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SchizophreniaPhase 3MAP-S-01NCT01320982

Minocycline, Acetylsalicylic Acid or Pramipexole vs Placebo in Patients With Schizophrenia or Schizoaffective Disorder

A Phase 3 study testing minocycline, pramipexole and acetylsalicylic acid in people with Schizophrenia and Schizoaffective Disorder, run by Sheba Medical Center at 14 sites in 2 countries.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The objective of the study is to evaluate the efficacy of Pramipexole, Minocycline and Aspirin compared to placebo, as add-on to anti-psychotics in the treatment of patients with schizophrenia. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
Schizophrenia, Schizoaffective Disorder
What is being tested?
minocycline, pramipexole and acetylsalicylic acid
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
400 participants
Where
14 sitesin 2 countries
Study dates
Mar 2011to Jul 2012
Phase
Phase 3
Are there results?
None posted in the registry

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

  • Male or female, 18-65 years of age, inclusive
  • Females who are abstinent or practicing an established method of birth control (oral contraceptive tablets, hormonal implant device, hormone patch, injectable contraceptive, intrauterine device.
  • Willing and able to provide informed consent, after the nature of the study has been fully explained
  • Current DSM-IV-TR diagnosis of schizophrenia or schizoaffective disorder as confirmed by modified Structured Clinical Interview for DSM Disorders (SCID) and having had at least 2 prior schizophrenic episodes, or continually ill for at least 6 months.
  • Symptoms: 4 (moderate) or above on Clinical Global Impression scale (CGI-S)and 4 (moderate)or above score on two of the following four Positive and negative syndrome scale (PANSS) items: delusions, hallucinatory behaviors, conceptual disorganization or suspiciousness/ persecution, and/or a total PANSS negative symptoms score of 18.
  • Must be on any antipsychotic drug, for at least 2 weeks prior to the baseline visit, at doses within the Patient Outcome Research Team (PORT) criteria, whenever possible. Patients receiving higher doses will have their records reviewed to insure that their dose is required and, if possible, will be stabilized on a lower dose prior to study entry.
  • Inpatients or outpatients. Inpatients will be randomized 3 days or more after admission

Who cannot join

  • Unwilling or unable, in the opinion of the Investigator, to comply with study instructions
  • Pregnant or breast-feeding
  • Unstable medical disease (malignancy, poorly controlled diabetes, active ischemic cardiac disease, or cardiomyopathy, serious pulmonary disease, kidney disease, impaired liver functioning. History of hemorrhagic CVA or peptic ulcer disease.
  • Patients treated with: any of the trial medications i.e. pramipexole/minocycline/ acetylsalicylic acid, NSAIDs, anti-coagulants, sucralfate, cimetidine, amantadine, mexiletine.
  • Likely allergy or sensitivity to raloxifene/pramipexole/minocycline/acetylsalicylic acid.
  • At significant risk of committing suicide, or in the opinion of the Investigator, currently is at imminent risk of suicide or harming others.
  • Patients with a current DSM-IV substance or alcohol abuse. Patients with a history of and/or current recreational use of cannabinoids or alcohol, and/or patients who smoke cigarettes can be included.
  • Concurrent delirium, mental retardation, drug-induced psychosis, or history of clinically significant brain trauma documented by CT or MRI.

Trial locations and contacts

14 sites in 2 countries.

