Advanced Parkinson's DiseasePhase 3NCT00660673
Open Label Continuation Treatment Study With Levodopa-Carbidopa Intestinal Gel in Advanced Parkinson's Disease
A Phase 3 study testing Levodopa-Carbidopa Intestinal Gel (LCIG), CADD-Legacy® 1400 ambulatory infusion pump and Percutaneous Endoscopic Gastrostomy with jejunal extension tube (PEG-J) in people with Advanced Parkinson's Disease, run by AbbVie at 61 sites in 11 countries.
Trial summary
The primary objective of this study is to provide continued access to levodopa-carbidopa intestinal gel (LCIG), to participants who have already participated in an open-label efficacy and safety study with the same treatment (Study S187.3.003 [NCT00360568] or Study S187.3.004 [NCT00335153]). Read more about this study
- Who is it for?
- Ages 30 to 99 years
- Conditions the study is for
- Advanced Parkinson's Disease
- What is being tested?
- Levodopa-Carbidopa Intestinal Gel (LCIG), CADD-Legacy® 1400 ambulatory infusion pump and Percutaneous Endoscopic Gastrostomy with jejunal extension tube (PEG-J)
- Type of treatment
- Injection or infusion, Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 262 participants
- Where
- 61 sitesin 11 countries
- Study dates
- 13 Nov 2009to 30 Nov 2021
- Phase
- Phase 3
- Are there results?
- Yes, posted in the registrySummary in the doctors' view
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 30 to 99 years
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- The participant should have completed participation in Study S187.3.003 or S187.3.004; and, in the opinion of the Principal Investigator, would benefit from long-term treatment with LCIG.
- For Canada, participants will be allowed to participate in the S187.3.005 study with a minimum of 6 months of exposure to LCIG in the S187.3.004 study.
- The participant must be able to understand the nature of the study and must provide written informed consent prior to the conduct of any study related procedures. If the participant does not have the capacity to provide informed consent, full informed consent must be obtained from the participant's legally authorized representative. Consenting will be performed according to local regulations.
Who cannot join
- Medical, laboratory, psychiatric, or surgical issues deemed by the investigator to be clinically significant and which could interfere with the participant's participation in the study.
Trial locations and contacts
61 sites in 11 countries.
61 sites in 11 countries
United States31 sites
Georgia Regents University /ID# 49938
Augusta, Georgia, 30912
Univ Maryland School Medicine /ID# 49934
Baltimore, Maryland, 21201
Johns Hopkins University /ID# 49937
Baltimore, Maryland, 21287
University of Alabama at Birmingham /ID# 49941
Birmingham, Alabama, 35294
Bradenton Research Center, Inc /ID# 49929
Bradenton, Florida, 34205
University of Vermont Medical Center /ID# 49912
Burlington, Vermont, 05401-1473
Northwestern University Feinberg School of Medicine /ID# 49944
Chicago, Illinois, 60611-2927
Rush University Medical Center /ID# 49930
Chicago, Illinois, 60612
University of Cincinnati /ID# 49914
Cincinnati, Ohio, 45267-0585
Cleveland Clinic Main Campus /ID# 76173
Cleveland, Ohio, 44195
The Research Center of Southern California /ID# 49928
Encinitas, California, 92024
Colorado Neurological Institute /ID# 49927
Englewood, Colorado, 80113
Neurologic Consultants, PA /ID# 49918
Fort Lauderdale, Florida, 33308
The Parkinson's & Movement Disorder Institute - Fountain Valley /ID# 49915
Fountain Valley, California, 92708
University of Florida - Archer /ID# 49935
Gainesville, Florida, 32610
University of Florida /ID# 49922
Jacksonville, Florida, 32209
King County Public Hospital /ID# 49917
Kirkland, Washington, 98034
University of Kentucky Chandler Medical Center /ID# 49940
Lexington, Kentucky, 40536
Universtiy of Southern California /ID# 49913
Los Angeles, California, 90033
North Shore University Hospital /ID# 49932
Manhasset, New York, 11030
Froedtert Memorial Lutheran Hospital /ID# 49924
Milwaukee, Wisconsin, 53226
The Mount Sinai Hospital /ID# 49942
New York, New York, 10029
Columbia Univ Medical Center /ID# 49943
New York, New York, 10032-3725
University of Nebraska Medical Center /ID# 49911
Omaha, Nebraska, 68198
Charlotte Neurological Service /ID# 49916
Port Charlotte, Florida, 33980
Raleigh Neurology Associates /ID# 49923
Raleigh, North Carolina, 27607
Louisiana State Univ HSC /ID# 49945
Shreveport, Louisiana, 71130
Washington University-School of Medicine /ID# 49933
St Louis, Missouri, 63110
University of South Florida /ID# 49919
Tampa, Florida, 33612
Georgetown University Hospital /ID# 49931
Washington D.C., District of Columbia, 20007
Wake Forest Univ HS /ID# 49939
Winston-Salem, North Carolina, 27157
Czechia5 sites
Fakultni Nemocnice u Svate Anny /ID# 50085
Brno, 656 91
Fakultni nemocnice Hradec Kralove /ID# 50088
Hradec Králové, 500 05
Pardubicka krajska nemocnice, a.s.
