Long Term Follow up for the Detection of Delayed Adverse Events in Cal-1 Recipients

NCT02390297 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 11

Last updated 2025-10-10

No results posted yet for this study

Summary

Long term safety follow-up of Cal-1 recipients

Conditions

  • HIV-1 Infection
  • Receipt of Cal-1 Modified Hematopoietic Cellular Products

Interventions

GENETIC

Blood tests

Collection of blood samples for general health (complete blood count) and Cal-1 specific analyses

Sponsors & Collaborators

  • Calimmune, Inc.

    lead INDUSTRY

Principal Investigators

  • Raphael Landovitz, MD · University of California, Los Angeles

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-04-30
Primary Completion
2031-10-31
Completion
2031-10-31

Countries

  • United States

Study Locations

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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 NCT02390297 on ClinicalTrials.gov