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Clinical Trials/NCT03283397
NCT03283397
Terminated
Phase 3

A Phase IIIb, Multi-center, International, Randomized, Assessor-blind, Active-controlled Parallel Arm Clinical Study to Evaluate the Efficacy, Safety and Tolerability of Neuropeptide Combination of Metenkefalin and Tridecactide (EK-12) in Comparison to Interferon Beta-1a (REBIF®) in Patients With Relapsing Remitting Multiple Sclerosis (RRMS)

Bosnalijek D.D1 site in 1 country301 target enrollmentMarch 26, 2019

Overview

Phase
Phase 3
Intervention
EK-12
Conditions
Multiple Sclerosis, Relapsing-Remitting
Sponsor
Bosnalijek D.D
Enrollment
301
Locations
1
Primary Endpoint
Superiority of efficacy of EK-12 to interferon beta-1a in patients with RRMS
Status
Terminated
Last Updated
last year

Overview

Brief Summary

Multiple sclerosis is a chronic autoimmune, inflammatory neurological disease of the central nervous system. It is the most common disabling neurologic disease of young people. This study is planned for the evaluation of efficacy, safety and tolerability of neuropeptide combination of metenkefalin and tridecactide (EK-12) as compared to INF beta-1a (REBIF®) in patients with RRMS. The primary objective of this study is to prove the superiority of efficacy of neuropeptide combination of metenkefalin and tridecactide (EK-12) compared to INF beta-1a (REBIF®) in patients with RRMS on the basis of annualized protocol defined relapse rate by 144 weeks.

Registry
clinicaltrials.gov
Start Date
March 26, 2019
End Date
July 1, 2023
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients from both genders with a confirmed and documented diagnosis of MS as defined by the Revised McDonald criteria (2010), with relapse onset disease or a relapsing-remitting disease course, between 18 and 55 years of age at screening (inclusive).
  • Ambulatory patients with EDSS score of 0 to 4.5 at both screening and randomization visits.
  • Patients who meet one of the following disease activity criteria:
  • At least 1 documented relapse within the last 12 months prior to screening or;
  • At least 1 documented relapse occurred within the last 24 months prior to screening and documented evidence of at least 1 Gadolinium Enhancing (GdE) lesion on brain MRI scan within the last 12 months prior to randomization.
  • Patients with a confirmed stable neurological condition, who are relapse-free and not on a corticosteroid treatment \[intravenous (IV), intramuscular (IM) and/or per os (PO)\] or adrenocorticotrophic hormone (ACTH) treatment, at least 30 days prior to randomization.
  • Women of child-bearing potential (e.g. women who are not postmenopausal or surgically sterilized) must practice an acceptable method of birth control for 30 days before taking the study drug and two acceptable methods of birth control during the duration of the study and until 30 days after the last dose of study medication. Acceptable methods of birth control include: intrauterine devices, barrier method (condom with spermicide or diaphragm with spermicide) and hormonal methods of birth control (e.g. oral contraceptive, contraceptive patch, and long-acting injectable contraceptive).
  • Patients must be able to sign and date a written Informed Consent Form (ICF) prior to entering the study.
  • Patients must be willing and able to comply with the study protocol requirements for the duration of the study

Exclusion Criteria

  • Patients with progressive forms of MS.
  • Patients with disease duration of ≥10 years.
  • Inability to complete an MRI examination. Contraindications for MRI examination include but are not restricted to overweight, pacemaker, cochlear implants, presence of foreign substances in the eye, intracranial vascular clips, surgery within 6 weeks of entry into the study, coronary stent implanted within 8 weeks prior to the time of the intended MRI, etc.
  • Patients with neuromyelitis optica (NMO) or NMO spectrum disorders.
  • Use of experimental or investigational drugs and/or participation in drug clinical studies within 6 months prior to randomization.
  • Use of immunosuppressive agents or cytotoxic agents, including cyclophosphamide within 6 months prior to randomization.
  • Use of either of the following agents within 2 years prior to randomization: natalizumab, rituximab, ocrelizumab, atacicept, belimumab, or ofatumumab.
  • Use of teriflunomide within 2 years prior to randomization, except if active washout (with either cholestyramine or activated charcoal) was done 2 months or more prior to randomization.
  • Previous treatment with glatiramer acetate, interferon-beta (either 1a or 1b), fingolimod, dimethyl fumarate or intravenous immunoglobulin (IVIG) within 2 months prior to randomization.
  • Chronic (more than 30 consecutive days) systemic (IV, IM or PO) corticosteroid treatment within 30 days prior to randomization.

Arms & Interventions

EK-12

This arm will be treated with 12 mg EK-12 in 2 mL 0.9 % NaCl solution (SC, three times per week) for 144 weeks

Intervention: EK-12

INF Beta-1a

This arm will be treated with 44 mg INF Beta-1a in 0.5 mL solution (SC, three times per week) for 144 weeks

Intervention: INF beta-1a

Outcomes

Primary Outcomes

Superiority of efficacy of EK-12 to interferon beta-1a in patients with RRMS

Time Frame: weeks 12, 24, 36, 48, 60, 72, 84, 96, 108, 120, 132, 144

The primary objective of this study is to prove the superiority of efficacy of neuropeptide combination of metenkefalin and tridecactide (EK-12) compared to interferon beta-1a (INF beta-1a, 44 mcg, REBIF®) in patients with RRMS on the basis of annualized protocol defined relapse rate (ARR) by 144 weeks.

Secondary Outcomes

  • T1 lesions(weeks 12, 24, 36, 48, 60, 72, 84, 96, 108, 120, 132, 144)
  • EDSS score(weeks 12, 24, 36, 48, 60, 72, 84, 96, 108, 120, 132, 144)
  • clinical attacks(weeks 12, 24, 36, 48, 60, 72, 84, 96, 108, 120, 132, 144)
  • T2 lesions(weeks 12, 24, 36, 48, 60, 72, 84, 96, 108, 120, 132, 144)

Study Sites (1)

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