REGENXBIO announced early completion of dosing in the confirmatory study of RGX-202, a gene therapy for Duchenne muscular dystrophy, due to strong patient demand. The company plans to submit a Biologics License Application (BLA) under the accelerated approval pathway in Q3 2026, aiming for FDA approval in the second half of 2027. RGX-202 showed promising safety and efficacy data, including significant microdystrophin expression and functional improvements in patients. REGENXBIO is preparing for commercial launch with in-house manufacturing capabilities.
The global automotive microcontrollers market is projected to grow from USD 15.49 billion in 2025 to USD 34.31 billion by 2035, at a CAGR of 8.28%. Growth is fueled by increasing adoption of advanced driver-assistance systems (ADAS), vehicle electrif...
Sodexo has secured a major global contract to provide catering services across more than 130 Meta sites in over 30 countries. This large-scale partnership includes diverse locations such as headquarters, campuses, data centers, and conference centers...
Viasat and BMW Group have successfully demonstrated the first integrated automotive satellite voice call, allowing drivers to make calls directly through the car's infotainment system even in areas without cellular coverage. This advancement, utilizi...
Iran has warned it will retaliate fiercely if the US targets its infrastructure, following President Trump's threat to strike Iranian power plants and bridges next week if negotiations fail. The US recently conducted airstrikes against Iranian milita...
Solana (SOL) maintains its price in the mid-$70 range, supported by several key developments. These include Circle's recent issuance of $500 million in USDC on the Solana network, increasing liquidity and transactional demand. Additionally, instituti...
