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Spots Global Cancer Trial Database for A Study of XMT-1660 in Participants With Solid Tumors

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Trial Identification

Brief Title: A Study of XMT-1660 in Participants With Solid Tumors

Official Title: A Phase 1, First-in-human, Dose Escalation and Expansion, Multicenter Study of XMT-1660 in Participants With Solid Tumors

Study ID: NCT05377996

Interventions

XMT-1660

Study Description

Brief Summary: A Study of XMT-1660 in Solid Tumors

Detailed Description: This first-in-human (FIH) study will test the safety and side effects of a drug called XMT-1660. A side effect is anything a drug does to the body besides treating the disease. Participants in the study will have cancer that has come back after a period of time during which the cancer could not be detected (recurrent), spread in the body near where it started (advanced) or spread through the body (metastatic). The study will have two parts. The first part called Dose Escalation will find out how much XMT-1660 should be given to participants. The second part called Dose Expansion will use the dose found in the first part to find out how safe XMT-1660 is and if it works to treat solid tumor cancers.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

UC Irvine Health-Chao Family Comprehensive Cancer Center, Orange, California, United States

UCLA, Santa Monica, California, United States

Florida Cancer Specialists, Sarasota, Florida, United States

Moffitt Cancer Center, Tampa, Florida, United States

Winship Cancer Institute, Emory University, Atlanta, Georgia, United States

Northwestern University, Chicago, Illinois, United States

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

Henry Ford Health Hospital, Detroit, Michigan, United States

New York University Langone Health, New York, New York, United States

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

Stephenson Cancer Center Oklahoma University Health, Oklahoma City, Oklahoma, United States

Avera Cancer Institute, Sioux Falls, South Dakota, United States

Tennessee Oncology, PLLC, Nashville, Tennessee, United States

Texas Oncology, P.A., Dallas, Texas, United States

Huntsman Cancer Institute, Salt Lake City, Utah, United States

NEXT Oncology Virginia, Fairfax, Virginia, United States

Summit Cancer Centers, Spokane, Washington, United States

Contact Details

Name: Robert Burger, MD

Affiliation: Mersana Therapeutics

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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