An Open-Label, 8-Week Study of Safety and Efficacy of Pimavanserin Treatment in Adults with Parkinson’s Disease and Depression
Abstract
Background:
Many patients with Parkinson’s disease (PD) experience depression.
Objective:
Evaluate pimavanserin treatment for depression in patients with PD.
Methods:
Pimavanserin was administered as monotherapy or adjunctive therapy to a selective serotonin reuptake inhibitor or serotonin/noradrenaline reuptake inhibitor in this 8-week, single-arm, open-label phase 2 study (NCT03482882). The primary endpoint was change from baseline to week 8 in Hamilton Depression Scale–17-item version (HAMD-17) score. Safety, including collection of adverse events and the Mini-Mental State Examination (MMSE) and Movement Disorder Society-sponsored revision of the Unified Parkinson’s Disease Rating Scale Part III (MDS-UPDRS III) scores, was assessed in patients who received ≥1 pimavanserin dose.
Results:
Efficacy was evaluated in 45 patients (21 monotherapy, 24 adjunctive therapy). Mean (SE) baseline HAMD-17 was 19.2 (3.1). Change from baseline to week 8 (least squares [LS] mean [SE]) in the HAMD-17 was –10.8 (0.63) (95% CI, –12.0 to –9.5; p < 0.0001) with significant improvement seen at week 2 (p < 0.0001) and for both monotherapy (week 8, –11.2 [0.99]) and adjunctive therapy (week 8,–10.2 [0.78]). Most patients (60.0%) had ≥50% improvement at week 8, and 44.4% of patients reached remission (HAMD-17 score ≤7). Twenty-one of 47 patients experienced 42 treatment-emergent adverse events; the most common by system organ class were gastrointestinal (n = 7; 14.9%) and psychiatric (n = 7; 14.9%). No negative effects were observed on MMSE or MDS-UPDRS Part III.
Conclusion:
In this 8-week, single-arm, open-label study, pimavanserin as monotherapy or adjunctive therapy was well tolerated and associated with early and sustained improvement of depressive symptoms in patients with PD.
INTRODUCTION
Parkinson’s disease (PD) is a progressive neurodegenerative disorder characterized primarily by motor deficits; however, behavioral symptoms associated with the disease are frequent, severe, and disabling [1]. Mood disorders, including depression, occur in 30% to 50% of patients [1, 2]. Depression can emerge at any phase of the disease [1] and is associated with faster progression of physical symptoms, disability, and diminished quality of life [3]. Conversely, improvement of depression in patients with PD correlates with reduced physical disability and improved quality of life [3].
Despite the significant need for treatment, no medications are currently approved by the United States Food and Drug Administration (US FDA) for depression in patients with PD. A paucity of studies have examined currently approved antidepressants for treating depression in patients with PD [4–7] and suggest either no benefit or only marginal effects.
Widespread neurodegeneration and monoaminergic dysregulation, particularly in the mesolimbic system, can contribute to depression [8, 9]. While the exact pathophysiology is unknown, key features of depression, including depressed mood, apathy, and anhedonia, are known to be related to serotonergic transmission that is dysregulated in PD [9–11]. Compounds with potent antagonist/inverse agonist activity at 5-hydroxytryptamine 2A (5-HT2A) receptors, and to varying degrees at 5-hydroxytryptamine 2C (5-HT2C) receptors, but with lower affinity for monoamine transporters, have shown antidepressant effects in major depressive disorder patient populations [12, 13].
Pimavanserin is a selective 5-HT2A receptor antagonist/inverse agonist with limited affinity for 5-HT2C receptors [14]. Based on its mechanism of action, pimavanserin may have antidepressant activity. In a phase 2 randomized, controlled trial, adjunctive pimavanserin treatment improved symptoms of major depressive disorder (MDD) in patients with an inadequate response to selective serotonin reuptake inhibitor (SSRI) or serotonin/norepinephrine reuptake inhibitor (SNRI) treatment [15]. The current study was intended to preliminarily assess the efficacy and safety of pimavanserin being investigated for the treatment of depression in patients with PD.
METHODS
Study design
This was an 8-week, open-label, single-arm phase 2 study to evaluate the efficacy and safety of pimavanserin for treatment of depression in patients with PD. During the study, patients were given pimavanserin 34 mg (two 17 mg tablets) with instructions to take the medication orally at approximately the same time daily. Assessments were conducted every 2 weeks, and patients received a safety follow-up call 2 weeks after the last dose of pimavanserin (Fig. 1).
Fig. 1
Study design. PD, Parkinson’s disease; SNRI, serotonin/norepinephrine reuptake inhibitor; SSRI, selective serotonin reuptake inhibitor.
The study was conducted between March 9, 2018, and July 24, 2019 (ClinicalTrials.gov identifier: NCT03482882). All procedures were conducted in accordance with the Declaration of Helsinki and applicable International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use and Good Clinical Practice guidelines. The protocol was approved by each site’s ethics committee or institutional review board and all participants provided informed consent.
Patient eligibility
Patients in the United States aged ≥50 years with PD and depression [16] were recruited. Patients were required to have a clinical diagnosis of PD for ≥1 year with ≥3 symptoms of PD (rest tremor, rigidity, bradykinesia or akinesia, or postural/gait abnormalities), be on anti-PD medication for ≥1 year, and exhibit a Mini-Mental State Examination (MMSE [17]) score of ≥21.
PD patients with depressive symptoms (score of ≥15 on the Hamilton Depression Scale–17-item version (HAMD-17 [18]) and who met the National Institute of Neurological Disorders and Stroke-National Institute of Mental Health criteria for depression in patients with PD [16]) were eligible to enroll. Those taking a single SSRI or SNRI within the US FDA approved labeling for the treatment of major depressive disorder were eligible if their current treatment was inadequate. If patients were taking more than one antidepressant, they were eligible to enroll if they were being discontinued from one agent before the baseline visit in a clinically appropriate manner.
Patients were excluded if they were taking or had taken an antipsychotic medication (within 3 weeks or 5 half-lives of the baseline visit [whichever is longer]); had a history of PD psychosis, schizophrenia, bipolar I or II disorder, another psychotic disorder, or substance use disorder (within the last 6 months); or were actively suicidal. Individuals with a history of stroke, a family history of a long QT syndrome, or a myocardial infarction were also excluded. Full inclusion/exclusion criteria are listed in Supplementary Table 1. Adjunctive medications for Parkinson’s disease or depression were kept stable for the duration of the study if possible.
Outcomes and assessments
The primary objective of the study was to assess the efficacy of pimavanserin treatment, as monotherapy or adjunctive therapy, in improving depression symptoms in adults with PD. The primary endpoint was assessed based on the change from baseline to week 8 in depression symptoms as measured by the HAMD-17 [18]. The proportion of patients showing ≥50% improvement in the HAMD-17 score was evaluated as a secondary endpoint. A post hoc analysis examined the proportion of patients who reached remission, defined as a HAMD-17 score of ≤7 [19]. The HAMD-17 was administered at screening, baseline, and weeks 2, 4, 6, and 8.
Secondary endpoints evaluated the effect of pimavanserin treatment on clinicians’ global assessment of illness, sleep quality, and overall quality of life. Global impression of illness was assessed by the Clinical Global Impression–Improvement (CGI-I) score and change from baseline on the Clinical Global Impression–Severity (CGI-S) score [20]. Changes in sleep quality were evaluated as change from baseline in the Scale for Outcomes of PD-Sleep Scale (SCOPA) score, including global sleep (GS) quality, nighttime sleep (NS) quality, and daytime sleepiness (DS) [21]. Patients’ quality of life was assessed by a caregiver as change from baseline in the EuroQol-5 Dimensions-5 Levels Proxy version 1 visual analog scale (EQ-5D-5L-VAS) [22]. The CGI-S and CGI-I were assessed at baseline and weeks 2, 4, 6, and 8. SCOPA and EQ-5D-5L-VAS were assessed at baseline and at weeks 4 and 8.
