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A Safety Study of sNN0029 Administration Via Intracerebroventricular Route to Patients With ALS

Phase 1
Terminated
Conditions
Amyotrophic Lateral Sclerosis
Interventions
Drug: Placebo
Registration Number
NCT01999803
Lead Sponsor
Newron Sweden AB
Brief Summary

This is a phase I, multicentre randomised, double-blind, placebo-controlled trial to assess the safety and tolerability of continuous i.c.v. administration of sNN0029 infusion solution at a dose of 4µg/day in patients with Amyotrophic Lateral Sclerosis (ALS).

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
15
Inclusion Criteria
  • Clinical diagnosis of ALS classified as definite, or probable with or without additional laboratory evidence, according to the revised World Federation of Neurology (WFN) El Escorial criteria.
  • If patients are being treated with riluzole, they must have been on a stable dose for at least the past 30 days prior to screening.
  • The patient is, in the opinion of the investigator, medically fit to undergo the surgery required for stereotactic implantation of the catheter and infusion pump.
Exclusion Criteria
  1. Impaired respiratory function judged to pose a risk to the patient during anaesthesia for the device implantation.

  2. Hypertension defined as blood pressure >160 mmHg systolic or >90 mmHg diastolic.

  3. Values for coagulation parameters including platelet count, normalised prothrombin complex (PK-INR), activated partial thromboplastin time (APTT) outside normal ranges.

  4. Ophthalmological examination (fundus photography, visual acuity and perimetry) with any clinically significant findings that imply safety concerns for this study.

  5. Diagnosis of diabetes mellitus.

  6. History of structural brain disease other than ALS, including tumours and hyperplasia.

  7. An MRI of the brain and cervical spine, and an Magnetic Resonance Angiography (MRA) of the brain with findings of tumours or potential sources of pathological bleedings, or abnormality that may interfere with the assessments of safety or efficacy or that would, in the judgment of the investigator, represent a surgical risk to the patient. If an MRI and/or MRA has been performed within 1 month prior to screening, the results from that examination can be used.

  8. Any disorder that precludes a surgical procedure (e.g., signs of sepsis or inadequately treated infection), alters wound healing (e.g., including bleeding disorders), or renders chronic i.c.v. delivery or device implants medically unsuitable.

  9. Presence of risk for increased or uncontrolled bleeding and/or risk of bleeding that cannot be not managed optimally due to:

    i. anatomical factors at or near the implant site (e.g., vascular abnormalities, neoplasms, or other abnormalities), ii. underlying disorders of the coagulation cascade, platelet function, or platelet count (e.g., haemophilia, Von Willebrand's disease, liver disease, or other medical conditions) iii. administration of any antiplatelet or anticoagulant medication in the preoperative period

  10. A personal history of thromboembolic disease. A family history of thromboembolic disease will prompt a laboratory assessment to exclude hereditary liability before the patient is declared eligible.

  11. Presence of additional risk factors for thromboembolism such as obesity (BMI > 35) or use of oestrogens including combined contraceptive pills.

  12. Presence of an implanted shunt for the drainage of CSF or an implanted Central Nervous System (CNS) catheter.

  13. Clinically significant abnormalities in haematology or clinical chemistry parameters as assessed by the investigator.

  14. Serological evidence of Hepatitis B virus (HBV), Hepatitis C virus (HCV) or Human immunodeficiency virus (HIV)

  15. Ongoing medical condition that according to the investigator would interfere with the conduct and assessments in the study. Examples are medical disability (e.g., severe degenerative arthritis, compromised nutritional state, peripheral neuropathy) that would interfere with the assessment of safety and efficacy of investigational product or device performance, or would compromise the ability of the patient to undergo study procedures (e.g., MRI), or to give informed consent.

  16. Participation in another clinical trial with an investigational drug or device within 3 months prior to screening visit.

  17. For women only: pregnant, breast feeding and/or for fecund women unwillingness to use adequate contraception during the trial such as:

    • Established use of oral, injected or implanted hormonal methods of contraception that do NOT contain oestrogens.
    • Placement of an intrauterine device.
    • Barrier methods of contraception: Condom or occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/suppository.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboPlaceboPlacebo administered by continuous intracerebral infusion during12 weeks
sNN0029 (VEGF)sNN00294 µg/d of sNN0029 administered by continuous intracerebral infusion during12 weeks
Primary Outcome Measures
NameTimeMethod
Number of Adverse Events (AEs)12 weeks

The safety and tolerability of i.c.v. administration of sNN0029 infusion solution at a dose of 4 µg/day delivered via a Medtronic SynchroMed® II Infusion System will be evaluated by comparing tabulated number of events over 12 weeks by body system, preferred term and by severity and relationship to study medication/device. Serious Adverse Events/Serious Adverse Device Events will also be presented in separate tabulations.

Secondary Outcome Measures
NameTimeMethod
VEGF165 levels in Cerebrospinal Fluid (CSF)12 weeks

Levels of the active ingredient of sNN0029 infusion solution (VEGF165) in CSF will be summarised using descriptive statistics by time point and treatment.

Medical Device performance12 weeks

Device performance (number of values +/-25% of expected) will be presented by time point and treatment.

Trial Locations

Locations (2)

Philip Van Damme

🇧🇪

Leuven, Belgium

Leonard van den Berg

🇳🇱

Utrecht, Netherlands

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