Pardubice, 532 03
Vseobecna fakultni nemocnice v Praze /ID# 50086
Prague, 128 21
Fakultni Nemocnice v Motole /ID# 50084
Prague, 150 06
Russia5 sites
Scientific Research Medical Complex Your Health /ID# 50104
Kazan', 420097
Institution of the Russian Academy of Medical Sciences Scientific Centre of Neurology /ID# 50102
Moscow, 125367
Military Medical Academy n.a. Kirov /ID# 50103
Saint Petersburg, 194044
I.P. Pavlov First St. Petersburg State Medical University /ID# 50107
Saint Petersburg, 197022
City Clinical Hospital #40 /ID# 50106
Saint Petersburg, 197706
New Zealand4 sites
Auckland City Hospital /ID# 50093
Auckland, 1023
New Zealand Brain Research Institute/ID# 50090
Christchurch, 8011
Waikato Hospital /ID# 50091
Hamilton, Waikato Region, 3240
Wellington Hospital /ID# 50092
Wellington, 6021
Australia3 sites
Royal Adelaide Hospital /ID# 50083
Adelaide, South Australia, 5000
Austin Hospital /ID# 50082
Heidelberg, Victoria, 3084
Westmead Hospital /ID# 50081
Westmead, New South Wales, 2145
Canada3 sites
University of Alberta /ID# 78476
Edmonton, Alberta, T6G 2B7
CHUM - Notre-Dame Hospital /ID# 74513
Montreal, Quebec, H2X 0A9
Toronto Western Hospital /ID# 75913
Toronto, Ontario, M5T 2S8
Portugal3 sites
Hospitais da Universidade de Coimbra /ID# 50098
Coimbra, 3000-075
Hospital de Santa Maria /ID# 50099
Lisbon, 1649-035
Centro Hospitalar Universitario de Sao Joao, EPE /ID# 50101
Porto, 4200-319
Poland2 sites
Miejskie Centrum Medyczne im. dr. Karola Jonschera w Lodzi /ID# 50096
Lodz, Łódź Voivodeship, 93-113
NZOZ Centrum Medyczne HCP /ID# 50094
Poznan, Greater Poland Voivodeship, 61-485
Thailand2 sites
King Chulalongkorn Mem Hosp /ID# 50108
Bangkok, 10330
Siriraj Hospital /ID# 50109
Bangkok, 10700
United Kingdom2 sites
The Walton Centre NHS Foundation /ID# 50003
Liverpool, L9 7LJ
National Hospital for Neurology & Neurosurgery
London, WC1N 3BG
About this study
Official title: Open-Label Continuation Treatment Study With Levodopa - Carbidopa Intestinal Gel In Subjects With Advanced Parkinson's Disease And Severe Motor-Fluctuations Who Have Exhibited A Persistent And Positive Effect To Treatment In Previous Studies
The primary objective of this study is to provide continued access to levodopa-carbidopa intestinal gel (LCIG), to participants who have already participated in an open-label efficacy and safety study with the same treatment (Study S187.3.003 [NCT00360568] or Study S187.3.004 [NCT00335153]).
- Conditions
- Advanced Parkinson's Disease
- Being tested
- Levodopa-Carbidopa Intestinal Gel (LCIG), CADD-Legacy® 1400 ambulatory infusion pump, Percutaneous Endoscopic Gastrostomy with jejunal extension tube (PEG-J)
- Keywords
- levodopa/carbidopa intestinal gel, Severe Motor Fluctuations, Levodopa, Carbidopa, Parkinson's Disease, Dyskinesia
- Medical subject headings
- Parkinson Disease, Dyskinesias
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Levodopa-Carbidopa Intestinal Gel (LCIG)Drug
Also called Carbidopa-Levodopa Enteral Suspension (CLES), Duopa®, Duodopa®
LCIG for upper-intestinal infusion is a suspension of levodopa (20 mg/mL) and carbidopa (5 mg/mL) in an aqueous gel that is dispensed in a medication cassette reservoir containing 100 mL of LCIG.
CADD-Legacy® 1400 ambulatory infusion pumpDevice
Portable infusion pump (CADD-Legacy Pump Model 1400) connected to the LCIG medication cassette reservoir.