Medical history and demographic information were collected during screening. The MMSE [17] and Columbia-Suicide Severity Rating Scale (C-SSRS) scores [23] were used to screen for cognitive impairment and suicidal ideation. Both measures were also collected as safety assessments. The MMSE was administered at screening, baseline, week 4, and week 8. The C-SSRS was administered at screening, baseline, and weeks 2, 4, 6, and 8. The Massachusetts General Hospital Antidepressant Treatment Response Questionnaire (MGH ATRQ) [24, 25] was used as a screening assessment. The MGH ATRQ assesses response to antidepressant treatment retrospectively using specific anchor points throughout treatment history to define the adequacy of the dose and duration of each antidepressant course. Patients exhibiting a maximum improvement of <75% with an existing antidepressant were included in the adjunctive therapy group.
Safety endpoints, including the MMSE, C-SSRS, physical examinations, vital signs, clinical laboratory tests, electrocardiograms, and incidence of adverse events (AEs) were monitored throughout the study. A treatment-emergent AE (TEAE) was defined as an AE with onset date during treatment or within 30 days of the last study drug dose date. The relationship to treatment was reported by the investigator. A serious AE was defined as an AE that was fatal, was immediately life-threatening, resulted in disability or permanent damage, required hospitalization, was a congenital anomaly or birth defect in an offspring, or was medically significant.
The Movement Disorder Society (MDS)–sponsored revision of the Unified Parkinson’s Disease Rating Scale (UPDRS) Part III (MDS-UPDRS III) [26], a comprehensive measure of motor indices, was also included to assess any decline in motor function. This assessment was completed in the “on” state and was conducted at baseline, week 4, and week 8; change from baseline was analyzed.
Statistical analysis
Patients who received ≥1 dose of pimavanserin and completed a baseline and ≥1 postbaseline HAMD-17 assessment were included in the efficacy analysis. The mixed model repeated measures (MMRM) method was used to analyze primary and secondary endpoints. The total score of each measure was analyzed, with change from baseline as the dependent variable and baseline total score (of the dependent variable), visit (weeks 2, 4, 6, and 8), and baseline total score-by-visit interaction as independent variables. Treatment effects were reported as the least squares (LS) mean (standard error [SE]) change from baseline to week 8. The CGI-I was analyzed using the MMRM with CGI-I score as the dependent variable, and with independent variables of baseline CGI-S score, visit, and baseline CGI-S score-by-visit interaction. Significance level was set to 0.05 and p values reported for pre-planned secondary outcomes were unadjusted for multiple comparisons.
The proportion of patients showing a response to treatment was reported by visit. Responders were defined as patients who exhibited ≥50% reduction from baseline score in the HAMD-17. Observed cases (patients with missing values at a given visit were excluded) and missing values imputed as nonresponders were included.
In a post hoc analysis, the proportion of patients reaching remission, defined as a HAMD-17 score ≤7, was reported by visit. Missing values were imputed as nonremitters. Improvement on individual items of the HAMD-17 was also analyzed post hoc using an MMRM similar to the primary endpoint.
Patients who received ≥1 dose of pimavanserin were included in the safety analysis. Safety endpoints were summarized using descriptive statistics. The MMSE and MDS-UPDRS Part III were analyzed using an MMRM similar to the primary endpoint.
