CompletedPhase 3Optic neuritisNCT019625712013-002515-10

What it found

Missed its main goal

The main measure did not show a significant benefit.

“Mean pRNFL atrophy was 15·93 μm (SD 14·91) in the erythropoietin group and 14·65 μm (15·60) in the placebo group (adjusted mean treatment difference 1·02 μm; 95% CI -5·51 to 7·55; p=0·76).”
Read by software from the paper's abstract

week 26

GroupnValue
Erythropoietin5215.93 μm (SD 14.91)
Placebo5114.65 μm (15.60)

adjusted mean treatment difference 1.02 μm (95% CI -5.51–7.55)

p = 0.76

Total participants: 108

Read by software from the paper's abstract

What was tested

Treatment tested

  • Epoetin alfa

    Erythropoietin receptor agonist

Placebo or sham

  • Placebo

What it measured

Main measures

  • Global retinal nerve fibre layer thickness (RNFLT-G)

    6 months

    Retina scans (OCT)
  • Low contrast visual acuity (LCVA)

    6 months

    Vision
  • 1) RNFLT-G-12 of contralateral healthy eye at baseline minus RNFLT-G-12 of the affected eye 6 months after randomisation

Other measures (12)

  • Absolute values of the global retinal nerve fibre layer thickness

    6 months

    Retina scans (OCT)
  • Retinal nerve fibre layer thickness in the papillomacular bundle

    6 months

    Retina scans (OCT)
  • Retinal nerve fibre layer thickness in the temporal quadrant

    6 months

    Retina scans (OCT)
  • Total macular volume

    6 months

  • Visual acuity

    6 months

    Vision
  • Contrast sensitivity

    6 months

  • Mean visual field defect

    6 months

  • Latency [ms] and amplitude [µV] of visual evoked potentials (VEP)

    6 months

    Myelin repair
  • Expanded Disability Status Scale (EDSS) score

    6 months

    Disability progression
  • Quality of life

    6 months

    Quality of life (reported by participants)

Who could take part

Optic neuritis · 18 to 50

Patients eligible for inclusion in this trial must meet all of the following criteria: 1. Written informed consent obtained according to international guidelines and local laws 2. Male and female patients aged ≥ 18 to ≤ 50 years 3. Patients with ON 4. First symptoms of ON ≤ 10 days prior to the first administration of investigational product 5. High contrast visual acuity (HCVA) of ≤ 0.5 (decimal system) 6. Adequate OCT measurements available Patients eligible for this trial must not meet any of the following criteria: 1. Patient without legal capacity who is unable to understand the nature, significance and consequences of the trial 2. Simultaneous participation in another interventional trial which could interfere with this trial and/or participation in a clinical trial within the last 3 months before enrolment in this trial 3. Refractive anomalies: Hyperopia > 5 dpt, myopia \< -7 dpt, astigmatism > 3 dpt 4. Media opacity 5. Severe papillitis 6. Previous ON 7. Any other optic nerve and retinal disease 8. Pre-existing MS or any other neurological disease 9. Congenital diseases: * thrombophilia * phenylketonuria 10. Acquired diseases: * autoimmune diseases, * cardiovascular diseases, * diabetes mellitus, * uncontrolled hypertension (with blood pressure > 140 / 90 mm Hg (cf. chapter 7.7.5)), * any malignancy, * epilepsy, * known tuberculosis with ongoing or unknown activity, * acute gastrointestinal ulceration within the last 3 months prior to randomisation, * acute viral, bacterial or fungal infection, * known infection with Human Immunodeficiency Virus (HIV), Hepatitis B Virus, or Hepatitis C Virus, * history of colitis ulcerosa, diverticulitis, or acute enteroanastomosis, * known osteoporosis, * history of thromboembolic events, * elevated haemoglobin level (>17 g/dl in men or >15 g/dl in women) * polycythaemia * any other significant illness potentially interfering with any trial assessment or trial treatment 11. Performing semi-professional or professional sporting activities or physical training 12. Pre-treatment with corticosteroids in the last 30 days prior to the onset of optic neuritis 13. Pre-treatment with EPO 14. Known or persistent abuse of medication, drugs or alcohol 15. Active immunization within 2 weeks prior to randomisation 16. Significant surgery within 4 weeks prior to randomisation 17. Blood donation or bloodletting within 4 weeks prior to screening 18. Pre-treatment with immunosuppressive or immunomodulatory agents 19. Persons who are in a relationship of dependence/employment with the sponsor or the investigator This section concerns only female patients who are able to have a child: 20. Current or planned pregnancy; nursing period within 3 months from investigational product administration 21. Unwillingness to use one of the following safe combination methods of contraception within 3 months from investigational product administration to achieve a PEARL index of \<1: female condom, diaphragm or coil, each used in combination with a spermicide; hormonal intra-uterine device or hormonal contraception in combination with a mechanical method of contraception

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

This clinical trial aims at preventing visual dysfunction and optic nerve degeneration associated with autoimmune optic neuritis by systemic i.v. administration of 33.000 IU erythropoietin over 3 days. The primary objective is to determine the efficacy of erythropoietin compared to placebo given as add-on to methylprednisolone as assessed by measurements of retinal nerve fibre layer thickness and low contrast visual acuity 6 months after acute optic neuritis.

Papers

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History

    1. Started

      Nov 2014

    2. Main results due

      Jun 2018

    3. Finished

      Nov 2019

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