Rollover Protocol for Subjects Who Have Responded on Study 4218s - A Phase 2 Study
Completed · Phase 2
Conditions studied: Neuroendocrine Tumors
In brief
Subjects achieving a clinical response in study OX4218s with a biomarker reduction or symptom response are eligible to enroll in this rollover study to continue once every three weeks fosbretabulin infusions for up to one year.
Key facts
- Study ID
- NCT02279602
- Run by
- Mateon Therapeutics
- People needed
- 7
- Starts
- 2014-12-01
- Expected to finish
- 2016-08-01
- Last updated by the study team
- 2018-04-17
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subject has been treated in the OXiGENE-sponsored Phase 2 study OX4218s
You may not qualify if…
- Subject has not received fosbretabulin treatment in the study OX4218s
Where it is running
- Stanford University School of Medicine — Stanford, California, United States
- Markey Cancer Center, Clinical Research Office — Lexington, Kentucky, United States
- Montefiore — The Bronx, New York, United States
- Duke University Medical Center — Durham, North Carolina, United States
- Froedtert Hospital, Medicial College of Wisconsin — Milwaukee, Wisconsin, United States
Full record on ClinicalTrials.gov
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