Sign in

NCT02390297Active, not recruiting

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

Long Term Follow-up for the Detection of Delayed Adverse Events in Recipients of CD4+ T Lymphocytes and/or CD34+ Hematopoietic Stem/Progenitor Cells Transduced With LVsh5/C46, a Dual Anti-HIV Gene Transfer Construct

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

Long term safety follow-up of Cal-1 recipients

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
11 (actual)
First submitted
11 Mar 2015
Start date
Apr 2015
Primary completion date
Oct 2031
Lead sponsor
Calimmune, Inc.
Diseases
HIV
NCT number
NCT02390297

What you commit to

  • Study type: Observational
  • Participants enrolled: 11
  • From Apr 2015 to the primary completion date, Oct 2031
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study design.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Inability to understand and provide informed consent

Who the study is looking for

  • Signed informed consent
  • Previous treatment with the Cal-1 modified hematopoietic cellular products

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
UCLA CARE Center
Coordinator of this site? Confirm its status
Los AngelesUnited StatesUnknown status
Quest Clinical Research
Coordinator of this site? Confirm its status
San FranciscoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.