Wandercraft Receives FDA Clearance for Eve Personal Exoskeleton
Wandercraft’s Eve exoskeleton enables wheelchair users to regain upright mobility and perform daily activities hands-free using self-balancing technology.
Wandercraft’s Eve exoskeleton enables wheelchair users to regain upright mobility and perform daily activities hands-free using self-balancing technology.
US FDA has approved Lupin’s Sodium Zirconium Cyclosilicate for Oral Suspension as a bioequivalent to AstraZeneca’s Lokelma for the treatment of high levels of potassium in the blood, or hyperkalemia, in adults.
Tudriqev is approved for use in combination with nivolumab to treat adults with unresectable advanced cutaneous melanoma after progression on an anti-PD-1-based regimen.
If approved, BOTOX Cosmetic would become the only neurotoxin with five aesthetic indications and the first and only approved for masseter muscle prominence in the US.
Lilly is currently evaluating olomorasib in the Phase 1/2 LOXO-RAS-20001 trial involving patients with KRAS G12C-mutant non-small cell lung cancer (NSCLC) and other advanced solid tumours.
Chicago-based biopharmaceutical company Meitheal holds exclusive US commercialization rights for Garzulys through its exclusive license agreement with Emerge, the BLA holder.
Teleflex has received Biologics License Application (BLA) approval for EZPLAZ Freeze Dried Plasma (FDP) from the USFDA.
ELISIO-HX dialyzer, featuring NIPRO’s proprietary membrane technology, enhances middle molecule removal while remaining fully compatible with routine hemodialysis practice.
Johnson & Johnson plans a phased commercial rollout of the OTTAVA system with select customers in the United States while working in parallel to advance into additional indications.
Roche’s new PCR test simultaneously detects organisms associated with Bacterial vaginosis (BV) and Candida vaginitis (CV) from a single vaginal swab sample.