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Depression Predicts Lung Transplant Quality of Life

Depression and Quality of Life

June 18, 2005 - Duke University Medical Center researchers have shown that depression is a significant predictor of worse quality of life and perceived shortness of breath in patients awaiting lung transplantation. The negative effects of depression are above and beyond other factors, such as lung function and the underlying disease, they said.

Additionally, the researchers believe that efforts to treat the depression could possibly improve the outcomes after lung transplantation. While their study focused on patients awaiting transplantation, the researchers say that what they are learning about depression could also help other patients with severe lung disease, such as the estimated 16 million Americans who suffer from chronic obstructive pulmonary disease (COPD).

"These findings represent an example of how psychological factors can impact physical health," said pulmonologist Scott Palmer, M.D., medical director of Duke's lung transplantation program. "The effect of depression is quite striking in predicting a lung patient's quality of life as well as their perceived shortness of breath.

"The findings also suggest that while we have many medical treatments for these patients, if we don't address the issue of anxiety and depression we might have less impact on their quality of life, and possibly their ultimate outcomes," Palmer added.

Palmer prepared the results of the Duke study for presentation today (May 20) during the 98th annual international conference of the American Thoracic Society.

Their report is the first analysis of data being collected on patients awaiting lung transplants enrolled in a five-year, $2.6 million trial funded by the National Heart, Lung and Blood Institute. The trial's goal is to determine whether a telephone-based program of stress and anxiety reduction conducted prior to transplant has any effect on outcomes after surgery. During the course of the trial, Duke and Barnes-Jewish Hospital at Washington University, St. Louis, the two largest lung transplant centers in the U.S., plan to enroll 600 patients.

"Patients waiting for a transplant are under so much stress and anxiety," said collaborator James Blumenthal, Ph.D. "They worry about when the call will come or whether they'll survive the operation. In most cases, patients must relocate to the transplant center to wait for an available organ, which takes them away from their usual emotional support systems."

For this "snapshot" of the psychological and physical status of the first 99 patients enrolled in the trial on Duke's waiting list, patients took a battery of tests to measure their depression and anxiety, as well as questionnaires covering quality of life issues for lung patients and perceived shortness of breath.

The median number of days that patients had been on the waiting list was 77 days. Nationally, patients awaiting lung transplant wait an average of 18 months from the time they are listed to undergo the operation.

The researchers then performed statistical analyses to determine which of the following variables seemed to best predict quality of life and shortness of breath issues: social support, depression, gender, age, time on waiting list, underlying disease and lung function.

"Our analysis suggests that while lung function and underlying disease are important predictors of pulmonary quality of life and shortness of breath, depression appears to be a stronger predictor," Palmer said. "We need more studies to evaluate different interventions to see if they have any impact on quality of life and post-transplant outcomes."

The current trial, whose results should be available in two years, will be the first to gauge whether psychological interventions can improve the outcomes of lung transplant patients. Other possible interventions include medications or exercise, which has been proven effective in treating depression. The researchers add that there is an integral link between psychological status and lung function.

"Often, when a lung patient is short of breath, he or she becomes anxious or agitated, which can then cause them to breathe faster and shallower? it can then quickly become of vicious cycle," Blumenthal said. "Anything we can do to lessen the degree of anxiety for lung patients should be of benefit to their perceived quality of life."

Duke performed its first lung transplant procedure in 1992. In the ensuing 10 years, the Duke program has become the largest in the country, having performed more of the surgeries than any other program in each of the past two years.

_________________

ATLANTA - DukeMed News


Myogen Reports Positive Results for Darusentan Phase 2b Trial in Resistant Hypertension
DENVER, Aug. 18, 2005 /PRNewswire-FirstCall/ -- Myogen, Inc. today announced positive top line results of its Phase 2b trial evaluating darusentan in resistant hypertension.

Actelion Ltd.: JACC Publication on Tracleer in Children with PAH
ALLSCHWIL, Switzerland, Aug. 16, 2005 (PRIMEZONE) -- Actelion Ltd. (Other OTC:ALIOF) (SWX:ATLN) announced today that the Journal of the American College of Cardiology (JACC) has published a new study that investigated the long-term outcome of children with pulmonary arterial hypertension (PAH) treated with the dual endothelin receptor antagonist Tracleer (bosentan) with or without concomitant prostanoid therapy.

Predix Pharmaceuticals Initiates Phase III Clinical Trial of PRX-00023 in Generalized Anxiety Disorder; Provides Positive, Preliminary Findings from Phase II Study
LEXINGTON, Mass. & RAMAT GAN, Israel--(BUSINESS WIRE)--Aug 15, 2005 - Predix Pharmaceuticals, a drug discovery and development company, today announced the initiation of its first pivotal Phase III trial of PRX-00023, the company's novel 5-HT1A agonist, in patients with generalized anxiety disorder (GAD).

