White House deputy chief of staff Stephen Miller doubled down on President Trump’s renewed threats to make Greenland a U.S. territory ...

The US Food and Drug Administration (FDA) has cleared GenEditBio Limited’s Investigational New Drug (IND) application to ...

GenEditBio Limited ("GenEditBio"), a clinical-stage biotechnology startup focusing on genome-editing therapeutic solutions, today announced that the U.S.

An update from Pharmaust Limited ( ($AU:NUZ) ) is now available. Neurizon Therapeutics has provided a regulatory update on NUZ-001, its ...

EMA provided overall agreement with the proposed Phase 3 clinical trial of VCN-01 in combination with gemcitabine/nab-paclitaxel for the first-line treatment of metastatic PDAC, including sample size ...

In the world of biomechanics and medicine, there are challenges in the designing microrobots that are effective in drug ...

The US Food and Drug Administration intends to put a “black box” warning on Covid-19 vaccines, according to two people familiar with the agency’s plans, the latest move by President Donald Trump’s ...

The U.S. Food and Drug Administration is often described as the most influential scientific regulator in the world. Its decisions shape global drug development, investment, and patient access. But in ...

The design team was appointed through an international invited competition and selected from an initial group of 40 architectural teams and a shortlist of seven, with architects from every continent ...

Dec. 4 (UPI) --The Exzolt Cattle-CA1, aka Fluralaner, topical drug has received conditional approval from federal regulators to prevent and treat New World Screwworm and cattle fever tick infestations ...

The FDA has proposed cutting fees for early-stage companies conducting clinical development in the U.S. instead of abroad. The proposal is designed to incentivize U.S. drug development by tacking on ...