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Spots Global Cancer Trial Database for Rollover Study to Provide Continued Access to Napabucasin for Patients Enrolled in Boston Biomedical-sponsored Protocols

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Trial Identification

Brief Title: Rollover Study to Provide Continued Access to Napabucasin for Patients Enrolled in Boston Biomedical-sponsored Protocols

Official Title: A Rollover Study to Provide Continued Access to Napabucasin for Patients Enrolled in Boston Biomedical-sponsored Napabucasin Protocols

Study ID: NCT04299880

Conditions

Oncology

Study Description

Brief Summary: This is an open-label, multi-center, multi-national, non-randomized rollover study designed to allow continued access to napabucasin for patients who have participated in a Boston Biomedical-sponsored study and are being treated with napabucasin (monotherapy or combination) and who are deriving continued clinical benefit in the parent study at the time of closure.

Detailed Description: This is an open-label, multi-center, multi-national, non-randomized rollover study designed to allow continued access to napabucasin for patients who have participated in a Boston Biomedical-sponsored study and are being treated with napabucasin (monotherapy or combination) and who are deriving continued clinical benefit in the parent study at the time of closure. Individual patients will continue to be treated with napabucasin (monotherapy or combination) in accordance with the parent study under which they were enrolled. If the dose was reduced in the parent protocol, the dose of the last visit of the parent study will be used. Patients will be monitored to determine long term safety and tolerability of napabucasin.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

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

Maine Center for Cancer Medicine, Scarborough, Maine, United States

OHSU Knight Cancer Institute, Portland, Oregon, United States

Centre Antoine Lacassagne, Nice, , France

Kanagawa Cancer Center, Yokohama, Kanagawa, Japan

Kyorin University Hospital, Tokyo, , Japan

Taipei Veterans General Hospital, Taipei City, , Taiwan

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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