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NCT00002296 · ClinicalTrials.gov registry record · NA
The Safety and Effectiveness of Isoprinosine in Patients With Weakened Immune Systems and Lymph Node Disease
A NA study, sponsored by Newport Pharmaceuticals International.
- Completed
- Registry status
- NA
- Development phase
NCT00002296: Completed NA study, sponsored by Newport Pharmaceuticals International.
NCT00002296 is a NA study that has completed, run by Newport Pharmaceuticals International. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00002296, a NA study, has completed, sponsored by Newport Pharmaceuticals International.
- COMPLETED
- Registry status
- NA
- Development phase
Study Summary
The objective of this Phase III, randomized, double-blind, placebo-controlled study in patients with immunologic deficiency is to determine the effect of Isoprinosine in producing an immuno-restorative response within the study observation period (including the 2-month period following cessation of the 28 days of treatment), measured by one or more of the following immunological parameters: * Increase in natural killer (NK) cell activity. * Increase in total T-cells (OKT-11). * Increases in absolute number and percentage of T-helper cells (OKT-4).
Interventions
- DRUG Inosine pranobex
Trial Details
| Field | Value |
|---|---|
| Phase | NA |
What the finished NCT00002296 record still lists
NCT00002296 is an interventional study that assigns participants to a tested intervention. An enrollment target was not published in the registry record, which is common for early-stage or observational entries.
The record links to 0 conditions, and to 1 intervention - of which Inosine pranobex is the first listed.
NCT00002296 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00002296 about?
NCT00002296 is a clinical study titled "The Safety and Effectiveness of Isoprinosine in Patients With Weakened Immune Systems and Lymph Node Disease". The objective of this Phase III, randomized, double-blind, placebo-controlled study in patients with immunologic deficiency is to determine the effect of Isoprinosine in producing an immuno-restorative response within the study observation period (including the 2-month period following cessation of ...
What is the current status of trial NCT00002296?
This trial is currently completed. It is a NA study.
What interventions are being tested in trial NCT00002296?
The interventions under investigation include: Inosine pranobex (DRUG).
Who is sponsoring clinical trial NCT00002296?
This trial is sponsored by Newport Pharmaceuticals International, which has 6 total clinical trials registered on ClinicalTrials.gov.