Evolution of Cellular and Viral Resistance in HIV-infected Patients With Lymphoma

NCT ID: NCT01330342

Last Updated: 2012-06-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

40 participants

Study Classification

OBSERVATIONAL

Study Start Date

2011-05-31

Study Completion Date

2014-05-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The study's chief objective is to observe the evolution of cellular (in terms of expression of transmembrane transporters and their transcriptional regulators) and viral resistance (in terms of development of mutations in the HIV genome that may confer resistance to future treatment for HIV) in HIV-infected patients with lymphoma.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The study team will take two or three tubes of blood on three occasions during the course of chemotherapy. The total amount of blood required for this research project is 64mL (approximately 4 tablespoons).

This will allow better understanding of the changes that take place in the blood and the HIV virus itself. It is hoped that this will provide new insights that may aid the understanding and treatment of HIV patients with lymphoma.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

HIV Lymphoma

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

HIV patients without lymphoma

HIV-infected subjects on cART without a diagnosis of lymphoma

No interventions assigned to this group

HIV patients with lymphoma

HIV seropositive individuals with lymphoma

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* The ability to understand and sign a written informed consent form, prior to participation in any screening procedure and must be willing to comply with all study requirements.
* Documented HIV-1 infection.
* Diagnosis of lymphoma (with the exclusion of the five subjects that will be controls).
* On cART or about to start cART as part of clinical routine care before the initiation of chemotherapy.

Exclusion Criteria

\- Receiving anti-tuberculosis treatment.
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

St Stephens Aids Trust

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Marta Boffito, Dr

Role: PRINCIPAL_INVESTIGATOR

St Stephen's AIDS Trust

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

St Stephen's Centre

London, , United Kingdom

Site Status RECRUITING

Countries

Review the countries where the study has at least one active or historical site.

United Kingdom

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Marta Boffito, Dr

Role: CONTACT

020 3315 6507

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Marta Boffito, Dr

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

SSAT 042

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.