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Trial record 3 of 61 for:    Lixisenatide

Study to Evaluate the Effect of Lixisenatide in Patient With Parkinson's Disease (LixiPark)

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ClinicalTrials.gov Identifier: NCT03439943
Recruitment Status : Recruiting
First Posted : February 20, 2018
Last Update Posted : July 30, 2018
Sponsor:
Collaborators:
Cure Parkinson
Réseau NS-Park
EUCLID
Sanofi
Information provided by (Responsible Party):
University Hospital, Toulouse

Brief Summary:
The main objective of the study is to evaluate the effect of lixisenatide (20 μg/d), versus placebo, administered as add-on therapy with the usual antiparkinsonian treatment, on the progression of motor disability in patients with early PD in order to assess its potential "disease-modifying" effect.

Condition or disease Intervention/treatment Phase
Parkinson Disease Drug: Lixisenatide Drug: placebo Phase 2

Detailed Description:

This study will be a French, multicenter parallel groups, 2-arm, randomized, placebo-controlled, double-blind, proof-of-concept (POC) phase II trial evaluating the effect of lixisenatide, in patients with early PD.

The treatment period will be followed by a wash-out period of 2 months.

JUSTIFICATION/CONTEXT Parkinson's disease (PD) is a common neurodegenerative disease. Currently available symptomatic treatments allow improving motor and to a lesser extent non-motor function in PD patients.

None of these treatments can slow down the underlining disease process and the relentless progression of motor and non-motor disability.

Several mechanisms including the aggregation of misfolded alphasynuclein, mitochondrial dysfunction, oxidative stress and neuroinflammation have been related to the pathogenesis of PD. Recent evidence further suggests the implication of cerebral insulin resistance in the neurodegenerative process, while glucagon-like peptide 1 receptor (GLP1-R) agonists that are approved for the treatment of type 2 diabetes have neuroprotective properties in animal models of PD (Aviles-Olmos et al., 2013a). Moreover, the results of a recent clinical pilot trial suggest that treatment with the GLP-1R agonist exenatide for 12 months improves motor function in patients with moderate PD . GLP1-R are widely expressed in the central nervous system and GLP1-R agonists such as liraglutide, lixisenatide and exenatide have measurable brain concentrations, which makes them suitable for treating brain disorders.

Lixisenatide is a well-tolerated GLP-1R agonist that can be administered once-daily (subcutaneous injection). It has demonstrated positive effects on learning and memory through an increase of hippocampal neurogenesis in preclinical models of obesity/diabetes. Furthermore, lixisenatide increases neurogenesis and decreases microglial activation in rodent models of Alzheimer's disease (APPswe/PS1ΔE9 mice and Aβ25-35 rats) (. At the same dose, lixisenatide showed higher effectiveness at activating brain GLP-1R than liraglutide and exenatide, and showed more effective neuroprotection in a variety of in-vitro models of neurodegeneration (WO2013/030409A1).

Thus, this randomized, double-blind, clinical trial now aim to evaluate the effects of lixisenatide, versus placebo, on both motor and non-motor PD symptoms in patients at an early stage of PD.

This study will involve centers of the French national Parkinson's disease and movement disorders research network (Ns-Park network).


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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 158 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Multicenter, Randomised, Placebo-controlled, Double Blinded, Parallel Arm Proof-of-concept Trial of Lixisenatide in Patients With Early Parkinson's Disease
Actual Study Start Date : June 13, 2018
Estimated Primary Completion Date : September 2021
Estimated Study Completion Date : December 2021

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Lixisenatide
Lixisenatide (10μg/d for 14 days and then 20μg/d): once daily subcutaneous
Drug: Lixisenatide
Patients randomized in the Lixisenatide group will receive 10μg/day for 14 days and then 20μg/day administered by once-daily subcutaneous injections during 12 months. If patients are unable to tolerable the dose of 20μg/day, this dose can be reduced to 10μg/day
Other Name: injection drug

Placebo Comparator: Placebo
Placebo: once daily subcutaneous injection
Drug: placebo
Patients randomized in the placebo group will receive the corresponding placebo administered subcutaneously (once daily subcutaneous injection).
Other Name: placebo injection




Primary Outcome Measures :
  1. Change from baseline to end-point (M12) in the MDS-UPDRS III motor ( Movement Disorder Society-Unified Parkinson's disease rating scale) [ Time Frame: 12 month ]

    The main objective of the study is to evaluate the effect of lixisenatide (20 μg/d), versus placebo, administered as add-on therapy with the usual antiparkinsonian treatment, on the progression of motor disability in patients with early PD in order to assess its potential "disease-modifying" effect.

    The primary endpoint of this study is the change from baseline to end-point (M12) in the MDS-UPDRS III motor examination score, evaluated in the best ON condition in patients with early Parkinson's Disease.




Information from the National Library of Medicine

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Ages Eligible for Study:   40 Years to 75 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients with PD according to UKPDSBB criteria (male or female).
  • Patient with a Hoehn and Yahr Stage <3 in the ON condition.
  • Patients aged from 40 to 75 years old.
  • Early-stage PD patients: diagnosis of PD for less than 3 years, without dyskinesia and motor fluctuations.
  • Patients treated with an "optimized" stable dopaminergic medication regimen (dopamine agonist and/or L-dopa and/or MAOB inhibitor) for at least 1 month before baseline.
  • Patients expected to remain on stable doses of antiparkinsonian medications for at least the first 6 months of the study and preferably for the 12 months of follow-up.
  • Patients (or caregiver) able to self-administer lixisenatide injection.
  • Patients with health insurance.
  • Patients who signed the written informed consent form.

Exclusion Criteria:

  • Patients suffering from other parkinsonian syndromes other than PD.
  • Patients expected not to be able to remain on stable doses of symptomatic antiparkinsonian medications for at least 6-month.
  • Patients with a Body Mass Index < 18.5
  • Patients suffering from type 1 or type 2 diabetes.
  • Malnutrition as assessed clinically by the investigator or any sub-investigator and by Mini Nutritional Assessment Short Form (MNA-SF) score <12 (the judgement of the investigator prevails over questionnaire scores).
  • Weight change of more than 5 kg in body weight during the last 3 months prior to screening.
  • Known history of drug or alcohol abuse within 6 months prior to the time of screening.
  • Patients with hyperthyroidism or uncontrolled hypothyroidism. Note: Patients diagnosed with hypothyroidism need to be on a stable thyroid replacement therapy for at least 6 weeks.
  • Patients with severe depression according to DSM criteria.
  • Patients with cognitive impairment (MoCA score <26).
  • Severe gastrointestinal disease (e.g. gastroparesis).
  • Patients previously exposed to a GLP-1 agonist.
  • Patients with severely impaired renal function (estimated creatinine clearance <30ml/min).
  • Patients with a medical history of active liver disease (other than non-alcoholic hepatic steatosis), including chronic active hepatitis B or C (assessed by medical history), primary biliary cirrhosis, or ongoing symptomatic gallbladder disease.
  • Patients with any clinically significant ECG abnormality.
  • Laboratory findings at the time of screening:

Amylase and/or lipase: >3 times the upper limit of the normal (ULN) laboratory range ALT or AST: >3 times ULN Total bilirubin: >1.5 times ULN (except in case of Gilbert's syndrome) Calcitonin: >20 pg/mL (5.9 pmol/L) Hemoglobin: <11 g/dL (male/female) and/or neutrophils <1,500/mm3 and/or platelets <100,000/mm3 Triglyceride (TG): >600 mg/dL (6.78 mmol/L). History of unexplained pancreatitis, chronic pancreatitis or pancreatectomy.

