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HIV InfectionsNCT00002060

A Multi-Center Randomized Double-Blind Placebo-Controlled Study To Investigate the Effect of Isoprinosine in Patients With AIDS Related Complex (ARC)

A study testing Inosine pranobex in people with HIV Infections, run by Newport Pharmaceuticals International at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The objective is to determine the effect of Isoprinosine (inosine pranobex) in homosexual male patients with AIDS related complex (ARC) in delaying the onset of AIDS. Secondly, to determine the effect of Isoprinosine in decreasing the severity and/or incidence of lesser opportunistic infections and/or other conditions… Read more about this study

Who is it for?
Ages 18 to 75 years, men only
Conditions the study is for
HIV Infections
What is being tested?
Inosine pranobex
How many people
Not given
Where
1 siteUnited States
Study dates
Start not givento not given
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 75 years
  • Men only
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

None listed.

Who cannot join

  • Concurrent Medication:
  • Excluded:
  • Cardiac glycosides.
  • Patients with the following are excluded:
  • AIDS.
  • Presenting with chronic candida infection-colo/rectal, oral/pharyngeal, cutaneous (finger/toenails) - for = or > 3 months who have not responded to therapy.
Show all 21Show fewer
  • Critical illness.
  • Hemophilia.
  • Prior Medication:
  • Excluded within 1 month of study entry:
  • Steroids.
  • Cytotoxic immunosuppressive agents.
  • Radiotherapy and/or systemic antiviral medication.
  • Immunomodulators (including Isoprinosine).
  • Prior Treatment:
  • Excluded within 1 month of study entry:
  • Radiotherapy.
  • History of gout, uric acid urolithiasis, uric acid nephrolithiasis, or renal dysfunction.
  • Lymphoid malignancy.
  • Homosexual male patients with AIDS related complex (ARC).
  • Current IV drug abuse.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Newport Pharmaceuticals International Inc

    Laguna Hills, California, 92656

Other trials in United States

About this study

The objective is to determine the effect of Isoprinosine (inosine pranobex) in homosexual male patients with AIDS related complex (ARC) in delaying the onset of AIDS. Secondly, to determine the effect of Isoprinosine in decreasing the severity and/or incidence of lesser opportunistic infections and/or other conditions associated with ARC.

Conditions
HIV Infections
Being tested
Inosine pranobex
Keywords
AIDS-Related Opportunistic Infections, Inosine Pranobex, Homosexuality, Acquired Immunodeficiency Syndrome, AIDS-Related Complex
Medical subject headings
HIV Infections, AIDS-Related Opportunistic Infections, Homosexuality, Acquired Immunodeficiency Syndrome, AIDS-Related Complex

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Inosine pranobexDrug

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted31 Aug 2001 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Masking
Double blind
IDs, dates and publications
ClinicalTrials.gov ID
NCT00002060
Sponsor's protocol ID
008D
Other IDs
ISO-111-USA
Status last verified
Jun 1989
First submitted
2 Nov 1999
Last updated
24 Jun 2005
Results posted
No

Questions about this trial

What is this clinical trial studying?

A study testing Inosine pranobex in people with HIV Infections, run by Newport Pharmaceuticals International at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 0 inclusion and 21 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Jun 2005. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2005.

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Clinical Trial NCT00002060 | AzTrials