Trial | NCT02655471  Report issue

Title

Effect of Raltegravir in Patients With Acute Tropical Spastic Paraparesis - Human T-Lymphotropic Virus 1 Infection
Effect of Raltegravir in Patients With Myelopathy/Tropical Spastic Paraparesis Associated With Infection by Human T-Lymphotropic Virus 1 (HTLV-1). Pilot Study

  • Phase

    Early Phase 1

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    10
This is a pilot study of intervention in a group of patients with tropical spastic paraparesis/ myelopathy to evaluate virologic and clinical response of raltegravir plus zidovudine in this group of patients.
The study will the investigators develop in The Tropical Medicine Institute Alexander von Humboldt that is a referral center in Peru for diseases associated to Human T-Lymphotropic Virus 1 Infection (HTLV-1). The Institute has a cohort of around 600 patients currently being followed up and around 20 to 25 new patients are admitted every year with this disease.

This is a pilot study of intervention in a group of patients with tropical spastic paraparesis/ myelopathy to evaluate virologic and clinical response of raltegravir plus zidovudine in this group of patients on the follow-up of 48 weeks.
Study Started
Jul 01
2017
Primary Completion
Mar 15
2019
Study Completion
Mar 15
2019
Last Update
May 22
2019

Drug "Raltegravir" and "Zidovudine"

Through measure of pro-viral load and clinical score, we evaluate about safety and efficacy of combination of Raltegravir 400 mg BID and zidovudine 300 mg BID in patients with recent onset of Tropical Spastic paraparesis due HTLV-1 during 48 weeks

  • Other names: "Raltegravir", "Zidovudine"

HTLV-1 plus Tropical Spastic paraparesis Experimental

Patients with recent onset of Tropical Spastic paraparesis due HTLV-1 will receive combination of "Raltegravir" and "Zidovudine" during 48 weeks

Criteria 

Inclusion Criteria:

human t lymphotrophic virus 1 confirmed
Tropical Spastic Paraparesis of recent onset (less than 4 years)

Exclusion Criteria:

Pregnant or breastfeeding or unwilling to use contraception.
Treatment with immunosuppressive, immunomodulatory or experimental treatments within the last 6 months of enrolment in the study.
Patients presenting with medical disorder such as poorly controlled diabetes or arterial hypertension, severe cardiac insufficiency, unstable ischemic heart disease, abnormal liver function tests (>2.5 times upper limit normal (ULN)) and abnormal complete blood count (in particular leukopenia, as defined by a lymphocyte count <500, neutrophil <1.5 or platelet count < 100, or thrombocytopenia < 1.5 low limit normal (LLN), or any medical condition which, in the opinion of the chief investigator, would pose additional risk to the patient.
Presence of human immunodeficiency virus antibodies.
Patients with active hepatitis B or/and C with liver function tests >2.5 times ULN
Exposure to any other investigational drug within 30 days of enrolment in the study.
No Results Posted