Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide (MARITIME-2-EXTENSION)
A Phase 3, Randomized, Double-Blind Extension Trial to Evaluate the Long-term Efficacy, Safety, and Tolerability of Maridebart Cafraglutide in Participants With Obesity or Overweight With Type 2 Diabetes Mellitus
The primary objective of this trial is to evaluate the long-term efficacy, safety, and tolerability of maridebart cafraglutide in participants with obesity and type 2 diabetes mellitus. Trial 20210182 is extension of trial 20210184 (NCT06858878).
연구 개요
연구 유형
등록 (추정된)
단계
- 3단계
연락처 및 위치
연구 연락처
- 이름: Amgen Call Center
- 전화번호: 866-572-6436
- 이메일: medinfo@amgen.com
연구 장소
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Arizona
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Gilbert, Arizona, 미국, 85296
- 모병
- Gilbert Center for Family Medicine
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California
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Canoga Park, California, 미국, 91304
- 모병
- San Fernando Valley Health Institute
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Cerritos, California, 미국, 90703
- 모병
- Core Healthcare Group
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La Mesa, California, 미국, 91942
- 모병
- Velocity Clinical Research Chula Vista
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Modesto, California, 미국, 95355
- 모병
- Paradigm Clinical Research
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Pomona, California, 미국, 91767
- 모병
- Empire Clinical Research
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Florida
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Miami, Florida, 미국, 33135
- 모병
- Optimus U Corporation
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Miami, Florida, 미국, 33015
- 모병
- San Marcus Research Clinic Inc
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Miami Lakes, Florida, 미국, 33016
- 모병
- Indago Research and Health Center
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Orlando, Florida, 미국, 32825
- 모병
- Florida Institute for Clinical Research
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Weston, Florida, 미국, 33331
- 모병
- Encore Medical Research of Weston LLC
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Winter Park, Florida, 미국, 32789
- 모병
- Conquest Research - Winter Park
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Illinois
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Skokie, Illinois, 미국, 60077
- 모병
- Endeavor Health
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Iowa
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West Des Moines, Iowa, 미국, 50266
- 모병
- Iowa Diabetes Research
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Kansas
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Lenexa, Kansas, 미국, 66219
- 모병
- JCCT- Juno Northwest Houston
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Newton, Kansas, 미국, 67114
- 모병
- Alliance for Multispecialty Research Newton
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Wichita, Kansas, 미국, 67226
- 모병
- Alliance for Multispecialty Research LLC
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Louisiana
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Monroe, Louisiana, 미국, 71201
- 모병
- Ima Clinical Research- Monroe
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Maryland
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Annapolis, Maryland, 미국, 21401
- 모병
- Annapolis Internal Medicine, LLC
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Missouri
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Kansas City, Missouri, 미국, 64114
- 모병
- Alliance for Multispecialty Research - Kansas City
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Nevada
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Las Vegas, Nevada, 미국, 89148
- 모병
- Palm Research Center Inc
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New Jersey
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Trenton, New Jersey, 미국, 08611
- 모병
- Premier Research
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North Carolina
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Morehead City, North Carolina, 미국, 28557
- 모병
- West Clinical Research
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Ohio
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Cincinnati, Ohio, 미국, 45242
- 모병
- Velocity Clinical Research - Cincinnati
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Cincinnati, Ohio, 미국, 45246
- 모병
- Velocity Clinical Research - Springdale
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Rhode Island
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East Greenwich, Rhode Island, 미국, 02818
- 모병
- Velocity Clinical Research - Providence
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Texas
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Austin, Texas, 미국, 78704
- 모병
- Elligo Clinical Research Center
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Bellaire, Texas, 미국, 77401
- 모병
- Johnson County Clinical Trials Juno Bellaire
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Corpus Christi, Texas, 미국, 78414
- 모병
- Osvaldo A Brusco MD PA
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Denison, Texas, 미국, 75020
- 모병
- Soma Clinical Trials, LLC
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Virginia
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Burke, Virginia, 미국, 22015
- 모병
- Manassas Clinical Research Center Inc
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Birmingham, 영국, B21 9RY
- 모병
- FutureMeds Birmingham
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Ehime
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Matsuyama, Ehime, 일본, 790-0034
- 모병
- Mikannohana Clinic, Diabetes, Endocrinology and Metabolism
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Fukuoka
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Kitakyusyu-shi, Fukuoka, 일본, 807-0072
- 모병
- Morizono Medical Clinic
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Hiroshima
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Aki-gun, Hiroshima, 일본, 735-8585
- 모병
- Mazda Hospital of Mazda Motor Corporation
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Ibaraki
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Mito, Ibaraki, 일본, 310-0826
- 모병
- Nakamoto Medical Clinic
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Naka, Ibaraki, 일본, 311-0113
- 모병
- Nakakinen Clinic
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Tsuchiura-shi, Ibaraki, 일본, 300-0835
- 모병
- Ohishi Naika Clinic
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Kumamoto
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Kumamoto, Kumamoto, 일본, 860-0863
- 모병
- Morinaga Ueno Clinic
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Osaka
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Kashiwara-shi, Osaka, 일본, 582-0005
- 모병
- Shiraiwa Medical Clinic
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Shizuoka
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Shizuoka, Shizuoka, 일본, 424-0855
- 모병
- Suruga Clinic
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Tokyo
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Meguro-ku, Tokyo, 일본, 153-0053
- 모병
- Yutenji Medical Clinic
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Mitaka-shi, Tokyo, 일본, 181-0013
- 모병
- Medical Corporation Ouitsukai Kanno Naika
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Ontario
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Hamilton, Ontario, 캐나다, L8L 5G4
- 모병
- Hamilton Medical Research Group
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San Juan, 푸에르토 리코, 00909
- 모병
- Latin Clinical Trial Center
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
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Signed informed consent form (ICF) indicating compliance with the requirements and restrictions listed in the ICF and this protocol.