RESULTS
Patients
Forty-seven patients were enrolled in the study from 14 sites in the United States. Forty-five patients were included in the efficacy analyses. Patients had a mean (standard deviation [SD]) age at baseline of 69.3 (8.3) years and a mean (SD) MMSE score of 27.6 (2.5). The mean (SD) time since PD diagnosis and duration of depression with PD diagnoses was 7.8 (5.5) years and 5.4 (6.8) years, respectively (Table 1). At baseline, patients were “Moderately Depressed” on average, with a mean (SD) HAMD-17 score of 19.2 (3.1), and a range of 15 (“Mild Depression”) to 27 (“Severe Depression”) [19]. The mean (SD) time since the first use of an antidepressant was 5.4 (5.9) years. Forty patients completed the study and 7 (14.9%) discontinued. Reasons for discontinuation were adverse event (n = 3, 6.4%), protocol violation (n = 2, 4.3%), loss to follow up (n = 1, 2.1%), or other event (medical monitor decision, n = 1, 2.1%).
Table 1
Baseline demographics and disease characteristics
| Characteristic | N = 45 |
| Age, y | |
| Mean (SD) | 69.3 (8.3) |
| Range | 51–89 |
| Age category, n (%) | |
| <70 | 20 (44.4) |
| ≥70 | 25 (55.6) |
| Male, n (%) | 23 (51.1) |
| Female, n (%) | 22 (48.9) |
| Race, n (%) | |
| White | 41 (91.1) |
| Black or African American | 2 (4.4) |
| Asian | 1 (2.2) |
| Other | 1 (2.2) |
| Age at PD onset, mean (SD), y | 61.5 (9.9) |
| Duration of PD, mean (SD), y | 7.8 (5.5) |
| Age at onset of depression with PD (SD), y | 63.9 (10.9) |
| Duration of depression with PD (SD), y | 5.4 (6.8) |
| MMSE score, mean (SD) | 27.6 (2.5) |
| MDS-UPDRS Part III score, mean (SD) | 30.5 (17.3) |
| Assessment score, mean (SD) | |
| HAMD-17 | 19.2 (3.1) |
| CGI-S | 4.1 (0.5) |
| SCOPA-NS | 6.1 (3.4) |
| SCOPA-DS | 5.2 (3.7) |
| SCOPA-GS | 3.9 (1.5) |
| EQ-5D-5L-VAS | 63.9 (16.3) |
CGI-S, Clinical Global Impression–Severity; HAMD-17, Hamilton Depression Scale–17-item version; MDS-UPDRS, Movement Disorder Society–sponsored revision of the Unified Parkinson’s Disease Rating Scale; MMSE, Mini-Mental State Examination; PD, Parkinson’s disease; SCOPA-DS, Scale for Outcomes in Parkinson’s Disease–daytime sleepiness; SCOPA-GS, Scale for Outcomes in Parkinson’s Disease–global sleep; SCOPA-NS, Scale for Outcomes in Parkinson’s Disease–nighttime sleep; EQ-5D-5L-VAS, EuroQol-5 Dimensions-5 Levels Proxy version 1 visual analog scale; SD, standard deviation.
Twenty-six enrolled patients were administered pimavanserin as adjunctive therapy with one of the following: bupropion, duloxetine, escitalopram, fluoxetine, paroxetine, sertraline, or vortioxetine. Dosage and number of patients taking each are presented in Supplementary Table 2. Twenty-four patients (53.3%) taking pimavanserin as adjunctive therapy were included in the primary efficacy analysis. The MGH ATRQ revealed that 14 (58.3%) of 24 patients included in the adjunctive therapy group reported, a maximum improvement <50% with their existing antidepressant medication at screening and 10 (41.7%) of 24 patients reported a maximum improvement of 50% to <75%. Patients had been taking antidepressant medication for a minimum of 3 months, and the mean (SE) duration of antidepressant use was 49.0 (12.68) months. For those who discontinued a second antidepressant, the second antidepressant was discontinued within the 21-day screening period prior to the baseline visit. In patients in the adjunctive therapy group, the baseline mean (SD) HAMD-17 score was 19.2 (3.8), with a range of 15 to 27.
