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BAY94-9343 (Anetumab ravtansine) for Solid Tumors
Phase 2
Waitlist Available
Research Sponsored by Bayer
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 approximately 3 years (from first study treatment until safety follow-up)
Awards & highlights
Study Summary
This study is evaluating whether anetumab ravtansine is safe and efficient for patients with solid tumors.
Eligible Conditions
- Solid Tumors
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ approximately 3 years (from first study treatment until safety follow-up)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~approximately 3 years (from first study treatment until safety follow-up)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of Participants With TEAEs, TESAEs and Drug-related TEAEs and TESAEs
Secondary outcome measures
Overall Survival
Trial Design
1Treatment groups
Experimental Treatment
Group I: Cancer patientsExperimental Treatment1 Intervention
Adult patients with solid cancer who received anetumab-ravtansine treatment in a completed Bayer study
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Who is running the clinical trial?
BayerLead Sponsor
2,235 Previous Clinical Trials
25,325,554 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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