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Revelation Biosciences secured FDA acceptance for its Gemini therapy and reported positive trial results, advancing its development for kidney injury and infections.
Revelation Biosciences confirmed it has achieved a quorum for its December 3, 2025, special meeting and urged shareholders to vote by December 2.
The company reported FDA acceptance of its end-of-phase 1 meeting package for its Gemini therapy, aiming to advance development for acute kidney injury.
It also shared positive top-line results from its PRIME study and raised $9.6 million through a warrant inducement.
Gemini is being evaluated for acute and chronic kidney disease and post-surgical infections.
Forward-looking statements caution that actual results may vary due to clinical, regulatory, financial, and competitive risks.
Revelation Biosciences obtuvo la aceptación de la FDA para su terapia Gemini e informó resultados positivos de los ensayos, avanzando en su desarrollo para lesiones e infecciones renales.