United Therapeutics Completes European Mutual Recognition for Remodulin
SILVER SPRING, Md. and RESEARCH TRIANGLE PARK, N.C., Aug. 10, 2005 /PRNewswire-FirstCall/ -- United Therapeutics Corporation announced today that the European Union Mutual Recognition Procedure (MRP) has been completed for Remodulin (treprostinil sodium) Injection for the subcutaneous treatment of NYHA Class III Primary Pulmonary Hypertension patients.

Actelion: Second Study with bosentan (Tracleer) Demonstrating a Statistically Significant Reduction of New Digital Ulcers in Patients with Systemic Sclerosis
ALLSCHWIL, Switzerland, Aug. 9, 2005 (PRIMEZONE) -- Actelion Ltd announced today the preliminary result of a double-blind, placebo-controlled, randomized, multi-center, 190-patient Phase III study, RAPIDS-2, with the dual endothelin receptor antagonist bosentan (Tracleer) in systemic sclerosis patients suffering from digital ulceration.

Icagen Reports Second Quarter 2005 Financial Results
RESEARCH TRIANGLE PARK, N.C., Aug. 9, 2005 /PRNewswire-FirstCall/ -- Icagen, Inc. today reported financial results for the second quarter ended June 30, 2005. Revenues for the second quarter of 2005 totaled $1.7 million.

ICOS Corporation Reports Results for 2005 Second Quarter; Lilly ICOS Nears Profitability, Quarterly Loss Narrows to $1.7 Million
BOTHELL, Wash.--(BUSINESS WIRE)--Aug 4, 2005- ICOS Corporation today released its financial results for the three and six months ended June 30, 2005 and summarized recent events.

Predix Pharmaceuticals Files for Initial Public Offering
LEXINGTON, Mass. & RAMAT GAN, Israel--(BUSINESS WIRE)--Aug 3, 2005 - Predix Pharmaceuticals, a drug discovery and development company, today announced that it has filed a registration statement with the Securities and Exchange Commission (SEC) relating to the proposed initial public offering of primary shares of its common stock.

Myogen Reports 2005 Second Quarter Results
DENVER, Aug. 1, 2005 /PRNewswire-FirstCall/ -- Myogen, Inc. , a biopharmaceutical company focused on the discovery, development and commercialization of small molecule therapeutics for the treatment of cardiovascular disorders, today reported 2005 second quarter results.

Committee for Medicinal Products for Human Use Summary of Opinion for Revatio - International Nonproprietary Name (INN): sildenafil citrate
LONDON, July 27, 2005 - On 27 July 2005 the Committee for Medicinal Products for Human Use adopted a positive opinion, recommending to grant a marketing authorisation for the medicinal product Revatio 20 mg film-coated tablets intended for treatment of patients with pulmonary hypertension.

Encysive Files for European Marketing Approval of Thelin
HOUSTON, July 28, 2005 /PRNewswire-FirstCall/ -- Encysive Pharmaceuticals today announced that it has completed the submission of a Marketing Authorization Application (MAA) with the European Agency for the Evaluation of Medicinal Products (EMEA) for Thelin (sitaxsentan) 100 mg as a once daily oral treatment for patients with pulmonary arterial hypertension (PAH).

FDA Sends Warning Letter to Actelion Over Tracleer Web Page
ROCKVILLE, Md., July 26, 2005 - The Food and Drug Administration today posted on its website a warning letter sent to Actelion Pharmaceuticals over a Tracleer product page on the Actelion website.

Committee for Orphan Medicinal Products July 2005 Meeting
LONDON, July 22, 2005 - The fifty-ninth meeting of the Committee for Orphan Medicinal Products (COMP) took place on 12-13 July 2005.

Myogen Announces Completion of Enrollment for Pivotal Phase 3 ARIES-2 Trial of Ambrisentan in PAH
DENVER, July 21, 2005 /PRNewswire-FirstCall/ -- Myogen, Inc. , a biopharmaceutical company focused on the discovery, development and commercialization of small molecule therapeutics for the treatment of cardiovascular disorders, today announced the completion of enrollment of 187 patients in ARIES-2, one of the Company's two pivotal Phase 3 trials of ambrisentan in patients with pulmonary arterial hypertension (PAH).

Pfizer Inc Second-Quarter 2005 Performance Report
NEW YORK, July 20, 2005 /PRNewswire-FirstCall/ -- Pfizer today reported financial results for the second quarter of 2005.

Sepracor Announces Second Quarter 2005 Operating Results
MARLBOROUGH, Mass.--(BUSINESS WIRE)--Jul 19, 2005 - Sepracor Inc. (Nasdaq: SEPR) today announced its consolidated financial results for the second quarter of 2005.

Predix Pharmaceuticals Announces Initiation of Phase Ib Clinical Trial in Alzheimer's Patients; Provides Initial Dose Study Update
LEXINGTON, Mass. & RAMAT GAN, Israel--(BUSINESS WIRE)--Jul 13, 2005 - Predix Pharmaceuticals, a drug discovery and development company, has initiated the second of two Phase Ib multiple dose studies with PRX-03140, its highly selective, proprietary serotonin 4 (5-HT4) receptor agonist intended to treat Alzheimer's disease and other disorders of memory and cognition.

