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Juvmo (tavapadon)

Parkinson's disease

Also known as CVL-751
Manufacturer
AbbVie
Last updated
218 sources

Cost-effectiveness analyses and utility weights

Published cost-effectiveness analyses and health-state utility weights that a model of this product could cite, adapt, or compare against, grouped by how each article relates to the product and its indication. Every value is quoted from the article it cites, and section 3 lists the searches that found the articles.

14 cost-effectiveness analyses and 10 studies reporting utility weights · 15 sources

Overview

ItemDetail
Literature searchedTufts Medical Center Cost-Effectiveness Analysis Registry, searched October 21, 2026; the queries are listed in section 3.
Cost-effectiveness analyses14
Studies reporting utility weights10

Cost-effectiveness analyses

Analyses of Juvmo (tavapadon and CVL-751)

No evidence found.

Treatments for the same indication

Pramipexole versus levodopa as initial treatment in early Parkinson's disease, United States: Noyes et al. (2004)

Relevance: Evaluates pramipexole against levodopa as initial therapy in early Parkinson's disease within a United States randomized trial, the setting of the TEMPO-1 and TEMPO-2 trials and of the early-disease model in the ICER evidence report cited in section 4.1.

Levodopa versus levodopa-sparing therapy, and dopamine agonists versus monoamine oxidase type B inhibitors, in early Parkinson's disease, United Kingdom: McIntosh et al. (2021)

Relevance: Evaluates dopamine agonists against monoamine oxidase B inhibitors, and levodopa against levodopa-sparing therapy, as initial treatment of newly diagnosed Parkinson's disease in a United Kingdom randomized trial, the classes listed as current treatment options in section 2.

Access: Free full text

“PD MED is a pragmatic, open-label randomized, controlled trial in which patients newly diagnosed with PD were randomly assigned between levodopa-sparing therapy” (opens the source at this quote in a new tab)

“The economic analysis was performed from a health and personal social services perspective (PSS), as recommended by the National Institute for Health and Care Excellence (NICE) in the United Kingdom.” (opens the source at this quote in a new tab)

“Unit costs were attached to resource use volumes using UK 2011 prices, and both costs and benefits were discounted at an annual rate of 3.5%, consistent with NICE guidance.” (opens the source at this quote in a new tab)

“Aggregated QALYs and costs were estimated for each trial participant up to 7 years from randomization or death if earlier.” (opens the source at this quote in a new tab)

“Over a mean observation period of 4 years, levodopa was associated with significantly higher quality-adjusted life-years (difference, 0.18; 95% CI, 0.05–0.30; P < 0.01) and lower mean costs (£3390; £2671–£4109; P < 0.01) than levodopa-sparing therapies” (opens the source at this quote in a new tab)

“The probability that levodopa is cost-effective was estimated at 100% for all threshold values for a QALY considered” (opens the source at this quote in a new tab)

“There was no significant difference in quality-adjusted life-years between those allocated dopamine agonists and monoamine oxidase type B inhibitors (0.02; −0.17 to 0.13 in favor of dopamine agonists; P = 0.81); however costs were significantly lower for those allocated monoamine oxidase type B inhibitors (£2321; £1628–£3015; P < 0.01) because of the higher costs of dopamine agonists.” (opens the source at this quote in a new tab)

“For UK threshold values of £20,000 and £30,000 per incremental QALY, the probability that allocation to MAOBI is cost-effective compared with DA was 92% and 81%, respectively” (opens the source at this quote in a new tab)

“Initial treatment with levodopa is highly cost-effective compared with levodopa-sparing therapies.” (opens the source at this quote in a new tab)

Pramipexole versus baseline levodopa-based treatment in early and in advanced Parkinson's disease, United States: Hoerger et al. (1998)

Relevance: Evaluates pramipexole against levodopa-based standard care separately in early and in advanced Parkinson's disease in the United States, the early and later stages at which the TEMPO trials studied tavapadon as monotherapy and as an adjunct to levodopa.

“We developed a cost-effectiveness (CE) model in the US setting that linked Unified Parkinson's Disease Rating Scale (UPDRS) Part II (activities of daily life) and III (motor) scores to disease progression, costs and patient utility.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“We performed separate analyses for patients with early and advanced PD.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“The study was conducted from the societal perspective, although data presentation allows interpretation of cost effectiveness from either the societal or payer perspective.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“For patients with both early and advanced PD, treatment with pramipexole had higher costs but was more effective than baseline treatment.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“For patients with early onset of PD, the incremental total CE ratio for pramipexole was $US8837/QALY.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“For patients with advanced PD, the incremental CE ratio was $US12 294/QALY (1997 costs).” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

Rasagiline versus pramipexole as first-line monotherapy in early Parkinson's disease, United Kingdom: Haycox et al. (2009)

Relevance: Evaluates first-line monotherapy with rasagiline against pramipexole in early Parkinson's disease from a United Kingdom healthcare payer perspective, classes listed as current treatment options in section 2.

