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A Study to Assess Adverse Events and Change in Disease Activity With Treatment Combinations With Telisotuzumab Adizutecan in Adults Participants With Pancreatobiliary Cancers

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NCT07769502 · readout ≤ 834 d

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

Phase
Phase 2
Status
Not yet recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
168estimated
Sites
4
Countries
Canada, China, 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
Start2026-09-22estimatedWhen the study began enrolling
Primary completionNov 2028estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionNov 2028estimatedThe whole study's end, after follow-up
First posted2026-08-18actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-18actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Pancreatobiliary Cancers
  • Pancreatic Ductal Adenocarcinoma

Interventions

  • Drug: Telisotuzumab Adizutecan
  • Drug: Gemcitabine
  • Drug: Nab-Paclitaxel

Primary outcomes

what the primary-completion date above is the date OF
Overall Response (OR) Assessed by Blinded Independent Central Review (BICR) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1
measured Up to approximately 3 years
Number of Participants with Adverse Events (AEs)
measured Up to approximately 3 years

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