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A I/II Phase Clinical Study to Evaluate the Safety and Efficacy of RC288 in the Treatment of Solid Tumors

StatusRecruiting
PhasePhase 1/2
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Recruitment opened Primary endpoints: details revised at 2 of 6 entries · Trial sites expanded: 1 → 14 locations · Start date changed from estimate of Apr 30, 2026 to Apr 27, 2026 · 1 more Show 4 more changesShow less
    • Primary endpoints: details revised at 2 of 6 entries
    • Trial sites expanded: 1 → 14 locations
    • Start date changed from estimate of Apr 30, 2026 to Apr 27, 2026
    • Eligibility criteria expanded, about 28 words
  2. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The primary objective is to evaluate the safety and tolerability of RC288; determine the maximum tolerated dose (MTD) and/or maximum administered dose (MAD) of RC288; and determine the recommended phase 2 dose (RP2D), and assess the efficacy of RC288 at the RP2D dose;
Trial Details
NCT Number NCT07537881
Lead Sponsor RemeGen Co., Ltd.
Conditions Solid Tumors
Enrollment 326 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov