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The initiation of the trial follows an official approval of the study by the Ethical Committee of the Laniado-Sanz Medical Centre in Netanya, Israel. The study is expected

The agreement has been reached under the special protol assessment procedure, a process under which the FDA provides evaluation and guidance on clinical trial protocols for phase III

According to the company, results from the trial provide strong support for clinical investigation, clearly illustrating the prospects for siRNA therapeutics to address unmet clinical need, but also

In exchange, Vical has obtained non-exclusive, sub-licensable rights to use the technology for vaccines against HIV, giving both companies freedom to operate in the field. “These options allow

Patients using the Lilly/Alkermes inhaled insulin system achieved blood sugar levels similar to patients treated with injected insulin. In addition, 80% of patients in this study expressed a

ImClone Systems intends to use the UltiMAb system to develop human antibody product candidates against its disease targets, which are primarily in the area of oncology. Under the

Cytori, in collaboration with researchers from the University of California in Los Angeles, has illustrated that adipose (fat) derived stem and regenerative cells can improve left ventricular function

The application has been submitted under the European Medicines Agency’s (EMEA’s) centralized procedure for product approval, which provides review and approval for all countries within the EU. The

The drug reduces glucose levels in the blood, and also increases levels of high-density lipoprotein, or ‘good’ cholesterol. Pargluva is an investigational oral medication that, if approved, would