The Safety and Effectiveness of SPC3 in HIV-1 Infected Patients

HIV Infections Clinical Trial

Official title:

Study of the Safety and Effects of Two Doses of SPC3, Administered Daily Intravenously in HIV-1 Seropositive Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00002363
• Other study ID #: 257A
• Secondary ID: SPC3-US1
• Status: Completed
• Phase: Phase 1
• First received: November 2, 1999
• Last updated: June 23, 2005

Study information

• Verified date: April 1999
• Source: NIH AIDS Clinical Trials Information Service
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

To assess the effects of two doses of synthetic peptide construction 3 ( SPC3 ) on HIV-1 plasma levels (as measured by RNA PCR Amplicor) and on lymphocyte subsets in patients with initial viral load above 10,000 copies/ml. To study the safety of SPC3 and the kinetics of HIV-1 plasma level changes.

Description:

The first five patients receive SPC3 daily for 3 weeks. If that dose is tolerated, the dose is increased and given to the next 5 patients for 3 weeks. The remaining ten patients receive a dose of SPC3 based on response to the previous two dose levels. Patients are followed through day 28.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 65 Years

Eligibility

Inclusion Criteria

Concurrent Medication:

Allowed:

• Antiretrovirals provided regimen has been stable for at least 6 weeks prior to study screening.

Patients must have:

• HIV seropositivity for at least 6 months.

• CD4 >= 100 cells/mm3.

• HIV RNA PCR (Amplicor) > 10,000 copies/ml.

• No significant active opportunistic infection or tumor at study entry.

FDA DISCLAIMER:

• The FDA encourages the inclusion of females of childbearing potential in study protocols, but the sponsor of this protocol specifically excludes females of childbearing potential from this study and includes only females who are sterile. Any questions about these inclusion/exclusion criteria should be directed to the study's contact person.

Prior Medication:

Allowed:

• Prior antiretrovirals.

Exclusion Criteria

Co-existing Condition:

Patients with the following conditions are excluded:

Inability to communicate with investigator or deemed likely to be noncompliant on study.

Concurrent Medication:

Excluded:

• Any drug that may interact with SPC3 (e.g., suramin).

Patients with the following prior condition are excluded:

History of relevant drug hypersensitivity.

Prior Medication:

Excluded:

• Investigational drug within the past 4 weeks.

Study Design

Endpoint Classification: Pharmacokinetics Study, Primary Purpose: Treatment

Related Conditions & MeSH terms

• HIV Infections

Intervention

Drug:
• Peptide Construction 3, Synthetic

Locations

Country	Name	City	State
United States	Brown Univ School of Medicine	Providence	Rhode Island

Sponsors (1)

Lead Sponsor	Collaborator
Columbia Research Laboratories

Country where clinical trial is conducted

United States,