SchizophreniaPhase 2NCT02970305
Efficacy and Safety of Pimavanserin as Adjunctive Treatment for the Negative Symptoms of Schizophrenia (ADVANCE)
A Phase 2 study testing Pimavanserin in people with Schizophrenia, run by ACADIA Pharmaceuticals Inc. at 101 sites in 10 countries.
Trial summary
To evaluate the efficacy and safety of adjunctive pimavanserin compared with adjunctive placebo in the treatment of the negative symptoms of schizophrenia Read more about this study
- Who is it for?
- Ages 18 to 55 years
- Conditions the study is for
- Schizophrenia
- What is being tested?
- Pimavanserin
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 403 participants
- Where
- 101 sitesin 10 countries
- Study dates
- 4 Nov 2016to 28 Oct 2019
- Phase
- Phase 2
- 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 18 to 55 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Adult patients, between 18 and 55 years of age
- A clinical diagnosis of schizophrenia with a minimum duration of 1 year
- Has predominant negative symptoms according to predefined study criteria
- The main background antipsychotic with which the subject is being treated must be one of the antipsychotics listed below:
- Aripiprazole
- Aripiprazole long-acting injectables:
Show all 15Show fewer
- Abilify Maintena®
- Aristada®
- Risperidone
- Risperidone long-acting injection
- Olanzapine
- Lurasidone
- Cariprazine
- Brexpiprazole
- Asenapine
Who cannot join
- Patient has a psychiatric disorder other than schizophrenia
- A urine drug screen (UDS) result at Baseline that indicates the presence of any tested prohibited substance of potential abuse, except marijuana
- Patients with a result indicating the presence of marijuana are permitted if they agree to abstain from marijuana use during the study and the medical monitor approves the subject's participation
- Patient has current evidence of a serious and/or unstable psychiatric, neurologic, cardiovascular, respiratory, gastrointestinal, renal, hepatic, hematologic, or other medical disorder, including cancer or malignancies, which would affect the patient's ability to participate in the program
- Patient has had a myocardial infarction in the last six months
- Patient has a family or personal history or symptoms of long QT syndrome
- Patient has been hospitalized due to inadequate family support or care at the patient's primary residence, during the 8 weeks prior to screening
- Patients will be evaluated at screening to ensure that all criteria for study participation are met. Patients may be excluded from the study based on these assessments (and specifically if it is determined that their baseline health and psychiatric condition do not meet all pre-specified entry criteria).
Trial locations and contacts
101 sites in 10 countries.
101 sites in 10 countries
United States33 sites
Study site
Albuquerque, New Mexico, 87109
Study site
Ann Arbor, Michigan, 48105
Study site
Atlanta, Georgia, 30328
Study site
Atlanta, Georgia, 30331
Study site
Bellflower, California, 90706
Study site
Berlin, New Jersey, 08009
Study site
Charleston, South Carolina, 29407
Study site
Charlotte, North Carolina, 28211
Study site
Chicago, Illinois, 60611
Study site
Decatur, Georgia, 30030
Study site
Downingtown, Pennsylvania, 19335
Study site
Durham, North Carolina, 27704
Study site
Hialeah, Florida, 33016
Study site
Hoffman Estates, Illinois, 60169
Study site
Irving, Texas, 75062
Study site
Las Vegas, Nevada, 89102
Study site
Lauderhill, Florida, 33319
Study site
Lemon Grove, California, 91945
Study site
Marietta, Georgia, 30060
Study site
Miami, Florida, 33122
Study site
Miami, Florida, 33136
Study site
Norwalk, California, 90650
Study site
Oklahoma City, Oklahoma, 73116
Study site
Phoenix, Arizona, 85012
Study site
Richardson, Texas, 75080
Study site
Rochester, New York, 14618
Study site
Rogers, Arkansas, 72758
Study site
San Diego, California, 92103
Study site
San Diego, California, 92123
Study site
