The HAM Infliximab Study

Phase 2

Terminated

• Conditions: HTLV-I-associated Myelopathy
• Interventions: Drug: Infliximab

• Registration Number: NCT00823641
• Lead Sponsor: Imperial College London

Brief Summary

An open-label, non-randomised, uncontrolled, proof-of-concept study of eight patients with 'definite' HTLV-I-associated myelopathy/Tropical Spastic Paraparesis (HAM/TSP). Eligible patients will have either early disease (of less than 2 years duration) or progressive disease (with observed clinical deterioration during the preceding 3 months.

Following 2 baseline assessments including Magnetic Resonance Imaging (MRI) of the spinal cord and a lumbar puncture for examination of the fluid around the brain (CSF) participants will be treated with a total of 7 infusions of the anti-TNF-alpha antibody infliximab over a period of 48 weeks. After the last on therapy assessment at 48 weeks participants will be followed up for a further 24 weeks. Study assessments will be clinical, virological, immunological and radiological. MRIs of the spinal cord will be obtained at weeks 12 and 72. CSF will be examined, on therapy, at week 12.

Detailed Description

Not available

Study Timeline

• Study Start: 2008-10
• Study First Submitted: 2009-01-14
• Study First Submitted QC: 2009-01-14
• Study First Posted: 2009-01-15
• Primary Completion: 2011-03
• Study Completion: 2011-03
• Status Verified: 2013-04
• Last Update Submitted: 2013-04-12
• Last Update Posted: 2013-04-15

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 3

Inclusion Criteria

• Are able to give informed consent

• Are 16 years or older

• Have 'definite' HAM/TSP according to the criteria of "Definite HAM/TSP" agreed in Belem 200361

• Have early or progressing disease as defined here:

  • "Early HAM/TSP": Patients must have motor disability (minimum of stiffness or weakness) for less than 2 years. (Bladder symptoms if the original and only presenting symptoms as assessed by history are not included)

• "Progressing HAM/TSP"

• New or worsening motor symptoms in a patient with definite HAM of > 2 years duration within the last 3 months

Exclusion Criteria

• Hepatitis B or hepatitis C infection
• HIV infection
• Overt sepsis, abscesses or opportunistic infections
• Active TB (untreated or on treatment)
• Strongyloides stercoralis (untreated)
• Known hypersensitivity to inflixmab, other murine proteins or to any of the excipients
• Malignancy
• Moderate or severe heart failure (NYHA class III/IV)
• Pregnancy or breastfeeding
• Unhealed surgical wounds
• Planned impending surgery - treatment would be withheld for 2-4 weeks prior to major surgery and started/restarted post-operatively if no evidence of infection and wound healing is satisfactory
• Current immunosuppressive or immunomodulatory therapy

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Infliximab	Infliximab	Infliximab 3mg/kg infused intravenously at weeks 0, 2 and 8 and then every 8 weeks until and including week 40 of the study

Primary Outcome Measures

Name	Time	Method
Incidence of clinical failure	48 weeks

Secondary Outcome Measures

Name	Time	Method
Change in timed 10m walk	12, 24, 48 and 72 weeks
Clinical Safety	48 weeks
HTLV-I viral load in CSF	12 weeks
HTLV-I viral load in peripheral blood	12, 24, 48 and 72 weeks
% CD4+ T- lymphocytes expressing CD25	24, 48 and 72 hours

Trial Locations

Locations (1)

Imperial College Healthcare NHS Trust; 🇬🇧 London, United Kingdom