Percutaneous Endoscopic Gastrostomy with jejunal extension tube (PEG-J)Device
All participants previously had a PEG-J placed in one of the prior LCIG studies.
| Study group | Role | What they receive |
|---|---|---|
| Levodopa-Carbidopa Intestinal Gel | Experimental | Initial dosing is based on the dosing regimen that the participant received during the previous LCIG study. Dosing is individually optimized and can be adjusted at any time during the study as clinically indicated. The total dose/day of LCIG is composed of 3 individually adjusted doses. The morning dose is administered as a bolus infusion, usually 5 to 10 mL (100 to 200 mg levodopa). The maintenance dose is adjustable in steps of 2 mg/hour (0.1 mL/hour), within a range of 1 to 10 mL/hour (20 to 200 mg levodopa/hour) and is usually 2 to 6 mL/hour (40 to 120 mg levodopa/hour). Participants will be allowed to self-administer extra doses of LCIG to address immediate medical needs, normally 0.5 to 2.0 mL.
Participants will receive LCIG until it is commercially available. Receives: Drug: Levodopa-Carbidopa Intestinal Gel (LCIG); Device: CADD-Legacy® 1400 ambulatory infusion pump; Device: Percutaneous Endoscopic Gastrostomy with jejunal extension tube (PEG-J) |
What is being measured
The primary outcome is the main question the study is designed to answer.
Number of Participants With Treatment-emergent Adverse Events
Treatment-emergent adverse events (TEAEs) are defined as adverse events (AEs) which started on or after the date of the first LCIG Infusion in this study and within 30 days of the date of the last PEG-J exposure.
At least possibly drug-related is defined as TEAEs assessed as having a "Possible" or "Probable" or missing relationship to study drug.
Serious AEs included any untoward medical occurrence that:
- Resulted in death
- Was life-threatening
- Required inpatient hospitalization or prolongation of an existing hospitalization
- Resulted in persistent or significant disability/incapacity
- was a congenital anomaly/birth defect
The severity of all AEs was characterized as mild, moderate or severe according to the following definitions:
- Mild: usually transient and do not interfere with daily activities.
- Moderate: low level of inconvenience or concern to the subject, may interfere with daily activities.
- Severe: events interrupt the subject's usual daily activity.
Measured: From first dose of LCIG in this study up to 30 days after the date of last PEG-J exposure; median duration of treatment was 1178 days, with a maximum of 4217 days (11.5 years).
Secondary outcomes (21)
Number of Participants With Device Complications
Device complications include complications with the pump, intestinal tube, PEG-J or stoma.
Measured: From first dose of LCIG in this study up to 30 days after the date of last PEG-J exposure; median duration of treatment was 1178 days.
Number of Participants With Sleep Attacks
Participants were asked whether they experienced any events in which they fell asleep suddenly or unexpectedly, including while engaged in some activity (e.g., eating/drinking, speaking, or driving) or at rest, with or without any previous warning of sleepiness. If yes, participants were asked if they suffered any "bad" outcome or problem from the falling asleep event.
Measured: Baseline (final assessment period of the previous open-label LCIG study) and every 6 months until final visit; median duration of treatment was 1178 days.
Number of Participants With Intense Impulsive Behavior
To monitor for the development of intense impulsive behavior the Minnesota Impulsive Disorder Interview (MIDI) was administered. The MIDI is a semi-structured clinical interview assessing pathological gambling, trichotillomania, kleptomania, pyromania, intermittent explosive disorder, compulsive buying, and compulsive sexual behavior.
Measured: Baseline (final assessment of the previous open-label LCIG study) and every 6 months until final visit; median duration of treatment was 1178 days.
Number of Participants Who Developed Melanoma
A comprehensive assessment for the presence of melanoma was performed at least once a year by a dermatologist.
Measured: Once per year during the study; median duration of treatment was 1178 days.
Number of Participants With Treatment-emergent Adverse Events of Special Interest (TE AESI)
Adverse events of special interest (AESIs) were identified using standardized Medical Dictionary for Regulatory Activities (MedDRA) queries (SMQ) or company MedDRA queries (CMQs). The AESI in the following categories were identified on the basis of review of the clinical program and postmarketing observations where the treatment system is commercially available.
- Procedure and device associated events
- Polyneuropathy, included preferred terms in either the peripheral neuropathy or GuillainBarre syndrome standardized MedDRA query (narrow search), such as polyneuropathy, decreased vibratory sense, peripheral neuropathy, peripheral sensory neuropathy, neuralgia, demyelinating polyneuropathy, and sensory disturbance
- Weight loss
- Cardiovascular fatalities
- Respiratory tract aspiration including aspiration pneumonia/pneumonitis.
Measured: From first dose of LCIG in this study up to 30 days after the date of last PEG-J exposure; median duration of treatment was 1178 days, with a maximum of 4217 days (11.5 years).
