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Female lung transplant recipients at greater risk of acute lung injury

25 May 2005 - Female lung transplant recipients are significantly more likely to suffer from a type of injury to the transplanted lung called primary graft dysfunction than male lung transplant patients, according to a study to be presented at the American Thoracic Society International Conference on May 24.

The study found that female lung transplant recipients who received a lung from either a male or female donor were almost 60% more likely to suffer from primary graft dysfunction, compared with male recipients who received their lung from a male donor.

"There are a number of possible reasons why women are at increased risk," said lead researcher Catherine Kuntz, M.D., Pulmonary Fellow at the Hospital of the University of Pennsylvania. "It may involve women's hormones or differences in their immune systems."

The study included data on all 7,482 adult lung transplants performed in the United States between 1994 and 2002. The researchers took into account factors such as the donor's age, race, cause of death, and the recipient's age, race and reason for lung transplant, as well as the size matching between the donor and recipient.

Overall, approximately 10% of transplant recipients suffered from primary graft dysfunction, which is an acute severe lung injury that occurs within the first 72 hours after the transplant and has a high mortality.

Once the lung is taken out of the donor, it is put on ice, and during this time, no blood flows through the organ. When the lung is transplanted into the recipient and all the blood vessels are reattached, injury to the lung may become apparent. Lung graft dysfunction is associated with a high death rate, prolonged hospital stay and other serious complications.

"We need further investigation into what it is about women that increases the risk," Dr. Kuntz said. "We need to look at factors such as whether the women have gone through menopause, and how many children they've had."

According to the United Network for Organ Sharing (UNOS) there are currently 3,688 Americans waiting for a lung transplant for diseases including cystic fibrosis, chronic obstructive pulmonary disease (COPD), primary pulmonary hypertension and pulmonary fibrosis.

Contact: Jim Augustine
619-525-6216
American Thoracic Society
http://www.thoracic.org


Little Jack has a double transplant

A LITTLE boy who was given just weeks to live as a baby is set to undergo a life-saving double transplant operation.

Jack Waller was rushed to London's Great Ormond Street Hospital with a police escort yesterday to receive a new heart and lungs.

The South Yorkshire five-year-old - nicknamed "Backpack Boy" because of the vital medical equipment he has had to carry on his back in a rucksack - was placed on the transplant list just one month ago after his condition declined dramatically.
His mother Diane was telephoned at their home in Brampton, between Barnsley and Rotherham, at breakfast time and told the organs had become available.

Her sister Joanne Read told The Star: "We've been feeling every emotion you can possibly imagine.

"We're relieved because he needs this, but it's a big operation and of course we feel for the family of the donor child."
For the past four years Jack has been hooked up to a backpack 24 hours a day which shoots drugs into his heart every three minutes.

The Cortonwood Infants and Junior School student is the face of Bluebell Wood Children's Hospice Appeal, which is aiming to build a facility in Dinnington to care for poorly youngsters.
He suffers from primary pulmonary hypertension and experts say a transplant is his last chance of survival.

Just six children in the UK had a double heart and lung transplant last year and the average waiting time was 546 days.


Scientific Publication on Long-term Bosentan Use in PPH
ALLSCHWIL, Switzerland, Feb. 1, 2005 - Actelion Ltd (SWX: ALTN) announced today the publication of the scientific paper evaluating disease outcome of patients with advanced primary pulmonary arterial hypertension receiving Tracleer(bosentan).

Fitch Affirms Wyeth's 'A-/F2' Senior Unsecured & CP Ratings
CHICAGO--(BUSINESS WIRE)--Jan 31, 2005 - Fitch Ratings has affirmed Wyeth's 'A-' senior unsecured credit rating and 'F2' commercial paper rating.

Wyeth Reports Results for the 2004 Fourth Quarter and Full Year
MADISON, N.J., January 31, 2005 /PRNewswire-FirstCall/ -- Wyeth today reported results for the 2004 fourth quarter and full year. Worldwide net revenue increased 7% to $4.6 billion for the 2004 fourth quarter and 10% to $17.4 billion for the 2004 full year.

