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Study to Assess Adverse Events and How Intravenously (IV) Infused Telisotuzumab Adizutecan (ABBV-400) Moves Through the Body of Adult Participants With Unresectable Locally Advanced/Metastatic Colorectal Cancer

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NCT06464692 · readout ≤ 499 d

Sponsored by AbbVie (industry) · ABBV — their whole pipeline →.

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
31actual
Sites
8
Country
China

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
Start2024-09-30actualWhen the study began enrolling
Primary completionDec 2027estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionDec 2027estimatedThe whole study's end, after follow-up
First posted2024-06-18actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-11actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Colorectal Cancer

Intervention

  • Drug: Telisotuzumab Adizutecan

Primary outcomes

what the primary-completion date above is the date OF
Dose-Limiting Toxicity (DLT) of Telisotuzumab Adizutecan in Stage 1
measured Up to 24 Months
Maximum observed plasma or serum concentration (Cmax) of Telisotuzumab Adizutecan Conjugate
measured Up to 24 Months
Time to Cmax (Tmax) of Telisotuzumab Adizutecan Conjugate
measured Up to 24 Months
Area Under the Concentration-Time Curve (AUC) of Telisotuzumab Adizutecan Conjugate
measured Up to 24 Months
Total Antibody of Telisotuzumab Adizutecan
measured Up to 24 Months
Unconjugated Payload of Telisotuzumab Adizutecan
measured Up to 24 Months

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