A Phase 1/2 Randomized, Blinded, Placebo Controlled Study of Ipilimumab in Combination With Epacadostat or Placebo in Subjects With Unresectable or Metastatic Melanoma
Status: | Terminated |
---|---|
Conditions: | Skin Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 3/28/2019 |
Start Date: | March 2012 |
End Date: | December 27, 2016 |
The study design includes an open-label, dose escalation phase followed by a blinded,
randomized phase, which combines epacadostat (an oral IDO1 inhibitor) with an approved
therapy and compares to approved therapy plus placebo in metastatic melanoma patients.
randomized phase, which combines epacadostat (an oral IDO1 inhibitor) with an approved
therapy and compares to approved therapy plus placebo in metastatic melanoma patients.
Inclusion Criteria:
- Male or female subjects, aged 18 years or older with unresectable or metastatic
melanoma.
- A life expectancy of >12 weeks.
- Laboratory ranges and medical criteria met, as defined within the protocol.
- Subject may have received more than 1 prior regimen of systematic treatment for
unresectable or metastatic melanoma.
- For Phase 2 period of the study only, Subjects must have archival tumor tissue
available and collected with the prior 6 months or accessible disease for
pre-treatment, study biopsy.
Exclusion Criteria:
- Pregnant or nursing women.
- Current investigational trial participation with another investigational product or
subjects who have received any anticancer medications within 21 days prior to
screening (6 weeks for mitomycin-C or nitrosoureas.)
- Subjects receiving monoamine oxidase inhibitors (MAOI)s; subjects who have ever had
Serotonin Syndrome after receiving one or more serotonergic drugs.
- Subjects who have received prior immune checkpoint inhibitors (eg anti-CTLA-4,
anti-PD-1, anti- PD-L1 and others) who have had Grade 3 or 4 hepatotoxicity, immune
colitis requiring infliximab, endocrine toxicity not controlled by replacement, any
other Grade 4 immune adverse events (AEs) or ocular toxicity
- Subjects with protocol-specified active autoimmune process except vitiligo or
thyroiditis.
- Subjects with concurrent conditions that would jeopardize the safety of the safety of
the subject or compliance with the protocol.
We found this trial at
7
sites
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