Number of Participants With Any Suicidal Ideation or Behavior
The Columbia-Suicide Severity Rating Scale (C-SSRS) was implemented with Protocol Amendment 3 (20 March 2012) in order to assess suicidal behavior and ideation.
Suicidal ideation includes the wish to be dead, nonspecific active suicidal thoughts, active ideation without intent to act, active ideation with some intent to act, and active ideation with specific plan or intent. Suicidal behavior includes actual attempts, interrupted attempts, aborted attempts, completed suicide, and preparatory acts or behaviors.
The number of participants with affirmative responses on the C-SSRS at any time during the treatment period is reported.
Measured: Every 6 months (beginning with implementation of Protocol Amendment 3) until final visit; median duration of treatment was 1178 days.
Number of Participants With Potentially Clinically Significant Vital Sign Values
A vital sign value was considered potentially clinically significant if it satisfied the pre-specified criteria presented in the table and was also more extreme than the participant's corresponding Baseline value.
Measured: Baseline and every 6 months until final visit; median duration of treatment was 1178 days.
Number of Participants With Potentially Clinically Significant Hematology Laboratory Values
A laboratory value was considered potentially clinically significant if it satisfied the pre-specified criteria presented in the table and was also more extreme than the participant's corresponding Baseline value.
Measured: Baseline and every 6 months until final visit; median duration of treatment was 1178 days.
Number of Participants With Potentially Clinically Significant Chemistry Laboratory Values
A laboratory value was considered potentially clinically significant if it satisfied the pre-specified criteria presented in the table and was also more extreme than the participant's corresponding baseline value.
ULN = upper limit of normal
Measured: Baseline and every 6 months until final visit; median duration of treatment was 1178 days.
Number of Participants With Vitamin Levels Outside of the Normal Range
Special tests for vitamin deficiencies (folic acid, vitamin B6, vitamin B12, methylmalonic acid [MMA], and homocysteine) were implemented with Protocol Amendment 2 (27 July 2011). The number of participants with vitamin levels outside of the normal range at any time post-baseline is reported for each vitamin tested.
Measured: Every 6 months (beginning with implementation of Protocol Amendment 2) until final visit; median duration of treatment was 1178 days.
Number of Participants Receiving Concomitant Anti-Parkinson's Disease Medications by Treatment Year
Participants could use oral levodopa-carbidopa for scheduled or supplemental bedtime/overnight doses after the pump was disconnected for the night, or as rescue medication in case of acute deterioration caused by failure of the LCIG system such as tubes and/or the pump or the onset of an acute illness.
The initiation of additional concomitant PD medication was allowed at the discretion of the Investigator if medically indicated.
Measured: Year 1, Year 2, Year 3, Year 4, Year 5, Year 6, Year 7, Year 8, Year 9, Year 10, > Year 10 (maximum time on treatment was approximately 11.5 years).
Change in Average Daily "Off" Time Based on the Parkinson's Disease Symptom Diary at End of Treatment
The PD symptom diary asks participants (or their caregivers) to indicate their status upon waking and every 30 minutes during their normal waking time according to the following categories: asleep, "off", "on" without dyskinesia, "on" with non-troublesome dyskinesia, or "on" with troublesome dyskinesia.
"Off" time was defined as time when medication had worn off and was no longer providing benefit with regard to mobility, slowness, and stiffness.
PD diary times were normalized to a 16-hour waking day and averaged for the 3 days prior to each study visit.
A negative change for "off" time indicates improvement. The PD diary assessment was implemented with Protocol amendment 4 (December 2013) for participants at United States (US) sites only.
Measured: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Average Daily "On" Time Without Troublesome Dyskinesia Based on the Parkinson's Disease Symptom Diary at End of Treatment
The PD diary asks participants (or their caregivers) to indicate their status upon waking and every 30 minutes during their normal waking time according to the following categories: asleep, "off", "on" without dyskinesia, "on" with non-troublesome dyskinesia, or "on" with troublesome dyskinesia.
"On" time is when medication is providing benefit with regard to mobility, slowness and stiffness. Dyskinesia is involuntary twisting, turning movements which are an effect of medication and occur during "on" time. Non-troublesome dyskinesia does not interfere with function or cause meaningful discomfort.
"On" time without troublesome dyskinesia is the sum of "on" time without dyskinesia and "on" time with non-troublesome dyskinesia. PD diary times were normalized to a 16-hour waking day and averaged for the 3 days prior to each study visit. A positive change indicates improvement.
The PD diary was implemented with Protocol amendment 4 (December 2013) for participants at US sites only.