“The aim of this study was to compare the cost effectiveness, from a UK healthcare payer perspective, of two antiparkinsonian treatment strategies in early PD: first-line monotherapy with rasagiline, a novel monoamine oxidase B inhibitor; and the non-ergoline dopamine receptor agonist pramipexole.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“An economic Markov model was developed as a pragmatic tool to derive comparative information on the effectiveness, utility and costs of these two strategies over a 5-year period.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“Rasagiline was the dominant strategy.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“Compared with pramipexole, use of the rasagiline strategy was estimated to reduce costs by 18% per patient over 5 years and was associated with an additional 10% delay in dyskinesia onset (0.41 years; 95% CI 0.27, 0.55).” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“In addition, use of the rasagiline strategy was found to generate a 5% gain in QALYs over 5 years compared with the pramipexole strategy (3.7 +/- 0.02 vs 3.51 +/- 0.03).” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

Dopamine agonists added to levodopa versus levodopa alone in Parkinson's disease, Japan: Shimbo et al. (2001)

Relevance: Evaluates dopamine agonists added to levodopa against levodopa alone in Japan, the drug class with which the ICER model of levodopa-treated Parkinson's disease with motor fluctuations in section 4.1 compares tavapadon.

“We used a Markov model to simulate the course of Parkinson's disease and to compare the cost effectiveness of dopamine agonists added to levodopa with that of levodopa alone in Japan.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“The model assumed that 60-year-old men with Parkinson's disease in Hoehn-Yahr (HY) stages 2 to 5 using levodopa were administered dopamine agonists or continued on levodopa alone.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“The incremental cost effectiveness of dopamine agonists used for 10 years was then estimated.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“In the patients in HY stage 2, the incremental cost effectiveness of dopamine agonists was 18,610,000 to 19,320,000 yen per quality-adjusted life-year (QALY)” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“In patients in HY stage 3 or higher, the use of dopamine agonists was dominant over levodopa alone mainly due to reduced cost for care.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“The use of a generic formulation of bromocriptine was dominant over levodopa alone even in the patients with HY stage 2 disease.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

Opicapone versus entacapone as adjuncts to levodopa/carbidopa in Parkinson's disease with OFF time, United States: Hansen et al. (2021)

Relevance: Evaluates opicapone against entacapone as adjuncts to levodopa/carbidopa, based on reduction in OFF time, from a United States payer perspective, an analysis section 4.1 cites.

Access: Free full text

“To assess from a US payer perspective the relative cost-effectiveness of the catechol-O-methyltransferase inhibitors opicapone and entacapone when used adjunctively to levodopa/carbidopa (LD/CD) in patients with Parkinson’s disease (PD), based on the drugs’ effects to reduce absolute OFF-time hours in PD patients.” (opens the source at this quote in a new tab)

“A Markov model was created to estimate cost-effectiveness of adjunctive opicapone treatment compared with adjunctive entacapone treatment in a synthetic cohort of 1,000 patients with PD taking LD/CD.” (opens the source at this quote in a new tab)

“Cost data (in 2018 US dollars)” (opens the source at this quote in a new tab)

“Outcomes were projected over a 25-year lifetime horizon and discounted at 3% annually.” (opens the source at this quote in a new tab)

“Opicapone treatment was associated with an average of 1,187 fewer OFF-time hours per patient and an increase of 0.07 QALYs compared with entacapone.” (opens the source at this quote in a new tab)

“Total lifetime costs for opicapone were $3,100 higher than entacapone, resulting in an incremental cost-effectiveness ratio of $46,900 per QALY.” (opens the source at this quote in a new tab)

“Probabilistic sensitivity analysis suggested a 60–65% probability that opicapone was cost-effective relative to entacapone at any willingness-to-pay threshold ≥$5,000.” (opens the source at this quote in a new tab)

Rasagiline or entacapone added to levodopa, and levodopa/carbidopa/entacapone, versus levodopa monotherapy in advanced Parkinson's disease with motor fluctuations, United States: Groenendaal et al. (2010)

Relevance: Evaluates rasagiline or entacapone added to levodopa, and levodopa/carbidopa/entacapone, against levodopa monotherapy in advanced Parkinson's disease with motor fluctuations in the United States, the levodopa-treated population with motor fluctuations studied in TEMPO-3.