Santa Ana, California, 92705
Study site
Tampa, Florida, 33613
Study site
Torrance, California, 90502
Study site
Wichita, Kansas, 67214
Ukraine15 sites
Study site
Dnipro, 49005
Study site
Hlevakha, 08631
Study site
Kharkiv, 61068
Study site
Kherson, 73488
Study site
Kyiv, 01133
Study site
Kyiv, 02192
Study site
Kyiv, 04080
Study site
Kyiv, 08631
Study site
Lviv, 79017
Study site
Lviv, 79021
Study site
Odesa, 65014
Study site
Oleksandrivka, 67513
Study site
Poltava, 36013
Study site
Smila, 20708
Study site
Vinnytsia, 21005
Russia11 sites
Study site
Plekhanovo, Lipetsk Oblast, 399313
Study site
Roshchino, Leningradskaya Oblast', 188820
Study site
Saint Petersburg, 192019
Study site
Saint Petersburg, 193167
Study site
Saint Petersburg, 195112
Study site
Saint Petersburg, 197341
Study site
Samara, 443016
Study site
Smolensk, 214019
Study site
Stavropol, 355000
Study site
Yaroslavl, 150003
Study site
Yekaterinburg, 620030
Bulgaria8 sites
Study site
Plovdiv, 4000
Study site
Sofia, 1202
Study site
Sofia, 1408
Study site
Sofia, 1431
Study site
Sofia, 1680
Study site
Targovishte, 7700
Study site
Tserova Koria, 5047
Study site
Varna, 9020
Hungary8 sites
Study site
Budapest, Pest County, 1036
Study site
Budapest, Pest County, 1083
Study site
Budapest, 1084
Study site
Budapest, 1135
Study site
Debrecen, 4032
Study site
Gyula, 5700
Study site
Kalocsa, Bács-Kiskun Megya, 6300
Study site
Pécs, 7633
Czechia6 sites
Study site
Hradec Králové, Vekose, 50341
Study site
Pilsen, 31200
Study site
Prague, 10000
Study site
Prague, 10600
Study site
Prague, 16000
Study site
Říčany, 25101
Serbia6 sites
Study site
Belgrade, 11 000
Study site
Belgrade, 11000
Study site
Kovin, 26 220
Study site
Kovin, 26220
Study site
Kragujevac, 34 000
Study site
Niš, 18 000
Poland5 sites
Study site
Bialystok, 15-756
Study site
Bydgoszcz, 85-080
Study site
Lublin, 20-080
Study site
Lublin, 20-582
Study site
Pruszcz Gdański, 83-000
Spain5 sites
Study site
Barcelona, 08830
Study site
Madrid, 28007
Study site
Oviedo, 33011
Study site
Valladolid, 47016
Study site
Zamora, 49021
Canada4 sites
Study site
Chatham, Ontario, N7L1C1
Study site
Montreal, Quebec, H3QA 1A1
Study site
Penticton, British Columbia, V2A4M4
Study site
Toronto, M6J 1H4
About this study
Official title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Pimavanserin as Adjunctive Treatment for the Negative Symptoms of Schizophrenia
To evaluate the efficacy and safety of adjunctive pimavanserin compared with adjunctive placebo in the treatment of the negative symptoms of schizophrenia
- Conditions
- Schizophrenia
- Being tested
- Pimavanserin, Placebo
- Medical subject headings
- Schizophrenia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PimavanserinDrug
Pimavanserin 34 mg, 20 mg, or 10 mg, taken as two tablets, once daily by mouth
PlaceboDrug
Placebo, taken as two tablets, once daily by mouth
| Study group | Role | What they receive |
|---|---|---|
| Pimavanserin | Experimental | Drug- pimavanserin 34 mg, 20 mg, or 10 mg taken as two tablets + background antipsychotic, once daily by mouth Receives: Drug: Pimavanserin |
| Placebo | Placebo comparator | Placebo, taken as two tablets + background antipsychotic, once daily by mouth Receives: Drug: Placebo |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change From Baseline to Week 26 in the Negative Symptom Assessment-16 (NSA-16) Total Score
The NSA-16 is a semi-structured interview and a validated scale containing 16 items for evaluating negative symptoms of schizophrenia, i.e. the reduction or absence of emotional expression and volitional behaviors normally present in a healthy person. Items are scored based on behaviors during the interview (items 1-4, 6, 7, 9, 11, 15, 16) or previous 7 days (items 5, 8, 10, 12-14) on a 6-point scale from 1 to 6. The NSA-16 total score is the sum of item scores. It can range from 16 to a maximum of 96, with higher scores denoting more severe negative symptoms in schizophrenia.
