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A Phase I Trial of CT900, a Novel α-Folate Receptor-Mediated Thymidylate Synthase Inhibitor, in Patients with Solid Tumors with Expansion Cohorts in Patients with High-Grade Serous Ovarian Cancer.

Susana BanerjeeVasiliki MichalareaJoo Ern AngAlvaro H Ingles GarcesAndrea BiondoIonut-Gabriel FuninganaMartin LittleRuth RuddleFlorence I RaynaudRuth RiisnaesBora GurelSue ChuaNina TunariuJoanna C PorterToby ProutMona ParmarAnna ZachariouAlison TurnerBen JenkinsStuart McIntoshEd AinscowAnna R MinchomJuanita LopezJohann S de BonoRobert JonesEmma C HallNatalie CookBristi BasuUdai Banerji
Published in: Clinical cancer research : an official journal of the American Association for Cancer Research (2022)
The dose of 12 mg/m2/q2Wk was declared the recommended phase II dose/schedule. At this dose/schedule, CT900 exhibited an acceptable side effect profile with clinical benefit in patients with high/medium α-FR expression and warrants further investigation.
Keyphrases
  • phase ii
  • high grade
  • clinical trial
  • open label
  • low grade
  • phase iii
  • computed tomography
  • image quality
  • dual energy
  • contrast enhanced
  • poor prognosis
  • study protocol
  • randomized controlled trial
  • placebo controlled