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Phase 2Not yet recruitingPriority 2 · High priorityNCT07529405

A Study of VG712 in Patients With Mycosis Fungoides

ClinicalTrials.gov

Plain-language summary

This Phase 2 trial is comparing VG712 and Mogamulizumab against other options for people whose cutaneous T-cell lymphoma (skin lymphoma) has come back or has not responded to previous treatment. Patients are randomly assigned to different treatment groups to see which approach works best. It is available at 1 US location.

Who can join (key eligibility)

  • Age 18 Years or older
  • Lymphoma came back or did not respond to prior treatment
  • Must be well enough for treatment (adequate performance status)

Final eligibility is determined by the trial team. This list is a starting point only.

What's being tested

VG712 (DRUG): Recombinant anti-CD3 immunotoxin fusion protein composed of bivalent UCHT1 single-chain variable fragments linked to a modified diphtheria toxin (A-dmDT390). VG712 is administered intravenously to selectively deplete CD3-positive T cells. | Mogamulizumab (DRUG): Humanized monoclonal antibody targeting CCR4, administered intravenously for the treatment of T-cell lymphomas, including mycosis fungoides.

Drugs / treatments
VG712, Mogamulizumab
Treatment length
Ask the trial team for details
Visit frequency
Ask the trial team for details

At a glance

Phase
Phase 2
Status
Not yet recruiting
Design
Randomized, open-label
Enrollment target
386 patients
Primary endpoint
Progression-Free Survival (PFS)
Ages
18 Years to —
Start date
2026-07-30
Est. completion
2032-12-30

Locations

1 US sites · 1 total

Florida

Contact

Sponsor
Virogen Biotechnology Inc. (INDUSTRY)
Contact
Su Chen | chensu@virogenbio.com | 1-925-699-2195

Tags

CTCLRelapsed/Refractory
TrialCompass — Clinical Trial Summary

A Study of VG712 in Patients With Mycosis Fungoides

NCT07529405

Phase: Phase 2 | Status: Not yet recruiting | Priority: High

Plain-language summary

This Phase 2 trial is comparing VG712 and Mogamulizumab against other options for people whose cutaneous T-cell lymphoma (skin lymphoma) has come back or has not responded to previous treatment. Patients are randomly assigned to different treatment groups to see which approach works best. It is available at 1 US location.

Who can join

  • Age 18 Years or older
  • Lymphoma came back or did not respond to prior treatment
  • Must be well enough for treatment (adequate performance status)

What's being tested

VG712 (DRUG): Recombinant anti-CD3 immunotoxin fusion protein composed of bivalent UCHT1 single-chain variable fragments linked to a modified diphtheria toxin (A-dmDT390). VG712 is administered intravenously to selectively deplete CD3-positive T cells. | Mogamulizumab (DRUG): Humanized monoclonal antibody targeting CCR4, administered intravenously for the treatment of T-cell lymphomas, including mycosis fungoides.

Drugs / treatments: VG712, Mogamulizumab

Treatment length: Ask the trial team for details

Visit frequency: Ask the trial team for details

Trial design

Randomized, open-label

Enrollment target: 386 patients

Primary endpoint: Progression-Free Survival (PFS)

Ages: 18 Years to —

Start date: 2026-07-30 | Est. completion: 2032-12-30

Locations

1 US sites · 1 total

Florida

Contact

Su Chen | chensu@virogenbio.com | 1-925-699-2195

Sponsor: Virogen Biotechnology Inc. (INDUSTRY)

Tags

CTCL · Relapsed/Refractory

View on ClinicalTrials.gov

https://clinicaltrials.gov/study/NCT07529405

Prepared using TrialCompass (trialcompass.com) on July 4, 2026. For informational purposes only. Always discuss with your healthcare team.
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Data sourced from ClinicalTrials.gov.

For informational purposes only. Not medical advice — always consult your healthcare team.

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Data last updated: June 2026

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