Measured: From baseline to Week 26
Secondary outcomes (12)
Change From Baseline to Week 26 in the Personal and Social Performance Scale (PSP) Score
The PSP is a validated 100-point (1 to100) single-item rating scale to assess the psychosocial functioning of subjects with schizophrenia. Ratings are based on 4 main areas i.e. (a) socially useful activities, including work and study; (2) personal and social relationships, (3) self-care; and (4) disturbing and aggressive behaviors. The time period assessed is "past month". Higher scores denote better psychosocial functioning
Measured: From baseline to Week 26
Proportion of Negative Symptom Assessment-16 (NSA-16) Responders at Week 26
The NSA-16 is a semi-structured interview and a validated scale containing 16 items for evaluating negative symptoms of schizophrenia, i.e. the reduction or absence of emotional expression and volitional behaviors normally present in a healthy person. Items are scored based on behaviors during the interview (items 1-4, 6, 7, 9, 11, 15, 16) or previous 7 days (items 5, 8, 10, 12-14) on a 6-point scale from 1 to 6. The NSA-16 total score is the sum of item scores. It can range from 16 to a maximum of 96, with higher scores denoting more severe negative symptoms in schizophrenia.
NSA-16 responders were defined as patients with at least 20, 30, 50, or 75% percentage improvement in NSA-16 total score from baseline.
Measured: From baseline to Week 26
Change From Baseline to Week 26 in NSA-16 Global Negative Symptoms Rating
The global negative symptoms rating of the NSA-16 assesses overall severity on a 7-point scale from 1 to 7, with higher scores denoting more severe negative symptoms in schizophrenia.
Measured: From baseline to Week 26
Change From Baseline (CFB) to Week 26 in NSA-16 Domain Scores
The NSA-16 is a semi-structured interview and a validated scale containing 16 items for evaluating negative symptoms of schizophrenia, i.e. the reduction or absence of emotional expression and volitional behaviors normally present in a healthy person. Items are scored based on behaviors during the interview (items 1-4, 6, 7, 9, 11, 15, 16) or previous 7 days (items 5, 8, 10, 12-14) on a 6-point scale from 1 to 6. The NSA-16 domain scores are the sum of item scores in each domain i.e. communication (min score 4, max score 24), emotion/affect (min 3, max 18), social involvement (min 3, max 18), motivation (min 4, max 24), and retardation (min 2, max 12); with higher scores denoting more severe negative symptoms in schizophrenia.
Measured: From baseline (BL) to Week 26
Change From Baseline to Week 26 in the Clinical Global Impression of Schizophrenia Scale-Severity (CGI-SCH-S) of Negative Symptoms Score
The CGI-SCH-S is a clinician-rated, 7-point scale to evaluate positive, negative, depressive, cognitive symptoms and overall severity in schizophrenia. For the purpose of this study, only the negative symptoms were evaluated. The score could range from 1 (normal, not ill) to 7 (among the most severely ill).
Measured: From baseline to Week 26
Clinical Global Impression of Schizophrenia Scale-Improvement (CGI-SCH-I) of Negative Symptoms Score at Week 26
The CGI-SCH-I is a clinician-rated, 7-point scale to evaluate change from baseline in positive, negative, depressive, cognitive symptoms and overall severity in schizophrenia. For the purpose of this study, only the changes in negative symptoms from baseline were evaluated. The score could range from 1 (very much improved) to 7 (very much worse).
Measured: From baseline to Week 26
Proportion of CGI-SCH-I Responders (CGI-SCH-I Score of 1 or 2) at Week 26; Observed Cases
The CGI-SCH-I is a clinician-rated, 7-point scale that is designed to evaluate change from baseline in positive, negative, depressive, cognitive symptoms and overall severity in schizophrenia. For the purpose of this study, only the changes in negative symptoms from baseline were evaluated. The 7-point scores range from 1 (very much improved) to 7 (very much worse); responders were defined as those with CGI-SCH-I of 1 or 2.
