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SchizophreniaPhase 3PROSIPALNCT01081769

Prevention of Relapse With Injectable Paliperidone Palmitate Versus Oral Antipsychotics

A Phase 3 study testing paliperidone palmitate injection and oral antipsychotics in people with Schizophrenia, run by Janssen-Cilag International NV at 94 sites in 25 countries.

Completed

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

Official record
Search all trials

Trial summary

The purpose of this study is to assess the efficacy (how well the drug works; primarily through the time to relapse) of long-acting injectable paliperidone palmitate compared to treatment as usual with orally administered antipsychotics in monotherapy over 24 months in the treatment of recently diagnosed (1-5 years… Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Schizophrenia
What is being tested?
paliperidone palmitate injection and oral antipsychotics
Could I receive a placebo?
No, everyone receives an active treatment
How many people
769 participants
Where
94 sitesin 25 countries
Study dates
Feb 2010to Feb 2013
Phase
Phase 3
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Have been meeting the diagnostic criteria for schizophrenia for 1 to 5 years before screening, and have a history of treatment with antipsychotics
  • Have a history of two or more relapses requiring psychiatric hospitalization in the preceding 24 months, which may include the current acute episode
  • Experiencing at screening an acute schizophrenic episode with a Positive And Negative Syndrome Scale (PANSS) total score at screening between 70 and 120, inclusive
  • Be healthy on the basis of physical examination, medical history and vital signs performed at screening
  • Woman must be postmenopausal (for at least 1 year) or surgically sterile or abstinent or be practicing an effective method of birth control, must agree to continue to use the same method of contraception throughout the study and must have a negative urine pregnancy test at screening
  • be able to fill out questionnaires
  • Men must agree to use a double barrier method of birth control and to not donate sperm during the study and for 3 months after receiving the last dose of study drug

Who cannot join

  • Patients that have never been treated with antipsychotics before
  • Treatment resistant patient and/or currently (i.within the last 3 months) treated with clozapine
  • Substance dependence within 6 months prior to entry and current intravenous drug use or abuse
  • allergies, hypersensitivity, or intolerance to risperidone or paliperidone or excipients
  • treatment with a long-acting injectable antipsychotic within three injection cycles prior to screening
  • newly started psychotherapy program within the two months preceding the treatment phase baseline
Show all 10Show fewer
  • evidence of clinically significant hepatic, renal, cardiac, vascular, pulmonary, gastrointestinal, endocrine, neurologic, hematologic, rheumatologic, psychiatric, or metabolic disturbances in the past 6 months (as determined by medical history, clinical laboratory or ECG results, or physical examination) that would increase the risk associated with taking study medication or would confound the interpretation of the study
  • history or current symptoms of tardive dyskinesia or neuroleptic malignant syndrome
  • involuntarily hospitalized patient
  • pregnant or breast-feeding females

Trial locations and contacts

94 sites in 25 countries.