Measured: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Average Daily "On" Time With Troublesome Dyskinesia Based on the Parkinson's Disease Symptom Diary at End of Treatment
The PD diary asks participants (or their caregivers) to indicate their status upon waking and every 30 minutes during their normal waking time according to the following categories: asleep, "off", "on" without dyskinesia, "on" with non-troublesome dyskinesia, or "on" with troublesome dyskinesia.
"On" time is when medication is providing benefit with regard to mobility, slowness and stiffness. Dyskinesia is involuntary twisting, turning movements which are an effect of medication and occur during "on" time. Troublesome dyskinesia interferes with function or causes meaningful discomfort.
PD diary times were normalized to a 16-hour waking day and averaged for the 3 days prior to each study visit. A positive change indicates improvement.
The PD diary was implemented with Protocol amendment 4 (December 2013) for participants at US sites only.
Measured: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part I Score at End of Treatment
The UPDRS is an Investigator-used rating tool to follow the longitudinal course of PD. It is made up of the following sections:
- Mentation, Behavior, and Mood;
II) Activities of Daily Living;
III) Motor Examinations;
IV) Complications of Therapy sections (including dyskinesias).
The Part I Score is the sum of the answers to the 4 questions that comprise Part I, each of which are measured on a 5-point scale (0-4). The Part I score ranges from 0-16 and higher scores are associated with more disability. A negative change from Baseline indicates improvement.
The UPDRS was implemented with Protocol amendment 4 (December 2013) for participants at US sites only.
Measured: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part II Score at End of Treatment
The UPDRS is an Investigator-used rating tool to follow the longitudinal course of PD. It is made up of the following sections:
- Mentation, Behavior, and Mood;
II) Activities of Daily Living;
III) Motor Examinations;
IV) Complications of Therapy sections (including dyskinesias).
The Part II score is the sum of the answers to the 13 questions that comprise Part II, each of which are measured on a 5-point scale (0-4). The Part II score ranges from 0-52 and higher scores are associated with more disability. A negative change from Baseline indicates improvement.
The UPDRS was implemented with Protocol amendment 4 (December 2013) for participants at US sites only.
Measured: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part III Score at End of Treatment
The UPDRS is an Investigator-used rating tool to follow the longitudinal course of PD. It is made up of the following sections:
- Mentation, Behavior, and Mood;
II) Activities of Daily Living;
III) Motor Examinations;
IV) Complications of Therapy sections (including dyskinesias).
UPDRS Part III consists of 14 questions. Questions 20 - 26 are multi-part questions in that they are evaluated separately for multiple body parts. Counting each of these assessments leads to a total of 27 answers for Part III. The UPDRS Part III score is the sum of the 27 answers provided to the 14 Part III questions, each of which are measured on a 5-Point scale (0-4). The Part III score ranges from 0-108 and higher scores are associated with more disability. A negative change from Baseline indicates improvement.
The UPDRS was implemented with Protocol amendment 4 (December 2013) for participants at US sites only.
Measured: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Total Score at End of Treatment
The UPDRS is an Investigator-used rating tool to follow the longitudinal course of PD. It is made up of the following sections:
- Mentation, Behavior, and Mood;
II) Activities of Daily Living;
III) Motor Examinations;
IV) Complications of Therapy sections (including dyskinesias).
The UPDRS total score is the sum of the responses to the 31 questions (44 answers) that comprise Parts I - III of the scale. The total score ranges from 0 - 176 with 176 representing the worst (total) disability, and 0 no disability. A negative change from Baseline indicates improvement.
The UPDRS was implemented with Protocol amendment 4 (December 2013) for participants at US sites only.
Measured: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part IV Score at End of Treatment
The UPDRS is an Investigator-used rating tool to follow the longitudinal course of PD. It is made up of the following sections:
- Mentation, Behavior, and Mood;
II) Activities of Daily Living;
III) Motor Examinations;
IV) Complications of Therapy sections (including Dyskinesias).
The UPDRS Part IV Score is the sum of all answers to the 11 questions that comprise Part IV, 4 of which are measured on a 5-point scale (0 - 4) and 7 which are measured on a 2-point scale (0 - 1). The Part IV score ranges from 0 - 23 with higher scores associated with more disability. A negative change from Baseline indicates improvement.
The UPDRS was implemented with Protocol amendment 4 (December 2013) for participants at US sites only.
Measured: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part IV Dyskinesia Score at End of Treatment
The UPDRS is an Investigator-used rating tool to follow the longitudinal course of PD. It is made up of the following sections:
- Mentation, Behavior, and Mood; II) Activities of Daily Living; III) Motor Examinations; IV) Complications of Therapy sections (including Dyskinesias); and
The UPDRS Part IV dyskinesia Score is the sum of Questions 32 (What proportion of the waking day are dyskinesias present?), 33 (How disabling are the dyskinesias? ), and 34 (How painful are the dyskinesias?) on UPDRS Part IV, each of which are measured on a 5-point scale (0-4). The Part IV dyskinesia score ranges from 0 - 12 and higher scores are associated with more disability. A negative change from Baseline indicates improvement.