Twenty-one patients (46.7%) who received pimavanserin as monotherapy were included in the primary efficacy analysis. In these patients, baseline mean (SD) HAMD-17 score was 19.1 (2.1), with a range of 16 to 23.
Changes in depressive symptoms in PD
In the primary analysis, which included both monotherapy and adjunctive therapy, patients showed a significant improvement in depression symptoms, as indicated by a significant reduction in the HAMD-17 score at week 8 (LS mean [SE] change, –10.8 [0.63]; 95% CI, –12.0 to –9.5; p < 0.0001), with significant improvement seen as early as week 2 (–7.3 [0.85]; 95% CI, –9.0 to –5.6; p < 0.0001) (Fig. 2A). Patients showed significant improvement on all 17 individual items of the HAMD-17 in the post hoc analysis (Fig. 2B).
Fig. 2
Change from baseline in HAMD-17 (A) total score over 8 weeks and (B) individual item scores at week 8 in all patients included in efficacy analyses. BL, baseline; HAMD-17, Hamilton Depression Scale–17-item version; LS, least squares; SE, standard error.
Patients receiving pimavanserin as monotherapy showed significant improvement in depression symptoms, as indicated by a reduction at week 8 in the HAMD-17 (LS mean [SE] change, –11.2 [0.99]; 95% CI, –13.3 to –9.1; p < 0.0001). Again, significant improvements were seen starting at week 2 (Fig. 3A). Patients receiving pimavanserin as adjunctive therapy also exhibited a significant reduction in HAMD-17 score at week 8 (LS mean [SE] change, –10.2 [0.78]; 95% CI, –11.8 to –8.6; p < 0.0001), with significant improvement starting at week 2 (Fig. 3B).
Fig. 3
Change in HAMD-17 from baseline by treatment with pimavanserin as (A) monotherapy and (B) adjunctive therapy. BL, baseline; HAMD-17, Hamilton Depression Scale–17-item version; LS, least squares; SE, standard error.
By week 2, 16 of 45 patients (35.6%; 95% CI, 23.2 to 50.2) showed a response to treatment (HAMD-17 improvement ≥50% from baseline). This level of improvement was observed in 22 patients (48.9%; 95% CI, 35.0 to 63.0) at week 4, 25 patients (55.6%; 95% CI, 41.2 to 69.1) at week 6, and 27 patients (60.0%; 95% CI, 45.5 to 73.0) at week 8. Remission (HAMD-17 score ≤7) was achieved by 10 of 45 patients (22.2%; 95% CI, 12.5 to 36.3) at week 2, 14 patients (31.1%; 95% CI, 19.5 to 45.7) at week 4, and 20 patients (44.4%; 95% CI, 30.9 to 58.8) at weeks 6 and 8. Two patients at week 2 and 6 patients at weeks 4 and 6 were imputed as nonresponders/nonremitters, respectively.
Changes in secondary clinical outcomes
In the overall study population, symptom severity was decreased, as indicated by a LS mean [SE] change from baseline at week 8 in the CGI-S of –1.7 [0.16] (95% CI, –2.1 to –1.4; p < 0.0001) (Fig. 4A), though the significance level for all secondary outcomes was not adjusted for pre-planned multiple comparisons. Consistent with this, the CGI-I score also indicated improvement following 8 weeks of pimavanserin treatment (LS mean [SE], 2.0 [0.16]; 95% CI, 1.7 to 2.3) (Fig. 4B). Reductions were also observed for both monotherapy and adjunctive therapy (Table 2).
Fig. 4
Impact on (A) CGI-S and (B) CGI-I scores over 8 weeks in all patients included in efficacy analyses. BL, baseline; CGI-I, Clinical Global Impression–Improvement; CGI-S, Clinical Global Impression–Severity; LS, least squares; SE, standard error.