The analysis includes observed cases; missing cases were not imputed.
Measured: From baseline to Week 26
Change From Baseline to Week 26 in the Positive and Negative Syndrome Scale (PANSS) Total Score
The PANSS is a 30-item scale to evaluate the presence, absence, and severity of schizophrenia symptoms. Items are scored over the past week (7 days) on a 7-point scale from 1 (absent) to 7 (extreme). The PANSS total score is the sum of scores and ranges from a minimum of 30 to a maximum of 210. Higher scores denote more severe symptoms.
Measured: From baseline to Week 26
Change From Baseline (CFB) to Week 26 in PANSS Subscale Scores
The PANSS is a 30-item scale to evaluate the presence, absence, and severity of schizophrenia symptoms. Items are scored over the past week (7 days) on a 7-point scale from 1 (absent) to 7 (extreme). The PANSS has 3 subscales that are the sums of the respective item scores, including the positive scale (min 7, max 49), negative scale (min 7, max 49), and general psychopathology scale (min 16, max 112). Higher scores denote more severe symptoms.
Measured: From baseline (BL) to Week 26
Change From Baseline to Week 26 in Brief Assessment of Cognition in Schizophrenia (BACS) Composite Score
The BACS is a performance-based assessment of treatment-related changes in cognition, assessing 6 domains of verbal memory and learning; working memory; motor function; verbal fluency; attention and speed of processing; and executive function. The 6 domains with their raw scores are: verbal memory 0-75; digit sequencing 0-28; token motor 0-100; verbal fluency 0-225; symbol coding 0-110; Tower of London 0-22. For each domain, higher scores reflect better cognition. Raw scores are converted to age and sex-corrected normalized scores. The BACS composite score is calculated as the mean of the normalized scores from the 6 subscale scores, standardized so that the mean of the BACS composite score in the healthy normative sample is 50 and the standard deviation is 10.
Measured: From baseline to Week 26
Change From Baseline to Week 26 in 10-item Drug Attitude Inventory (DAI-10) Score
The DAI-10 contains 6 items (1, 3, 4, 7, 9, and 10) that a subject who is fully adherent to the prescribed medication would answer as "True" and 4 items (2, 5, 6, and 8) that a subject who is fully adherent to the prescribed medication would answer as "False." A correct answer is scored +1 and an incorrect answer is scored -1. The total score is the sum of pluses and minuses, which can range from -10 to 10 in increments of 2. A positive total score indicates a positive subjective response (adherent) and a negative total score indicates a negative subjective response (non-adherent). Higher scores denote better adherence.
Measured: From baseline to Week 26
Change From Baseline to Week 26 in Karolinska Sleepiness Scale (KSS) Score
The KSS is a self-reported subjective measure of a subject's level of drowsiness. Respondents must choose statements that most accurately describe their level of sleepiness over the past 7 days. Scoring was based on a 9-point verbally anchored scale ranging from 1 (extremely alert) to 9 (very sleepy, great effort to keep awake, fighting sleep). Higher scores denoted more drowsiness.
Measured: From baseline to Week 26
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Nov 2016 (estimated)
- Study start4 Nov 2016
- Primary completion16 Oct 2019
- Study completion28 Oct 2019
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 (3)Papers the sponsor has linked to this study.
- Other trials for SchizophreniaStudies of the same condition, open and under way.
- 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 2
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 403 participants (actual)
Sponsor and investigators
- Lead sponsor
- ACADIA Pharmaceuticals Inc.
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02970305
- Sponsor's protocol ID
- ACP-103-038
- Other IDs
- 2016-003436-20, 2016
- Status last verified
- Dec 2020
- First submitted
- 18 Nov 2016
- Last updated
- 22 Dec 2020
- Results posted
- Yes, on ClinicalTrials.gov
- Data monitoring committee
- Yes
- Individual data sharing
- No
Publications
Bugarski-Kirola D, Abbs B, Odetalla R, Liu IY, Darwish M, DeKarske D. Adherence to Background Antipsychotic and Pimavanserin in Patients with Schizophrenia: Post Hoc Analyses from the ENHANCE and ADVANCE Studies. Patient Prefer Adherence. 2024 Jan 19;18:207-216. doi: 10.2147/PPA.S436041. eCollection 2024.