Katya Rubinstein, MA contact

972-3-5303454

rubins.katya@gmail.com

14 sites in 2 countries

Romania13 sites
  • Clinica de Psihiatrie

    Arad

    Delia Podea, MD, 0722 583 757, deliapodea@gmail.com

    Delia Podea, MD

  • Spitalul de Psihiatrie Botosani, Sectia Psihiatrie

    Botoșani

    Nicolae Vlad, MD, 0741 335 034, v_nicolae@yahoo.com

    Nicolae Vlad, MD

  • Spitalul Clinic de Psihiatrie "Prof. Dr. Alex. Obregia"

    Bucharest

    Dan Prelipceanu, MD, 0722 300 227, prelipceanudan@yahoo.com

    Dan Prelipceanu, MD

  • Spitalul Clinic de Psihiatrie "Prof. Dr. Alex. Obregia"

    Bucharest

    Gabriela Marian, MD, 0723 569 620, gabi.marian@yahoo.com

    Marian Gabriela, MD

  • Spitalul Clinic de Psihiatrie "Prof. Dr. Alex. Obregia"

    Bucharest

    Maria Ladea, MD, 0724 371 042, marialadea@gmail.com

    Maria Ladea, MD

  • Spitalul Clinic de Psihiatrie "Prof. Dr. Alex. Obregia"

    Bucharest

    Dorina-Valerica Sima, MD, 0723 859 570, dorinasima@yahoo.com

    Dorina-Valerica Sima, MD

  • Spitalul Clinic de Psihiatrie "Prof. Dr. Alex. Obregia"

    Bucharest

    Maria-Silvia Trandafir, MD, 0724 275 572, silviatrandafir2004@yahoo.com

    Maria-Silvia Trandafir, MD

  • Spitalul Clinic de Psihiatrie "Prof. Dr. Alex. Obregia"

    Bucharest

    Ana-Liana Giurgiuca, MD, 0722 378 967, giurgiuca_liana@yahoo.com

    Ana-Liana Giurgiuca, Md

  • Spitalul Clinic de Psihiatrie "Prof. Dr. Alex. Obregia"

    Bucharest

    Valentin Matei, MD, 0723 640 918, petcu_camelia@yahoo.com

    Valentin Matei, MD

  • Sp. Jud. "Prof. Dr.O. Fodor"

    Cluj-Napoca

    Mircea-Alexandru Birt, MD, 0721 012 220, mirceabirt@yahoo.com

    Mircea-Alexandru Birt, MD

  • Spitalul Clinic Judetean de Urgenta Cluj

    Cluj-Napoca

    Ioana-Valentina Miclutia, MD, 0722 796 067, ioanamiclu@yahoo.com

    Ioana-Valentina Miclutia, MD

  • Spitalul Clinic de Psihiatrie Socola, Iasi

    Iași

    Serban Turliuc, MD, 0745 203 002, serban_turliuc@yahoo.com

    Serban Turliuc, MD

  • Spitalul Clinic de Psihiatrie Socola, Iasi

    Iași

    Nicoleta Cartas, MD, 0724 576 261, nicoletacartas_socola@yahoo.com

    Nicoleta Cartas, MD

Other trials in Romania

Israel1 site
  • Sheba Medical Center

    Ramat Gan, 52621

    Mark Weiser, MD, +972-52-6666575, mweiser@netvision.net.il

    Katya Rubinstein, MA, +972-3-5303454, rubins.katya@gmail.com

Other trials in Israel

About this study

Official title: A Randomized Trial Administering Minocycline, Acetylsalicylic Acid or Pramipexole vs Placebo as add-on to Antipsychotics in Patients With Schizophrenia or Schizoaffective Disorder

The objective of the study is to evaluate the efficacy of Pramipexole, Minocycline and Aspirin compared to placebo, as add-on to anti-psychotics in the treatment of patients with schizophrenia.

Read the detailed description

Inflammatory processes have been implicated as a cause of schizophrenia (Fan, Goff et al. 2007), and the COX-2 inhibitor, Celecoxib, has been shown to reduce symptoms of schizophrenia (Muller, Krause et al. 2010). Aspirin, which is also a non-steroidal anti-inflammatory drug(NSAID), irreversibly inhibits Cyclooxygenase-1 (COX-1) and modifies the enzymatic activity of Cyclooxygenase-2 (COX-2), thus inhibiting the formation of prostaglandins and reduces inflammatory reaction. In a study funded by the Stanley Medical Research Institute (SMRI) recently published, Laan at all (Laan, Grobbee et al. 2010) administered add-on 1000mg/d of Aspirin to patients with schizophrenia receiving anti-psychotics, and reported reductions in Positive and negative syndrome scale (PANSS) total and PANSS positive scores without substantial side effects.

