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Antibody-drug conjugate

TR1801-ADC for Solid Tumors

Phase 1
Waitlist Available
Research Sponsored by Open Innovation Partners, 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 3.5 years
Awards & highlights
No Placebo-Only Group

Summary

This trial tests TR1801-ADC, an experimental drug, in patients with certain solid tumors that have the c-Met marker. The drug aims to kill cancer cells by targeting the c-Met marker.

Eligible Conditions
  • Unspecified Adult Solid Tumor Protocol Specific

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3.5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3.5 years for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Characterize safety of TR1801-ADC in patients with advanced solid tumor malignancies which express c-Met
Establish maximum tolerated dose
Secondary study objectives
Evaluate clinical activity of TR1801-ADC
Evaluate pharmacokinetics of TR1801-ADC
Immunogenicity

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: TR1801-ADCExperimental Treatment1 Intervention
Humanized anti-c-Met monoclonal antibody conjugated to a cleavable pyrrolobenzodiazepine toxin

Find a Location

Who is running the clinical trial?

Open Innovation Partners, Inc.Lead Sponsor
Tanabe Research Laboratories USA IncLead Sponsor
Open Innovation PartnersUNKNOWN
~2 spots leftby Nov 2025
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