Clinical Trial of Apomorphine Subcutaneous Infusion in Patients With Advanced Parkinson's Disease (TOLEDO)

Multicentre,Parallel-group,Double-blind,Placebo-controlled Phase III Study to Evaluate the Efficacy and Safety of Apomorphine sc Infusion in Parkinson's Disease Patients With Motor Complications Not Well Controlled on Medical Treatment

The primary objective of the trial was to investigate the efficacy of apomorphine continuous subcutaneous infusion compared to placebo in Parkinson's Disease patients with motor fluctuations not well controlled on medical treatment.

The secondary objective of the study was to investigate the safety and tolerability of apomorphine continuous subcutaneous therapy.

Study Overview

• Status: Completed
• Conditions: Parkinson's Disease
• Intervention / Treatment: Drug: Apomorphine hydrochloride; Drug: Placebo

Detailed Description

The primary efficacy variable is the mean change in time spent "OFF" from baseline (start of blinded treatment) to the end of a 12 weeks' double-blind treatment period based on patient diaries. Patients recorded their motor symptoms in half-hour blocks as OFF, ON without dyskinesia, ON without troublesome dyskinesia, or sleeping using the Hauser Parkinson's Disease home diary.

Key secondary Endpoints (tested hierarchically):

• Change in time spent "ON without troublesome dyskinesia"
• Patient Global Impression of Change

Other Endpoints:

• Percentage of patients with response to therapy, defined as a mean OFF time reduction of at least 2 hours
• Change in oral levodopa and levodopa equivalent dose

• Study Type: Interventional
• Enrollment (Actual): 107
• Phase: Phase 3

Contacts and Locations

Study Locations

• Austria
  • Graz, Austria
    • Medizinische Universität Graz / Univ. Klinik für Neurologie
  • Innsbruck, Austria
    • Medizinische Universität Innsbruck
  • Vienna, Austria, 1220
    • Donauspital / SMZ-Ost, Abteilung für Neurologie, Sekretariat (Stock 1, Ebene 4)
• Denmark
  • Copenhagen, Denmark
    • Bispebjerg University Hospital, Movement Disorder Centre
• France
  • Clermont-Ferrand Cedex 1, France
    • CHRU Clermont- Ferrand Gabriel-Montpied
  • Rennes Cedex 9, France
    • CHU de Rennes, Hopital Pontchaillou
  • Toulouse Cedex 9, France
    • CHU Toulouse, Hôpital Purpan, Centre d'Investigation Clinique
• Germany
  • Beelitz-Heilstätten, Germany
    • Neurologisches Fachkrankenhausfür Bewegungsstörungen / Parkinson
  • Bremerhaven, Germany
    • Klinikum Bremerhaven-Reinkenheide gGmbH, Neurologische Klinik
  • Kassel, Germany
    • Paracelsus Elena-Klinik Kassel
  • München, Germany
    • Schön Klinik München Schwabing / Neurologie und Klinische Neurophysiologie
• Netherlands
  • Groningen, Netherlands
    • Universitair Medisch Centrum
  • Heerlen, Netherlands
    • Atrium MC Parkstad
  • Rotterdam, Netherlands
    • Erasmus MC
• Spain
  • Barcelona, Spain
    • Hospital Clinic de Barcelona
  • Madrid, Spain
    • Hospital Universitario Fundación Jiménez Díaz
• United Kingdom
  • Liverpool, United Kingdom
    • The Walton Centre NHS Foundation Trust
  • London, United Kingdom
    • Kings College Hospital NHS Foundation Trust
  • London, United Kingdom
    • St George's Heathcare NHS Trust
  • Newcastle, United Kingdom
    • Newcastle University, Clinical Ageing Research Unit (CARU)