Minocycline is a second-generation tetracycline that exerts anti-inflammatory and antimicrobial effects while having a distinct neuroprotective profile. Minocycline effects the glutaminergic system, through inhibition of neuronal nitric oxide synthase (nNOS) and blocking of nitric oxide (NO)- induced neurotoxicity (Du et al, 1998; Jiang et al., 2005), and thus has been suggested as a potential treatment for schizophrenia. One published study (Levkovitz, Mendlovich et al. 2010), and another, unpublished study by Bill Deakin found that add-on treatment of 200mg/d of Minocycline was beneficial for symptoms and cognition in schizophrenia, and a study by Miayoka et al (Miyaoka, Yasukawa et al. 2008) administered open-label 450 mg/day Minocycline, and found improvement on positive symptoms.

Indirect pharmacological evidence suggests a relative excess of dopaminergic activity as being implicated in the pathogenesis of some of the symptoms of schizophrenia, and all effective antipsychotics effect dopamine D2 receptors. Pramipexole is a pre-synaptic dopamine auto-receptor agonist hypothesized to improve in symptoms in schizophrenia patients. In an open label study, Kasper at all (Kasper, Barnas et al. 1997) showed statistically significant improvement in PANSS scores in patients not stabilized on haloperidol. Other data indicate that add-on Pramipexole improves symptoms of depression and cognition, in patients with affective disorders (Goldberg, Frye et al. 1999; Sporn, Ghaemi et al. 2000; Goldberg, Burdick et al. 2004; Zarate, Payne et al. 2004), and Malhotra et al, unpublished data.

All of these studies were relatively small, and were performed by investigators with an interest in the compound. The objective of this study is to replicate them in large trial by investigators with no specific interest in the compounds. This proposed study is a multi-arm study, in which patients will be randomized to one of the three study drugs: Pramipexole, Minocycline and Aspirin, or placebo as part of the same protocol. A design by which several active compounds are all compared to the same placebo arm has been utilized before for schizophrenia (Meltzer, Arvanitis et al. 2004). This design has several advantages: in addition to reduced costs and time it exposes fewer patients to placebo, and enables direct comparison between the compounds and not only to the placebo.

Being tested
minocycline, pramipexole, acetylsalicylic acid, placebo
Keywords
Schizophrenia, schizoaffective disorder
Medical subject headings
Schizophrenia, Psychotic Disorders

What participants receive

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

  • minocyclineDrug

    minocycline 100 mg/bid

  • pramipexoleDrug

    pramipexole 0.125, 0.25, 0.5 and 0.75 mg/bid

  • acetylsalicylic acidDrug

    acetylsalicylic acid 500mg/ bid

  • placeboDrug

    placebo bid

Study groups in NCT01320982
Study groupRoleWhat they receive
minocyclineActive comparatorminocycline
Receives: Drug: minocycline
pramipexoleActive comparatorpramipexole
Receives: Drug: pramipexole
acetylsalicylic acidActive comparatoracetylsalicylic acid
Receives: Drug: acetylsalicylic acid
PlaceboPlacebo comparatorPlacebo
Receives: Drug: placebo

What is being measured

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

  1. Positive and Negative Syndrome Scale (PANSS)total score

    Change from baseline in Positive and Negative Syndrome Scale (PANSS)total score at 8 weeks

    Measured: Positive and Negative Syndrome Scale (PANSS) total score at week 8

  2. Positive and Negative Syndrome Scale (PANSS)total score

    Change from baseline in Positive and Negative Syndrome Scale (PANSS)total score at 16 weeks.