94 sites in 25 countries

Ukraine11 sites
  • Study site

    Dnipropetrovsk

  • Study site

    Donetsk

  • Study site

    Hlevakha

  • Study site

    Kharkiv

  • Study site

    Kherson

  • Study site

    Kiev

  • Study site

    Lviv

  • Study site

    Odesa

  • Study site

    Poltava

  • Study site

    Simferopol

  • Study site

    Uzhhorod

Other trials in Ukraine

Russia8 sites
  • Study site

    Ekaterinburg Na

  • Study site

    Krasnodar

  • Study site

    Nizny Novgorod

  • Study site

    Saint Petersburg

  • Study site

    Samara

  • Study site

    Saratov

  • Study site

    Tomsk

  • Study site

    Yaroslavl

Other trials in Russia

France6 sites
  • Study site

    Colombes

  • Study site

    La Seyne-sur-Mer

  • Study site

    Limoges

  • Study site

    Metz

  • Study site

    Paris

  • Study site

    Saint-Avé

Other trials in France

Spain6 sites
  • Study site

    Barcelona

  • Study site

    Burgos

  • Study site

    Elche

  • Study site

    Madrid

  • Study site

    Sant Boi de Llobregat

  • Study site

    Zamora

Other trials in Spain

Czechia5 sites
  • Study site

    Brno

  • Study site

    Litoměřice

  • Study site

    Olomouc

  • Study site

    Prague

  • Study site

    Přerov

Other trials in Czechia

Israel5 sites
  • Study site

    Bat Yam

  • Study site

    Beer Yaakov

  • Study site

    Hod HaSharon

  • Study site

    Ramat Gan

  • Study site

    Tirat Hacarmel

Other trials in Israel

Romania5 sites
  • Study site

    Arad

  • Study site

    Bucharest

  • Study site

    Jebel

  • Study site

    Oradea

  • Study site

    Sibiu

Other trials in Romania

Belgium4 sites
  • Study site

    Bertrix

  • Study site

    Ghent

  • Study site

    Liège

  • Study site

    Ostend

Other trials in Belgium

Germany4 sites
  • Study site

    Berlin

  • Study site

    Bochum

  • Study site

    Mannheim

  • Study site

    München

Other trials in Germany

Hungary4 sites
  • Study site

    Budapest

  • Study site

    Kalocsa

  • Study site

    Nagykálló

  • Study site

    Sopron

Other trials in Hungary

Poland4 sites
  • Study site

    Chełmno

  • Study site

    Gdansk

  • Study site

    Torun

  • Study site

    Ząbki

Other trials in Poland

South Korea4 sites
  • Study site

    Goyang

  • Study site

    Incheon

  • Study site

    Kyounggi

  • Study site

    Seoul

Other trials in South Korea

United Kingdom4 sites
  • Study site

    Birmingham

  • Study site

    Exeter

  • Study site

    London

  • Study site

    Warrington

Other trials in United Kingdom

Bulgaria3 sites
  • Study site

    Burgas

  • Study site

    Plovdiv

  • Study site

    Radnevo

Other trials in Bulgaria

Slovakia3 sites
  • Study site

    Bratislava

  • Study site

    Michalovce

  • Study site

    Rimavská Sobota

Other trials in Slovakia

Taiwan3 sites
  • Study site

    Taichung

  • Study site

    Taipei

  • Study site

    Taoyuan

Other trials in Taiwan

Turkey (Türkiye)3 sites
  • Study site

    Istanbul

  • Study site

    Manisa Turkey

  • Study site

    Zonguldak

Other trials in Turkey (Türkiye)

Egypt2 sites
  • Study site

    Alexandria

  • Study site

    Cairo

Other trials in Egypt

Estonia2 sites
  • Study site

    Talinn

  • Study site

    Tartu

Other trials in Estonia

Lithuania2 sites
  • Study site

    Šiauliai

  • Study site

    Vilnius

Other trials in Lithuania

South Africa2 sites
  • Study site

    Cape Town

  • Study site

    Pretoria

Other trials in South Africa

Austria1 site
  • Study site

    Vienna

Other trials in Austria

Croatia1 site
  • Study site

    Zagreb

Other trials in Croatia

Greece1 site
  • Study site

    Thessalonikis

Other trials in Greece

Jordan1 site
  • Study site

    Amman

Other trials in Jordan

About this study

Official title: A 24-month, Prospective, Randomized, Active-Controlled, Open-Label, Rater-Blinded, Multicenter, International Study of the Prevention of Relapse Comparing Long-Acting Injectable Paliperidone Palmitate to Treatment as Usual With Oral Antipsychotic Monotherapy in Adults With Schizophrenia

The purpose of this study is to assess the efficacy (how well the drug works; primarily through the time to relapse) of long-acting injectable paliperidone palmitate compared to treatment as usual with orally administered antipsychotics in monotherapy over 24 months in the treatment of recently diagnosed (1-5 years since diagnosis) schizophrenia.

