News

The study’s data monitoring committee (DMC) recommended for termination of the trial early because of lack of efficacy. Gilead is however continuing the phase 2 trials of the

HD affects muscle coordination and leads to deterioration of mental abilities and physical control. IONIS-HTT Rx, which is currently in phase 1/2a study, is an antisense drug designed

This program is evaluating vadadustat (formerly AKB-6548) in non-dialysis patients with anemia related to chronic kidney disease (NDD-CKD). In addition, the U.S. Food and Drug Administration (FDA) recently

Furthermore, high diversity among CTCs was not associated with resistance to taxane-based chemotherapy. This suggests that patients likely to fail anti-androgen therapies but potentially benefit from chemotherapy can

Matinas BioPharma president and CEO Roelof Rongen said: "In preclinical studies, MAT2501 was shown to have oral bioavailability and provide targeted delivery of the powerful antibiotic, amikacin, directly

Validation confirms that the submission is complete and initiates the Centralized Review process by the EMA’s Committee for Medicinal Products for Human Use (CHMP). Under Centralized Review, the

Under the terms of the agreement, Merus and Gustave Roussy will collaborate on the design and conduct of basic, preclinical and translational research studies and early clinical studies

Gilead filed a new drug application for the treatment, a combination of the company’s Sovaldi with velpatasvir, in October last year. A final decision from the FDA is

The immuno-oncology collaboration intends to advance development of novel immune checkpoint therapies. Baxalta agreed to make an upfront payment of $175m to Symphogen in exchange for exclusive rights