A Study of Intravenous VRT106 for Locally Advanced or Metastatic Solid Tumors
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: VRT106.
- Who it may be relevant to
- Registry conditions: Solid Tumors. Basic parameters: 18 years — 75 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
An Open-labeled Phase I Clinical Trial Evaluating the Safety, Tolerability, Biodistribution Characteristics, Biological EEffects, and Initial Efficacy of VRT106 for Injection in the Treatment of Locally Advanced/Metastatic Solid Tumors by Intravenous Administration
Overview
A Phase I Study of the Safety and Tolerability of VRT106 Administered Intravenously for Treatment of Patients With Locally Advanced or MetastaticSolid Tumors
Detailed description
To evaluate VRT106 for injection in patients with locally advanced/metastatic solid tumours for safety and tolerability, exploring the maximum tolerated dose (MTD)/maximum administered dose (MAD)/optimal bioavailable dose (OBD) and/or the recommended phase II clinical dose (RP2D) to provide a recommended dose for subsequent clinical trials.
Interventions
- Biological VRT106
Intravenous drip administration
Primary outcome measures
- Evaluate the safety and tolerability of escalating doses of VRT106 in Patients with advanced malignanttumors [Time frame: About 2 years]
Eligibility criteria
Inclusion criteria
- Subjects voluntarily participate in the clinical study; fully understand and be informed about the study and sign the ICF; and are willing to follow and have the ability to complete all trial procedures.
- Males and females are aged at 18-75 years (including borderline values) at the time of signing the ICF, male or female.
- Subjects are histologically or cytologically confirmed to be intolerable or refractory to the standard systemic treatment.
- Subjects have at least one measurable lesion.
- ECOG score of 0 to 28 days prior to first dose of IMP.
- An expected survival time of ≥ 12 weeks.
- Have sufficient organ function.
- Female patients of childbearing potential with a negative serum pregnancy test within 7 days prior to first dose of study drug.
- Subjects of childbearing potential (males and females) agree to use effective birth control with their partner from signing informed consent to at least 90 days after the last dose.
Exclusion criteria
- Subject has received any antitumor therapy within 4 weeks prior to the first dose of IMP.
- Subject has previously received oncolytic virus or other gene drug therapy.
- Subject has received treatment with other unlisted clinical investigational drugs/devices within 4 weeks prior to the first dose of IMP.
- Subject is known to have an allergic reaction to any of the components of IMP.
- Women who are breastfeeding.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
China · 1 center
- The Third Affiliated Hospital of Sun Yat-sen University — Guangzhou
Identifiers
NCT: NCT06826313 · VRT106-CN01