Read the detailed description

This is a randomized (study drug assigned by chance), open-label (both physician and patient know the name of the assigned drug), rater-blinded (the person who assesses the condition of the patient does not know the name of the assigned drug), active-controlled, parallel-group, multicenter, prospective international study of paliperidone palmitate versus treatment as usual with oral antipsychotic agents in monotherapy in the prevention of relapse (return of symptoms). Patients who have been recently diagnosed with schizophrenia (within 5 years) and are suffering from a schizophrenic relapse (return of symptoms of schizophrenia) will be enrolled. This study consists of a 2-week initial acute oral treatment phase, followed by a treatment phase (core phase) until relapse or up to maximally 24 months, whichever comes first. Prior to a 2-week oral treatment phase, patients will be randomly (by chance) assigned in a 1:1 ratio to receive treatment with paliperidone palmitate injection (once-monthly) or oral antipsychotic medication (daily). Patients randomized to paliperidone palmitate will first receive oral paliperidone ER once daily for 2 weeks followed by paliperidone palmitate injections at a dose of 150 mg eq. on Day 1, 100 mg eq. on Day 8 both in the deltoid muscle and 75 mg eq. on Day 38 and doses in a dose range of 25 to 150 mg eq. in either the deltoid or the gluteal muscle thereafter. Patients randomized to oral comparator arm will receive oral antipsychotics (haloperidol, paliperidone ER, risperidone, olanzapine, quetiapine or aripiprazole) as per investigator discretion and prescribed according to the label. Total treatment duration is maximally 24 months. During the 24 month treatment phase, investigators will be allowed to flexibly decrease or increase the dose of paliperidone palmitate with one dose level in the range of 25 to 150 mg eq. or the oral antipsychotic in the respective locally approved dose range, all according to the patient's clinical needs. The primary endpoint of the 24-month treatment phase will be the time to relapse. Safety will be monitored by evaluating Adverse Events (AEs), rating of extrapyramidal symptoms (symptoms like abnormal muscle movements, abnormal movements of the tongue or jaw, slow or sustained muscle contractions, muscle spasms, shaking, abnormal movements of the eyes, involuntary muscle contractions, slow movements, or restlessness), vital signs measurements (including heart rate and blood pressure), body weight and physical examination findings. A urine pregnancy test will be performed in females of childbearing potential. Adverse events (unintended, but not necessarily unexpected, results of therapy that can be unpleasant or dangerous), associated concomitant medications, and symptoms of relapse will be recorded as needed.

Conditions
Schizophrenia
Being tested
paliperidone palmitate injection, oral antipsychotics
Keywords
Schizophrenia, paliperidone palmitate, Invega, Intramuscular injection, Oral antipsychotics, Relapse
Medical subject headings
Schizophrenia, Recurrence

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • paliperidone palmitate injectionDrug

    injection with 150 mg equivalent on Day 1, 100 mg equivalent on Day 8, 75 mg equivalent on Day 38 and flexible dosing with 25, 50, 75, 100 or 150 mg equivalent once monthly thereafter

  • oral antipsychoticsDrug

    daily treatment according to local label for maximally 24 months

Study groups in NCT01081769
Study groupRoleWhat they receive
Paliperidone PalmitateExperimentalpaliperidone palmitate injection with 150 mg equivalent on Day 1 100 mg equivalent on Day 8 75 mg equivalent on Day 38 and flexible dosing with 25 50 75 100 or 150 mg equivalent once monthly thereafter
Receives: Drug: paliperidone palmitate injection
Oral AntipsychoticsActive comparatororal antipsychotics daily treatment according to local label for maximally 24 months
Receives: Drug: oral antipsychotics

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Time to First Relapse Event

    Number of days from baseline (day 1 of core phase) to relapse as evaluated according the Csernansky criteria. A patient was considered to have relapsed if they met one or more of the following criteria: (1) psychiatric hospitalization; (2) an increase in the level of psychiatric care and an increase of 25 percent (%) from baseline in the Positive And Negative Syndrome Score (PANSS) total score (or an increase of 10 points if the baseline score was 40 or less); (3) deliberate self-injury; (4) suicidal or homicidal ideation that was clinically significant in the investigator's judgment; (5) violent behavior resulting in clinically significant injury to another person or property damage; (6) substantial clinical deterioration, defined as a change score of 6 ("much worse") or 7 ("very much worse") on the Clinical Global Impressions Scale (CGI-C); and/or (7) the required dose of the antipsychotic exceeds the maximum approved dose.

    Measured: from baseline (Day 1 of core phase) up to maximally 24 months.

  2. Number of Participants With a Relapse Event

    Number of participants with a relapse event with relapses evaluated according the Csernansky criteria. A patient was considered to have relapsed if they met one or more of the following criteria: (1) psychiatric hospitalization; (2) an increase in the level of psychiatric care and an increase of 25% from baseline in the PANSS total score (or an increase of 10 points if the baseline score was 40 or less); (3) deliberate self-injury; (4) suicidal or homicidal ideation that was clinically significant in the investigator's judgment; (5) violent behavior resulting in clinically significant injury to another person or property damage; (6) substantial clinical deterioration, defined as a change score of 6 ("much worse") or 7 ("very much worse") on the Clinical Global Impressions Scale (CGI-C); and/or (7) the required dose of the antipsychotic exceeds the maximum approved dose.

