Safety Study of the HemoModulator System for the Treatment of Patients With Human Immunodeficiency Virus (HIV)

NCT00858923 | Unknown Phase 1 DMC

• 1 other identifier: G080104
• Study Type: interventional
• Target: 10
• Locations: 1 country
• Sites: 1

Brief Summary

Tulane University Health Sciences Center/Louisiana Community AIDS Research Center Program, New Orleans, LA is seeking patients for an HIV study. The purpose of the study is to test the safety and effectiveness of an experimental ultra-violet light device designed to reduce virus in your blood.

Conditions

HIV; HIV Infections

Keywords

Extracorporeal Photophoresis; immuno-therapy; treatment naive

Outcome Measures

Primary Outcomes (1)

• Determine the therapy effectiveness on HIV-1 plasma viral load using PCR analysis Determine the therapy effects on CD4+, CD8+ cells and CD4/CD8 ratio

  Once a week for 10 weeks

Interventions

Energex HemoModulator DEVICE

To use ultraviolet light to reduce HIV virus in the patient's blood

Also known as: Extracorporeal photophoresis

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Diagnosis of HIV-1 has been confirmed positive by ELISA and by Western Blot
• Subject is not yet eligible for HAART
• Subject's viral count at pre-baseline measured by RT-PCR is
• ,000 copies /ml
• Subject has a CD4+ count ≥ 400 cells/mm3
• Subject's pre-screen EIA and RIBA test has proven negative for Hepatitis C virus
• Female subjects with reproductive potential (and any male sexual partners) must agree to use a barrier device with spermicide (e.g., condoms, cervical cap, diaphragm) as the primary form of contraception, in addition to any other methods used, during treatment and until the end of the study to prevent pregnancy
• Subject has taken no other anti-viral device or pharmacologic treatments in the 2 months prior to the first scheduled Hemo-Modulator study treatment
• Subject agrees not to receive any other anti-viral device or anti-viral pharmacologic treatment (including herbal remedies) throughout the 21-week study period
• Subject weighs at least 90 lbs (40.9 kg) at study initiation
• Subject agrees to comply with study protocol requirements including all follow up visits through Day 60 of study duration

You may not qualify if:

• Subjects with any other major illness (e.g., malignancy, renal failure, tuberculosis, porphyria, severe cardiac disease, severe neurological disease, or Hepatitis C) that would prevent completion of the study or bias efficacy assessments
• Subjects with any other medical condition that the Investigator believes would make the patient unable to safely tolerate the extracorporeal blood volume required during the procedure \[e.g., severe cardiovascular disease, history of congestive heart failure, or severe anemia (hemoglobin \< 90 g/L)\]
• Subject with porphyria cutanea tarda (PCT), since PCT is associated with increased sensitivity to light and skin reactions such redness, pain, swelling and blistering after exposure to ultraviolet light
• Subject has clinically abnormal hemotologic or chemistry laboratory values, defined as any parameter for these tests that exceeds Grade 1 (DAIDS Table for Grading the Severity of Adult Adverse Events, December 2004)
• Subject has taken a steroid drug (other than Estrogen or Progesterone) within 7 days prior to study enrollment, or may require such medications during the course of study participation
• Subject has taken a drug listed as photosensitizing in the Physician's Desk Reference (PDR) within 7 days prior to a Hemo-Modulator Treatment session
• Subjects that habitually use excessive alcohol
• Subjects that use illicit drugs or have an ongoing drug abuse problem
• Subjects that have an acute systemic bacterial infection (septicemia)
• Subjects that have been immunized for influenza within 7 days prior to study enrollment or is likely to require such immunization during the course of study participation
• Subject is currently participating in another clinical investigation of a medical device, drug or biologic, or has participated in such a study within the 3 months prior to study enrollment
• Subject is pregnant or plans on becoming pregnant within the next twelve months; or is lactating
• Subject has a clotting deficiency
• Subject is allergic to heparin

Sponsors & Collaborators

• Energex Systems, Inc.: lead

Study Sites (1)

Tulane University Health Sciences Center/LaCarp

New Orleans, Louisiana, 70112, United States

Location

MeSH Terms

Conditions

HIV Infections

Interventions

Photopheresis

Condition Hierarchy (Ancestors)

Blood-Borne Infections; Communicable Diseases; Infections; Sexually Transmitted Diseases, Viral; Sexually Transmitted Diseases; Lentivirus Infections; Retroviridae Infections; RNA Virus Infections; Virus Diseases; Genital Diseases; Urogenital Diseases; Immunologic Deficiency Syndromes; Immune System Diseases

Intervention Hierarchy (Ancestors)

PUVA Therapy; Ultraviolet Therapy; Phototherapy; Therapeutics; Extracorporeal Circulation; Surgical Procedures, Operative

Study Design

• Study Type: interventional
• Phase: phase 1
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY

Study Record Dates

• First Submitted: March 6, 2009
• First Posted: March 10, 2009
• Study Start: July 1, 2008
• Primary Completion: July 1, 2009
• Study Completion: November 1, 2009
• Last Updated: April 8, 2009

Record last verified: 2009-03

Locations

US (1)