Table 2
Change in CGI-S and CGI-I scores over 8 weeks of treatment with pimavanserin as monotherapy vs adjunctive therapy
| Monotherapy | Adjunctive Therapy | |||
| CGI-S | n | Change from baseline | n | Change from baseline |
| LS mean (SE) | LS mean (SE) | |||
| Week 2 | 20 | –1.1 (0.18) | 23 | –0.9 (0.23) |
| Week 4 | 20 | –1.5 (0.19) | 19 | –1.5 (0.21) |
| Week 6 | 18 | –1.7 (0.20) | 21 | –1.5 (0.18) |
| Week 8 | 19 | –1.9 (0.21) | 20 | –1.6 (0.22) |
| CGI-I | n | LS mean (SE) | n | LS mean (SE) |
| Week 2 | 19 | 2.4 (0.21) | 23 | 2.6 (0.26) |
| Week 4 | 20 | 2.1 (0.20) | 19 | 2.3 (0.23) |
| Week 6 | 18 | 1.9 (0.19) | 21 | 2.2 (0.22) |
| Week 8 | 19 | 1.8 (0.20) | 20 | 2.2 (0.25) |
Clinicians rated the severity of the patient’s depression and improvement of symptoms from baseline on a scale of 1–7, with lower scores indicating improvement. CGI-I, Clinical Global Impression–Improvement; CGI-S, Clinical Global Impression–Severity; LS, least squares; SE, standard error.
Patients also reported an improvement in sleep quality. LS mean [SE] change from baseline in GS quality (SCOPA-GS) at week 8 was –1.0 [0.23] (95% CI, –1.5 to –0.6; p < 0.0001) (Fig. 5A). Both NS (SCOPA-NS; LS mean [SE], –2.1 [0.48], 95% CI, –3.1 to –1.1; p < 0.0001) (Fig. 5B) and DS (SCOPA-DS; LS mean [SE], –2.2 [0.33], 95% CI, –2.8 to –1.5; p < 0.0001) (Fig. 5C) were also improved at week 8. Similarly, pimavanserin treatment improved caregivers’ perception of patients’ quality of life, as indicated by an increase from baseline in EQ-5D-5L-VAS score at week 8 (LS mean [SE], 7.0 [2.46]; 95% CI, 2.1 to 12.0; p = 0.0068) (Fig. 6).
Fig. 5
Change from baseline to week 8 in (A) SCOPA-GS, (B) SCOPA-NS, and (C) SCOPA-DS in all patients included in efficacy analyses. BL, baseline; LS, least squares; SCOPA-DS, Scale for Outcomes in Parkinson’s Disease–daytime sleepiness; SCOPA-GS, Scale for Outcomes in Parkinson’s Disease–global sleep; SCOPA-NS, Scale for Outcomes in Parkinson’s Disease–nighttime sleep; SE, standard error.
Fig. 6
Change from baseline to week 8 in EQ-5D-5L-VAS in all patients included in efficacy analyses. BL, baseline; EQ-5D-5L-VAS, EuroQol-5 Dimensions-5 Levels version 1 visual analog scale; LS, least squares; SE, standard error.
Safety
The safety analyses included 47 patients. Twenty-one patients experienced 42 TEAEs, with most in the system organ classes (SOC) of gastrointestinal (n = 7, 14.9%) and psychiatric (n = 7, 14.9%). The most common events by preferred term, across all SOC, were fall (n = 4, 8.5%), nausea (n = 3, 6.4%), diarrhea (n = 2, 4.3%), edema (n = 2, 4.3%), skin abrasion (n = 2, 4.3%), and urinary tract infection (n = 2, 4.3%) (Table 3). Twelve events in 8 patients were considered to be related to treatment. One serious TEAE of colitis was reported and was not considered to be related to treatment. No deaths were reported.
