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A Biomarker Study in Men With Localized Prostate Cancer Treated With Aglatimagene Besadenovec

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NCT07332000 · readout ≤ 12 d

Sponsored by Candel Therapeutics, Inc. (industry) · CADL — their whole pipeline →.

Phase
Phase 2
Status
Recruiting
Study type
Interventional
Design
Non randomized · None · Basic science
Enrollment
45estimated
Sites
7
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
Start2025-10-30actualWhen the study began enrolling
Primary completionAug 2026estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionAug 2026estimatedThe whole study's end, after follow-up
First posted2026-01-12actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-03-20actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Prostate Cancer Patients Treated by Radiotherapy
  • Prostate Cancer (Adenocarcinoma)

Interventions

  • Biological: aglatimagene besadenovec + valacyclovir — also filed as CAN-2409 plus prodrug
  • Radiation: External Beam Radiation Therapy (EBRT)

Primary outcome

what the primary-completion date above is the date OF
Biodistribution of aglatimagene besadenovec
measured Up to 3 months post last injection of aglatimagene besadenovec.

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