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 26 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Male or female patients aged ≥30 years
• Diagnosis of idiopathic PD of >3 years' duration, defined by the UK Brain Bank criteria (with the exception of >1 affected relative being allowed), without any other known or suspected cause of Parkinsonism
• Hoehn & Yahr stage up to 3 in the ON and 2 to 5 in the OFF state
• Motor fluctuations not adequately controlled on medical treatment including levodopa which was judged by the treating physician to be optimal
• Average of OFF time > 3 hours/day based on screening and baseline diary entries with no day with < 2 hours of OFF time recorded
• Stable medication regimen, with a stable dose of levodopa administered in at least 4 intakes, for at least 28 days prior to baseline. All oral or transdermal antiparkinsonian drugs were permitted, with the exception of budipine. This regimen might include the use of levodopa/DDCI rescue medication, if this occurred up to 2 times a day, at doses of up to 200 mg levodopa/day
• Patients must be able to differentiate between the ON and OFF state and between troublesome and non-troublesome dyskinesias
• Male and female patients must be compliant with a highly effective contraceptive method (oral hormonal contraception alone is not considered highly effective and must be used in combination with a barrier method) during the study and for the 12-month OLP, if sexually active
• Females of childbearing potential must have a negative serum human chorionic gonadotropin (hCG) or urine pregnancy test at screening
• Ability to accurately complete a paper diary on designated days (with assistance from caregivers, if required), recording periods when they are "ON without troublesome dyskinesia", "ON with troublesome dyskinesia", OFF, and sleeping
• Written informed consent prior to enrolment, after being provided with detailed information about the nature, risks, and scope of the clinical trial as well as the expected desirable and adverse effects of the study treatments
• Patients considered reliable and capable of adhering to the protocol, visit schedule, and medication intake according to the judgment of the investigator

Exclusion Criteria:

• History of respiratory depression
• Hypersensitivity to apomorphine or any excipients of the medicinal product
• High suspicion of other parkinsonian syndromes
• Presence of severe freezing or clinically relevant postural instability leading to falls during the ON state
• Concomitant therapy or within 28 days prior to baseline with: apomorphine pen injections; alpha-methyl dopa, metoclopramide, reserpine, neuroleptics, methylphenidate, or amphetamine; intrajejunal levodopa
• Previous use of apomorphine pump treatment
• History of deep brain stimulation or lesional surgery for PD
• Any medical condition that is likely to interfere with an adequate participation in the study, including e.g. current diagnosis of unstable epilepsy; clinically relevant cardiac dysfunction and/or myocardial infarction or stroke within the last 12 months
• Symptomatic, clinically relevant and medically uncontrolled orthostatic hypotension
• Patients with a borderline QT interval corrected for heart rate according to Bazett's formula (QTcB) of >450 msec for male and >470 msec for female at screening or history of long QT syndrome; or >450 msec absolute duration
• Clinically relevant hepatic dysfunction (total bilirubin >2.0 mg/dL, alanine transaminase [ALT] and aspartate transaminase [AST] >2 times the upper limit of normal)
• Clinically relevant renal dysfunction (serum creatinine >2.0 mg/dL)
• Pregnant and breastfeeding women
• Clinically relevant cognitive decline, defined as MMSE ≤24 or according to Diagnostic and Statistical Manual of Mental Disorders (DSM) IV criteria for dementia
• Active psychosis or history of at least moderate psychosis in the past year, or with medically uncontrolled severe depression; very mild illusions or hallucinations in the sense of "feelings of passage or presence" with fully retained insight are not an exclusion criterion
• Known history of melanoma
• Any investigational therapy in the 4 weeks prior to randomization
• History or current drug or alcohol abuse or dependencies

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Active Comparator: Apomorphine hydrochloride; Apo-go® Apomorphine hydrochloride 5 mg/ml solution for infusion in pre-filled syringe	Drug: Apomorphine hydrochloride; Apomorphine hydrochloride 5 mg/ml solution for infusion in pre-filled syringe; Other Names: Apo-go
Placebo Comparator: Placebo; Placebo: saline infusion	Drug: Placebo; Sodium chloride 9 mg/ml