Table 3
Summary of treatment-emergent adverse events
| Patients with Treatment-Emergent Adverse Events (TEAEs), n (%) | Safety Population (N = 47) |
| Any TEAE | 21 (44.7) |
| Any serious TEAE | 1 (2.1) |
| TEAEs by MedDRA preferred term | |
| Fall | 4 (8.5) |
| Nausea | 3 (6.4) |
| Diarrhea | 2 (4.3) |
| Edema | 2 (4.3) |
| Skin abrasion | 2 (4.3) |
| Urinary tract infection | 2 (4.3) |
| Abdominal pain | 1 (2.1) |
| Abnormal dreams | 1 (2.1) |
| Blood glucose increased | 1 (2.1) |
| Blood pressure increased | 1 (2.1) |
| Colitis | 1 (2.1) |
| Constipation | 1 (2.1) |
| Contusion | 1 (2.1) |
| Dizziness | 1 (2.1) |
| Gastritis | 1 (2.1) |
| Gout | 1 (2.1) |
| Hallucination, auditory | 1 (2.1) |
| Hallucination, visual | 1 (2.1) |
| Hypertonia | 1 (2.1) |
| Hypothyroidism | 1 (2.1) |
| Illusion | 1 (2.1) |
| Insomnia | 1 (2.1) |
| Laceration | 1 (2.1) |
| Mental impairment | 1 (2.1) |
| Muscle strain | 1 (2.1) |
| Non-cardiac chest pain | 1 (2.1) |
| Palpitations | 1 (2.1) |
| Peripheral swelling | 1 (2.1) |
| Presyncope | 1 (2.1) |
| Rapid eye movement sleep behavior | 1 (2.1) |
| disorder | |
| Suicidal ideation | 1 (2.1) |
| Supraventricular extrasystoles | 1 (2.1) |
| Vomiting | 1 (2.1) |
MedDRA, Medical Dictionary for Regulatory Activities, Version 20.0.
No change from baseline was observed in cognitive function, as measured by the MMSE, at either week 4 (LS mean [SE], 0.3 [0.26]; p = 0.2078) or week 8 (LS mean [SE], 0.4 [0.25]; p = 0.1266). Furthermore, no clinically significant changes induced by pimavanserin regarding cardiovascular safety were reported. No patients exhibited a QTcF of >500 ms or a change from baseline of >60 ms at any point during the study. At baseline, the mean (SE) QTcF interval was 411.0 (3.01) ms. After 8 weeks of pimavanserin treatment, the mean (SE) QTcF interval was 416.8 (3.33) ms, with a mean change from baseline of 8.4 (2.26) ms (range, –18 to 39).
In the safety analysis, no negative effect of pimavanserin on motor function was observed. In contrast, we observed a statistically significant improvement in motor function, as measured by the MDS-UPDRS III, at both week 4 (p = 0.0023) and week 8 (p = 0.0007) (Fig. 7).
Fig. 7
Change from baseline to week 8 in MDS-UPDRS Part III in all patients included in safety analysis. BL, baseline; LS, least squares; MDS-UPDRS Part III, Movement Disorder Society (MDS)-sponsored revision of the Unified Parkinson’s Disease Rating Scale (UPDRS) Part III; SE, standard error.
DISCUSSION
These data from a single-arm, open-label 8-week study suggest that pimavanserin is associated with early and sustained improvement of depression symptoms in patients with PD. By week 8, 60.0% of patients showed ≥50% improvement in symptoms on the HAMD-17, and 44.4% of patients reached remission (HAMD-17 score ≤7) at week 6, which was sustained through week 8. Further, similar improvements were seen in patients administered pimavanserin as monotherapy and patients administered pimavanserin as adjunctive therapy with an SSRI or SNRI. Treatment was associated with improvements in global assessments of disease severity, quality of sleep, and overall quality of life.
Few studies evaluating currently approved antidepressants for the treatment of PD patients with depression have been conducted, and these studies have shown no or marginal improvement of depressive symptoms [4, 7]. Importantly, antidepressant treatments may take several weeks to achieve efficacy for those who do experience some therapeutic benefits [27]. The latency period between the initiation treatment and the onset of the therapeutic benefit exacerbates the public health burden and increases risks for suicide or self-harm [27]. In this study, improvements in depressive symptoms emerged by the first study visit, 2 weeks after the start of treatment, with continued improvement throughout the 8-week study. These results suggest that pimavanserin has the potential for rapid antidepressant efficacy in patients with PD.