The UPDRS was implemented with Protocol amendment 4 (December 2013) for participants at US sites only.
Measured: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Parkinson's Disease Questionnaire (PDQ-39) Scores at End of Treatment
The PDQ-39 is a self-administered questionnaire that comprises 39 items addressing the following eight domains of health that patients consider to be adversely affected by the disease:
- Mobility (e.g., fear of falling when walking) - 10 questions
- Activities of daily living (e.g., difficulty cutting food) - 6 questions
- Emotional well-being (e.g., feelings of isolation) - 6 questions
- Stigma (e.g., social embarrassment) - 4 questions
- Social support - 3 questions
- Cognition - 4 questions
- Communication - 3 questions
- Bodily discomfort - 3 questions
Each question is answered on a 5-point scale from 0 (Never) to 4 (Always / Cannot Do At All). Scores are calculated by summing the answers to the questions in the domain and converting to a scale from 0 to 100. Higher scores are associated with the more severe symptoms of the disease such as tremor and stiffness. The PDQ-39 summary index (range 0-100) includes responses to all 39 items. A negative change indicates improvement.
Measured: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Apr 2008 (estimated)
- Study start13 Nov 2009
- Primary completion30 Nov 2021
- Study completion30 Nov 2021
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Advanced Parkinson's DiseaseStudies of the same condition, open and under way.
- More trials run by AbbVieThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 262 participants (actual)
Sponsor and investigators
- Lead sponsor
- AbbVie
- Sponsor type
- Industry (pharma, biotech, devices)
- Collaborators
- IQVIA, formerly Quintiles
- Responsible party
- Sponsor
- Investigators
- ABBVIE INC., Study director, AbbVie
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00660673
- Sponsor's protocol ID
- S187.3.005
- Other IDs
- 2008-001329-33, 2008
- Status last verified
- Nov 2022
- First submitted
- 15 Apr 2008
- Last updated
- 2 Dec 2022
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Yes: AbbVie is committed to responsible data sharing regarding the clinical trials we sponsor. This includes access to anonymized, individual and trial-level data (analysis data sets), as well as other information (e.g., protocols, analyses plans, clinical study reports), as long as the trials are not part of an ongoing or planned regulatory submission. This includes requests for clinical trial data for unlicensed products and indications.
Publications
Fernandez HH, Boyd JT, Fung VSC, Lew MF, Rodriguez RL, Slevin JT, Standaert DG, Zadikoff C, Vanagunas AD, Chatamra K, Eaton S, Facheris MF, Hall C, Robieson WZ, Benesh J, Espay AJ. Long-term safety and efficacy of levodopa-carbidopa intestinal gel in advanced Parkinson's disease. Mov Disord. 2018 Jul;33(6):928-936. doi: 10.1002/mds.27338. Epub 2018 Mar 23.
PubMed 29570853
Study at a glance
From the registry record, last updated by the sponsor on 2 Dec 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Open-Label Continuation Treatment Study With Levodopa - Carbidopa Intestinal Gel In Subjects With Advanced Parkinson's Disease And Severe Motor-Fluctuations Who Have Exhibited A Persistent And Positive Effect To Treatment In Previous Studies
- ClinicalTrials.gov ID
- NCT00660673
- Acronym / sponsor ID
- S187.3.005
- Conditions
- Advanced Parkinson's Disease
- Keywords
- levodopa/carbidopa intestinal gel, Severe Motor Fluctuations, Levodopa, Carbidopa, Parkinson's Disease, Dyskinesia
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 262 participants (actual)
- Lead sponsor
- AbbVieIndustry (pharma, biotech, devices)
- Collaborators
- IQVIA, formerly Quintiles
- Study start
- 13 Nov 2009 (actual)
- Primary completion
- 30 Nov 2021 (actual)
- Study completion
- 30 Nov 2021 (actual)
- First posted
- 17 Apr 2008 (estimated)
- Results
- Posted 2 Dec 2022
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The primary objective of this study is to provide continued access to levodopa-carbidopa intestinal gel (LCIG), to participants who have already participated in an open-label efficacy and safety study with the same treatment (Study S187.3.003 [NCT00360568] or Study S187.3.004 [NCT00335153]).
