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A Pilot Open Label Trial of HIV Therapy With d4T (Stavudine), ddI (Didanosine), Nelfinavir and Hydroxyurea in Subjects With Early Asymptomatic HIV Infection
This study has been completed.
Study NCT00002176   Information provided by Bristol-Myers Squibb
First Received: November 2, 1999   Last Updated: October 1, 2007   History of Changes

November 2, 1999
October 1, 2007
 
 
 
 
Complete list of historical versions of study NCT00002176 on ClinicalTrials.gov Archive Site
 
 
 
A Pilot Open Label Trial of HIV Therapy With d4T (Stavudine), ddI (Didanosine), Nelfinavir and Hydroxyurea in Subjects With Early Asymptomatic HIV Infection
A Pilot Open Label Trial of HIV Therapy With d4T (Stavudine), ddI (Didanosine), Nelfinavir and Hydroxyurea in Subjects With Early Asymptomatic HIV Infection

To assess the magnitude and duration of the antiviral activity in plasma and the incidence and time to total suppression of detectable HIV RNA in plasma. To assess the long-term safety and tolerability of this combination therapy and the magnitude and duration of the effect of this therapy over CD4 cell counts.

 
 
Interventional
Treatment, Randomized, Open Label, Active Control, Single Group Assignment, Safety Study
HIV Infections
  • Drug: Hydroxyurea
  • Drug: Nelfinavir mesylate
  • Drug: Stavudine
  • Drug: Didanosine
 
 

*   Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.
 
Completed
 
 
 

Inclusion Criteria

Patients must have:

  • Documented HIV infection.
  • CD4 count > 500 cells/mm3.
  • No HIV-associated symptoms.
  • Written, informed consent from parent or legal guardian for patients < 18 years old.
  • Availability for follow-up for at least 96 weeks.

Exclusion Criteria

Co-existing Condition:

Patients with the following conditions and symptoms are excluded:

  • Presence of a newly diagnosed AIDS-defining opportunistic infection requiring acute therapy at the time of enrollment.
  • Intractable diarrhea.
  • Signs and symptoms of bilateral peripheral neuropathy >= Grade 2.
  • Inability to tolerate oral medication.
  • Hemophilia, other bleeding disorder, or no accessible tonsillar or lymph node tissue.

Patients with the following prior conditions are excluded:

History of acute or chronic pancreatitis. 1. Use of potent neurotoxic drugs is not permitted.

  • No other anti-HIV therapy allowed.
  • Nelfinavir should not be administered concurrently with rifampin or rifabutin, terfenadine (Seldane), astemizole (Hismanal), cisapride (Propulsid), triazolam (Halcion), and midazolam (Versed).

    1. Any prior antiretroviral therapy.

  • Prior vaccination with a candidate HIV therapeutic vaccine.
  • Previous therapy with agents with significant systemic myelosuppressive, neurotoxic, pancreatotoxic, hepatotoxic or cytotoxic potential within 3 months of study start or the expected need for such therapy at the time of enrollment.
  • Previous therapy with rifampin or rifabutin, terfenadine (Seldane), astemizole (Hismanal), cisapride (Propulsid), triazolam (Halcion), and midazolam (Versed) within 14 days prior to study entry or at any time while on study.

Active alcohol or substance abuse.

Both
16 Years and older
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00002176
 
244C, AI455-062
Bristol-Myers Squibb
 
Principal Investigator: . ., . .
Bristol-Myers Squibb
October 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP