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Alberto Martinez-Castelao

Publications and source records attributed to Alberto Martinez-Castelao.

2 recordsLinked to original sources

Losartan reduces the burden and cost of ESRD: public health implications from the RENAAL study for the European Union.

Type 2 diabetes is the leading cause of end-stage renal disease (ESRD) in most industrialized countries in Europe. The RENAAL (Reduction of Endpoints in NIDDM with the Angiotensin II Antagonist Losartan) Study evaluated the renal protective effects of losartan versus placebo on a background of non-ACE-I/non-AIIA conventional antihypertensive therapy in 1513 patients with type 2 diabetes and nephropathy. Losartan reduced the incidence of doubling of serum creatinine, end-stage renal disease (ESRD), or death by 16% (P=0.022) and reduced the risk of progression to ESRD, defined as the initiation of dialysis or transplantation, by 29% (P=0.002). We set out to estimate the potential effect of losartan on the burden and costs associated with ESRD over 3.5 years in the European Union (EU). The risk reduction in new cases of ESRD was calculated by combining type 2 diabetes population estimates for the EU with the percent absolute risk reduction of ESRD in patients treated with losartan as observed in RENAAL. The number of days each patient experienced ESRD was defined as the length of time from onset of ESRD until the minimum of death or 3.5 years. ESRD-free person-years avoided with losartan treatment were calculated by combining the population estimate with the ESRD days avoided divided by number of days in a year. ESRD costs from Germany were used to approximate the potential cost savings from reduced time with ESRD and fewer ESRD cases on a EU wide basis. There are approximately 700,000 diagnosed type 2 diabetes patients with proteinuria (urine albumin/creatinine >or=300 mg/g) in the EU. The addition of losartan to the treatment regimen of these patients is expected to lead to a reduction of 44,100 cases of ESRD, 64,400 fewer person-years with ESRD, and reduce ESRD-related costs by euro 2.6 billion over 3.5 years based on RENAAL data. Treatment with losartan not only reduced the incidence of ESRD, but also can result in substantial cost savings in the European Union.

Angiotensin II Type 1 Receptor Blockers↗

Conivaptan (Yamanouchi).

Yamanouchi is developing conivaptan, an orally active vasopressin V1A and V2 antagonist for the potential treatment of heart failure, edema and hyponatremia. The company anticipated launch of the product for hyponatremia in 2002 [362201]. By May 2001, Yamanouchi was continuing phase II trials in Japan for hyponatremia and heart failure, and in the US and Europe for heart failure, and phase III trials in the US and Europe for hyponatremia [411763]. In July 2000, it had been reported that conivaptan was undergoing phase III trials in both the US and Europefor hyponatremia and heart failure [377561]. In April 1998, Warner-Lambert (now Pfizer) acquired the rights to YM-087 for US, South America, Europe and Africa, while Yamanouchi retains copromotion rights, but by November 2000, Pfizer had cancelled its licensing contract to market the drug in the US [397901]. In September 2001, analysts at Morgan Stanley predicted launch of conivaptan for hyponatremia in the US between 2004 and 2005 [422782]. In October 2001, analysts at Credit Suisse First Boston predicted that an NDA would be filed in 2002 followed by launch in 2003, with peak annual sales of $50 million and $300 million for hyponatremia and heart failure, respectively [427028].

Animals↗