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NCT06600568Recruiting

Novel Therapeutic Approach for Human T-cell Malignancies

Identification of Targetable Vulnerabilities in Redox Homeostasis Pathways as a Novel Therapeutic Approach for Human T-cell Malignancies

Source: ClinicalTrials.gov · Last updated 6 Aug 2026

Brief summary (registry, in English)

This multicenter translational study, with prospective and retrospective samples, aims to identify new strategies to selectively eliminate neoplastic T cells by modulating intracellular ROS levels. Interactions between drugs capable of activating the apoptotic process (e.g., Venetoclax) and drugs capable of altering ROS homeostasis (e.g., inhibitors of the enzyme glucose-6-phosphate dehydrogenase) will be examined. The most promising compounds will be selected based on results obtained in vitro on cell lines and PDX already available in the laboratory, and then will be assayed ex vivo in cells obtained from patients with resistant/refractory T-cell neoplasms.

Status (registry)
Recruiting
Study type
Observational
Enrollment
120 (estimated)
First submitted
11 Sept 2024
Start date
Mar 2025
Primary completion date
Mar 2027
Lead sponsor
Istituto Oncologico Veneto IRCCS
NCT number
NCT06600568

What you commit to

  • Study type: Observational
  • Planned participants: 120
  • From Mar 2025 to the primary completion date, Mar 2027
  • 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, not your situation.

Who cannot take part

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

Other illness

  • -Serious illness or medical condition that does not allow the patient to be managed according to standard treatment protocols, including uncontrolled active infection.

Who the study is looking for

  • Patients with pre- and post-thymic T-cell leukemia/lymphoma
  • Patients of both sexes
  • Age of patients older than 18 years
  • Patient is willing to provide written and signed informed consent for participation in the study

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Istituto Nazionale Tumori Fondazione G. Pascale
Coordinator of this site? Confirm its status
NaplesItalyRecruiting
Istituto Oncologico Veneto
Coordinator of this site? Confirm its status
PadovaItalyRecruiting

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