Regeneron’s clinical trials are at the core of this mission. Regeneron is grateful to all clinical trial participants — ...

Trials with retrospective registration or with registration in a database that is not publicly accessible cannot be considered. Interim analyses should be pre-specified in the study protocol.

The multi-centre trial was conducted to evaluate the safety and performance of the EmStop embolic protection system.

Backed by a Strong Balance Sheet, MIRA Accelerates Toward Becoming a Clinical-Stage Company and Advancing Breakthroughs in Pain and Depression Treatment ...

After a three-year negotiation, the FDA has dropped its objection to allowing patients to self-titrate dosing of smoked ...

Per the study protocol, two patients in Cohort 1 received administered ... Based on FDA interactions prior to trial initiation, the decision to open Cohort 3 will follow consultation and alignment ...

A phase 1 trial of α-lactalbumin vaccine for the treatment of patients with triple-negative breast cancer demonstrated safety ...

Canadian neurosurgeons in partnership with Elon Musk's Neuralink have regulatory approval to recruit six patients with ...

Confirmed relative bioavailability to the reference standard, dose proportional increases in pharmacokinetic exposure, and no food effectMarks ...