PubMed 38264323Darwish M, Bugarski-Kirola D, Passarell J, Owen J, Jaworowicz D, DeKarske D, Stankovic S. Pimavanserin Exposure-Response Analyses in Patients With Schizophrenia: Results From the Phase 2 ADVANCE Study. J Clin Psychopharmacol. 2022 Nov-Dec 01;42(6):544-551. doi: 10.1097/JCP.0000000000001611. Epub 2022 Oct 3.
PubMed 36190440Bugarski-Kirola D, Arango C, Fava M, Nasrallah H, Liu IY, Abbs B, Stankovic S. Pimavanserin for negative symptoms of schizophrenia: results from the ADVANCE phase 2 randomised, placebo-controlled trial in North America and Europe. Lancet Psychiatry. 2022 Jan;9(1):46-58. doi: 10.1016/S2215-0366(21)00386-2. Epub 2021 Nov 30.
PubMed 34861170
Study at a glance
From the registry record, last updated by the sponsor on 22 Dec 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Pimavanserin as Adjunctive Treatment for the Negative Symptoms of Schizophrenia
- ClinicalTrials.gov ID
- NCT02970305
- Acronym / sponsor ID
- ACP-103-038
- Conditions
- Schizophrenia
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 403 participants (actual)
- Lead sponsor
- ACADIA Pharmaceuticals Inc.Industry (pharma, biotech, devices)
- Study start
- 4 Nov 2016 (actual)
- Primary completion
- 16 Oct 2019 (actual)
- Study completion
- 28 Oct 2019 (actual)
- First posted
- 22 Nov 2016 (estimated)
- Results
- Posted 22 Dec 2020
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To evaluate the efficacy and safety of adjunctive pimavanserin compared with adjunctive placebo in the treatment of the negative symptoms of schizophrenia
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Pimavanserin | Experimental | Drug: PimavanserinDrug- pimavanserin 34 mg, 20 mg, or 10 mg taken as two tablets + background antipsychotic, once daily by mouth |
| Placebo | Placebo comparator | Drug: PlaceboPlacebo, taken as two tablets + background antipsychotic, once daily by mouth |
Who may qualify
- Ages
- 18 to 55 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (15 listed)
- Adult patients, between 18 and 55 years of age
- A clinical diagnosis of schizophrenia with a minimum duration of 1 year
- Has predominant negative symptoms according to predefined study criteria
- The main background antipsychotic with which the subject is being treated must be one of the antipsychotics listed below:
Key exclusion criteria (8 listed)
- Patient has a psychiatric disorder other than schizophrenia
- A urine drug screen (UDS) result at Baseline that indicates the presence of any tested prohibited substance of potential abuse, except marijuana
- Patient has current evidence of a serious and/or unstable psychiatric, neurologic, cardiovascular, respiratory, gastrointestinal, renal, hepatic, hematologic, or other medical disorder, including cancer or malignancies, which would affect the patient's ability to participate in the program
- Patient has had a myocardial infarction in the last six months
- Patient has a family or personal history or symptoms of long QT syndrome
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 |
|---|---|---|
| PimavanserinPimavanserin 34 mg, 20 mg, or 10 mg, taken as two tablets, once daily by mouth | Drug | Pimavanserin |
| PlaceboPlacebo, taken as two tablets, once daily by mouth | Drug | Placebo |
Primary outcome
Change From Baseline to Week 26 in the Negative Symptom Assessment-16 (NSA-16) Total Score
Time frame: From baseline to Week 26
The NSA-16 is a semi-structured interview and a validated scale containing 16 items for evaluating negative symptoms of schizophrenia, i.e. the reduction or absence of emotional expression and volitional behaviors normally present in a healthy person. Items are scored based on behaviors during the interview (items 1-4, 6, 7, 9, 11, 15, 16) or previous 7 days (items 5, 8, 10, 12-14) on a 6-point scale from 1 to 6. The NSA-16 total score is the sum of item scores. It can range from 16 to a maximum of 96, with higher scores denoting more severe negative symptoms in schizophrenia.
