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The double-blind, randomized and placebo-controlled trial showed dose-proportional pharmacokinetic exposure over the tested dose range. In the trial, the terminal half-life was approximately 20 hours. The trial investigated

The trial aims to evaluate the safety and efficacy of CRLX101 in patients with advanced NSCLC whose disease has progressed following one or two prior regimens of therapy.

Jones joined Acura in April 2008 as the senior vice president and COO and was reponsible for products development, which use the company’s proprietary abuse deterrent technologies. Acura’s

The deal allows Phillips to broaden its medical business manufacturing capabilities. Medisize provides services to drug delivery devices, primary pharmaceutical packaging, medical and diagnostic devices and airway management.

As per the terms of the agreement, Probiomed is responsible for seeking regulatory approval for Fanapt in Mexico. However, Vanda will be responsible for supplying the drug to

As per the terms of the agreement, Antares Pharma is entitled to receive milestone payments on achieving regulatory approval and certain sales level from Watson. Antares Pharma is

Cephalosporin API manufacturing plant manufactures a range of oral and sterile Cephalosporin APIs and caters to the developed markets like US, Europe and Japan. The closure notice has

The new hub – India Distribution Center (IDC) – will ramp up the availability, timely delivery and quality of products to customers in the region. Life Technologies operates

The company will conduct the test runs by the end of this month to investigate whether the plant is maintaining GMP. Additionally, the company will also verify its