Victims, Attorneys Praise New Ruling in Fen-Phen Litigation; Ruling Allows Key Evidence in Thousands of Heart Valve Cases, Says Majority Counsel
DALLAS, May 26, 2004 /PRNewswire/ -- The following was released today by Majority Counsel:

Ambrisentan Phase II Results Presented at ATS 2004
DENVER, May 24, 2004 /PRNewswire-FirstCall/ -- Myogen, Inc. (NASDAQ:MYOG) , a biopharmaceutical company focused on the discovery, development and commercialization of small molecule therapeutics for the treatment of cardiovascular disorders, announced that Lewis Rubin, M.D. presented detailed results of AMB-220, the Company's Phase II safety and efficacy study of ambrisentan in patients with pulmonary arterial hypertension (PAH), at a mini symposium on "Emerging Therapies for PAH" at the American Thoracic Society (ATS) 2004 International Conference.

Record Fen-Phen Judgment Upheld; Judge and Jury Outraged By Evidence Proving Wyeth Knowingly Sold Harmful Drug, Says Majority Counsel
BEAUMONT, Texas, May 17, 2004 /PRNewswire/ -- The following was released today by Majority Counsel:

Freedland, Farmer, Russo & Sheller PL Prepares Phen-fen Case Similar To Recent $1 Billion Verdict; Family Sues Drug-maker, Hospital and Doctor for Mother's Death
WESTON, Fla.--(BUSINESS WIRE)--Apr 30, 2004 - Coming on the heels of a Texas jury's $1 billion award to the family of a woman who died after taking one of the now banned phen-fen diet drugs, Freedland, Farmer, Russo & Sheller PL await a trial date for a strikingly similar case against Wyeth-Ayerst Laboratories.

Wyeth to Appeal Verdict in Diet Drug Case
MADISON, N.J., April 27, 2004 /PRNewswire-FirstCall/ -- Wyeth (NYSE:WYE) said today it will appeal today's verdict in the case of Jerry Coffey (representing the estate of Cynthia Cappel-Coffey), et al. v. Wyeth, et al.

Landmark Judgment in Fen-Phen Trial
BEAUMONT, Texas, April 27 /PRNewswire/ -- The following was released today by Majority Counsel: A Beaumont, Texas jury today returned a more than $1 billion verdict against Wyeth-Ayerst Laboratories in a landmark Fen-Phen trial. Experts predict that this outcome against drug-maker Wyeth will set the standard by which the company will be judged in the tens of thousands of Fen-Phen cases currently in the court system awaiting trial dates.

Phen-Fen's Hazards Emerge Anew; Family Sues Drug-Maker, Hospital & Doctor for Mother's Death According to Freedland, Glassman, Farmer & Sheller
WESTON, Fla.--(BUSINESS WIRE)--March 22, 2004--After almost a decade of stories of death and illness, billions of dollars in settlements, and persistent fears about Phen-Fen's damaging effects on those who've used it, news is emerging about lingering health risks related to the once-popular diet drug.

Actelion announces Full Year 2003 financial results
ALLSCHWIL/BASEL, SWITZERLAND - March 2, 2004 - Actelion Ltd (SWX: ATLN) today announced its financial results for the year 2003. With net revenues of CHF 307.5 million (FY 2002: CHF 132.4 m) and operating expenses of CHF 309.2 million (FY 2002: 164.5 m), the company reported an operating loss of CHF 1.7 million (FY 2002 loss: 32.0 m), mainly the result of a one-time In-Process R&D charge, related to the acquisition of Axovan in late 2003.

Profile Signs Inhaler Agreement with Schering
WEST SUSSEX, England, Oct. 24, 2003--Profile Therapeutics plc ("Profile"), which develops and commercialises specialist inhaled therapies, is delighted to announce the signing of an agreement with Schering Health Care Ltd. ("Schering"), a division of Schering AG.

HIV Patients with Pulmonary Arterial Hypertension (PAH): Results of Treatment with Oral Tracleer (bosentan)
ALLSCHWIL/BASEL, Switzerland, Sept. 2, 2003 - Actelion Ltd (SWX: ATLN) today announced results of a study assessing its oral dual endothelin receptor antagonist (ERA) Tracleer® (bosentan) in the treatment of pulmonary arterial hypertension (PAH) related to HIV (human immunodeficiency virus) infection.

