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Study details
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Intratumoral T3011 Trial

ImmVira Pharma Co. Ltd
NCT IDNCT04370587ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1/2

Target enrollment

30

Study length

about 6.3 years

Ages

18+

Locations

6 sites in AZ, MA, PA +2

What this study is about

This trial is testing a treatment called T3011 given directly into the tumor, alone or with pembrolizumab (an intravenous medication), in people with advanced solid tumors. The goal is to see if this treatment is safe and has some effect on the cancer.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Receive T3011
  • 2.Take T3011 + pembrolizumab

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

pembrolizumab (Immune checkpoint inhibitor; blocks PD-1 to boost T-cell attack on cancer)

Drug routes

infusion

Endpoints

Primary: Characterize the safety and tolerability of T3011 in combination with pembrolizumab, Characterize the safety and tolerability of T3011 in combination with pembrolizumab in participants who progress on T3011 alone, Safety and tolerability of T3011 dose(s) selected from Phase 1 in disease specific cohorts, Safety and tolerability of escalating doses T3011

Secondary: Disease control rate (DCR), Duration of response (DOR), Overall Survival (OS), Overall response rate (ORR), Presence of neutralizing antibodies of anti-PD-1 antibody for antidrug antibodies (ADAs) development, Progression-free survival (PFS)

Body systems

Oncology