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FDA accepts Akesis’ diabetic drug IND

DGD Research of San Antonio has begun screening patients in a Phase IIa, controlled US clinical trial measuring efficacy (using the gold-standard euglycemic-hyperinsulinemic clamping procedure), as well as

Cephalon submits SNDA for Fentora

Fentora supplemental new drug application (sNDA) includes data from three randomized, placebo-controlled clinical trials and one long-term open-label safety study with a total of 941 opioid tolerant patients.

Allos starts Phase I trial in solid tumors

In this study, patients with either advanced solid tumors or non-Hodgkin’s lymphoma (NHL) will receive a three-hour intravenous (IV) infusion of RH1 administered once every 21 days. Patients

Lexicon files IND for rheumatoid arthritis drug

This initial trial is designed to evaluate the safety, tolerability, and pharmacokinetics of LX2931. Lexicon expects to initiate clinical trials with LX2931 following FDA review. Philip Brown, vice

Crucell signs distribution deal with Sanquin

Cofact is Sanquin’s prothrombin complex of blood factors II, VII, IX and X which is currently in MRP (mutual recognition procedure) registration, in a number of Crucell’s key