Recruiting at 6 sites Phase 1, Phase 2 Advanced Solid Malignancies

Trial studying safety and effects for Advanced Solid Malignancies

Official title A Study to Evaluate the Safety, Tolerability, and Efficacy of BMS-986523 Alone and in Combination With Anti-Cancer Agents in Participants With Advanced Solid Malignancies

ClinicalTrials.gov ID: NCT07223047

What this study is testing

What is BMS-986523?

An investigational medicine being studied for advanced solid cancers.

Plain-language explanation of the investigational treatment. It is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
The study aims to see how safe and well tolerated BMS‑986523 is, and whether it works against advanced solid cancers.
Who it's for
Adults who have advanced solid cancers such as non‑small cell lung cancer, colorectal cancer, or pancreatic ductal adenocarcinoma.
What's involved
Participants will receive BMS‑986523, either by itself or together with other cancer drugs, and will have regular visits and medical tests to monitor safety and effectiveness.
  • Phase 2: a mid-size study of how well it works

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older

You may be able to join if

  • Participants must have a histologically confirmed diagnosis of a locally advanced and unresectable or metastatic solid tumor malignancy with a known...
  • Participants must, for Arm D, have a PD-L1 expression (≥50%).
  • Participants must have previously received, be ineligible for, or decline (after having been provided adequate information to make an informed...

You likely can't join if

  • Participants must not have untreated central nervous system (CNS) metastases.
  • Participants must not have concurrent malignancy (present during screening) requiring treatment or history of prior malignancy active within 2 years...
  • Participants must not have a history of, or any evidence of, interstitial lung disease or active, non-infectious pneumonitis.
  • Participants must not have a history of prior severe cutaneous adverse reactions (SCARs), including Stevens-Johnson Syndrome (SJS) and toxic...
  • Other protocol-defined Inclusion/Exclusion criteria apply.

The study team makes the final eligibility decision.

Where it is enrolling

  • Baltimore, Maryland, United States
  • San Antonio, Texas, United States
  • West Valley City, Utah, United States
  • Fairfax, Virginia, United States
  • Vancouver, British Columbia, Canada
  • Toronto, Ontario, Canada

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part, but confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

This study is enrolling now at Baltimore, Maryland, United States; San Antonio, Texas, United States; West Valley City, Utah, United States; Fairfax, Virginia, United States; Vancouver, British Columbia, Canada; Toronto, Ontario, Canada. Enter your location above to see the nearest enrolling site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool that is independent of the study sponsor. Details come from ClinicalTrials.gov. The study team decides eligibility, and your own doctor gives medical advice.