  • Personal or immediate family history of medullary thyroid cancer or genetic conditions that predispose to medullary thyroid cancer (e.g. multiple endocrine neoplasia syndromes).
  • Hyperlipidemia.
  • Females who are pregnant, breast feeding or of child bearing age without effective contraception.
  • Patients treated per os in the evening by drugs requiring a rapid action (at the discretion of the investigator).
  • Participants who lack the capacity to give informed consent.
  • Any medical or psychiatric condition which may compromise participation in the study or the safety, at the discretion of the investigator.
  • Known abnormality on CT or MRI brain imaging that is considered likely to compromise compliance with any aspect of the trial.
  • Prior intra-cerebral surgical intervention for PD.
  • Participant under legal guardianship or incapacitation.
  • Patients who are participating or have participated in another interventional clinical trial within 30 days prior to baseline.
  • Previous enrolment in the present trial.
  • Allergic reaction to the active substance or to any of the excipients of lixisenatide

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03439943


Contacts
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Contact: Olivier. RASCOL, MD, PHD 05 61 14 59 62 ext 33 olivier.rascol@univ-tlse3.fr
Contact: Wassilios MEISSNER, MD, PHD 05 57 82 12 53 ext 33 wassilios.meissner@chu-bordeaux.fr

Locations
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France
University Hospital of Amiens Not yet recruiting
Amiens, France
Contact: Pierre Krystkowiak, MD, PHD         
University Hospital of Besancon Not yet recruiting
Besancon, France
Contact: Thierry Moulin, MD, PHD         
University Hospital of Bordeaux Not yet recruiting
Bordeaux, France
Contact: Wassilios Meissner, MD, PHD         
University Hospital of Caen Not yet recruiting
Caen, France
Contact: Gilles Defer, MD, PHD         
University Hospital of Clermont-Ferrand Not yet recruiting
Clermont-Ferrand, France
Contact: Franck Durif, MD, PHD         
Creteil- Henri Mondor Hospital Not yet recruiting
Créteil, France
Contact: Philippe Remy, MD, PHD         
University Hospital of Lille Not yet recruiting
Lille, France
Contact: Luc Defebvre, MD, PHD         
University Hospital of Limoges Not yet recruiting
Limoges, France
Contact: Frédéric Torny, MD, PHD         
University Hospital of Lyon Not yet recruiting
Lyon, France
Contact: Stéphane Thobois, MD, PHD         
University Hospital of Marseille Not yet recruiting
Marseille, France
Contact: Jean-Philippe Azulay, MD PHD         
University Hospital of Montpellier Not yet recruiting
Montpellier, France
Contact: Christian Geny, MD, PHD         
University Hospital of Nancy Not yet recruiting
Nancy, France
Contact: Lucie Hopes, MD         
University Hospital of Nantes Not yet recruiting
Nantes, France
Contact: Philippe Damier, MD, PHD         
University Hospital of Nice Not yet recruiting
Nice, France
Contact: Caroline Giordana, MD         
Pitié Salpêtrière Hospital Not yet recruiting
Paris, France
Contact: Jean-Christophe Corvol, MD, PHD         
University Hospital of Poitiers Not yet recruiting
Poitiers, France
Contact: Jean-Luc Houeto, MD, PHD         
University Hospital of Rennes Not yet recruiting
Rennes, France
Contact: Sophie Drapier, MD         
University Hospital of Rouen Not yet recruiting
Rouen, France
Contact: David Maltête, MD, PHD         
University Hospital of Strasbourg Not yet recruiting
Strasbourg, France
Contact: Christine Tranchant, MD, PHD         
CHU Toulouse Recruiting
Toulouse, France, 31000
Contact: Olivier Rascol, MD, PHD         
Sponsors and Collaborators
University Hospital, Toulouse
Cure Parkinson
Réseau NS-Park
EUCLID
Sanofi
Investigators
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Principal Investigator: Olivier. RASCOL, MD, PHD University Hospital, Toulouse

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Responsible Party: University Hospital, Toulouse
ClinicalTrials.gov Identifier: NCT03439943     History of Changes
Other Study ID Numbers: RC31/16/8912
First Posted: February 20, 2018    Key Record Dates
Last Update Posted: July 30, 2018
Last Verified: July 2018

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Additional relevant MeSH terms:
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Lixisenatide
Parkinson Disease
Parkinsonian Disorders
Basal Ganglia Diseases
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Movement Disorders
Neurodegenerative Diseases
Hypoglycemic Agents
Physiological Effects of Drugs