New analysis suggests treatment with Tracleer (bosentan) is associated with improved survival in primary pulmonary hypertension patients
ALLSCHWIL/BASEL, SWITZERLAND - May 19, 2003 - Actelion Ltd (SWX: ATLN) today announced the analysis of long-term follow-up data of primary pulmonary hypertension patients from Tracleer® pivotal registration studies.

Aradigm and geneRx+ Announce Drug Delivery Collaboration for Gene-Based Therapeutics
HAYWARD, Calif. and ATLANTA, Sept. 26, 2002 /PRNewswire-FirstCall/ -- Aradigm Corporation (NASDAQ: ARDM) , a leader in pulmonary drug delivery and geneRx+, an innovator in protein and gene-based technologies, today

Deadline Set for Those Who Opted Out of the Fen-Phen Settlement, Says Attorney Michael Hackard
SACRAMENTO, Calif., Jan. 10, 2002 -- People who have opted out of the class-action lawsuit against American Home Products and

Deaths, Lawsuits on Rise as Fen-Phen Withdrawal Approaches 4-Year Anniversary; Cases Against Diet Drug Manufacturer Could Double, Says Leading Pharmaceutical Attorney Michael Hackard
SACRAMENTO, Sept. 10, 2001 -- Two wrongful death complaints filed today in California could signal a renewed wave of lawsuits against American Home Products just as the pharmaceutical company coaxes investors back with predictions that its legal troubles over Fen-Phen/Redux are coming to an end.

The Faces of Fen-Phen; All They Wanted Was to Lose Weight; Now Their Families Face a Bigger Loss
SACRAMENTO, Calif., Sept. 10, 2001 -- Donald Holmes of San Juan Bautista was the 63-year-old owner of a trucking company

AMERICAN HOME PRODUCTS CORPORATION REPORTS STRONG OPERATING RESULTS
MADISON, N.J., Jan. 25, 2001 -- American Home Products Corporation (the Company) (NYSE: AHP) today reported net revenue and results of operations for the 2000 fourth quarter and full year.

National Diet Drug Class Action Against French Pharmaceutical Giant Cleared to Proceed Access to Justice for 155,000 Canadians
TORONTO, Nov. 22, 2000 - Access to justice for more than 155,000 Canadians who took the diet pills Ponderal and Redux which are alleged to cause serious illnesses is now a reality following an important ruling released today from Madam Justice Susan Gray of the Ontario Divisional Court.

American Home Products Corporation Reports Continued Strong Sales and Earnings From Continuing Operations for the 2000 Third Quarter and First Nine Months
MADISON, N.J., Oct. 19, 2000 -- American Home Products Corporation (the Company) (NYSE: AHP) today reported sales and earnings results for the 2000 third quarter and first nine months.

United Therapeutics Corporation: Pulmonary Hypertension Clinical Trial Discussed at Seminar Associated With European Cardiology Conference
SILVER SPRING, Md. and RESEARCH TRIANGLE PARK, N.C., Aug. 28, 2000 -- United Therapeutics Corporation (Nasdaq: UTHR) announced today that results of its Phase III clinical trial of Uniprost (also known as UT-15) for pulmonary hypertension -- the largest double blinded placebo-controlled pulmonary hypertension study -- were presented today at a satellite symposium organized for clinicians attending the European Society of Cardiology's annual meeting in Amsterdam, The Netherlands.

Glaxo Wellcome's Flolan Now Approved for a New Use
Research Triangle Park, NC, (May 2, 2000)-Glaxo Wellcome Inc. announced today that Flolan‚ brand epoprostenol sodium for Injection, a treatment for severe cases of primary pulmonary hypertension (New York Heart Association (NYHA) classes III & IV), has now received approval for a new indication, the long-term intravenous treatment of pulmonary hypertension secondary to scleroderma spectrum of diseases (PH/SSD, NYHA classes III & IV) for patients who do not respond to conventional therapy.

American Home Products CEO Forced to Testify in Fen-Phen Case
HOUSTON, March 13, 2000 -- Fleming & Associates, L.L.P., lead counsel for two severely injured Sioux Falls, South Dakota, women who ingested Fen-Phen, has successfully petitioned the court to order John R. Stafford, chairman, president and CEO of American Home Products Corporation (NYSE: AHP) (AHP), to undergo an immediate deposition by plaintiffs’ attorney George M. Fleming.


 

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