A Randomized, Dose-ranging Study of Alferon LDO in Asymptomatic HIV+ Subjects

This study has been terminated.
Sponsor:
Information provided by (Responsible Party):
Hemispherx Biopharma
ClinicalTrials.gov Identifier:
NCT00215852
First received: September 16, 2005
Last updated: August 27, 2013
Last verified: August 2013
  Purpose

To conduct a randomized dose-ranging study to evaluate the safety and activity of orally administered low dose interferon alfa-n3 as an immunomodulator in subjects with asymptomatic HIV-1 infection. The primary endpoints of the study will include an increase or upregulation in genes known to be mediators of interferon response. Secondary endpoints will include the absolute CD4 count and plasma HIV RNA levels.


Condition Intervention Phase
HIV Infections
Drug: Alferon LDO
Phase 2

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: A Randomized, Dose-Ranging Study of Alferon® LDO [Low Dose Interferon Alfa-n3 (Human Leukocyte Derived)] in Asymptomatic HIV+ Subjects

Resource links provided by NLM:


Further study details as provided by Hemispherx Biopharma:

Primary Outcome Measures:
  • Gene expression analysis [ Time Frame: Days 0, 2, 5, 11, 12 and 16 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • CD4 Level [ Time Frame: Days 0, 11 and 16 ] [ Designated as safety issue: No ]

Enrollment: 17
Study Start Date: July 2005
Study Completion Date: April 2009
Primary Completion Date: April 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: 1
500 IU
Drug: Alferon LDO
500 IU, taken orally each evening, for 10 consecutive days while holding in the mouth for at least 2 minutes prior to swallowing, for 10 daysday 5 of each 28 day cycle.
Active Comparator: 2
1000 IU
Drug: Alferon LDO
500 IU, taken orally each evening, for 10 consecutive days while holding in the mouth for at least 2 minutes prior to swallowing, for 10 daysday 5 of each 28 day cycle.
Active Comparator: 3
2000 IU
Drug: Alferon LDO
500 IU, taken orally each evening, for 10 consecutive days while holding in the mouth for at least 2 minutes prior to swallowing, for 10 daysday 5 of each 28 day cycle.

Detailed Description:

This study will be an open-label, randomized outpatient study in HIV infected subjects using a range of doses of Alferon LDO. The first nine (9) patients enrolled will not be randomized. Instead, the first three (3) patients will receive 500 IU, the second three (3) patients will receive 1000 IU, and the final three (3) patients will receive 2000 IU. Once three (3) patients at a given dose level have received at least 8 doses without grade 3 toxicity, patients may be enrolled at the next higher dose level. Following enrollment of the first nine (9) patients, additional patients will be randomized to receive one of the three (3) dose levels of Alferon® LDO. The Alferon LDO (natural interferon alfa-n3) will be in a buffer solution and taken orally once each day for 10 consecutive days at doses equal to 500 IU, 1000 IU, or 2000 IU.

Pretherapy baseline evaluations will be performed within the three (3) week period prior to randomization.

Drug will be dispensed for a ten day treatment period, during which time any clinical symptoms and adverse events will be evaluated. Laboratory samples (2.5 ml blood) for microarray analysis evaluations will be made twice during baseline and 12-14 hours following doses 1, 4, and 10 on study days 2, 5, and 11, respectively.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. 18 years of age or older.
  2. HIV-1 plasma RNA > 500 copies/ml (Roche Amplicor assay) or similar assay within 45 days of starting oral dosing.
  3. Karnofsky performance status of 100
  4. Subjects must be asymptomatic with regard to HIV related clinical symptoms including the following opportunistic infections: Oral candidiasis (thrush), cutaneous herpes simplex, fever, diarrhea, weight loss ≥ 10% of body weight, seborrheic dermatitis, chronic mucocutaneous fungal infections or Kaposi's sarcoma. Subjects with a history of AIDS are not eligible.
  5. Serum creatinine ≤ 1.5 ULN; serum bilirubin ≤ 2.0 ULN.
  6. Total WBC ≥ 3000/mm3, platelet count ≥ 100,000/mm3 and granulocytes ≥ 1500 mm3.
  7. Absolute CD4 cell count greater than 400 (based on the average CD4 count from the two pretherapy tests).
  8. Hemoglobin > 10.0 g/dl.
  9. AST < 4 times upper normal limit.
  10. ALT < 4 times upper normal limit.
  11. Serum Albumin > 2.0 g/dl.
  12. Written informed consent.
  13. Females must either be of non-child bearing potential, or utilize an effective form of contraception and have a negative pregnancy test within 14 days of entry.
  14. For those subjects who are on antiretroviral therapy, they must have been on a stable dose schedule for at least 90 days prior to study entry and must continue on the same schedule during the treatment phase of this study.

