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Safety and Efficacy of Mitazalimab in Combination With Chemotherapy in Pancreatic Cancer Patients

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NCT04888312

Sponsored by Alligator Bioscience AB (industry) · ATORX.ST — their whole pipeline →.

Phase
Phase 1/2
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
94actual
Sites
14
Countries
Belgium, France, Spain

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
Start2021-09-17actualWhen the study began enrolling
Primary completion2026-06-01estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-06-30estimatedThe whole study's end, after follow-up
First posted2021-05-17actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-10-08actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Metastatic Pancreatic Ductal Adenocarcinoma

Intervention

  • Biological: CD40 agonist mitazalimab in combination with chemotherapy — also filed as ADC-1013, JNJ-64457107

Primary outcomes

what the primary-completion date above is the date OF
Incidence of Dose Limiting Toxicities (DLTs) (Part 1: Phase 1b Dose escalation)
measured From first dose to end of dose limiting toxicity period (Day 1-21)
Objective response rate (ORR) (Part 2: Phase 2 Dose expansion)
measured From first dose to 28-56 days after end of study treatment

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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