    Measured: from baseline (Day 1 of core phase) up to maximally 24 months

Secondary outcomes (13)
  1. Percentage of Treatment Responders

    The proportion of patients achieving a treatment response, defined as a ≥30% decrease (i.e., improvement) in Positive and Negative Syndrome Scale (PANSS) total score from baseline to endpoint. The PANSS is a 30-item scale (Range 30-210) designed to assess various symptoms of schizophrenia including delusions, grandiosity, blunted affect, poor attention, and poor impulse control. The 30 symptoms are rated on a 7-point scale that ranges from 1 (absent) to 7 (extreme psychopathology). The PANSS total score consists of the sum of all 30 PANSS items. Higher scores indicate increased severity of schizophrenia symptoms.

    Measured: from baseline (day 1 of core phase) up to maximally 24 months

  2. Change From Baseline in PANSS Total Score

    Change from baseline in the PANSS: The PANSS is a 30-item scale (Range 30-210) designed to assess various symptoms of schizophrenia including delusions, grandiosity, blunted affect, poor attention, and poor impulse control. The 30 symptoms are rated on a 7-point scale that ranges from 1 (absent) to 7 (extreme psychopathology). The PANSS total score consists of the sum of all 30 PANSS items. Higher scores indicate worsening.

    Measured: Baseline, day 8, month 1, 2, 3, 4, 6, 9, 12, 15, 18, 21, 24

  3. Change From Baseline in PANSS Subscale Score

    Change from baseline in positive symptom, negative symptom and general psychopathology subscales of the PANSS scale. The PANSS scale is designed to assess symptoms of schizophrenia by means of the 30-items. The PANSS scale provides subscores for 3 subscales, that is, the positive symptoms subscale (7 items, range 7-49), the negative symptoms subscale (7 items, range 7-49), and the general psychopathology subscale (16 items, range 16-112). Each item of the scale is to be scored on a scale of 1 (absent) to 7 (extreme). Higher scores indicate higher severity of schizophrenia symptoms.

    Measured: Baseline (day 1 of core phase), day 8, month 12, 24

  4. Change From Baseline in PANSS Marder Factor Scores

    Change from baseline in schizophrenia symptoms were assessed through the following PANSS factor scores as described by Marder: (1) positive symptoms (range 8-56): sum of delusions, hallucinatory behavior, grandiosity, suspiciousness, stereotyped thinking, somatic concern, unusual thought content, lack of judgment and insight; (2) negative symptoms (range 7-49): sum of blunted affect, emotional withdrawal, poor rapport, passive social withdrawal, lack of spontaneity, motor retardation, and active social avoidance; (3) disorganized thoughts (range 7-49): sum of conceptual disorganization, difficulty in abstract thinking, mannerisms and posturing, disorientation, poor attention, disturbance of volition, and preoccupation; (4) uncontrolled hostility/excitement (range 4-28): sum of excitement, hostility, uncooperativeness and poor impulse control; (5) anxiety/depression (range 4-28): sum of anxiety, guilt feelings, tension, and depression. Higher scores indicate higher severity of symptoms

    Measured: Baseline (day 1 of core phase), day 8, month 12 and 24

  5. Change From Baseline in Clinical Global Impression Severity (CGI-S) Score

    The Clinical Global Impression Severity (CGI-S) rating scale is a 7 point global clinical assessment that measures the clinician's impression of the severity of illness exhibited by a participant. A rating of 1 is equivalent to "Normal, not at all ill" and a rating of 7 is equivalent to "Among the most extremely ill participants". Higher scores indicate higher impression of illness severity.

    Measured: Baseline (day 1 of core phase), day 8, month 1, 2, 3, 4, 6, 9, 12, 15, 18, 21, 24

  6. Clinical Global Impression-Change (CGI-C)

    The Clinical Global Impression-Change (CGI-C) rating scale is used to rate the change in severity of the patient's illness compared to baseline (day 1 of core phase) on a 7-point scale ranging from 1 (very much improved) to 7 (very much worse).

    Measured: Month 24 and endpoint

  7. Changes From Baseline in Personal and Social Performance (PSP) Total Score

    The Personal and Social Performance (PSP) scale assesses degree of a participant's dysfunction within 4 domains of behavior: socially useful activities, personal and social relationships, self-care, and disturbing and aggressive behavior. Score ranges from 1 to 100, divided into 10 equal intervals to rate degree of difficulty (1, absent to 6, very severe) in each of the 4 domains. Based on 4 domains there will be 1 total score. Participants with score of 71 to 100 have mild degree of difficulty; from 31 to 70, varying degrees of disability; less than or equal to 30, functioning so poorly as to require intensive supervision.

    Measured: baseline (day 1 of core phase), month 1, 3, 6, 9, 12, 15, 18, 21 and 24

  8. Change From Baseline in Short Form-36 Health Survey (SF-36)

    The Short Form-36 Health Survey (SF-36) is a measure of Participant-reported health status. It is a 36-item questionnaire measuring 8 domains (physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, and mental health). Two summary scale scores are computed based on weighted combinations of the 8 subscale scores: the Physical Component Summary and the Mental Component Summary. Each summary scale score ranges from 0 (worst) to 100 (best), with higher scores reflecting better health-related functional status.

    Measured: baseline (day 1 of core phase), month 6, 12 and 24

  9. Change From Baseline in EuroQol 5-Dimensional Questionnaire (EQ-5D) VAS Score

    The EQ-5D VAS records the respondent's self-rated health on a vertical, visual analog scale, with 0 representing the worst imaginable health state and 100 representing the best imaginable health state. The EQ VAS is used as a quantitative measure of health outcome as judged by the individual respondent.

    Measured: baseline (day 1 of core phase), month 6, 12 and 24

  10. Change From Baseline in EuroQol 5-Dimensional Questionnaire (EQ-5D) Index Score

    The EuroQol-5 is a five dimensional health state classification. Each dimension is assessed on a 3-point ordinal scale (1=no problems, 2=some problems, 3=extreme problems). The responses to the five EQ-5D dimensions were scored using a utility-weighted algorithm to derive an EQ-5D health status index score between 0 to 1, with 1.00 indicating "full health" and 0 representing dead. A higher score indicates an improvement in health in the Health Status Index.

    Measured: baseline (day 1 of core phase), month 6, 12 and 24

  11. Change From Baseline in Subjective Well-Being Under Neuroleptics-Short Form (SWN-S) Total Score

    The SWN-S is a patient self-rated scale developed to measure the subjective well-being for the previous 7 days of a patient under neuroleptic treatment. The SWN-S consists of 20 items (each item is rated from 1=not at all to 6=very much). The total score ranges from 20 to 120 with higher score indicating greater subjective well-being.

    Measured: baseline (day 1 of core phase), month 6, 12 and 24

  12. Change From Baseline in Patient's Treatment Satisfaction

    Patient's satisfaction with medication was assessed using the Treatment Satisfaction Questionnaire for Medication (TSQM). The TSQM is divided into 4 subscales (effectiveness, side effects, convenience, and global satisfaction), with the value of each subscale ranging from 0 to 100. Higher scores indicate greater treatment satisfaction.

    Measured: baseline (day 1 of core phase), month 12 and 24

  13. Change From Baseline in Physician's Treatment Satisfaction

    Physician's treatment satisfaction was assessed using the physician's treatment satisfaction scale which is designed to rate 4 aspects of treatment (efficacy, safety, mode of administration, and overall satisfaction), each on a scale ranging from 1 (extremely satisfied) to 7 (extremely dissatisfied).

    Measured: baseline (day 1 of core phase), month 12 and 24

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Mar 2010 (estimated)
  2. Study startFeb 2010
  3. Primary completionFeb 2013
  4. Study completionFeb 2013

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 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
769 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01081769
Sponsor's protocol ID
CR015199
Other IDs
R092670SCH3005, 2008-002247-16, 2008
Acronym
PROSIPAL
Status last verified
Feb 2015
First submitted
4 Mar 2010
Last updated
18 Feb 2015
Data monitoring committee
No

Publications

  • Lopena OJ, Alphs LD, Sajatovic M, Turkoz I, Sun L, Johnston KL, Sliwa JK, Najarian DM, Starr HL. Earlier Use of Long-Acting Injectable Paliperidone Palmitate Versus Oral Antipsychotics in Patients With Schizophrenia: An Integrated Patient-Level Post Hoc Analysis. J Clin Psychiatry. 2023 Sep 25;84(6):23m14788. doi: 10.4088/JCP.23m14788.

    PubMed 37756123

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing paliperidone palmitate injection and oral antipsychotics in people with Schizophrenia, run by Janssen-Cilag International NV at 94 sites in 25 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 7 inclusion and 10 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 18 Feb 2015. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 94 sites in Ukraine, Russia, France, Spain, Czechia and 20 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 18 Feb 2015). 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?

Time to First Relapse Event (time frame: from baseline (Day 1 of core phase) up to maximally 24 months.). The study lists 2 primary outcomes in all. 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 NCT01081769, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 18 Feb 2015.

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