    Measured: Positive and Negative Syndrome Scale (PANSS) total score at week 16

Secondary outcomes (24)
  1. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and negative syndrome scale(PANSS) positive sub-scale scoreat 2 weeks.

    Measured: Positive and Negative Syndrome Scale (PANSS)positive sub-scale score at week 2

  2. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and Negative Syndrome Scale(PANSS) positive sub-scale score at 4 weeks.

    Measured: Positive and Negative Syndrome Scale(PANSS) positive sub-scale score at week 4 .

  3. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and negative syndrome scale(PANSS) positive sub-scale score at 8 weeks.

    Measured: Positive and negative syndrome scale(PANSS) positive sub-scale score at week 8.

  4. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and negative syndrome scale(PANSS) positive sub-scale score at 16 weeks.

    Measured: Positive and negative syndrome scale(PANSS) positive sub-scale score at week 16.

  5. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and Negative Syndrome Scale (PANSS) negative sub-scale score at 2 weeks

    Measured: Positive and Negative Syndrome Scale (PANSS) negative sub-scale score at week 2

  6. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and Negative Syndrome Scale (PANSS) negative sub-scale score at 4 weeks

    Measured: Positive and Negative Syndrome Scale (PANSS) negative sub-scale score at week 4

  7. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and Negative Syndrome Scale (PANSS) negative sub-scale score at 8 weeks

    Measured: Positive and Negative Syndrome Scale (PANSS) negative sub-scale score at week 8

  8. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and Negative Syndrome Scale (PANSS) negative sub-scale score at 16 weeks

    Measured: Positive and Negative Syndrome Scale (PANSS) negative sub-scale score at week 16

  9. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and Negative Syndrome Scale (PANSS) general psychopathology sub-scale score at week 2

    Measured: Positive and Negative Syndrome Scale (PANSS) general psychopathology sub-scale score at 2 weeks

  10. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and Negative Syndrome Scale (PANSS) general psychopathology sub-scale score at 4 weeks

    Measured: Positive and Negative Syndrome Scale (PANSS) general psychopathology sub-scale score at week 4

  11. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and Negative Syndrome Scale (PANSS) general psychopathology sub-scale score at 8 weeks

    Measured: Positive and Negative Syndrome Scale (PANSS) general psychopathology sub-scale score at week 8

  12. Positive and Negative Syndrome Scale (PANSS)

    Change from baseline in Positive and Negative Syndrome Scale (PANSS) general psychopathology sub-scale score at 16 weeks

    Measured: Positive and Negative Syndrome Scale (PANSS) general psychopathology sub-scale score at week 16

  13. Clinical Global Impression Scale-Severity (CGI-S)

    Change from baseline in Clinical Global Impression Scale-Severity(CGI-S)at 2 weeks

    Measured: Clinical Global Impression Scale-Improvement (CGI-S) at week 2

  14. Clinical Global Impression Scale-Severity (CGI-S)

    Change from baseline in Clinical Global Impression Scale-Severity(CGI-S)at 5 weeks

    Measured: Clinical Global Impression Scale-Severity (CGI-S) at week 5

  15. Clinical Global Impression Scale-Severity(CGI-S)

    Change from baseline in Clinical Global Impression Scale-Severity(CGI-S)at 8 weeks

    Measured: linical Global Impression Scale-Severity(CGI-S) at week 8

  16. Clinical Global Impression Scale-Severity(CGI-S)

    Change from baseline in Clinical Global Impression Scale-Severity(CGI-S)at 12 weeks

    Measured: Change from baseline in Clinical Global Impression Scale-Severity(CGI-S) at week 12

  17. Clinical Global Impression Scale-Severity(CGI-S)

    Change from baseline in Clinical Global Impression Scale-Severity(CGI-S)at 16 weeks

    Measured: Change from baseline in Clinical Global Impression Scale-Severity(CGI-S) at week 16

