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The trial was conducted by Covance, and involved 74 healthy volunteers enrolled in the UK. The primary objective of this Phase I clinical trial was to demonstrate that

Approved by the FDA for postoperative nausea and vomiting, Aloxi injection 0.075mg is administered as a single IV dose immediately before induction of anesthesia to prevent PONV for

The project is part of the EuroTransBio Initiative and is coordinated by the Dutch company Crossbeta Biosciences. The objective is the development of novel vaccine technologies based on

Viren Grover, vice-chairman of Pinnacle Biologics, said: “We are pleased to conclude this agreement with Pharmexx, which allows us a cost effective way to support our sales and

This represents a purchase price of CHF130 per registered share. Following the closing of the agreement with Speedel’s major shareholders, Novartis, including the 9.7% stake in Speedel prior

Chenofalk is approved in Germany for the dissolution of gallstones, and Sigma-Tau’s German affiliate, Sigma-Tau Arzneimittel, will immediately assume distribution of this important medicine, ensuring there is no

Zinthionein capsules (25mg capsules twice daily) were compared to placebo capsules twice daily on a 1:1 randomization scheme in a prospective, randomized, double-blind, placebo-controlled trial involving a total

The new Phase I clinical trial will examine the safety and immunological response of breast and ovarian cancer patients to a combination of AE37 plus a peptide vaccine

The purchase price will be paid in two installments, $7 million at closing and $3 million six months after closing. At the election of the company, up to