Phase 1 Study of GEN2 in Patients With Advanced Solid Tumors

NCT06391918 | Terminated Phase 1 FDA Drug

• 1 other identifier: Protocol GVO-1102
• Study Type: interventional
• Target: 37
• Locations: 1 country
• Sites: 7

Brief Summary

Protocol GVO-1102 is a phase 1, open label, multi-center study in adult patients with locally advanced or metastatic solid tumors. This study includes two parts: dose escalation and dose expansion. In the dose escalation phase, GEN2 will be administered at increasing dose levels via intravenous infusion or intratumoral injection on Days 1, 3 and 8 every 4 weeks. Valganciclovir will start dosing on Day 12 and continue for 10 days (through Day 21). Once a recommended dose has been defined in approximately 35-45 patients, the dose expansion phase will initiate to further assess intravenous administration of GEN2 in specific tumor types. Approximately 15 patients per tumor type will be enrolled in the intravenous dose expansion phase.

Conditions

Solid Tumor, Adult

Outcome Measures

Primary Outcomes (1)

• Determine the recommended phase 2 dose (RP2D) of GEN2 by intravenous infusion and intratumoral injection.

  The RP2D will be determined by evaluating the number of subjects with treatment related adverse events and Dose Limiting Toxicities

  First 28 days.

Secondary Outcomes (9)

• Safety and tolerability as assessed by adverse event monitoring

  Up to 24 months

• Pharmacokinetics (PK) - Intravenous Administration Cohorts Only: area under the concentration-time curve from the time of dosing to 48 hours after dosing (AUC48h)

  Up to 24 months

• PK - Intravenous Administration Cohorts Only: Maximum Concentration (Cmax)

  Up to 24 months

• To assess replication competent retrovirus (RCR) in peripheral blood mononuclear cells (PBMCs)

  Up to 36 months

• To assess vector integration into genomic deoxyribonucleic acid (DNA) of PBMCs

  Up to 36 months

Interventions

GEN2 + Valganciclovir BIOLOGICAL

Gene therapy vector product

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Adult patients with a locally advanced or metastatic solid tumor that has progressed or was non-responsive to prior therapy
• Measurable disease as determined by response evaluation criteria in solid tumors (RECIST) v1.1.
• At least 18 years of age.
• Eastern Cooperative Oncology Group (ECOG) performance status score of 0 - 1.
• For patients with HCC: Child-Pugh Class A
• Available archived tumor tissue sample or a lesion that can be safely biopsied if the archived sample is not available.
• Adequate renal, liver and bone marrow function.
• Ability to swallow VGCV tablets.
• Willingness of men and women of child-bearing potential (WCBP) to observe conventional and highly effective birth control for the duration of treatment and for 12 months following the last dose of study treatment. Patients who are pregnant or lactating are excluded.
• For the dose expansion phase: Patients with hepatocellular carcinoma or cutaneous malignancy: no more than 2 prior systemic regimens for metastatic disease. Patients with breast cancer: no more than 2 prior cytotoxic regimens for metastatic disease (single-agent hormone therapy or hormone-based doublets do not count). Patients with cutaneous malignancies includes patients with melanoma, cutaneous squamous cell carcinoma, basal cell carcinoma and Merkel cell carcinoma.
• For the intratumoral injection dose escalation phase: patients with cutaneous malignancy, including patients with melanoma, cutaneous squamous cell carcinoma, basal cell carcinoma and Merkel cell carcinoma. Patients must have at least 1 measurable and injectable lesion and an additional site of measurable distant metastases for assessment of systemic immune response to therapy. Patients may not have received prior treatment with oncolytic therapy. Patients for whom tyrosine kinase inhibitor therapy would be considered standard of care should have received these agents prior to enrollment in this trial. Patients may not have a history of significant bleeding diathesis.

You may not qualify if:

• Investigational agent or anticancer therapy within 28 days or 5 elimination half-lives prior to Cycle 1 Day 1.
• Prior receipt of talimogene laherparepvec (TVEC) or any other oncolytic virus (including but not limited to RP1, RP2, or BNT111).; prior receipt of a live vaccine within 28 days prior to Cycle 1 Day 1.
• Washout from prior major surgery and radiotherapy (less than 28 days)
• Symptomatic primary central nervous system (CNS) tumor or metastases; symptomatic leptomeningeal carcinomatosis; untreated spinal cord compression. Patients with CNS lesions may be eligible if CNS lesions are asymptomatic or if neurological symptoms are stable, the patient is not receiving steroids to manage CNS symptoms, and no CNS surgery or radiation has been performed for 28 days (14 days for stereotactic radiation).
• Active uncontrolled systemic bacterial, viral, or fungal infection, which in the opinion of the Investigator makes it undesirable for the patient to participate in the trial
• Clinically significant active malabsorption syndrome or other conditions such as refractory nausea and vomiting, external biliary shunt, or significant bowel resection likely to affect gastrointestinal absorption of valganciclovir
• Known contraindications to the ganciclovir class
• For patients with hepatocellular carcinoma, patients with active hepatitis B are excluded; patients with evidence of prior exposure who have a negative hepatitis surface antigen (HbsAg) and who do not require antiviral therapy are allowed. Patients with hepatitis C are allowed but may not be on antiviral therapy during study participation and for two weeks prior to Cycle 1 Day 1.
• Known HIV positivity
• Current treatment with systemic steroids at or above 10 mg/day of prednisone (or its equivalent). Inhalational and topical steroids are acceptable

Sponsors & Collaborators

• GenVivo, Inc.: lead

Study Sites (7)

City of Hope

Duarte, California, 91010, United States

Location

University of Southern California-Keck School of Medicine

Los Angeles, California, 90033, United States

Location

UCLA Hematology-Oncology

Los Angeles, California, 90095, United States

Location

Indiana University Melvin and Bren Simon Comprehensive Cancer Center

Indianapolis, Indiana, 46202, United States

Location

University of Iowa Health Care

Iowa City, Iowa, 52242, United States

Location

SCRI Oncology Partners

Nashville, Tennessee, 37203, United States

Location

NEXT Oncology

Fairfax, Virginia, 22031, United States

Location

MeSH Terms

Interventions

Valganciclovir

Intervention Hierarchy (Ancestors)

Ganciclovir; Acyclovir; Guanine; Hypoxanthines; Purinones; Purines; Heterocyclic Compounds, 2-Ring; Heterocyclic Compounds, Fused-Ring; Heterocyclic Compounds

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 19, 2024
• First Posted: April 30, 2024
• Study Start: March 4, 2024
• Primary Completion: March 1, 2026
• Study Completion: March 1, 2026
• Last Updated: March 13, 2026

Record last verified: 2026-03

Data Sharing

• IPD Sharing: Will share
• Shared Documents: STUDY PROTOCOL, SAP
• Time Frame: Within one year of Last Patient off.

Locations

US (7)