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Mean Change in Daily OFF Time From Baseline (Start of Blinded Treatment) to the End of Double-blind Phase (Visit 10) Based on Patient Diaries Using MMRM mITT Population	The least squares mean reduction (improvement) in OFF time as reported by the patient using the Hauser Parkinson's disease home diary. Patients categorised their motor symptoms into OFF, ON with dyskinesia, ON without troublesome dyskinesia or sleeping using half hour blocks over 24 hours. Daily OFF time was computed from the average of valid motor diaries from the two days preceding each visit. Correct diary completion was evaluated during screening and observed by the investigator to ensure patients could categorise their motor symptoms correctly. A diary was considered valid if no more than 4 half-hour periods were either absent or duplicated. There were no invalid diaries at Baseline or Week 12.	Baseline and 12 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Mean Change in Daily Time Spent "ON Without Troublesome Dyskinesia" From Baseline to the End of the Double-blind Phase (Visit 10), Based on Patient Diaries Using MMRM mITT Population	The least squares mean change in "ON time without troublesome dyskinesia" as reported by the patient using the Hauser Parkinson's disease home diary. Each half hour of the day categorised as OFF, ON with dyskinesia, ON without troublesome dyskinesia or asleep. "ON time without troublesome dyskinesia" measures good ON time for a Parkinson's disease patient.	Baseline and 12 weeks
Patient Global Impression of Change (PGIC), Using the mITT Population	PGIC is a self-administered questionnaire measuring personal general state of health on a 7-point rating scale. The 7 ordinal categories from which patients must choose are 'very much improved', 'much improved', 'minimally improved', 'no change', 'minimally worse', 'much worse', and 'very much worse. Results are presented as the % of patients who reported at least minimal improvement in general health status at week 12 compared to Baseline. A Wilcoxon range sum test was performed to test for treatment differences from baseline to end of 12 weeks' treatment period.	Baseline and 12 weeks
Mean Change in Oral Levodopa Dose From Baseline to Visit 10 Using MMRM for the mITT Population	The least squares mean change in oral levodopa dose from Baseline to Visit 10 (week 12) was calculated excluding 3 centres who declined to participate in collecting the necessary details of PRN use of levodopa.	Baseline and 12 weeks
Mean Change in Levodopa Equivalent Dose From Baseline to Visit 10 (Week 12) Using MMRM in the mITT Population	Levodopa equivalent dose is an indication of the burden of medication taken to control symptoms of Parkinson's disease with all medications other than levodopa itself being converted to a calculated levodopa dose using the methodology published by Tomlinson et al, 2010. The computation of LED excludes the study drug.	Baseline and 12 weeks

Collaborators and Investigators

• Sponsor: Britannia Pharmaceuticals Ltd.
• Investigators: Principal Investigator: Regina Katzenschlager, Doz. Dr., Donauspital KH SMZ Ost, Neurologie

Publications and helpful links

General Publications

• Katzenschlager R, Poewe W, Rascol O, Trenkwalder C, Deuschl G, Chaudhuri KR, Henriksen T, van Laar T, Lockhart D, Staines H, Lees A. Long-term safety and efficacy of apomorphine infusion in Parkinson's disease patients with persistent motor fluctuations: Results of the open-label phase of the TOLEDO study. Parkinsonism Relat Disord. 2021 Feb;83:79-85. doi: 10.1016/j.parkreldis.2020.12.024. Epub 2021 Jan 12.
• Katzenschlager R, Poewe W, Rascol O, Trenkwalder C, Deuschl G, Chaudhuri KR, Henriksen T, van Laar T, Spivey K, Vel S, Staines H, Lees A. Apomorphine subcutaneous infusion in patients with Parkinson's disease with persistent motor fluctuations (TOLEDO): a multicentre, double-blind, randomised, placebo-controlled trial. Lancet Neurol. 2018 Sep;17(9):749-759. doi: 10.1016/S1474-4422(18)30239-4. Epub 2018 Jul 25.

Study record dates

Study Major Dates

• Study Start (Actual): March 3, 2014
• Primary Completion (Actual): June 6, 2016
• Study Completion (Actual): June 8, 2017

Study Registration Dates

• First Submitted: November 22, 2013
• First Submitted That Met QC Criteria: December 4, 2013
• First Posted (Estimate): December 9, 2013

Study Record Updates

• Last Update Posted (Actual): July 8, 2019
• Last Update Submitted That Met QC Criteria: April 17, 2019
• Last Verified: April 1, 2019

More Information

Terms related to this study

• Keywords: Parkinson's disease; motor fluctuations; medical treatment; apomorphine; not well controlled
• Additional Relevant MeSH Terms: Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Parkinsonian Disorders; Basal Ganglia Diseases; Movement Disorders; Synucleinopathies; Neurodegenerative Diseases; Parkinson Disease; Physiological Effects of Drugs; Neurotransmitter Agents; Molecular Mechanisms of Pharmacological Action; Autonomic Agents; Peripheral Nervous System Agents; Gastrointestinal Agents; Dopamine Agonists; Dopamine Agents; Emetics; Apomorphine
• Other Study ID Numbers: CT-37527-13-0124; 2013-000980-10 (EudraCT Number)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No