Long-Term Follow-Up Safety Study of Subjects Treated with SynKIR-110 in Cancer Studies

NCT06377202 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2024-11-07

No results posted yet for this study

Summary

The primary objective of this study is to evaluate the long-term safety of SynKIR- 110 administered to adult subjects with solid tumors expressing mesothelin.

Conditions

Sponsors & Collaborators

  • Verismo Therapeutics

    lead INDUSTRY

Principal Investigators

  • Laura Johnson, PhD · Verismo Therapeutics

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-15
Primary Completion
2038-12-15
Completion
2038-12-15

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06377202 on ClinicalTrials.gov