12 secondary outcomes
Change From Baseline to Week 26 in the Personal and Social Performance Scale (PSP) Score
Time frame: From baseline to Week 26
Proportion of Negative Symptom Assessment-16 (NSA-16) Responders at Week 26
Time frame: From baseline to Week 26
Change From Baseline to Week 26 in NSA-16 Global Negative Symptoms Rating
Time frame: From baseline to Week 26
Change From Baseline (CFB) to Week 26 in NSA-16 Domain Scores
Time frame: From baseline (BL) to Week 26
Change From Baseline to Week 26 in the Clinical Global Impression of Schizophrenia Scale-Severity (CGI-SCH-S) of Negative Symptoms Score
Time frame: From baseline to Week 26
Clinical Global Impression of Schizophrenia Scale-Improvement (CGI-SCH-I) of Negative Symptoms Score at Week 26
Time frame: From baseline to Week 26
Proportion of CGI-SCH-I Responders (CGI-SCH-I Score of 1 or 2) at Week 26; Observed Cases
Time frame: From baseline to Week 26
Change From Baseline to Week 26 in the Positive and Negative Syndrome Scale (PANSS) Total Score
Time frame: From baseline to Week 26
Change From Baseline (CFB) to Week 26 in PANSS Subscale Scores
Time frame: From baseline (BL) to Week 26
Change From Baseline to Week 26 in Brief Assessment of Cognition in Schizophrenia (BACS) Composite Score
Time frame: From baseline to Week 26
Change From Baseline to Week 26 in 10-item Drug Attitude Inventory (DAI-10) Score
Time frame: From baseline to Week 26
Change From Baseline to Week 26 in Karolinska Sleepiness Scale (KSS) Score
Time frame: From baseline to Week 26
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Dec 2020.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- Derived from this study: PubMed 38264323Bugarski-Kirola D, Abbs B, Odetalla R, Liu IY, Darwish M, DeKarske D. Adherence to Background Antipsychotic and Pimavanserin in Patients with Schizophrenia: Post Hoc Analyses from the ENHANCE and ADVANCE Studies. Patient Prefer Adherence. 2024 Jan 19;18:207-216. doi: 10.2147/PPA.S436041. eCollection 2024.
- Derived from this study: PubMed 36190440Darwish M, Bugarski-Kirola D, Passarell J, Owen J, Jaworowicz D, DeKarske D, Stankovic S. Pimavanserin Exposure-Response Analyses in Patients With Schizophrenia: Results From the Phase 2 ADVANCE Study. J Clin Psychopharmacol. 2022 Nov-Dec 01;42(6):544-551. doi: 10.1097/JCP.0000000000001611. Epub 2022 Oct 3.
- Derived from this study: PubMed 34861170Bugarski-Kirola D, Arango C, Fava M, Nasrallah H, Liu IY, Abbs B, Stankovic S. Pimavanserin for negative symptoms of schizophrenia: results from the ADVANCE phase 2 randomised, placebo-controlled trial in North America and Europe. Lancet Psychiatry. 2022 Jan;9(1):46-58. doi: 10.1016/S2215-0366(21)00386-2. Epub 2021 Nov 30.
- Individual participant dataSharing planned: No
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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.
The record lists no contact. Use the official record to reach the sponsor.
101 sites in 10 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2 study testing Pimavanserin in people with Schizophrenia, run by ACADIA Pharmaceuticals Inc. at 101 sites in 10 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 15 inclusion and 8 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 22 Dec 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 101 sites in United States, Ukraine, Russia, Bulgaria, Hungary and 5 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. Some participants in this study may receive a placebo. 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 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
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 22 Dec 2020). 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?
Change From Baseline to Week 26 in the Negative Symptom Assessment-16 (NSA-16) Total Score (time frame: From baseline to Week 26). 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 NCT02970305, which also lists 3 linked publications.
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 22 Dec 2020.