“To assess the cost utility of rasagiline or entacapone as adjunctive therapies to levodopa versus levodopa/carbidopa/entacapone (LCE) versus standard levodopa monotherapy in patients with advanced PD and motor fluctuations in the US.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“A 2-year stochastic Markov model was utilized to examine the cost effectiveness of treatments of advanced PD.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“Over 2 years, all therapy options showed greater effectiveness than levodopa alone.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“Rasagiline+levodopa and LCE were cost saving from a payor perspective, while entacapone+levodopa was cost saving from a societal perspective.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“Mean benefits over 2 years were 0.12 (90% credibility interval [CI] 0.07, 0.18) additional quality-adjusted life-years (QALYs) for rasagiline+levodopa, entacapone+levodopa and LCE” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“From a payor perspective, rasagiline+levodopa and LCE were dominant therapies over levodopa monotherapy, while entacapone+levodopa was effective at a higher cost.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

Entacapone added to standard treatment versus standard treatment alone in Parkinson's disease with off-time, United States: Palmer et al. (2002)

Relevance: Evaluates entacapone added to standard treatment in Parkinson's disease with motor fluctuations in the United States, the catechol-O-methyltransferase inhibitor class listed as an adjunctive option in section 2.

“To determine the cost effectiveness of adjunctive therapy with entacapone versus standard treatment (levodopa) without entacapone for patients in the US with Parkinson's disease (PD) who experience 'off-time' (re-emergence of the symptoms of PD) while receiving levodopa.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“A Markov model was used to estimate 5-year costs and effectiveness of standard treatment with and without entacapone.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“PD disability was measured using the daily proportion of off-time and Hoehn and Yahr scale scores.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“The analysis measured costs from a societal and third-party payer perspective, and effectiveness as gains in quality-adjusted life-years (QALYs) and years without progression to >25% off-time.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“From a societal perspective, entacapone therapy resulted in an incremental cost of US dollars 9327 per QALY gained compared with standard treatment.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“Treatment with entacapone also provided an additional 7.6 months with < or =25% off-time/day compared with standard treatment.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

Opicapone and entacapone versus no catechol-O-methyltransferase inhibitor, and opicapone versus entacapone, in advanced Parkinson's disease, South Korea: Kwak et al. (2024)

Relevance: Evaluates opicapone and entacapone against no catechol-O-methyltransferase inhibitor in advanced Parkinson's disease from a South Korean healthcare system perspective, an analysis section 4.1 cites.

Access: Not open access

Not quoted: The incremental costs, QALYs, and cost-effectiveness ratios are reported in the full text, which is closed access.

Levodopa/carbidopa/entacapone versus standard care in Parkinson's disease with wearing-off, United Kingdom: Findley et al. (2005)

Relevance: Evaluates levodopa/carbidopa/entacapone against standard care in Parkinson's disease with end-of-dose wearing-off from United Kingdom societal and National Health Service perspectives, the levodopa-treated population with motor fluctuations studied in TEMPO-3.

“A Markov model was developed to evaluate the cost-effectiveness of levodopa/carbidopa/entacapone (LCE;Stalevo), in the treatment of patients with Parkinson's disease (PD) and end-of-dose motor fluctuations (wearing-off).” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“The costs and outcomes of both treatments were projected over a period of 10 years from the perspective (a) of society as a whole and (b) of the UK National Health Service (NHS).” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“Treatment with LCE produced an average gain of +1.04 quality-adjusted life-years (QALYs) per patient (2.57 vs. 1.53) in the base-case analysis (discount rate 3.5%).” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“This gain was accompanied by a reduction in the total 10-year direct cost of care to society of 10198 pounds per patient” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“From the societal perspective, therefore, LCE was dominant, producing better clinical outcomes with lower costs.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“Although treatment with LCE resulted in an increase in direct costs per patient of 3239 pounds (25756 pounds versus 22517 pounds) to the NHS over the 10-year period analysed, the incremental cost-effectiveness ratio (ICER) of LCE was only 3105 pounds per QALY gained (approximately E4500).” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

Rasagiline or entacapone added to levodopa versus levodopa alone in Parkinson's disease with motor fluctuations, Finland: Hudry et al. (2006)

Relevance: Evaluates rasagiline and entacapone as adjuncts to levodopa in Parkinson's disease with motor fluctuations in Finland, covering the monoamine oxidase B and catechol-O-methyltransferase inhibitor classes listed in section 2.

