2008, it accepted a $6.5 billion acquisition offer from Eli Lilly and Company, and became a fully owned subsidiary of Eli Lilly and Company on November 24, 2008. Prior to the acquisition, it was traded on the NASDAQ stock exchange under the symbol IMCL.

Contents

Insider trading scandal

ImClone's stock price dropped sharply at the end of 2001 when its drug Erbitux, an experimental monoclonal antibody failed to get the expected Food and Drug Administration (FDA) approval. It was later revealed by the U.S. Securities and Exchange Commission that numerous executives sold their stock before the announcement of the decision after the close of trading on December 28.

Its founder, Samuel D. Waksal, was arrested in 2002 on insider trading charges for informing friends and family to sell their stock, and attempting to sell his own. His daughter, Aliza Waksal, sold $2.5 million in shares on December 27. His father, Jack Waksal, sold $8.1 million in shares over the 27th and 28th. Company executives had done the same. John B. Landes, the general counsel, sold $2.5 million in shares on December 6. Ronald A. Martell, the vice president for marketing and sales, sold $2.1 million in shares on December 11. Four other executives sold shares in the following weeks as well. Later, Samuel Waksal pleaded guilty to various charges, including securities fraud, and on June 10, 2003, was sentenced to seven years and three months in prison.

Martha Stewart, the founder of Martha Stewart Living Omnimedia (Waksal had dated Stewart's daughter) also became embroiled in the scandal after it emerged that she sold about $230,000 in ImClone shares on December 27, just a day before the announcement of FDA decision. Although Stewart maintained her innocence, she was found guilty and sentenced on July 16, 2004 to five months in prison, five months of home confinement, and two years probation for lying about a stock sale, conspiracy, and obstruction of justice.

Ultimately a new clinical trial and FDA filing prepared by Imclone's partner Merck KGaA ("German Merck," not to be confused with the US company of similar name) resulted in an FDA approval of Erbitux in 2004 for use in colon cancer.

A Congressional hearing on improprieties at ImClone, held in October 2002, unveiled a culture of corruption dating back to 1986. This was the year that ImClone CEO Waksal first forged the signature of the company's general counsel John Landes (one of the three original employees of the company) for financial gain. Nonetheless, Landes defended Waksal's illegal actions at the hearings before the Subcommittee on Oversight and Investigations, portraying the forgery as "a good-faith misunderstanding," to which Representative James Greenwood replied "My children know better than that, Mr. Landes." Further questioning about this and subsequent forgeries on Waksal's part revealed that neither Landes, the chief legal officer of the company, or the company's outside directors reported Waksal's actions to proper authorities or made any moves to have Waksal removed as CEO. Instead, testimony revealed that they initiated their own internal investigation, which was never concluded. The decades-long tolerance for Waksal's fraud, starting from the company's earliest days, provoked Representative Peter Deutsch to refer to the ongoing misconduct as "wacky."

The FDA's February 2004 announcement of approval for use of Erbitux for treatment of colrectal cancer reported that conclusions were drawn from a trial involving 329 patients, of which 10.8% responded when Erbitux was used by itself, delaying tumor growth by 1.5 months. When used in conjunction with a standard treatment irinotecan, 22.9% of patients responded and tumor growth was delayed by approximately 4.1 months.

In September 2001, Bristol-Myers Squibb committed $2 billion (including a $1 billion up-front cash payment) for less than 20% of ImClone due to what was called at the time the drug's "blockbuster" potential.

In January 2006, the company was put up for sale but failed to find any buyers, likely due to the fact that Erbitux by that time faced significant competition in the medical marketplace. ImClone directors withdrew the sale of the company in mid-2006.

In April 2007, The Wall Street Journal reported that "Bristol-Myers Squibb Co. and ImClone Systems Inc. said their cancer drug, Erbitux, failed to significantly prolong the lives of people with pancreatic cancer in a new study, marking yet another setback in the drug industry's efforts to find a better treatment for this deadly disease."

Compassionate use controversy

The FDA approved the aforementioned colorectal cancer drug, Erbitux, on February 12, 2004. In May 2001, while ImClone was still seeking approval for the drug (then known as IMC-C225), the CBS news program "60 Minutes" aired a story about two cancer patients' struggles to obtain "compassionate use" of the drug. One ultimately succeeded; the other failed despite repeated pleas to ImClone officials. It was alleged in the story that ImClone was arbitrary in who received the drug and had no written criteria for compassionate use.

Carl Icahn acquisition

On October 25, 2006, a group led by billionaire investor Carl Icahn acquired a majority of stock thereby giving him control of the board. Within hours of the announcement, interim CEO Joseph Fischer resigned, and Icahn announced that other members of the Board of Directors would not be re-elected.

Takeover offer from Bristol-Myers Squibb, and subsequent bidding showdown

On July 31, 2008, Bristol-Myers Squibb offered to take over ImClone for $60 a share cash. The offer was made by letter addressed to ImClone's chairman of the board, Carl Icahn.

On September 10, 2008, An undisclosed company and CEO offered to take over ImClone for $70 a share, financing approach was not disclosed. The offer was conditional on the results of a due diligence review of ImClone's business and technology by the undisclosed party, to be completed September 28th, 2008.

On September 23, 2008, Bristol-Myers Squibb upped its offer to take over ImClone to $62 a share. In addition, Bristol threatened to take the offer to the share holders for a proxy battle with the intention of replacing the current Board of Directors headed by Carl Icahn.

On October 6, 2008, ImClone agreed to be acquired by Eli Lilly for $6.5 billion ($70/share).

On November 24, 2008, ImClone was formally acquired by Eli Lilly, with all NASDAQ IMCL shares tendered for $6.5 billion ($70/share). ImClone is now a fully owned subsidiary of Eli Lilly and Company

Yeda/Aventis/Imclone Patent Dispute

Yeda Research and Development, a company set up to commercialize and market the products of research at the Weizmann Institute of Science in Israel[1], challenged the Aventis-owned patent, licensed by Imclone, for the use of anti-Epidermal growth factor receptor antibodies in combination with chemotherapy, to slow the growth of certain tumors. This is the so-called '866' patent[2] which was filed in 1989 by Rhone-Poulenc-Rorer and issued in 2001, on which Joseph Schlessinger was listed as first-named inventor. [3].

Joseph Schlessinger's former colleagues at the Weizmann Institute, in particular Michael Sela, claimed to have come up with this concept alongside Schlessinger when they worked together there years earlier, and Yeda challenged the Aventis patent in the United States. Schlessinger testified in court that the idea of combining the anti-EGFR antibody that his lab had developed with chemotherapy in cancer treatment was his own idea. However, the Weizmann Institute scientists provided extensive documentation that they had been developing this idea using an antibody against that Schlessinger's laboratory had developed and generated, and that he had given them for these studies[4][5]. Schlessinger claims to have initiated the idea of this use in combination therapy, but had not documented his research and ideas as thoroughly, leaving him forced to rely on his recollections of the events that led to the patent filing some 17 years before Yeda mounted their challenge.[6].

The court ruled that Yeda are the sole owners of the disputed patent in the U.S., while Yeda and Sanofi-Aventis co-own the 866 Patent's foreign counterparts. Following the ruling, ImClone and Sanofi-Aventis agreed to settle the dispute with Yeda, for $120 million, with each company paying Yeda $60 million.[7][8]. In return, ImClone were also granted a worldwide license to technology covered by the 866 Patent, and agreed to pay a small royalty on Erbitux sales to Yeda.

See also

External links

Articles

FDA

Data

References


 
 

 

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