Myogen Reports Results for Phase 3 Enoximone Trials in Chronic Heart Failure
DENVER, June 26, 2005 /PRNewswire-FirstCall/ -- Myogen, Inc. today announced top line results of ESSENTIAL I & II, the Company's two Phase 3 trials of enoximone capsules in patients with advanced chronic heart failure (CHF).

DATAMONITOR: Is Diagnosis Failing Heart Failure Patients?
LONDON, June 22, 2005--It is widely acknowledged that heart failure has reached epidemic proportions.

Actelion Launches Tracleer in PAH in Japan
ALLSCHWIL, Switzerland, June 8, 2005 (PRIMEZONE) -- Actelion Ltd (SWX:ATLN) (Other OTC:ALIOF) announced today that Tracleer (bosentan) is now available upon prescription to all patients in Japan.

CoTherix Initiates Phase II Trial for Ventavis in Expanded Indication
SOUTH SAN FRANCISCO, Calif., June 01, 2005 /PRNewswire-FirstCall/ -- CoTherix, Inc. announced today that it has initiated a Phase II trial for its marketed product, Ventavis (iloprost) Inhalation Solution, to potentially expand the indication to include pulmonary hypertension (PH) associated with idiopathic pulmonary fibrosis (IPF).

Biotech Continues Its Steady Improvement in May
SAN FRANCISCO, June 01, 2005 /PRNewswire/ -- "While Genentech continued to impress with another excellent month, the whole sector performed well with hardly a negative number in sight," noted G. Steven Burrill, CEO of Burrill & Company, a San Francisco based life sciences merchant bank.

Encysive Pharmaceuticals Submits New Drug Application for Thelin
HOUSTON, May 25, 2005 /PRNewswire-FirstCall/ -- Encysive Pharmaceuticals today announced that it has completed the submission of a New Drug Application (NDA) with the U.S. Food and Drug Administration (FDA) for Thelin (sitaxsentan) 100 mg as a once daily oral treatment for patients with pulmonary arterial hypertension (PAH).

Researchers Present Data That Support Inhaled Iloprost Therapy in Patients With Pulmonary Arterial Hypertension
SAN DIEGO, Calif., May 23, 2005 /PRNewswire-FirstCall/ -- CoTherix, Inc. announced today that researchers have presented results involving inhaled iloprost therapy for the treatment of pulmonary arterial hypertension (PAH), a debilitating and potentially fatal disease characterized by high blood pressure in the pulmonary arteries.

Long-term Tracleer (bosentan) Safety Profile Confirmed with Completion of Non-interventional Program in Almost 5,000 Patients

SAN DIEGO - May 23, 2005 - Actelion Ltd (SWX: ATLN) announced that data from almost 5,000 Tracleer®-treated patients amounting to 3,416 patient-years of treatment were presented on Monday at the American Thoracic Society (ATS) meeting in San Diego.

Encysive Pharmaceuticals Announces New STRIDE-2 Data Presented at American Thoracic Society International Conference

HOUSTON, May 23, 2005 /PRNewswire-FirstCall/ -- Encysive Pharmaceuticals today presented additional data from STRIDE-2, the Company's second randomized, pivotal Phase III clinical trial of Thelin (sitaxsentan) for the treatment of pulmonary arterial hypertension (PAH) at the annual International Conference of the American Thoracic Society (ATS) in San Diego.

Myogen Initiates Trial of Ambrisentan in Patients Who Previously Failed Other ERA Therapy
DENVER, May 19, 2005 /PRNewswire-FirstCall/ -- Myogen, Inc. , a biopharmaceutical company focused on the discovery, development and commercialization of small molecule therapeutics for the treatment of cardiovascular disorders, today announced the initiation of a clinical trial to evaluate ambrisentan in patients with pulmonary arterial hypertension (PAH) who have previously discontinued bosentan or sitaxsentan therapy due to liver function test (LFT) abnormalities, specifically elevated serum aminotransferase concentrations.
Data from Tarceva Clinical Trial Program Presented at American Society of Clinical Oncology Annual Meeting
ORLANDO, Fla.--(BUSINESS WIRE)--May 17, 2005 - OSI Pharmaceuticals (Nasdaq: OSIP) provided a second informational update summarizing highlights from presentations on Tarceva (erlotinib) made at the 41st Annual Meeting of the American Society of Clinical Oncology (ASCO) being held from May 14-17 in Orlando, Fla.

Phase III Trial of Avastin Plus Chemotherapy Showed 30 Percent Improvement in Overall Survival in First-Line Non-Squamous, Non-Small Cell Lung Cancer
ORLANDO, Fla., May 13, 2005 /PRNewswire-FirstCall/ -- Genentech, Inc. and Roche (SWX Zurich) today announced that data from a Phase III study (E4599) of Avastin (bevacizumab) plus paclitaxel and carboplatin chemotherapies in first-line non-squamous, non-small cell lung cancer (NSCLC) showed the study met its primary efficacy endpoint of improving overall survival.