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Levodopa-Carbidopa Intestinal Gel | Experimental | Drug: Levodopa-Carbidopa Intestinal Gel (LCIG), Device: CADD-Legacy® 1400 ambulatory infusion pump, Device: Percutaneous Endoscopic Gastrostomy with jejunal extension tube (PEG-J)Initial dosing is based on the dosing regimen that the participant received during the previous LCIG study. Dosing is individually optimized and can be adjusted at any time during the study as clinically indicated. The total dose/day of LCIG is composed of 3 individually adjusted doses. The morning dose is administered as a bolus infusion, usually 5 to 10 mL (100 to 200 mg levodopa). The maintenance dose is adjustable in steps of 2 mg/hour (0.1 mL/hour), within a range of 1 to 10 mL/hour (20 to 200 mg levodopa/hour) and is usually 2 to 6 mL/hour (40 to 120 mg levodopa/hour). Participants will be allowed to self-administer extra doses of LCIG to address immediate medical needs, normally 0.5 to 2.0 mL. Participants will receive LCIG until it is commercially available. |
Who may qualify
- Ages
- 30 to 99 years
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- The participant should have completed participation in Study S187.3.003 or S187.3.004; and, in the opinion of the Principal Investigator, would benefit from long-term treatment with LCIG.
- For Canada, participants will be allowed to participate in the S187.3.005 study with a minimum of 6 months of exposure to LCIG in the S187.3.004 study.
- The participant must be able to understand the nature of the study and must provide written informed consent prior to the conduct of any study related procedures. If the participant does not have the capacity to provide informed consent, full informed consent must be obtained from the participant's legally authorized representative. Consenting will be performed according to local regulations.
Key exclusion criteria (1 listed)
- Medical, laboratory, psychiatric, or surgical issues deemed by the investigator to be clinically significant and which could interfere with the participant's participation in the study.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Levodopa-Carbidopa Intestinal Gel (LCIG)Also: Carbidopa-Levodopa Enteral Suspension (CLES), Duopa®, Duodopa®LCIG for upper-intestinal infusion is a suspension of levodopa (20 mg/mL) and carbidopa (5 mg/mL) in an aqueous gel that is dispensed in a medication cassette reservoir containing 100 mL of LCIG. | Drug | Levodopa-Carbidopa Intestinal Gel |
| CADD-Legacy® 1400 ambulatory infusion pumpPortable infusion pump (CADD-Legacy Pump Model 1400) connected to the LCIG medication cassette reservoir. | Device | Levodopa-Carbidopa Intestinal Gel |
| Percutaneous Endoscopic Gastrostomy with jejunal extension tube (PEG-J)All participants previously had a PEG-J placed in one of the prior LCIG studies. | Device | Levodopa-Carbidopa Intestinal Gel |
Primary outcome
Number of Participants With Treatment-emergent Adverse Events
Time frame: From first dose of LCIG in this study up to 30 days after the date of last PEG-J exposure; median duration of treatment was 1178 days, with a maximum of 4217 days (11.5 years).
Treatment-emergent adverse events (TEAEs) are defined as adverse events (AEs) which started on or after the date of the first LCIG Infusion in this study and within 30 days of the date of the last PEG-J exposure. At least possibly drug-related is defined as TEAEs assessed as having a "Possible" or "Probable" or missing relationship to study drug. Serious AEs included any untoward medical occurrence that: * Resulted in death * Was life-threatening * Required inpatient hospitalization or prolongation of an existing hospitalization * Resulted in persistent or significant disability/incapacity * was a congenital anomaly/birth defect The severity of all AEs was characterized as mild, moderate or severe according to the following definitions: * Mild: usually transient and do not interfere with daily activities. * Moderate: low level of inconvenience or concern to the subject, may interfere with daily activities. * Severe: events interrupt the subject's usual daily activity.
21 secondary outcomes
Number of Participants With Device Complications
Time frame: From first dose of LCIG in this study up to 30 days after the date of last PEG-J exposure; median duration of treatment was 1178 days.
Number of Participants With Sleep Attacks
Time frame: Baseline (final assessment period of the previous open-label LCIG study) and every 6 months until final visit; median duration of treatment was 1178 days.
Number of Participants With Intense Impulsive Behavior
Time frame: Baseline (final assessment of the previous open-label LCIG study) and every 6 months until final visit; median duration of treatment was 1178 days.
Number of Participants Who Developed Melanoma
Time frame: Once per year during the study; median duration of treatment was 1178 days.
Number of Participants With Treatment-emergent Adverse Events of Special Interest (TE AESI)
Time frame: From first dose of LCIG in this study up to 30 days after the date of last PEG-J exposure; median duration of treatment was 1178 days, with a maximum of 4217 days (11.5 years).
Number of Participants With Any Suicidal Ideation or Behavior
Time frame: Every 6 months (beginning with implementation of Protocol Amendment 3) until final visit; median duration of treatment was 1178 days.
Number of Participants With Potentially Clinically Significant Vital Sign Values
Time frame: Baseline and every 6 months until final visit; median duration of treatment was 1178 days.
