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Study of CTX-471 in Patients With Neural Cell Adhesion Molecule (NCAM) Positive Neuroendocrine Neoplasms

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NCT07684170 · readout ≤ 773 d

Sponsored by Compass Therapeutics (industry) · CMPX — their whole pipeline →.

Phase
Phase 2
Status
Not yet recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
58estimated

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
StartSep 2026estimatedWhen the study began enrolling
Primary completionSep 2028estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionSep 2029estimatedThe whole study's end, after follow-up
First posted2026-07-06actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-06actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Neuroendocrine Neoplasm
  • Neuroendocrine Carcinomas
  • Neuroendocrine Tumors

Intervention

  • Drug: CTX-471

Primary outcomes

what the primary-completion date above is the date OF
Evaluate the clinical activity of CTX-471
measured Baseline until confirmed disease progression (up to 1 year)
Evaluate the safety of CTX-471
measured From first dose of CTX-471 (Cycle 1 Day 1, Cycle = 2 weeks) until 30 days after the last dose of CTX-471
Determine the recommended phase 2 dose (RP2D) for CTX-471
measured From first dose of CTX-471 (Cycle 1 Day 1, Cycle = 2 weeks) until 30 days after the last dose of CTX-471

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