First Results From PTK/ZK CONFIRM 1 Trial Presented at American Society of Clinical Oncology Show Positive Drug Effects in Advanced Colorectal Cancer
BERLIN, May 13, 2005 /PRNewswire-FirstCall/ --First results from the phase III CONFIRM 1 trial showed that PTK/ZK, a new oral targeted therapy designed to block the growth of blood and lymphatic vessels, demonstrated positive drug effects in patients with metastatic colorectal cancer combined with FOLFOX chemotherapy as first-line therapy. It was announced today by Schering AG (NYSE: SHR; FSE: SCH).

AGGRASTAT Injection Strategy Trial Data Published in JAMA
BALTIMORE, May 11, 2005 /PRNewswire-FirstCall/ -- Guilford Pharmaceuticals Inc. today announced the publication of results from the STRATEGY trial of AGGRASTAT Injection (tirofiban hydrochloride) in the Journal of the American Medical Association, (May 2005 - Vol. 293, No. 17 pgs. 2109 - 2117).

New Eloxatin and Taxotere Research to Be Presented at the Annual Meeting of the American Society of Clinical Oncology (ASCO)
PARIS, May 10, 2005 /PRNewswire-FirstCall/ -- The sanofi-aventis Group announced today that important results from Eloxatin (oxaliplatin for injection) and Taxotere(docetaxel) Injection Concentrate clinical studies, including studies on colorectal, breast, lung, prostate and gastric cancer, will be presented at the 41st Annual Meeting of the American Society of Clinical Oncology (ASCO).

ICOS Corporation Reports Results for 2005 First Quarter; Tadalafil to be Evaluated in a Pivotal Clinical Study in Pulmonary Arterial Hypertension
BOTHELL, Wash.--(BUSINESS WIRE)--May 5, 2005 - ICOS Corporation (Nasdaq:ICOS) today released its financial results for the three months ended March 31, 2005 and summarized recent events.

Kos Announces Strategic Commercialization and Research and Development Alliance with Biovail in Cardiovascular Arena
CRANBURY, N.J.--(BUSINESS WIRE)--May 3, 2005 - Kos Pharmaceuticals, Inc. (Nasdaq: KOSP) today announced that it has entered into a strategic commercialization and research and development alliance with Biovail Corporation (NYSE: BVF) and certain of its subsidiaries in the area of cardiovascular disease.

Myogen Reports 2005 First Quarter Results
DENVER, May 02, 2005 /PRNewswire-FirstCall/ -- Myogen, Inc. , a biopharmaceutical company focused on the discovery, development and commercialization of small molecule therapeutics for the treatment of cardiovascular disorders, today reported 2005 first quarter results.

Protein Design Labs Announces First Quarter 2005 Financial Results
FREMONT, Calif., May 02, 2005 /PRNewswire-FirstCall/ -- Protein Design Labs, Inc. (PDL) today reported a net loss of $83.9 million, or $0.87 per basic and diluted share, for the three months ended March 31, 2005, compared with a net loss of $12.6 million, or $0.13 per basic and diluted share, for the three months ended March 31, 2004.

Encysive Pharmaceuticals Reports First Quarter 2005 Financial Results: Conference Call Scheduled for Today at 4:30 p.m. Eastern
HOUSTON, April 28, 2005 (PRIMEZONE) -- Encysive Pharmaceuticals (Nasdaq:ENCY) today announced financial results for the first quarter ending March 31, 2005.

Cytopia Gets Green Light to Trial Promising New Cancer Drug
MELBOURNE, Australia, April 27, 2005 /PRNewswire/ -- Up to 30 patients with advanced incurable solid-tumours are to be involved in clinical trials of a potent new anticancer drug (CYT997), developed by Australian biotechnology company, Cytopia Limited.

FDA Sends United Therapeutics Corp. Warning Letter Over Remodulin Advertisement
ROCKVILLE, Md., April 26, 2005 - The Food and Drug Administration today posted a warning letter sent to United Therapeutics Corporation about an advertisement for Remodulin.

Sepracor Announces First Quarter 2005 Operating Results
MARLBOROUGH, Mass., April 25, 2005 /PRNewswire-FirstCall/ -- Sepracor Inc. today announced its consolidated financial results for the first quarter of 2005.

Novartis First Quarter 2005 Sales and Results
BASEL, Switzerland, April 21, 2005 – Commenting on the first-quarter results published today, Dr. Daniel Vasella, Chairman and CEO of Novartis, said, “We are off to a strong start in 2005. In Pharmaceuticals, we once more gained market share, especially through the dynamic performance of our oncology portfolio. Our plans to integrate Hexal and Eon Labs making Sandoz the world leader in generics are on track, and will further strengthen our ability to fulfill customer needs with a broad health-care portfolio in the context of an aging population and rising health-care needs. We anticipate delivering a competitive performance in 2005 with record sales and, on a comparable basis, record earnings.”

Enrollment Completed in Phase 2b Trial of Darusentan in Patients with Resistant Systolic Hypertension
DENVER, April 19, 2005 /PRNewswire-FirstCall/ -- Myogen, Inc. , a biopharmaceutical company focused on the discovery, development and commercialization of small molecule therapeutics for the treatment of cardiovascular disorders, today announced the completion of patient enrollment in DAR-201, the company's Phase 2b trial of darusentan in patients with resistant systolic hypertension.

Pfizer Inc First-Quarter 2005 Performance Report
NEW YORK, April 19, 2005 /PRNewswire-FirstCall/ -- Pfizer today reported financial results for the first quarter of 2005.

Study of Breast Cancer Patients Showed Regimen Including EMEND- aprepitant- Prevented Nausea and Vomiting After Chemotherapy in More Patients than a Standard Regimen
WHITEHOUSE STATION, N.J.--(BUSINESS WIRE)--Apr 18, 2005 - The results of an investigational study evaluating the effect of an antiemetic regimen including EMEND in the prevention of nausea and vomiting after chemotherapy in breast cancer patients were published today in the Journal of Clinical Oncology (JCO).

FDA Sends Warning Letter to United Therapeutics Corp. Over Remodulin Advertisement
ROCKVILLE, Md., April 14, 2005 - The Food and Drug Administration today posted a letter on its website sent to United Therapeutics Corporation over advertisements for Remodulin

Japanese Approval for Tracleer in PAH
ALLSCHWIL, SWITZERLAND - 11 April 2005 - Actelion Ltd (SWX: ATLN) announced today that the Japanese Ministry of Health, Labor and Welfare has granted formal approval for Tracleer (bosentan) in Pulmonary Arterial Hypertension (PAH).

FW: DHC Press Release

CEDAR KNOLLS, N.J., April 8, 2005 – Dimensional HealthCare (DHC), which specializes in the delivery of late-phase (IIIb/IV), community-based clinical trials for the pharmaceutical and medical device industries, has announced several changes that will further expand our ability to provide our clients with a high level of scientific expertise, while delivering creative and effective industry solutions through clinical research programs.

Researchers Uncover New Clinical Syndrome: Destruction of Red Blood Cells Tied to Severe Symptoms in Diverse Diseases and Conditions

CHESHIRE, Conn., April 5, 2005 -- Researchers have identified a new clinical syndrome that produces serious and sometimes fatal symptoms in a variety of seemingly unrelated diseases.

Predix Pharmaceuticals Initiates Phase Ib Clinical Trials of 5-HT4 Agonist for Alzheimer's Disease and Other Cognitive Disorders
WOBURN, Mass. & RAMAT GAN, Israel--(BUSINESS WIRE)--Mar 30, 2005 - Predix Pharmaceuticals, a drug discovery and development company, today announced the initiation of two Phase Ib multiple dose studies with PRX-03140, its highly selective, proprietary serotonin 4 (5-HT4) receptor agonist intended to treat Alzheimer's disease and other disorders of memory and cognition.

Interim Analysis of Phase III Trial Shows Avastin Plus Chemotherapy Extends Survival of Patients With First-Line Non-Squamous, Non-Small Cell Lung Cancer

SOUTH SAN FRANCISCO, Calif. and BASEL, Switzerland, March 14, 2005 /PRNewswire-FirstCall/ -- Genentech, Inc. and Roche (SWX Zurich) today announced that an interim analysis of a Phase III study of Avastin (bevacizumab) plus paclitaxel and carboplatin chemotherapies in first-line non-squamous, non-small cell lung cancer (NSCLC) met its primary efficacy endpoint of improving overall survival, or a reduction in the risk of death, compared to chemotherapy alone.

United Therapeutics Completes European Mutual Recognition for Remodulin
SILVER SPRING, Md. and RESEARCH TRIANGLE PARK, N.C., Aug. 10, 2005 /PRNewswire-FirstCall/ -- United Therapeutics Corporation announced today that the European Union Mutual Recognition Procedure (MRP) has been completed for Remodulin (treprostinil sodium) Injection for the subcutaneous treatment of NYHA Class III Primary Pulmonary Hypertension patients.

Committee for Medicinal Products for Human Use Summary of Opinion for Revatio - International Nonproprietary Name (INN): sildenafil citrate
LONDON, July 27, 2005 - On 27 July 2005 the Committee for Medicinal Products for Human Use adopted a positive opinion, recommending to grant a marketing authorisation for the medicinal product Revatio 20 mg film-coated tablets intended for treatment of patients with pulmonary hypertension.

FDA Sends Warning Letter to Actelion Over Tracleer Web Page
ROCKVILLE, Md., July 26, 2005 - The Food and Drug Administration today posted on its website a warning letter sent to Actelion Pharmaceuticals over a Tracleer product page on the Actelion website.

