Efficacy, Safety and Tolerability of Andrographolides Versus Placebo in Patients With Progressive Forms of MS

Primary Progressive Multiple Sclerosis Clinical Trial

Official title: Controlled, Randomized, Double-blind Clinical Trial, 24 Months Duration, to Compare the Efficacy, Safety and Tolerability of Andrographolide Versus Placebo in Patients With Progressive Forms of Multiple Sclerosis

Status Recruiting

Clinical Trial Summary

The purpose of this study is to compare the efficacy and safety of andrographolide 140 mg administered twice a day orally versus a placebo as a modifying treatment of the disease in patients with the progressive forms of Multiple Sclerosis (MS).

The principal outcome is to determine the efficacy, of andrographolide in retarding the progression of brain atrophy in patients with progressive forms of MS.

Clinical Trial Description

1. Evaluate the clinical efficacy of andrographolide 140 mg administered orally twice a day versus a placebo in:

• Delay in the disability capacity progression through the Expanded Disability Status Scale (EDSS) and Multiple Sclerosis Functional Composite (MSFC) at 24 months compared to the baseline.

• Delay in cognitive impairment by means of Paced Auditory Serial Addition Test (PASAT), Symbol Digit Modalities Test (SDMT) and depression (Beck) at 24 months compared to the baseline.

• Quality of life Multiple Sclerosis Impact Scale (MSIS 29) and fatigue (Krupp) through parameters reported by the patients at at 24 months compared to the baseline.

• Tolerability of andrographolide measured by the Treatment Satisfaction Questionnaire for Medication (TSQM) at 24 months.

• Delay in the decrease in brain volume measured by Magnetic Resonance (MR) at 24 months compared to the baseline.

• Number and volume of new lesions or larger size in T2 by MR at 24 months compared to the baseline.

• Number of new hipointense lesions in T1 or (gadolinium captive) by MR at 24 months compared to the baseline.

• Delay in the retineal thinning measured by Optical Coherence Tomography (OCT) and visual field at 24 months compared to the baseline.

• Safety of andrographolide at 24 months through the record of adverse effects in symptom dairy and programmed interviews.

2. Explore the pharmacokinetic of andrographolide 140 mg administered orally twice day in:

• bio availability and concentration of andrographolide in the patients with treatment.

• half-life, maximum concentration, clearance of andrographolide in equilibrium state.

3. Determine the immunomodulatory effects of andrographolide 140 mg administered twice a day orally on lymphocyte populations in patients through the:

• Determination of Th1, Th2, Th17 and Treg lymphocyte sub-populations.

• Determination of cytokines IFNgama, TNFalpha, IL2, IL17alpha and TGFbeta.

Population: adult patients, men and women with progressive forms of MS. The number of patients to be selected will be 68, to randomly assign 34 patients to each group. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Multiple Sclerosis
• Multiple Sclerosis, Chronic Progressive
• Multiple Sclerosis, Secondary Progressive
• Primary Progressive Multiple Sclerosis
• Sclerosis

• NCT number: NCT02273635
• Study type: Interventional
• Source: Innobioscience SpA
• Contact: Claudia A Carcamo, MD, PhD
• Phone: +56223546885
• Email: ccarcamo@med.puc.cl
• Status: Recruiting
• Phase: Phase 1/Phase 2
• Start date: September 2014
• Completion date: April 2017