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A Phase 1 of CTX-8371 in Patients With Advanced Malignancies

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NCT06150664 · readout ≤ 134 d

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

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
85estimated
Sites
10
Country
United States

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
Start2024-03-19actualWhen the study began enrolling
Primary completionDec 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionMay 2027estimatedThe whole study's end, after follow-up
First posted2023-11-29actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-28actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Non Small Cell Lung Cancer
  • Triple Negative Breast Cancer
  • Hodgkin Lymphoma
  • Head and Neck Squamous Cell Carcinoma
  • Malignant Melanoma

Intervention

  • Drug: CTX-8371

Primary outcomes

what the primary-completion date above is the date OF
Cohort 1: Evaluate the safety and tolerability of escalating doses of CTX-8371
measured From first dose of CTX-8371 (Cycle 1 Day 1, Cycle = 2 weeks) until 30 days after the last dose of CTX-8371, average of 6 months
Cohort 1: Determine the dose(s) of CTX-8371 to be further examined in Cohort 2 and Phase 2 studies
measured From first dose of CTX-8371 (Cycle 1 Day 1, Cycle = 2 weeks ) until 30 days after the last dose of CTX-8371 (average of 6 months )
Cohort 2: Evaluate the safety and tolerability of CTX-8371 at 3.0 mg/kg and 10.0 mg/kg
measured From first dose of CTX-8371 (Cycle 1 Day 1, Cycle = 2 weeks) until 30 days after the last dose of CTX-8371 (up to 2 years)

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