Long-term Tracleer (bosentan) Safety Profile Confirmed with Completion of Non-interventional Program in Almost 5,000 Patients
SAN DIEGO - May 23, 2005 - Actelion Ltd (SWX: ATLN) announced that data from almost 5,000 Tracleer®-treated patients amounting to 3,416 patient-years of treatment were presented on Monday at the American Thoracic Society (ATS) meeting in San Diego.

FDA Sends United Therapeutics Corp. Warning Letter Over Remodulin Advertisement
ROCKVILLE, Md., April 26, 2005 - The Food and Drug Administration today posted a warning letter sent to United Therapeutics Corporation about an advertisement for Remodulin.

FDA Sends Warning Letter to United Therapeutics Corp. Over Remodulin Advertisement
ROCKVILLE, Md., April 14, 2005 - The Food and Drug Administration today posted a letter on its website sent to United Therapeutics Corporation over advertisements for Remodulin

United Therapeutics Announces Approval of Remodulin in France
SILVER SPRING, Md. and RESEARCH TRIANGLE PARK, N.C., March 08, 2005 /PRNewswire- FirstCall/ -- United Therapeutics Corporation announced today that AFSSAPS, the French drug regulatory agency, has issued an approval letter for Remodulin (treprostinil sodium) Injection for subcutaneous treatment of NYHA Class III Primary Pulmonary Hypertension patients.

The Claims Facilitating Committee Announces Enthusiastic Support for Opt-Out Settlement Process
PHILADELPHIA, February 28, 2005 /PRNewswire/ -- The Claims Facilitating Committee (CFC), announced today that lawyers representing nearly half of all claimants who have pending lawsuits against Wyeth related to the ingestion of diet drugs have agreed to recommend that their clients participate in the settlement process negotiated between Wyeth and the CFC.

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.

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.

Profile Therapeutics plc: Prodose AAD System Receives US Regulatory Approval & Update on Offer Talks
West Sussex, England, April 28, 2004--Profile Therapeutics plc ("Profile"), which develops and commercialises specialist inhaled therapies, is pleased to announce that, as expected, it has received regulatory approval from the US Food and Drug Administration ("FDA") for its Prodose Adaptive Aerosol Delivery ("AAD ") system.

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 Therapeutics Plc: Update on Regulatory Process for Promixin
WEST SUSSEX, Feb. 19, 2004 - Profile Therapeutics plc ('Profile'), which develops and commercialises specialist inhaled therapies, today announces that it has received positive opinion for Promixin from the respective regulatory authorities in eight of the fourteen markets in which it submitted, and therefore anticipates full regulatory approval in these markets over the coming months.

Sitaxsentan Results in Pulmonary Arterial Hypertension Published in The American Journal of Respiratory and Critical Care Medicine
HOUSTON, Feb. 17, 2004 /PRNewswire-FirstCall/--Encysive Pharmaceuticals today announced the publication of an article titled "Sitaxsentan Therapy for Pulmonary Arterial Hypertension" in the February 15 issue of the American Thoracic Society's American Journal of Respiratory and Critical Care Medicine (AJRCCM) (Vol. 169, pp. 441-447).

CoTherix, Inc., Expands Management Team
BELMONT, Calif., Jan. 29, 2004 /PRNewswire/--CoTherix, Inc., announced today the addition of two senior management team members.

Emphycorp Receives Cystic FibrosisOrphan Drug Designation for N115
FLEMINGTON, N.J., Jan. 28, 2004--The FDA has granted Emphycorp Orphan Drug Designation for investigational drug N115 for the treatment of Cystic Fibrosis.

Profile Therapeutics plc: Trading Update for 6 months ended 31 December 2003
WEST SUSSEX, England, Jan. 8, 2004 - Profile Therapeutics plc ('Profile'), which develops and commercialises specialist inhaled therapies, is pleased to announce the following key highlights for the 6 months ended 31 December 2003:

Sitaxsentan Clinical Data Presented at American Heart Association Meeting
HOUSTON, Nov. 10, 2003--Encysive Pharmaceuticals (Nasdaq:ENCY) today announced that data from its Phase IIb/III STRIDE (Sitaxsentan To Relieve ImpaireD Exercise) trial in Pulmonary Arterial Hypertension (PAH) was presented Sunday at the American Heart Association's Scientific Sessions 2003 in Orlando.

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.

CoTherix Obtains U.S. Rights to Ventavis (iloprost)
BELMONT, Calif., Oct. 14, 2003-- /PRNewswire/ -- CoTherix, Inc. has acquired exclusive United States development and marketing rights to Ventavis (iloprost), a synthetic prostacyclin analogue for the treatment of primary pulmonary hypertension developed by Schering AG (FSE: SCH; NYSE: SHR).

