Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
PlainTrials
RecruitingPhase 1 / Phase 2interventionalRules rewrite

Phase 1 / Phase 2: testing Two IM injections Lenti-HPV-07 for HPV-Related Cervical Carcinoma

The goal of this clinical trial is to learn about the safety and how well it works of a potential new treatment called Lenti-HPV-07 in patients with a cancer induced by Human Papilloma Virus (HPV). The main questions aim to answer are: * Is Lenti-HPV-07 safe?

Official registry: https://clinicaltrials.gov/study/NCT06319963 · Theravectys S.A. · enrollment listed as 72

What this phase means

Phase 2: researchers already know a roughly safe dose (from phase 1). This stage asks whether the treatment actually helps the condition, and watches side effects more closely.

Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

What the registry says happens

If you join, the listed intervention(s) are Two IM injections Lenti-HPV-07, or One IM injection Lenti-HPV-07. The registry lists allocation as randomized. The goal of this clinical trial is to learn about the safety and how well it works of a potential new treatment called Lenti-HPV-07 in patients with a cancer induced by Human Papilloma Virus (HPV).

They plan to enroll about 72 people at 4 sites. Taking part typically means taking a study drug (or dummy pill) plus check-ins.

Official title (unrewritten)

An Open-Label Phase 1/2a Clinical Trial to Evaluate the Safety, Immunogenicity, and Preliminary Efficacy of a Lentiviral Vector-Based Therapeutic Vaccine Against Human Papilloma Virus (Lenti-HPV-07) in Participants With HPV-Associated Oropharyngeal Squamous Cell Cancer or Cervical Cancer

Interventions: Two IM injections Lenti-HPV-07, One IM injection Lenti-HPV-07

Primary outcome (registry wording): Safety and Tolerability

Who it is for (from inclusion criteria)

  • Ages 18 Years to any
  • histologically confirmed invasive HPV-related oropharyngeal or cervical cancer
  • how well you can do daily activities (ECOG score) of 0 or 1
  • adequate hepatic, renal, pulmonary, and bone marrow/hematological function

Public study contact (from the registry)

Anastasia DEMIDOV

+33

ademidova@theravectys.com

Published on ClinicalTrials.gov. Contact them as a possible participant. They decide eligibility.

Sites listed on ClinicalTrials.gov

4 listed

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FAQ about this NCT record

Is NCT06319963 still recruiting?

The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.

What phase is NCT06319963?

Phase 1 / Phase 2. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

Can PlainTrials tell me if I qualify for NCT06319963?

No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.

How to read a ClinicalTrials.gov record · Questions to ask the coordinator · Glossary