A Phase 1 Study of the Safety and Tolerability of CTX-10726

StatusRecruiting
PhasePhase 1
Started

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Record History

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  1. Minor Trial sites expanded: 5 → 8 locations
    • Eligibility criteria expanded, about 44 words
    • Secondary endpoints: details revised at 1 of 15 entries
  2. Minor Study sites: 6 to 5v12
  3. Minor Study sites: 5 to 6v11
  4. Minor Site details revised at 1 of 5 sitesv10
  5. Minor Study sites: 4 to 5
    • Start date changed from estimate of May 1, 2026 to May 28, 2026
    v9
Show 4 earlier versionsHide 4 earlier versions
  1. Minor Eligibility criteria expanded, about 210 words
    • Site details revised at 1 of 4 sites
    v8
  2. Notable Start date: Apr 1, 2026 to May 1, 2026
    • Study sites: 3 to 4
    v7
  3. Minor Study sites: 2 to 3v6
  4. Minor Site details revised at 1 of 2 sitesv5
  1. Notable Recruitment opened
    • Study sites: 1 to 2
    v4
  2. Minor Study sites: 0 to 1v3
  3. Notable Primary endpoints revised (3)
    • Secondary endpoints: details revised at 2 of 15 entries
    • Study title shortened, about 3 words
    v2
  4. Minor Study First Submitted
  • 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.
1,602 trials monitored
See 70 trials at risk
1,051 trials monitored
See 53 trials at risk
890 trials monitored
See 72 trials at risk
and 1 more disease
This is a Phase 1, open-label, first-in-human study of CTX-10726 monotherapy in patients with metastatic or locally advanced malignancies. The study will be conducted in 2 Cohorts: Cohort 1 Dose Escalation and Cohort 2 Dose Expansion.
Trial Details
NCT Number NCT07419841
Lead Sponsor Compass Therapeutics
Conditions
(from sponsor)
Gastroesophageal Cancer (GC), Hepatocellular Carcinoma (HCC), Endometrial Cancer, Renal Cell Carcinoma (RCC)
Related terms Carcinoma, Hepatocellular, Carcinoma, Renal Cell, Endometrial Neoplasms
Enrollment 70 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov