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A Study in Advanced or Metastatic Gastrointestinal Cancers Exploring Treatment Combinations With Pelareorep and Atezolizumab

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NCT07280377 · readout in 344 d

Sponsored by Oncolytics Biotech (industry) · ONCY — their whole pipeline →. With Crolll Gmbh, AIO-Studien-gGmbH.

Phase
Phase 1/2
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
122estimated
Sites
15
Country
Germany

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
Start2021-10-27actualWhen the study began enrolling
Primary completion2027-07-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-12-31estimatedThe whole study's end, after follow-up
First posted2025-12-12actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-19actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Anal Cancer Metastatic
  • Squamous Cell Carcinoma of the Anus Stage Unspecified
  • Pancreatic Cancer Metastatic
  • Unresectable Pancreatic Carcinoma

Interventions

  • Drug: Pelareorep
  • Drug: Atezolizumab — also filed as Tecentriq
  • Drug: Gemcitabine and nab-paclitaxel — also filed as Gemzar, Abraxane
  • Drug: Trifluridine Tipiracil — also filed as Lonsurf
  • Drug: mFOLFIRINOX Treatment Regimen

Primary outcomes

what the primary-completion date above is the date OF
Overall Response Rate (ORR) for Cohort 1, 2, 4, and 5
measured At week 16 (within each cohort)
Disease Control Rate (DCR) - Cohort 3
measured at week 16
Overall Survival (OS) - Cohort 5
measured Cohort 5: From the date of randomization through long term follow up at 2 years

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