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MEK inhibitor
MEK162, MEK inhibitor; oral for Ovarian Cancer
Phase 3
Waitlist Available
Research Sponsored by Pfizer
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from randomization until disease progression or death (up to 24 months)
Awards & highlights
Study Summary
This study is evaluating whether a drug called MEK162 can be used to treat ovarian cancer.
Eligible Conditions
- Ovarian Cancer
- Serous Carcinoma of the Fallopian Tube
- Serous Carcinoma of the Peritoneum
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from randomization until disease progression or death (up to 24 months)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from randomization until disease progression or death (up to 24 months)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Progression-free Survival (PFS) as Assessed by Blinded Independent Central Review (BICR)
Secondary outcome measures
Disease Control Rate (DCR)
Duration of Response (DOR)
Maximum Observed Plasma Concentration (Cmax) of MEK162
+8 moreTrial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: MEK162Experimental Treatment1 Intervention
Group II: Physician's choice chemotherapyActive Control1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
MEK162, MEK inhibitor; oral
2012
Completed Phase 1
~40
Find a Location
Who is running the clinical trial?
PfizerLead Sponsor
4,570 Previous Clinical Trials
10,910,099 Total Patients Enrolled
21 Trials studying Ovarian Cancer
2,786 Patients Enrolled for Ovarian Cancer
Pfizer Pfizer CT.gov Call CenterStudy DirectorPfizer
22 Previous Clinical Trials
6,266 Total Patients Enrolled
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