Phase 2B Safety and Efficacy Study of VGT-309 in Subjects With Cancer in the Lung.

Completed · Phase 2

Conditions studied: Lung Cancer, Lung Metastases

In brief

This is a Phase 2, multi-center, open-label study to evaluate the safety and efficacy of VGT-309, a tumor-targeted, activatable fluorescent imaging agent, in subjects undergoing surgery for proven or suspected cancer in the lung. Approximately 100 subjects will be enrolled to ensure at least 86 subjects are evaluable with the option to expand enrollment by protocol amendment if deemed necessary by the DSC to meet primary and/or secondary objectives.

Key facts

Study ID

NCT06145048

Run by

Vergent Bioscience, Inc.

People needed

89

Starts

2023-10-05

Expected to finish

2025-02-20

Last updated by the study team

2026-05-13

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Be willing and able to sign the informed consent and comply with study procedures.
• Be at least 18 years of age.
• Meet the following conditions:
• Female participants must be of non-childbearing potential, or, If of childbearing potential, be non-pregnant or non-lactating and agree to use highly effective contraception from screening through Day 30 after treatment.
• Male participants, if not surgically sterilized, and if engaging in sexual intercourse with a female partner of childbearing potential, must be willing to use highly effective contraception from screening through 30 days after treatment and agree not to donate semen during this waiting period.
• Highly effective contraception involves the use of a condom for the male, plus one of the following for the female:
• Oral, injectable, implantable, intravaginal, or transdermal hormonal contraceptives, or Intrauterine device or intrauterine hormone-releasing system NOTE: Subjects who abstain from heterosexual intercourse as their usual and preferred lifestyle, will not be required to use contraception as described above. They are required to maintain abstinence from screening through Day 30 after treatment.
• Note: Subjects in a same sex relationship, must use a barrier form of contraception (e.g., condom, diaphragm) to protect against the transfer of the study drug in any bodily fluids.
• Have a lung nodule or mass that might be considered primary lung cancer or lung metastases whether or not it is biopsy-proven before surgery.
• Be scheduled to undergo standard of care surgical resection for a lung nodule or mass with diagnostic and/or curative intent
• Have acceptable kidney and liver functions at study entry as evidenced by:
• ALT/AST < 1.5 times the upper limit of normal Calculated Creatinine Clearance (CrCl) ≥ 50 ml/min Total bilirubin < 1.5 times the upper limit of normal Have an ECOG score of 0-2. Meet all standard of care surgical and general anesthesia requirements. 7) Have not participated in an interventional clinical trial within the last 30 days.

You may not qualify if…

• Not a candidate for standard of care surgery based on opinion of the surgeon, anesthesiologist, or other consulting physician.
• Have a known allergy or reaction to ICG, other radiographic contrast agent, or any component of VGT-309.
• Have congenital long QT syndrome or QTcF > 470ms by history or at Screening ECG.
• Prisoners, institutionalized individuals, or are unable to consent for themselves.
• Have any other co-morbidity or habit that the Investigator believes will interfere with their ability to comply with and complete the study.

Where it is running

• City of Hope National Medical Center — Duarte, California, United States
• Orlando Health Cancer Institute — Orlando, Florida, United States
• Mayo Clinic — Rochester, Minnesota, United States
• Hospital of the University of Pennsylvania — Philadelphia, Pennsylvania, United States
• University of Texas MD Anderson Cancer Center — Houston, Texas, United States
• St. Vincent's Hospital — Melbourne, Victoria, Australia

Full record on ClinicalTrials.gov

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