Skip to content

Intranasal Peptide T in the Treatment of Painful Peripheral Neuropathy of AIDS

Intranasal Peptide T in the Treatment of Painful Peripheral Neuropathy of AIDS

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002083
Enrollment
Unknown
Registered
2001-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2005-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections, Peripheral Nervous System Disease

Keywords

Peptide T, HIV-1, Administration, Intranasal, Acquired Immunodeficiency Syndrome, Peripheral Nervous System Diseases

Brief summary

To compare the effects of intranasal peptide T and placebo in the treatment of painful peripheral neuropathy associated with human immunodeficiency virus (HIV) infection.

Interventions

Sponsors

Advanced Peptides
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients must have: * Documented HIV-1 infection. * CD4 count \< 500 cells/mm3. * HIV-1-associated distal symmetrical polyneuropathy, with peripheral neuropathy present for at least 6 weeks prior to study entry. * Pain severity of at least 8 on an analog scale. * Prior zidovudine therapy for at least the previous 3 months (unless patient has shown intolerance to zidovudine).

Exclusion criteria

Co-existing Condition: Patients with the following symptoms and conditions are excluded: * Neuropathy due to any other cause besides HIV infection. * Any symptom consistent with a new or active underlying opportunistic infection or malignancy that could interfere with the evaluation of neuropathy. * Clinical evidence of new or active CNS disease, potentially from opportunistic infection or neoplasm resulting from HIV infections, that could interfere with the evaluation of neuropathy. * Other CNS disease (e.g., myelopathy) that could complicate the evaluation of neuropathy. * Active life-threatening illness other than AIDS. Concurrent Medication: Excluded: * Dapsone. * Hydralazine. * Isoniazid (INH). * Current use of tricyclic antidepressants, anticonvulsants, or clonidine unless the patient has used the drug without a change in dose for at least 3 months prior to study entry. * Narcotics, unless the patient has been using them for at least 6 weeks prior to study entry. Prior Medication: Excluded: * ddI or ddC in the past 8 weeks. * Prior peptide T. * Prior tricyclic antidepressants, anticonvulsants, or clonidine unless they have been used for at least 3 months without change in dose. * Other investigational drugs within the past 30 days. Required: * Zidovudine (if intolerance not demonstrated). Required: * Zidovudine for at least the previous 3 months (unless patient has demonstrated intolerance to zidovudine). Chronic alcohol abuse, or current abuse of psychoactive recreational drugs as defined in DSM IIIR. Patients who may be regarded as unreliable for the study.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026