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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.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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

Other trials in United States

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

Other trials in Ukraine

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

Other trials in Russia

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

Other trials in Bulgaria

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

Other trials in Hungary

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

Other trials in Czechia

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

Other trials in Serbia

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

Other trials in Poland

Spain5 sites
  • Study site

    Barcelona, 08830

  • Study site

    Madrid, 28007

  • Study site

    Oviedo, 33011

  • Study site

    Valladolid, 47016

  • Study site

    Zamora, 49021

Other trials in Spain

Canada4 sites
  • Study site

    Chatham, Ontario, N7L1C1

  • Study site

    Montreal, Quebec, H3QA 1A1

  • Study site

    Penticton, British Columbia, V2A4M4

  • Study site

    Toronto, M6J 1H4

Other trials in Canada

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 groups in NCT02970305
Study groupRoleWhat they receive
PimavanserinExperimentalDrug- pimavanserin 34 mg, 20 mg, or 10 mg taken as two tablets + background antipsychotic, once daily by mouth
Receives: Drug: Pimavanserin
PlaceboPlacebo comparatorPlacebo, 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.

  1. 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)
  1. 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

  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. 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

  9. 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

  10. 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

  11. 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

  12. 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.

  1. First posted22 Nov 2016 (estimated)
  2. Study start4 Nov 2016
  3. Primary completion16 Oct 2019
  4. Study completion28 Oct 2019

Resources

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)
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
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 38264323
  • Darwish 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 36190440
  • Bugarski-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

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.

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