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Spots Global Cancer Trial Database for A Phase I/II Study of VLS-1488 in Subjects With Advanced Cancer

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Interventions

VLS-1488

Study Description

Brief Summary: This is a first-in-human phase I/II study to examine the safety, tolerability and preliminary efficacy of VLS-1488 in subjects with advanced cancers.

Detailed Description: This a first-in-human phase I/II study designed to assess the safety, tolerability and preliminary efficacy of VLS-1488 monotherapy and consists of two parts: Dose Escalation and Dose Expansion. Dose Escalation will examine the safety and tolerability of VLS-1488 in different solid tumor types at various dose levels through a series of Dose Escalation and Backfill Cohorts to identify the Maximum Tolerated Dose (MTD) and to select dose levels for Dose Expansion. The criteria for dose (de-)escalation will be based on a Bayesian Optimal Interval (BOIN) design. Dose Expansion will examine the safety, tolerability, Drug Drug Interaction (DDI) risk, Food Effect (FE) and preliminary efficacy of VLS-1488 in different tumor types and/or dose levels of interest through various expansion cohorts. VLS-1488 will be given orally in 28-day cycles. Dosing will be continued until disease progression, unacceptable toxicity, withdrawal of consent, or other stopping criteria are met.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

University of Colorado Cancer Center, Aurora, Colorado, United States

Yale Cancer Center, New Haven, Connecticut, United States

Community Health Network, Indianapolis, Indiana, United States

Johns Hopkins Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland, United States

University of Michigan, Ann Arbor, Michigan, United States

START Midwest, Grand Rapids, Michigan, United States

Memorial Sloan Kettering Cancer Center, New York, New York, United States

The Christ Hospital, Cincinnati, Ohio, United States

Women & Infants Hospital, Providence, Rhode Island, United States

M.D. Anderson Cancer Center, Houston, Texas, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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