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NCT03351855

HPV Specific Immune Lymphocytes (HPV-CTLs) in the Treatment of HPV

Status unknown Phase 1, PHASE2 Last updated 19 September 2019
What this trial tests

Phase 1, PHASE2 trial testing HPV-CTLs in Human Papilloma Virus in 100 participants. Status unknown.

Timeline
15 November 2017
Primary endpoint
31 July 2019
31 December 2021

Quick facts

Lead sponsorShenzhen Geno-Immune Medical Institute
PhasePhase 1, PHASE2
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment100
Start date15 November 2017
Primary completion31 July 2019
Estimated completion31 December 2021
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shenzhen Geno-Immune Medical Institute

Who can join

Adults 6 Months to 75, any sex, with Human Papilloma Virus. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this clinical trial is to evaluate the safety and efficacy of IV-infused autologous or allogenic HPV-CTLs.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Harnessing virus-specific T cells: expanding therapeutic strategies across diverse populations.
    Djassemi N, Hanisch B, Motta C, Maghzian N, et al · · 2025 · cited 2× · PMID 40864193 · DOI 10.1182/bloodadvances.2024013727

Verify or expand the search:

Other recruiting trials for Human Papilloma Virus

Currently open trials in the same condition.

Other Shenzhen Geno-Immune Medical Institute trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03351855.

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