Management of depression in patients with PD is a critical component of treatment that influences quality of life [3]. Although the HAMD-17 was not developed primarily for use in PD patients and includes some questions about symptoms that may overlap with the symptoms of PD [18], it has good sensitivity in PD populations [28–30]. Patients in in this study exhibited stable symptoms of PD but strong improvements on the HAMD-17 following pimavanserin treatment. Consistent with this, patients also experienced improvements on both physician-reported and patient-reported outcomes, such as the CGI and the SCOPA.
Pimavanserin was well tolerated and safety outcomes were consistent with those from other studies of pimavanserin treatment in patients with PD [31, 32]. The most common TEAEs were fall, nausea, diarrhea, edema, skin abrasion, and urinary tract infection. Interestingly, an improvement in motor function was observed, as indicated by an LS mean reduction from baseline to week 8 of 5.1 on the MDS-UPDRS Part III.
Although the pimavanserin treatment results compared with baseline were robust and were consistent with improvements seen in the recent placebo-controlled trial showing efficacy for pimavanserin as an adjunctive treatment in MDD [15], this study was an open-label, single-arm design trial. Because eligible patients were required to have depressive symptoms based on HAMD-17 score, regression to the mean may have contributed to improvements observed on this measure, although the consistent improvement observed across measures supports the strength of the results. The small sample size and lack of a placebo comparator group in this study limit the generalizability of the results. Placebo-controlled studies will be needed to further determine the efficacy of pimavanserin in treating depression in patients with PD.
Patients with PD represent a clinical population with an unmet need for effective pharmacotherapies to improve depressive symptoms. Overall, these results suggest that pimavanserin treatment may be a potential therapeutic opportunity for further evaluation for improvement of depression in patients with PD.
Disclosures
DD, BC, LJ, RN, VA: are employees of and hold stock and/or stock options in ACADIA Pharmaceuticals Inc.
JCN: was an employee of ACADIA Pharmaceuticals Inc. at the time of this study.
GA: has received research support from Accera, Allergan, Axovant, Eisai, Genentech, Intra- Cellular, Janssen, Lundbeck, Neurim, Neurotrope, Novartis, Otsuka, Roche, Suven, and TransTech and has served on the speakers bureau or as a consultant for ACADIA, Alkermes, Allergan, Avanir, Janssen, Lundbeck, Merck, Nestlé, Otsuka, Sunovion, Takeda, and Vanda.
JLA: has received research support from Abbott, AbbVie, ACADIA, Biogen, Boston Scientific, Denali, Impax, NeuroDerm, Sunovion, and Theravance and has received honoraria from Abbott, AbbVie, Acorda, Adamas, Allergan, Boston Scientific, Medtronic, Teva, and US WorldMeds.
MC is a consultant to ACADIA, Kyowa Kirin, Sunovion, and Reviva.
Data sharing statement
Data available on request from authors: The data that support the findings of this study are available from the corresponding author upon reasonable request.
ACKNOWLEDGMENTS
The authors gratefully acknowledge the patients and clinicians who participated in this study. ACADIA Pharmaceuticals Inc. (San Diego, CA, USA) provided funding for medical writing and editorial support in the development of this manuscript. Meghan Jones, PhD (Ashfield Healthcare Communications, Middletown, CT) provided writing support based on input from authors, and Mary Kacillas and Dena McWain (Ashfield Healthcare Communications) copyedited and styled the manuscript per journal requirements.
SUPPLEMENTARY MATERIAL
[1] The supplementary material is available in the electronic version of this article: https://dx.doi.org/10.3233/JPD-202058.
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