Exclusion Criteria:

  1. Pregnant or nursing women, or women not using an effective form of contraception.
  2. Less than 18 years of age.
  3. Active IV drug users.
  4. Absolute CD4 ≤ 400 mm3 (based on the average CD4 counts from the two pretherapy tests).
  5. Receipt of any immunosuppressive agent, chemotherapy, or systemic steroids within 45 days of study entry.
  6. Receipt of any immunomodulator such as BCG vaccine, isoprinosine, or similar experimental agents within 45 days of study entry.
  7. Evidence of chronic hepatitis, or other active gastrointestinal, renal, respiratory, endocrine, hematologic, cardiovascular, neurological, or psychiatric disorder that would limit the subject's ability to complete the study period.
  8. Unlikely or unable to comply with the requirements of the protocol.
  9. Patients unwilling or unable to give informed consent.
  10. Patients on any other concurrent experimental medication.
  11. Concurrent, chronic prophylactic use of any systemic antifungal medication (e.g. ketoconazole, fluconazole, clotrimazole) or of any systemic anti-viral (e.g. acyclovir or ganciclovir) except for antiretroviral therapy.
  12. Patients using any form of interferon therapy during the 6 weeks prior to study entry. If prior interferon therapy has been received, the subject must not have known development of antibodies to interferon.
  13. Hospitalized subjects, or those with an active viral infection other than HIV, within 2 weeks of study entry.
  14. Transfusion dependent subjects (subjects requiring > 1 unit of packed RBC per month within the 3 months prior to study entry).
  15. Subjects who are symptomatic of their HIV infection at study entry.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00215852

Locations
United States, Pennsylvania
Drexel University School of Medicine
Philadelphia, Pennsylvania, United States, 19102
Philadelphia FIGHTS
Philadelphia, Pennsylvania, United States, 19107
Sponsors and Collaborators
Hemispherx Biopharma
Investigators
Study Director: David R Strayer, MD Hemispherx Biopharma
  More Information

No publications provided

Responsible Party: Hemispherx Biopharma
ClinicalTrials.gov Identifier: NCT00215852     History of Changes
Other Study ID Numbers: LDO-101
Study First Received: September 16, 2005
Last Updated: August 27, 2013
Health Authority: United States: Food and Drug Administration

Keywords provided by Hemispherx Biopharma:
Alferon LDO
Low Dose Oral Interferon
Alfa-n3
Human Leukocyte Derived
HIV
Asymptomatic HIV
Treatment Experienced

Additional relevant MeSH terms:
HIV Infections
Acquired Immunodeficiency Syndrome
Lentivirus Infections
Retroviridae Infections
RNA Virus Infections
Virus Diseases
Sexually Transmitted Diseases, Viral
Sexually Transmitted Diseases
Immunologic Deficiency Syndromes
Immune System Diseases
Slow Virus Diseases
Interferons
Interferon-alpha
Antineoplastic Agents
Therapeutic Uses
Pharmacologic Actions
Antiviral Agents
Anti-Infective Agents
Immunologic Factors
Physiological Effects of Drugs

ClinicalTrials.gov processed this record on August 19, 2014