Apomorphine sublingual film versus apomorphine hydrochloride injection and levodopa inhalation powder for OFF episodes in Parkinson's disease, United States: Thach et al. (2021)

Relevance: Evaluates apomorphine sublingual film against apomorphine injection and levodopa inhalation powder as on-demand treatment of OFF episodes from a United States payer perspective, the on-demand therapies listed in section 2 and an analysis section 4.1 cites.

“The cost-effectiveness analysis model was built from a pooled US Medicare and commercial payer perspective.” (opens the original PMC page at this quote in a new tab)View highlighted excerpt for this quote

“The model used a 10-year time horizon” (opens the original PMC page at this quote in a new tab)View highlighted excerpt for this quote

“It was developed using a microsimulation model with a 3-month cycle length” (opens the original PMC page at this quote in a new tab)View highlighted excerpt for this quote

“Costs and benefits were discounted at a 3% annual rate over the time horizon.” (opens the original PMC page at this quote in a new tab)View highlighted excerpt for this quote

“treatment costs (US$45 865) compared with apomorphine hydrochloride injection (US$280 213; difference: US–$234 349) and levodopa inhalation powder (US$73 317; difference: US–$27 453) over the 10-year time horizon.” (opens the original PMC page at this quote in a new tab)View highlighted excerpt for this quote

“Over the same time period, apomorphine sublingual film was also associated with the highest utility, with incremental QALYs of 0.019 compared with apomorphine hydrochloride injection (4.107 vs 4.088 QALYs, respectively) and 0.235 compared with levodopa inhalation powder (4.107 vs 3.872 QALYs) (Table 3).” (opens the original PMC page at this quote in a new tab)View highlighted excerpt for this quote

“Considering both cost and utility outcomes, apomorphine sublingual film was dominant compared with both comparator arms, being less costly and more effective on average than apomorphine hydrochloride injection and levodopa inhalation powder.” (opens the original PMC page at this quote in a new tab)View highlighted excerpt for this quote

“Apomorphine sublingual film was projected to be dominant in 70% of patients versus apomorphine hydrochloride injection and 71% versus levodopa inhalation powder.” (opens the original PMC page at this quote in a new tab)View highlighted excerpt for this quote

The same disease in other populations or settings

Carbidopa/levodopa enteral suspension versus oral standard of care in advanced Parkinson's disease, United States: Pahwa et al. (2023)

Relevance: Evaluates carbidopa-levodopa enteral suspension against oral standard of care in advanced Parkinson's disease in the United States, a device-aided therapy listed in section 2 and an analysis section 4.1 cites.

Access: Free full text

“A published Markov model, comprising of 25 health states and a death state, (defined by a combination of the Hoehn and Yahr scale and waking time spent in OFF-time) was adapted to estimate the benefits for CLES versus oral SoC over a patient's lifetime in the US healthcare setting.” (opens the source at this quote in a new tab)

“to determine the average costs, life years (LYs) and quality-adjusted life years (QALYs) per patient with CLES and SoC, from the US payer perspective (using costs inputs specific for Medicare), thereby calculating the incremental cost-effectiveness ratio (ICER).” (opens the source at this quote in a new tab)

“Discount rate was applied annually for both costs and effects (3.0%), as per the Institute for Clinical and Economic Review guidelines.” (opens the source at this quote in a new tab)

“The model population comprised of patients with aPD and severe motor fluctuations, defined on the Hoehn and Yahr (HY) scale as ≥3 and OFF-time >4 hours (ie, 25% of 16-hour waking day).” (opens the source at this quote in a new tab)

“In the base case analysis, as compared to SoC, CLES was associated with an incremental cost of $6611, an incremental QALY gain of 0.86, and LY incremental gain of 1.25 over a lifetime time horizon, resulting in an ICER of $7711/QALY.” (opens the source at this quote in a new tab)

“CLES compared to SoC was associated with incremental costs ($1,031,791 vs. $1,025,180) and QALY gain (4.61 vs. 3.76), resulting in an incremental cost-effectiveness ratio of $7711/QALY.” (opens the source at this quote in a new tab)

Deep brain stimulation with medical therapy versus best medical therapy alone in advanced Parkinson's disease, United States: Pietzsch et al. (2016)

Relevance: Evaluates deep brain stimulation with medical therapy against best medical therapy alone in advanced Parkinson's disease from a United States Medicare payer perspective, a device-aided therapy listed in section 2.

