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Longitudinal PET Imaging of Antipsychotic Binding to the Dopamine-3 Receptor in Schizophrenia

2026년 7월 15일 업데이트: Ragy Girgis, New York State Psychiatric Institute
This is a clinical trial in which 40 participants with schizophrenia will be randomized to 15 days of treatment with cariprazine (CAR) or brexpiprazole (BREX) in a single-blind manner. [11C]PHNO PET scans will be obtained before treatment and after 1 day and 15 days of treatment to examine the effects of antipsychotic medications on the dopamine-3 receptor (D3R). The overall objectives of the current study are to: 1) measure the acute binding of CAR/BREX to the D3R; 2) measure D3R availability for evidence of upregulation following subchronic administration of CAR/BREX in the same set of patients; 3) examine relationships between subchronic binding of CAR/BREX to, and upregulation of, the D3R vs. D2R and changes in positive symptoms, negative symptoms, and cognitive deficits. Relationships between subchronic binding of CAR/BREX and EPS will be explored.

연구 개요

상세 설명

There is a great need for the development of new treatments for schizophrenia (SCZ). Aside from the recently approved muscarinic agonist xanomeline, all current treatments have been assumed to function by blocking dopamine-2 receptors (D2Rs). Interest in the dopamine-3 receptor (D3R) was encouraged by preclinical findings that D3R antagonists reverse cognitive impairment and improve negative symptoms. In vivo imaging of the D3R became possible with the development of [11C]-(+)-PHNO, a D3R-preferring radioligand. However, while numerous preclinical studies have demonstrated that the D3R is relevant to both the neurobiology and treatment of SCZ, in vivo studies initially and surprisingly reported that, after several weeks of administration, antipsychotic medications may not bind to the D3R and may paradoxically increase levels of the D3R. These findings were discrepant with our own findings in non-human primates and individuals with SCZ demonstrating that acute doses of antipsychotic medications bind to the D3R and D2R in ratios predicted by their in vitro binding profiles. In a later study conducted by our group, 10 days of chronic dosing of the D2R-preferring antipsychotic medication brexpiprazole (BREX) also led to increased levels of the D3R at 1mg and negligible binding at 4mg. Finally, in our study of the D3R-preferring antipsychotic medication cariprazine (CAR), there was robust binding to the D3R and D2R after both acute and subchronic dosing. These seemingly discrepant findings may be related to methodological differences, differences in the binding profiles of D2R- vs. D3R-preferring antipsychotic medications, or to homeostatic responses to chronic antipsychotic treatment (i.e., upregulation). Upregulation is a potentially critical, though underexamined, effect common to all D2R/D3R-binding antipsychotic medications, including partial agonists. It has been hypothesized to be largely responsible for differences in occupancy estimates from single and repeat dose studies and contribute to waning effects of antipsychotic medications and tardive dyskinesia. The goals of this proposal are to elucidate the contribution of D3R, compared to D2R, binding to antipsychotic action, both acutely (SA1) and subchronically (SA2), in the same patients. The relationship between occupancy, upregulation, and clinical effects (SA3, EA) will be investigated.

연구 유형

중재적

등록 (추정된)

100

단계

  • 1단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인

건강한 자원 봉사자를 받아들입니다

아니

설명

Inclusion Criteria:

  1. Individuals, any gender or sex, aged 18 to 55, inclusive at screen
  2. Capable of understanding the study procedures and able to provide informed consent
  3. Diagnosed with schizophrenia, schizoaffective, or schizophreniform disorder
  4. Negative urine toxicology
  5. Antipsychotic free (by choice and for reasons unrelated to the study), and for at least 3 weeks (4 for aripiprazole or LAIs) at the time of the baseline PET scan, inclusive of any antipsychotic-free time prior to consent. [Any patient who requires inpatient hospitalization or acute medication treatment for clinical stabilization during the medication free period will not be included in this study; any participant who in the clinical judgment of the PIs or any involved clinician is not stable or appropriate for a medication free period will not be included.]
  6. PANSS total score > 80 and < 120 (inclusive)

Exclusion Criteria:

  1. Diagnosis of substance use disorder within the previous month
  2. A history of poor or inadequate response or hypersensitivity to CAR or BREX for any reason
  3. EKG abnormality that is clinically significant including a QTc interval > 450 msec for men and > 470 msec for women,
  4. Pregnant or breast-feeding women. Women of child-bearing potential must have a negative serum β-hCG pregnancy test at Visit 1, must have been using an acceptable method of contraception for 30 days before the study (i.e., before the first PET or MRI scan, whichever comes first), and must agree to do so for the whole study and 30 days after (unless post-menopausal or surgically sterile)
  5. Any clinically significant or unstable medical/neurological illness, condition, or disorder that is anticipated to potentially compromise participant safety on study medication
  6. Any material in the body that is a contraindication for MRI procedures or participated in prior nuclear medicine procedures in the past year that exceed FDA-defined limits when combined with radiation dosimetry from PET scanning in this protocol to avoid exceeding annual dosimetry limits (metal screener repeated before MRI scan). Individuals exposed to radiation in the workplace in the previous year will be excluded.
  7. Acute risk for suicide (i.e., score of 4-5 within the previous month or 6 within the previous 3 months on the CSSRS) or violence/homicide (e.g., homicidal ideation), or history of severe violent behavior or behavioral dyscontrol while antipsychotic-free
  8. A history of treatment resistance to antipsychotics or who have a duration of illness of greater than 20 years
  9. Claustrophobia
  10. Use of nicotine products within the previous month (prior to first PET scan)