CoTherix, Inc., Raises $55M in Series C Fund Raising
BELMONT, Calif., Oct. 14, 2003-- /PRNewswire/ -- CoTherix, Inc., formerly known as Exhale Therapeutics, Inc., has closed its Series C round of financing, raising approximately $55 million.

Schering Receives EU Approval for Ventavis

BERLIN, Sept. 22, 2003 /PRNewswire-FirstCall/ -- Schering AG, Germany (NYSE: SHR; FSE: SCH) announced today that the European Commission in a Centralized Procedure approved Schering's new drug Ventavis(R) for marketing in all EU countries.

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.

Caremark Rx and AdvancePCS Announce Strategic Combination Creating $23 Billion Revenue Company
NASHVILLE, Tenn. & IRVING, Texas, Sept. 2, 2003--Caremark Rx, Inc. (NYSE: CMX), one of the nation's leading pharmaceutical services companies, and AdvancePCS (Nasdaq: ADVP), the nation's leading health improvement company, today announced the signing of a definitive merger agreement.

Actelion announces half-year result 2003
ALLSCHWIL/BASEL, SWITZERLAND - 29 July 2003 - Actelion Ltd (SWX: ATLN) today announced its financial result for the first six months of 2003. With operating revenues for H1 2003 of CHF 133.6 million (H1 2002: CHF 51.1 m) and operating expenses of CHF 105.5 million (H1 2002: 74.0m), the company reported an operating profit of CHF 10.1 million (H1 2002 loss: -29.7m).

Ventavis Receives a Positive Opinion From CPMP
BERLIN, May 27, 2003 /PRNewswire-FirstCall/ -- Schering AG, Germany (FSE: SCH, NYSE: SHR) announced today that Ventavis(R), a product for the treatment of patients with primary pulmonary hypertension, received a positive opinion from the Committee of Proprietary Medicinal Products (CPMP).

Ventavis Receives a Positive Opinion from CPMP
Berlin, Germany, May 23, 2003 - Schering AG, Germany (FSE: SCH, NYSE: SHR) announced today that Ventavis®, a product for the treatment of patients with primary pulmonary hypertension, received apositive opinion from the Committee of Proprietary Medicinal Products (CPMP).

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.

Additional Remodulin(R) Efficacy and Safety Data Published in Journal of Cardiovascular Pharmacology
RESEARCH TRIANGLE PARK, N.C., Jan. 24, 2003 /PRNewswire-FirstCall/ -- United Therapeutics Corporation (NASDAQ:UTHR) today announced that the article "Efficacy and Safety of Treprostinil: An Epoprostenol Analog for Primary Pulmonary Hypertension"

Remodulin(R) Long-Term Survival Data Presented At American Heart Association Conference
SILVER SPRING, Md., Nov. 20, 2002 /PRNewswire-FirstCall/ -- United Therapeutics Corporation (NASDAQ: UTHR) announced today that a preliminary assessment of potential survival benefit associated with Remodulin(R) (treprostinil sodium) Injection therapy

Successful prevention study with Tracleer* in scleroderma-related Digital Ulcerations presented at the American College of Rheumatology Actelion to continue further clinical development with its endothelin receptor antagonist in scleroderma-related indica
ALLSCHWIL, SWITZERLAND - 29 October 2002 - Actelion Ltd (SWX: ATLN) announced that Joseph H. Korn, MD, Professor of Medicine and Biochemistry, School of Medicine, Boston University, will present the

Actelion Reports Positive Data From Breathe-3 Clinical Study; Tracleer(TM) improves important hemodynamic parameters in children with PAH
ALLSCHWIL/BASEL, SWITZERLAND, June 5, 2002 /PRNewswire-FirstCall/ -- Actelion Ltd (SWX New Market: ATLN) announced today positive results from the clinical

EU Commission grants marketing approval for Tracleer™ – European Launch of break-through treatment for Pulmonary Arterial Hypertension to start in June
Allschwil, Switzerland – 20 May 2002 – Actelion Ltd (SWX New Market: ATLN) today announced that the European Commission has

American Home Products Corporation Reports Continued Growth in Net Revenue and Operating Results for The 2001 Fourth Quarter and Full Year
MADISON, N.J., Jan. 24, 2002 -- American Home Products Corporation (the Company) (NYSE: AHP) today reported net revenue and earnings results for the 2001 fourth quarter and full year.

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

Canadian Health Authority approves Actelion's Tracleer™ - First oral treatment for Pulmonary Arterial Hypertension
Allschwil, Switzerland - 3 December 2001 - Actelion Ltd (SWX New Market: ATLN) today announced that Tracleer™ (bosentan) tablets have

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

Interneuron Enters Into Comprehensive Redux Product Liability Agreement With American Home Products
LEXINGTON, Mass.--May 30, 2001-- Agreement Is Milestone in Resolution of Legal Actions Against Interneuron Company Now in a Position to Focus on Product Development Pipeline

Interneuron Enters Into Comprehensive Redux Product Liability Agreement With American Home Products
LEXINGTON, Mass.--May 30, 2001-- Agreement Is Milestone in Resolution of Legal Actions Against Interneuron Company Now in a Position to Focus on Product Development Pipeline

Actelion files for EU authorization for bosentan (Tracleer™) in pulmonary arterial hypertension
Allschwil, Switzerland - March 1, 2001 - Actelion Ltd, (SWX New Market: ATLN) announced today that it has filed for EU marketing authorization for its oral dual endothelin receptor antagonist bosentan (TracleerTM) in the treatment of pulmonary arterial hypertension. In the United States, a New Drug Application (NDA) for TracleerTM in the same indication was filed with the U.S. Food and Drug Administration in November of last year.