“We used a decision-analytic state-transition (Markov) model to project PD progression and associated costs for the two treatment strategies.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“We estimated the discounted incremental cost-effectiveness ratio (ICER) in U.S. dollars per quality-adjusted life-year (QALY) from the Medicare payer perspective, considering a ten-year horizon, and evaluated the robustness of our projections through extensive deterministic sensitivity analyses.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“Over ten years, DBS treatment led to discounted total costs of $130,510 compared to $91,026 for BMT and added 1.69 QALYs more than BMT, resulting in an ICER of $23,404 per QALY.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“This ICER was relatively insensitive to variations in input parameters, with neurostimulator replacement, costs for DBS implantation, and costs for treatment of disease-related falls having the greatest effects.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

“Across all investigated scenarios, including a five-year horizon, ICERs remained under $50,000 per QALY.” (opens the original PubMed page at this quote in a new tab)View highlighted excerpt for this quote

Related diseases and analogous treatments

No evidence found.

Utility weights

Utility weights from analyses of Juvmo (tavapadon and CVL-751)

No evidence found.

Utility weights for the same indication

No evidence found.

Utility weights for the same disease in other populations or settings

Utility weights by Hoehn and Yahr stage and proportion of the day in off-time, Parkinson's disease: Palmer et al. (2002)

Relevance: Utilities for Parkinson's disease by Hoehn and Yahr stage and proportion of the day in off-time, used in a United States analysis of adjunctive entacapone.

Access: Not open access

Not quoted: The utility weights are reported in the full text, which is closed access.

Utility weights by OFF-time category and for dyskinesia, advanced Parkinson's disease: Kwak et al. (2024)

Relevance: Utilities for Parkinson's disease by OFF-time category and for dyskinesia, used in a South Korean analysis of opicapone and entacapone.

Access: Not open access

Not quoted: The utility weights are reported in the full text, which is closed access.

Utility weights for monotherapy with and without motor fluctuations or dyskinesia, early Parkinson's disease: Haycox et al. (2009)

Relevance: Utilities in early Parkinson's disease for monotherapy with and without motor fluctuations or dyskinesia, used in a United Kingdom analysis of rasagiline and pramipexole.

Access: Not open access

Not quoted: The utility weights are reported in the full text, which is closed access.

Utility weights for initial pramipexole and initial levodopa treatment, early Parkinson's disease: Noyes et al. (2004)

Relevance: Utilities measured in trial participants with early Parkinson's disease treated initially with pramipexole or with levodopa.

Access: Not open access

Not quoted: The utility weights are reported in the full text, which is closed access.

Baseline utility weights for participants assigned a dopamine agonist or a monoamine oxidase type B inhibitor, early Parkinson's disease: McIntosh et al. (2021)

Relevance: Utilities measured in trial participants with newly diagnosed Parkinson's disease allocated to a dopamine agonist or a monoamine oxidase B inhibitor.

Access: Free full text

Utility weights by Hoehn and Yahr stage in men, Parkinson's disease: Shimbo et al. (2001)

Relevance: Utilities for Parkinson's disease by Hoehn and Yahr stage in men, used in a Japanese analysis of dopamine agonists added to levodopa.

Access: Not open access

Not quoted: The utility weights are reported in the full text, which is closed access.

Utility weights by daily duration of OFF episodes and per OFF hour reduced, Parkinson's disease: Thach et al. (2021)

Relevance: Utilities for Parkinson's disease by daily duration of OFF episodes and the utility gain per OFF hour reduced.

Disutilities for an increase in Hoehn and Yahr stage and in OFF time, advanced Parkinson's disease: Pahwa et al. (2023)

Relevance: Disutilities for an increase in Hoehn and Yahr stage and for an increase in OFF-time duration in Parkinson's disease, from a United States analysis.

Access: Free full text

Utility weights for related diseases and analogous treatments

No evidence found.

Search strategy

DatasetQueryResults
Methodstavapadon0
Ratiostavapadon0
Methods"Parkinsons disease" OR "Parkinson disease" OR parkinsonism7
MethodsParkinson50
Ratios"Parkinson"60
Ratios"Parkinson's disease" OR "Parkinson disease"86
Ratiospramipexole OR ropinirole OR rotigotine OR "dopamine agonist" OR "dopamine agonists"35
Ratiosrasagiline OR selegiline OR safinamide OR entacapone OR opicapone OR tolcapone OR istradefylline OR amantadine OR apomorphine53
Ratioslevodopa OR foslevodopa OR carbidopa53
Weights"Parkinson's disease" OR "Parkinson disease" OR Parkinson387
Methods"CVL-751" OR "PF-06649751" OR Juvmo0
Weights"Hoehn" OR "Hoehn and Yahr"164
Weights"OFF time" OR "off-time" OR "motor fluctuations" OR dyskinesia167
Ratios"deep brain stimulation"64