Number of Participants With Potentially Clinically Significant Hematology Laboratory Values
Time frame: Baseline and every 6 months until final visit; median duration of treatment was 1178 days.
Number of Participants With Potentially Clinically Significant Chemistry Laboratory Values
Time frame: Baseline and every 6 months until final visit; median duration of treatment was 1178 days.
Number of Participants With Vitamin Levels Outside of the Normal Range
Time frame: Every 6 months (beginning with implementation of Protocol Amendment 2) until final visit; median duration of treatment was 1178 days.
Number of Participants Receiving Concomitant Anti-Parkinson's Disease Medications by Treatment Year
Time frame: Year 1, Year 2, Year 3, Year 4, Year 5, Year 6, Year 7, Year 8, Year 9, Year 10, > Year 10 (maximum time on treatment was approximately 11.5 years).
Change in Average Daily "Off" Time Based on the Parkinson's Disease Symptom Diary at End of Treatment
Time frame: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Average Daily "On" Time Without Troublesome Dyskinesia Based on the Parkinson's Disease Symptom Diary at End of Treatment
Time frame: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Average Daily "On" Time With Troublesome Dyskinesia Based on the Parkinson's Disease Symptom Diary at End of Treatment
Time frame: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part I Score at End of Treatment
Time frame: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part II Score at End of Treatment
Time frame: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part III Score at End of Treatment
Time frame: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Total Score at End of Treatment
Time frame: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part IV Score at End of Treatment
Time frame: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Unified Parkinson's Disease Rating Scale (UPDRS) Part IV Dyskinesia Score at End of Treatment
Time frame: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Change in Parkinson's Disease Questionnaire (PDQ-39) Scores at End of Treatment
Time frame: Prior to initial LCIG infusion (in the previous study, before the first LCIG infusion), Baseline (final assessment of the previous open-label LCIG study), and end of treatment; median duration of treatment was 1178 days.
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 2 Dec 2022.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Results publication: PubMed 29570853Fernandez HH, Boyd JT, Fung VSC, Lew MF, Rodriguez RL, Slevin JT, Standaert DG, Zadikoff C, Vanagunas AD, Chatamra K, Eaton S, Facheris MF, Hall C, Robieson WZ, Benesh J, Espay AJ. Long-term safety and efficacy of levodopa-carbidopa intestinal gel in advanced Parkinson's disease. Mov Disord. 2018 Jul;33(6):928-936. doi: 10.1002/mds.27338. Epub 2018 Mar 23.
- Related InfoLink provided by the sponsor.
- Individual participant dataSharing planned: Yes. AbbVie is committed to responsible data sharing regarding the clinical trials we sponsor. This includes access to anonymized, individual and trial-level data (analysis data sets), as well as other information (e.g., protocols, analyses plans, clinical study reports), as long as the trials are not part of an ongoing or planned regulatory submission. This includes requests for clinical trial data for unlicensed products and indications.
Related trials for Advanced Parkinson's Disease
Not yet recruiting
Unilateral and Staged Bilateral Pallidothalamic Tractotomy Using Exablate MRgFUS in Advanced Parkinson's Disease.
Parkinson Disease
Not yet recruitingObservational study
Longitudinal Observation of Neurodegeneration in Parkinson's Disease Using Molecular Imaging and Blood Biomarkers
Idiopathic Parkinson Disease
RecruitingPhase 2
Neural Mechanisms of Aerobic Exercise Benefits in PD With DBS
Parkinson's Disease, Deep Brain Stimulation
Not yet recruitingPhase 1
A Phase 1 Study of NCR201 in Parkinson's Disease Patients With Prior DBS
PARKINSON DISEASE (Disorder), Cell Therapy
Active, not recruiting
Enhancing Referral Decision-making for Advanced Treatment in Parkinson's Disease Through Objective Measurements and Patient Reported Outcomes.
Parkinson Disease
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
ABBVIE INC. study director
AbbVie
61 sites in 11 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Levodopa-Carbidopa Intestinal Gel (LCIG), CADD-Legacy® 1400 ambulatory infusion pump and Percutaneous Endoscopic Gastrostomy with jejunal extension tube (PEG-J) in people with Advanced Parkinson's Disease, run by AbbVie at 61 sites in 11 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 2 Dec 2022. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 61 sites in United States, Czechia, Russia, New Zealand, Australia and 6 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
Yes. Results are posted in the registry (first posted 2 Dec 2022). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Number of Participants With Treatment-emergent Adverse Events (time frame: From first dose of LCIG in this study up to 30 days after the date of last PEG-J exposure; median duration of treatment was 1178 days, with a maximum of 4217 days (11.5 years).). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00660673, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 2 Dec 2022.