Indoleamine 2,3-Dioxygenase (IDO) Inhibitor in Advanced Solid Tumors
Completed · Phase 1
Conditions studied: Solid Tumor
In brief
This is an open-label Phase I study to evaluate the safety, tolerability, and pharmacokinetics of escalating oral doses of GDC-0919, an investigational agent intended to inhibit the indoleamine 2,3-dioxygenase 1 (IDO1) enzyme and help the human immune system attack solid tumor cells more effectively.
Key facts
- Study ID
- NCT02048709
- Run by
- Genentech, Inc.
- People needed
- 22
- Starts
- 2014-04-01
- Expected to finish
- 2016-02-01
- Last updated by the study team
- 2017-02-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Histologically or cytologically confirmed solid tumor that is relapsed/refractory to standard therapies or for which no approved or curative therapy exists
- Age > or = 18
- Eastern Cooperative Oncology Group (ECOG) performance status < 2
- Life expectancy > or = 12 weeks
- Adequate hematologic and organ function before initiation of GDC-0919
- For some patients only: Accessible lesions amenable to paired fresh tumor biopsies
You may not qualify if…
- Some prior cancer immunotherapies
- Untreated brain metastases
- Active or history of autoimmune disease
Where it is running
- Georgia Regents University — Augusta, Georgia, United States
Full record on ClinicalTrials.gov
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