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Prana ditches Alzheimer’s drug program

As part of the effort to manufacture GMP grade PBT1 (clioquinol) for clinical trials, Prana found unacceptably high levels of a di-iodo (toxic) form of PBT1. After further

FDA delays new Sanofi-Aventis sleep drug

An approvable letter outlines specific questions that have to be resolved before the FDA will approve a product for marketing. The FDA’s questions in this letter relate specifically

Karo Bio dips as Merck halts trials

Development of the compound was discontinued due to what the companies have described as “adverse findings” in on-going animal studies. Although this development program has been discontinued, Merck

Actelion cleared to market Tracleer in Japan

Tracleer (bosentan), the first oral dual endothelin receptor antagonist, is approved for the treatment of pulmonary arterial hypertension (PAH) (WHO class III and IV) and made available by

QLT and VasoGenix to develop heart failure treatment

The agreement covers the development of a sustained-release formulation of VasoGenix’s calcitonin gene related peptide (CGRP) using QLT’s Atrigel biodegradable sustained release drug delivery system. Under the terms