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Pedmark, a formulation of sodium thiosulfate (STS), is a water-soluble thiol compound that serves as a chemical reducing agent. Delayed administration (between four to eight hours) of high dose

In 2015, the consumer healthcare JV was established, as part of a three-part inter-conditional transaction between GSK and Novartis. The JV is a combination of Novartis' over-the-counter (OTC)

The round was oversubscribed. Adagene CEO Peter Luo said: "Adagene is built on a proprietary discovery engine that we have leveraged to discover highly differentiated portfolio of agonist

Breakthrough Therapy Designation is a process designed to expedite the development and review of drugs that are intended to treat a serious or life-threatening condition. It is based

Vobarilizumab is the firm’s anti-IL-6R Nanobody, which did not achieve the primary endpoint of dose response based on the modified BILAG-based combined lupus assessment (mBICLA) at week 24.

RiVax has previously been granted orphan drug designation from the US Food and Drug Administration (FDA). The European Commission grants orphan designations for medicines that treat a life-threatening

The companies undertake a wide range of operations to make clinical trials more efficient overall, using Hitachi's advanced digital technology such as AI, aiming to shorten the period

The Phase III IMpower150 study has achieved its co-primary endpoint of overall survival (OS) at the interim analysis and demonstrated that combined lung cancer treatment helped people with

The trial assessing the efficacy and safety of vareniclin for smoking cessation in nicotine dependent adolescents between 12 years and 19 years of age did not achieve its