A Phase 3 Study of Pembrolizumab + Epacadostat or Placebo in Subjects With Unresectable or Metastatic Melanoma (Keynote-252 / ECHO-301)
Status: | Active, not recruiting |
---|---|
Conditions: | Skin Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 5/10/2018 |
Start Date: | June 2016 |
End Date: | April 2019 |
A Phase 3 Randomized, Double-Blind, Placebo-Controlled Study of Pembrolizumab (MK-3475) in Combination With Epacadostat or Placebo in Subjects With Unresectable or Metastatic Melanoma (Keynote-252 / ECHO-301)
The purpose of the study is to assess the efficacy, safety, and tolerability when combining
pembrolizumab with epacadostat or placebo in subjects with unresectable or metastatic
melanoma
pembrolizumab with epacadostat or placebo in subjects with unresectable or metastatic
melanoma
Inclusion Criteria:
- Have histologically or cytologically confirmed melanoma
- Have unresectable Stage III or Stage IV melanoma, as per AJCC staging system not
amenable to local therapy
- A minimum of 1 measurable lesion by CT or MRI
- Provide a baseline tumor biopsy
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1
Exclusion Criteria:
- Has received prior systemic treatment for unresectable or metastatic melanoma (except
BRAF directed therapy)
- Has received prior therapy with an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or
IDO1 inhibitor or any other antibody or drug specifically targeting checkpoint
pathways other than anti-CTLA-4 which is permitted in the adjuvant setting
- Has received prior adjuvant therapy, monoclonal antibody or an investigational agent
or device within 4 weeks or 5 half-lives (whichever is longer)
- Has an active infection requiring systemic therapy
- Has known history of human immunodeficiency virus (HIV) (HIV 1/2 antibodies)
- Has known history of or is positive for Hepatitis B or Hepatitis C
- Is pregnant or breastfeeding or expecting to conceive or father children within the
projected duration of the study, starting with the screening visit through 120 days
after the last dose of study treatment
We found this trial at
35
sites
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