Study on BMS-986340 Alone and with Nivolumab or Docetaxel for Advanced Solid Tumors
Sponsor: Bristol-Myers Squibb
Sponsor score: 60
Inactive
ClinicalTrials ID:NCT04895709
This clinical trial is testing a new drug, BMS-986340, both by itself and in combination with other drugs, Nivolumab or Docetaxel, to see if it is safe and to find the best dose for treating advanced solid tumors.
Patient Parameters
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Program Overview
The aim of this study is to evaluate the safety and best dosage of a new drug, BMS-986340, when used alone or with other drugs, Nivolumab or Docetaxel, in patients with advanced solid tumors. This is the first time BMS-986340 is being tested in humans with these types of cancers.
Eligibility Criteria
Inclusion Criteria
- Must provide a fresh tumor sample before and during treatment for analysis.
- Must have a measurable tumor that can be biopsied, according to specific medical criteria.
- Must be in good overall health, with a performance status score of 0 or 1, meaning fully active or restricted in physically strenuous activity but ambulatory.
- Must have cancer that has progressed after the most recent treatment.
- Must have received standard treatments, except for those who have previously used Docetaxel for advanced cancer.
- Must have advanced or metastatic cancer and have tried all other available treatments or be unable to tolerate them.
Exclusion Criteria
- Women who are pregnant or breastfeeding.
- Have a primary cancer in the central nervous system (CNS).
- Have untreated cancer that has spread to the CNS.
- Have cancer that has spread to the membranes surrounding the brain and spinal cord.
- Have another active cancer or a history of cancer that was active within the last two years.
- Have an active or suspected autoimmune disease.
- Require treatment with steroids or other immune-suppressing drugs within a certain timeframe before starting the study.
- Have had an organ or tissue transplant.
- Have uncontrolled or serious heart disease.
- Have had major surgery within four weeks before starting the study.
- Have a history of lung diseases like interstitial lung disease or pulmonary fibrosis.
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