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Speed takes fast approach as the lone American in F-1

...Bleeding ulcers in his colon caused anemia and severe weight loss to his already compact 5-foot-10, 150-pound frame.

While driving, he had to worry about his bowels, too.

"But it's something that was a huge character builder, when you can walk around the racetrack and still perform wearing diapers and have self-dignity," Speed said, noting he's had no attacks in a year.

After surviving that disease and constant pressure to perform, Speed won't let the weight of great expectations slow him down.

"I don't personally try to think about the responsibility I hold, although I am aware of it," Speed said in a pre-race teleconference.

"I know that this is my opportunity in my life that I've been given and, if I mess it up, it's no one's fault but my own." With an all-too-perfect name in a sport best known in the United States recently for tire issues, Speed will try to succeed.

Indy Racing star Michael Andretti tried F-1 in 1993 and soon quit.

Only two Americans have won an F-1 title: Phil Hill in 1961 and Mario Andretti, Michael's father, in 1978.

The F-1 tour makes only one U.S.

stop - the United States Grand Prix at Indianapolis Motor Speedway on July 2.

"I am so looking forward to it," said Julie Speed, Scott's mother, who will attend that race.

Mike Speed will watch their son's debut in Bahrain, an island nation in the Persian Gulf.

"I'll be watching at home on a big screen at 3 a.m.

with some friends," Julie said.

"The last ...

CytoDyn CEO Acquires Cancer-Fighting Compound and Lilly Launches ...

...The approval covers patients with moderately to severely active forms of the disease who have failed other therapies.

One of the deadliest and rarest forms of cancer is the focus of a Phase III study initiated by Eli Lilly (NYSE:LLY) and Company recently.

Enzastaurin, an investigational, targeted, oral agent, will be evaluated at more than 100 sites worldwide for the treatment of relapsed glioblastoma multiforme (GBM), an aggressive and malignant form of brain cancer.

Lilly, a leading innovation-driven corporation, is developing a growing portfolio of first-in-class and best-in-class pharmaceutical products.

Merck & Co., Inc.

(NYSE:MRK) and Paratek Pharmaceuticals, Inc.

announced recently that Paratek has entered into an exclusive, worldwide collaborative development and license agreement with Merck -through an affiliate - for PTK 0796, a novel, broad-spectrum aminomethylcycline (AMC) antibiotic with oral and intravenous (IV) formulations currently in Phase I clinical testing.

About Financial News USA Financial News USA is a Next Generation Financial Communications firm focused on the distribution of market moving news.

Financial News USA has developed leading edge e-publishing tools including programming proprietary RSS feeds and enabling open source press release publishing across its network.

Financial News USA has been agg...

Shire Announces Status of Ongoing FDA Review of NDA for DAYTRANA ...

... Shire Announces Status of Ongoing FDA Review of NDA for DAYTRANA(TM) for the Treatment of ADHD Shire Announces Status of Ongoing FDA Review of NDA for DAYTRANA(TM) for the Treatment of ADHD PHILADELPHIA, Pennsylvania, and BASINGSTOKE, England, March 10 /PRNewswire-FirstCall/ - Shire plc (LSE: SHP, NASDAQ: SHPGY, TSX: SHQ) announced today that the U.S.

Food and Drug Administration (FDA) has confirmed that Shire's resubmission for DAYTRANA in response to information that the FDA requested in its December 23, 2005 approvable letter for DAYTRANA's New Drug Application is being treated as a Class I resubmission.

The review period for Class I resubmissions is 60 days, and since Shire's resubmission was made on February 9, 2006, the anticipated FDA action date is April 9, 2006.

DAYTRANA (methylphenidate transdermal system (MTS)) is an investigational transdermal patch formulation for methylphenidate designed for once-daily use to treat attention deficit hyperactivity disorder (ADHD) in children aged 6 to 12 years.

Shire is planning to launch DAYTRANA, if approved, during the first half of 2006.

DAYTRANA is licensed globally to Shire by Noven Pharmaceuticals, Inc.

Notes to Editors SHIRE PLC Shire's strategic goal is to become the leading specialty pharmaceutical company that focuses on meeting the needs of the specialist physician.

Shire focuses its business on central nervous system, gastrointestinal, general products and human genetic t...

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