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 다른
  • 할당: 무작위
  • 중재 모델: 병렬 할당
  • 마스킹: 하나의

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Cariprazine 1mg
Cariprazine 1mg daily for 15 days
Cariprazine is an antipsychotic medication
This is the radiotracer that will be used to examine antipsychotic binding to D2 and D3 receptors in this study. It is experimental and used for imaging purposes.
실험적: Cariprazine 2mg
Cariprazine 2mg daily for 15 days
Cariprazine is an antipsychotic medication
This is the radiotracer that will be used to examine antipsychotic binding to D2 and D3 receptors in this study. It is experimental and used for imaging purposes.
실험적: Cariprazine 3mg
Cariprazine 3mg daily for 15 days
Cariprazine is an antipsychotic medication
This is the radiotracer that will be used to examine antipsychotic binding to D2 and D3 receptors in this study. It is experimental and used for imaging purposes.
실험적: Cariprazine 4mg
Cariprazine 4mg daily for 15 days
Cariprazine is an antipsychotic medication
This is the radiotracer that will be used to examine antipsychotic binding to D2 and D3 receptors in this study. It is experimental and used for imaging purposes.
실험적: Brexpiprazole 1mg
Brexpiprazole 1mg daily for 15 days
This is the radiotracer that will be used to examine antipsychotic binding to D2 and D3 receptors in this study. It is experimental and used for imaging purposes.
Brexpiprazole is an antipsychotic medication
실험적: Brexpiprazole 2mg
Brexpiprazole 2mg daily for 15 days
This is the radiotracer that will be used to examine antipsychotic binding to D2 and D3 receptors in this study. It is experimental and used for imaging purposes.
Brexpiprazole is an antipsychotic medication
실험적: Brexpiprazole 3mg
Brexpiprazole 3mg daily for 15 days
This is the radiotracer that will be used to examine antipsychotic binding to D2 and D3 receptors in this study. It is experimental and used for imaging purposes.
Brexpiprazole is an antipsychotic medication
실험적: Brexpiprazole 4mg
Brexpiprazole 4mg daily for 15 days
This is the radiotracer that will be used to examine antipsychotic binding to D2 and D3 receptors in this study. It is experimental and used for imaging purposes.
Brexpiprazole is an antipsychotic medication

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Acute D2 and D3 Receptor Occupancy
기간: Day 1
Delta BPND in poscommissural putamen and midbrain
Day 1
Upregulation of D3 receptor following subchronic administration of antipsychotics
기간: Day 15
The availability of D3Rs following two weeks of antipsychotic treatment will be measured.
Day 15

2차 결과 측정

결과 측정
측정값 설명
기간
Positive and Negative Syndrome Scale (PANSS) Total Positive Symptoms
기간: 15 days
Correlations between changes in PANSS total positive symptoms and receptor binding will be examined.
15 days
Positive and Negative Syndrome Scale (PANSS) Total Negative Symptoms
기간: 15 days
Correlations between changes in PANSS total negative symptom scores and receptor binding will be examined.
15 days
MATRICS Cognitive Deficits (Composite Score)
기간: 15 days
Correlations between changes in cognitive deficits (MATRICS composite score) and receptor binding will be examined.
15 days

기타 결과 측정

결과 측정
측정값 설명
기간
Abnormal Involuntary Movement Scale (AIMS) Score
기간: 15 days
Correlations between changes in extrapyramidal side effect scores (AIMS) and receptor binding will be examined.
15 days
Simpson-Angus Scale (SAS) Score
기간: 15 days
Correlations between changes in extrapyramidal side effect scores (SAS) and receptor binding will be examined.
15 days
Barnes Akathisia Rating Scale (BARS) Score
기간: 15 days
Correlations between changes in extrapyramidal side effect scores (BARS) and receptor binding will be examined.
15 days

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 12월 1일

기본 완료 (추정된)

2030년 8월 30일

연구 완료 (추정된)

2030년 11월 30일

연구 등록 날짜

최초 제출

2026년 7월 11일

QC 기준을 충족하는 최초 제출

2026년 7월 15일

처음 게시됨 (실제)

2026년 7월 20일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 20일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 15일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

키워드

기타 연구 ID 번호

  • NYSPI2026-31
  • 1R01MH139651-01A1 (미국 NIH 보조금/계약)

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

예

IPD 계획 설명

Data will be shared via the NIH data archive.

IPD 공유 기간

Data will be shared after the study has been completed, as per NIH guidelines.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

예

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

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