Profile Therapeutics plc Interim results for the six months ended 31 December 2000
March 1, 2001--Profile Therapeutics plc ("Profile"), the drug delivery company specialising in "intelligent inhaler" systems, announces its interim results for the six months ended 31 December 2000.

United Therapeutics Completes Enrollment in Phase III Study Of First Oral Therapy for Early-Stage Pulmonary Hypertension
RESEARCH TRIANGLE PARK, N.C., Feb. 26, 2001-- United Therapeutics Corporation (Nasdaq: UTHR) announced today that it has completed enrollment in its Phase III study of oral beraprost in patients with pulmonary hypertension.

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.

Inspire Pharmaceuticals' CEO Christy Shaffer Talks to The Wall Street Transcript
NEW YORK--Dec. 18, 2000--The Wall Street Transcript has published an in-depth interview with Christy Shaffer, CEO of Inspire Pharmaceuticals (Nasdaq:ISPH), in which she talks at length about the company's future.

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.

PDI Selected By United Therapeutics as U.S. Commercialization Partner For Beraprost PDI Will Integrate Services to Maximize Potential of a New Drug to Treat Peripheral Vascular Disease
UPPER SADDLE RIVER, N.J. and SILVER SPRING, Md., Nov. 1, 2000 -- Professional Detailing, Inc. (Nasdaq: PDII) and United Therapeutics Corporation (Nasdaq: UTHR) today announced that they have signed a five year agreement for PDI to provide a broad range of pre-launch and launch commercialization services for beraprost, a novel compound under development for peripheral vascular disease in the United States.

FDA Grants Priority Review to United Therapeutics New Drug Application For Pulmonary Hypertension
RESEARCH TRIANGLE PARK, N.C., Oct. 19, 2000 -- United Therapeutics Corporation (Nasdaq: UTHR) announced today that it has been informed by the FDA that six month Priority Review has been granted for its New Drug Application (NDA) for pulmonary hypertension.

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.

Profile Therapeutics plc -- Preliminary results for the year ended 30 June 2000
September 14, 2000 - Profile Therapeutics plc (LSE: PTP) announces the Company/s first set of preliminary results since its successful flotation on the London Stock Exchange in March 2000.

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.

Gene for Primary Pulmonary Hypertension Discovered At Columbia Genome Center Exclusively Licensed To United Therapeutics
SILVER SPRING, Md., July 20, 2000 -- United Therapeutics Corporation (Nasdaq: UTHR) announced today that a gene responsible for primary pulmonary hypertension has been identified by a team working at Columbia University and the New York State Psychiatric Institute.

American Home Products Corporation Reports Strong Sales and Earnings from Continuing Operations for the 2000 Second Quarter and First Half
July 20, 2000 - Significant highlights for the 2000 second quarter and first half: -- Income from continuing operations rose 19% and 18%, respectively -- Worldwide net sales increased 14% for both periods -- Diluted earnings per share from continuing operations increased 19% and 20%, respectively -- Liquidity strengthened as the Company received $3.8 billion from the sale of its Cyanamid Agricultural Products business and a $1.8 billion merger termination fee during the 2000 first half -- Three FDA approvals broaden the pharmaceutical product base, including new drug approvals for acute myeloid leukemia and gastric acid reflux disease, and enhanced labeling in rheumatoid arthritis

United Therapeutics Announces Commencement of Flolan-to-Uniprost Transition Study in Pulmonary Hypertension
RESEARCH TRIANGLE PARK, N.C. and SILVER SPRING, Md., May 8, 2000 -- United Therapeutics Corporation (Nasdaq: UTHR) announced today that it had filed with the FDA to commence a clinical study to investigate the safety of transitioning pulmonary hypertension patients from the intravenous drug Flolan to the investigational subcutaneous drug Uniprost.

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.
 

Confidential Client Questionnaire

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Have you been diagnosed with pulmonary hypertension?
 
No     Yes
Have you been diagnosed with
Primary Pulmonary Hypertension
or Primary Arterial Hypertension?
 
No     Yes
Did you ever use fen phen, pondimin or redux?
 
No     Yes
Did you use other diet drugs?
 
No     Yes
Are you on Treatment such as Flolan, Tracleer, Remodulin, Revatio (Viagra), Ventavis, or other?
No     Yes
 
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