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Monoclonal Antibodies
AGEN2034 for Cervical Cancer
Phase 1 & 2
Waitlist Available
Research Sponsored by Agenus Inc.
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 duration of the trial, up to 4 years
Awards & highlights
Study Summary
This trial is testing a new treatment for cervical cancer in two parts. The first part is to see what dose is safe for people with cancer that has spread or is hard to treat. The second part is to see if the new treatment can help people with cancer that has come back or spread after other treatments.
Eligible Conditions
- Cancer
- Cervical Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ duration of the trial, up to 4 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~duration of the trial, up to 4 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Objective Response Rate (ORR), as determined by IERC, in the analysis population
Secondary outcome measures
Area under the drug concentration-time curve from time zero to time t (AUC(0-t)), area under the drug concentration-time curve from time zero to infinity (AUC(0-∞))
Area under the drug concentration-time curve within time span t1 to t2 at steady-state (AUC(τ1-τ2)-ss)
Disease Control Rate (DCR)
+15 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: MonotherapyExperimental Treatment1 Intervention
Dose of 3 mg/kg IV every 2 weeks for up to 24 months.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
AGEN2034
2017
Completed Phase 2
~220
Find a Location
Who is running the clinical trial?
Agenus Inc.Lead Sponsor
51 Previous Clinical Trials
4,600 Total Patients Enrolled
Medical DirectorStudy DirectorAgenus Inc.
2,777 Previous Clinical Trials
8,063,677 Total Patients Enrolled
Frequently Asked Questions
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