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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 first dose of study drug until confirmed cr or pr or >=5 weeks after first dose for sd (up to 29 months)
Awards & highlights
Study Summary
This trial is testing a new drug to see if it is safe and works against advanced solid tumors or lymphomas.
Eligible Conditions
- Lymphoma
- Solid Tumors
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from first dose of study drug until confirmed icr or ipr or >=5 weeks after first dose for isd (up to 29 months)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from first dose of study drug until confirmed icr or ipr or >=5 weeks after first dose for isd (up to 29 months)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Dose Escalation Part: Number of Participants With Dose-limiting Toxicities (DLTs)
Dose Expansion Part: DCR Based on iRECIST
Dose Expansion Part: DOR Based on iRECIST
+5 moreSecondary outcome measures
AUC(0-inf): Area Under the Plasma Concentration From Time Zero to Infinity Curve for E7766
Cmax: Maximum Observed Plasma Concentration for E7766
Dose Escalation Part: CL/F: Apparent Total Body Clearance for E7766
+19 moreTrial Design
2Treatment groups
Experimental Treatment
Group I: Dose Expansion: Advanced Solid Tumors or LymphomasExperimental Treatment1 Intervention
Dose identified from dose escalation part for E7766 will be used in dose expansion part.
Group II: Dose Escalation: Advanced Solid Tumors or LymphomasExperimental Treatment1 Intervention
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Who is running the clinical trial?
Eisai Inc.Lead Sponsor
515 Previous Clinical Trials
153,996 Total Patients Enrolled
17 Trials studying Lymphoma
969 Patients Enrolled for Lymphoma
H3 Biomedicine Inc.Industry Sponsor
6 Previous Clinical Trials
509 Total Patients Enrolled
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