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Beactica Therapeutics met with Sweden’s regulator on Oct. 7, 2025, to advance its experimental cancer drug BEA-17 toward human trials.
Beactica Therapeutics held its first formal meeting with Sweden’s medical regulator on October 7, 2025, to discuss the preclinical development of BEA-17, a new drug candidate targeting LSD1 and CoREST for cancer treatment.
The agency supported Beactica’s plans to move toward human trials, citing promising results in animal models of colon cancer and glioblastoma, where the drug enhanced immune and standard therapies.
BEA-17 is orally available and can cross the blood-brain barrier, and it holds U.S. FDA Orphan Drug Designation for glioblastoma.
The company, using its Eclipsor™ platform, aims to address serious unmet medical needs, but BEA-17 remains investigational with no proven safety or efficacy in humans.
Beactica Therapeutics se reunió con el regulador de Suecia el 7 de octubre de 2025 para avanzar su fármaco experimental contra el cáncer BEA-17 hacia ensayos en humanos.