  18. Clinical Global Impression Scale- Improvement (CGI-I)

    Change from baseline in Clinical Global Impression Scale- Improvement (CGI-I)at 2 weeks

    Measured: Clinical Global Impression Scale- Improvement (CGI-I) at week 2

  19. Clinical Global Impression Scale- Improvement (CGI-I)

    Change from baseline in Clinical Global Impression Scale- Improvement (CGI-I)at 5 weeks

    Measured: Clinical Global Impression Scale- Improvement (CGI-I) at week 5

  20. Clinical Global Impression Scale- Improvement (CGI-I)

    Change from baseline in Clinical Global Impression Scale- Improvement (CGI-I)at 8 weeks

    Measured: Clinical Global Impression Scale- Improvement (CGI-I)at week 8

  21. Clinical Global Impression Scale- Improvement (CGI-I)

    Change from baseline in Clinical Global Impression Scale- Improvement (CGI-I)at 12 weeks

    Measured: Clinical Global Impression Scale- Improvement (CGI-I) at week 12

  22. Clinical Global Impression Scale- Improvement (CGI-I)

    Change from baseline in Clinical Global Impression Scale- Improvement (CGI-I)at 16 weeks

    Measured: Clinical Global Impression Scale- Improvement (CGI-I)at week 16

  23. Brief Assessment of Cognition in Schizophrenia (BACS)

    Change from baseline in Brief Assessment of Cognition in Schizophrenia (BACS)at 8 weeks.

    Measured: rief Assessment of Cognition in Schizophrenia (BACS)at week 8

  24. Brief Assessment of Cognition in Schizophrenia (BACS)

    Change from baseline in Brief Assessment of Cognition in Schizophrenia (BACS)at 16 weeks.

    Measured: Brief Assessment of Cognition in Schizophrenia (BACS)at week 16

Timeline

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

  1. First posted23 Mar 2011 (estimated)
  2. Study startMar 2011
  3. Primary completionJun 2012 (estimated)
  4. Study completionJul 2012 (estimated)

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
Triple blind
Who is masked
Participant, Care provider, Investigator
Enrolment
400 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01320982
Sponsor's protocol ID
SHEBA-8273-10-MW-CTIL
Acronym
MAP-S-01
Status last verified
Mar 2011
First submitted
2 Feb 2011
Last updated
23 Mar 2011
Results posted
No
Data monitoring committee
No

Publications

  • Levi L, Zamora D, Nastas I, Gonen I, Radu P, Matei V, Ciobanu AM, Nacu A, Boronin L, Karakrah L, Davidson M, Davis JM, Weiser M. Add-On Pramipexole for the Treatment of Schizophrenia and Schizoaffective Disorder: A Randomized Controlled Trial. J Clin Psychiatry. 2022 Aug 1;83(5):21m14233. doi: 10.4088/JCP.21m14233.

    PubMed 35921506
  • Weiser M, Zamora D, Levi L, Nastas I, Gonen I, Radu P, Matei V, Nacu A, Boronin L, Davidson M, Davis JM. Adjunctive Aspirin vs Placebo in Patients With Schizophrenia: Results of Two Randomized Controlled Trials. Schizophr Bull. 2021 Jul 8;47(4):1077-1087. doi: 10.1093/schbul/sbaa198.

    PubMed 33479775

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing minocycline, pramipexole and acetylsalicylic acid in people with Schizophrenia and Schizoaffective Disorder, run by Sheba Medical Center at 14 sites in 2 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 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: status not confirmed, as of the sponsor's last update on 23 Mar 2011. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 14 sites in Romania, Israel. 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 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?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Mark Weiser, MD (972-52-6666575, mweiser@netvision.net.il), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Positive and Negative Syndrome Scale (PANSS)total score (time frame: Positive and Negative Syndrome Scale (PANSS) total score at week 8). 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 NCT01320982, which also lists 2 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 23 Mar 2011.

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