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Participants completing Study 20210184 must meet the following criteria:
- Completed the Week 72 visit in Study 20210184.
- Did not permanently discontinue the investigational product in the parent trial (20210184).
- Randomized within 7 days of week 72 visit in the parent trial.
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Participants must use protocol-specified contraception during treatment and for 16 weeks after the last dose of trial intervention.
Exclusion Criteria:
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Planned (during the trial) surgical, endoscopic, or device-based treatment for obesity.
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Body mass index (BMI) ≤ 18.5 kilograms per meter square (kg/m^2).
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Participant has known sensitivity to any of the products or components to be administered during dosing.
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History of ischemic optic neuropathy.
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Any malignancy diagnosed during the parent trial, except for the following treated with curative intent:
- Nonmelanoma skin cancers
- Breast ductal carcinoma in situ
- Cervical carcinoma in situ
- Prostate cancer in situ
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Newly identified (during the parent trial) multiple endocrine neoplasia syndrome type 2, or family history (first-degree relative[s]) history of medullary thyroid carcinoma (MTC).
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Patient Health Questionnaire-9 (PHQ-9) score ≥ 15 at the Week 72 visit from the parent trial (20210184) before randomization.
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Any suicidal ideation (category 4 or 5) or any suicidal behavior on the Columbia-Suicide Severity Rating Scale (C-SSRS), Since Last Visit version, at the Week 72 visit from the parent trial before randomization.
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Participant unlikely to be able to complete all protocol-required procedures, restrictions and requirements, in the judgment of the individual and investigator.
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History or evidence of any other clinically significant disorder, condition, disease (including, but not limited to known drug or alcohol abuse, eating disorders, and conditions identified during the parent trial) that, in the opinion of the investigator, would pose a risk to participant safety.
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Currently pregnant (confirmed with positive pregnancy test) or breastfeeding or planning to become pregnant or breastfeed while on trial until an additional 16 weeks after the last dose of trial intervention.
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Major surgical procedures planned during the trial.
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Participants with minor surgical procedures (not requiring general anesthesia or deep sedation) planned during the trial may be eligible at the discretion of the investigator.
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Investigative site personnel directly affiliated with the trial and/or their immediate family (ie, spouse, parent, child, or sibling, whether biological or legally adopted).
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 더블
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: Maridebart Cafraglutide Low Dose Q4W
Participants who received low dose of maridebart cafraglutide in the parent trial (20210184 [NCT06858878]) will continue to receive low dose of maridebart cafraglutide subcutaneously (SC) once in 4 weeks (Q4W). |
Administered subcutaneously.
다른 이름들:
|
|
실험적: Maridebart Cafraglutide Medium Dose Q4W
Participants who received medium dose of maridebart cafraglutide in the parent trial will be re-randomized in this trial to receive medium dose of maridebart cafraglutide SC Q4W. |
Administered subcutaneously.
다른 이름들:
|
|
실험적: Maridebart Cafraglutide Medium dose Q8W
Participants who received medium dose of maridebart cafraglutide in the parent trial will be re-randomized in this trial to receive medium dose of maridebart cafraglutide SC once in 8 weeks (Q8W). |
Administered subcutaneously.
다른 이름들:
|
|
위약 비교기: Placebo Q4W (Received Medium Dose Maridebart Cafraglutide in Parent Trial)
Participants who received medium dose of maridebart cafraglutide in the parent trial will be re-randomized in this trial to receive placebo SC Q4W. |
Administered subcutaneously. |
|
실험적: Maridebart Cafraglutide High Dose Q4W
Participants who received high dose of maridebart cafraglutide in the parent trial will be re-randomized in this trial to receive high dose of maridebart cafraglutide SC Q4W. |
Administered subcutaneously.
다른 이름들:
|
|
실험적: Maridebart Cafraglutide High Dose Q8W
Participants who received high dose of maridebart cafraglutide in the parent trial will be re-randomized in this trial to receive high dose of maridebart cafraglutide SC Q8W. |
Administered subcutaneously.
다른 이름들:
|
|
위약 비교기: Placebo Q4W (Received High Dose Maridebart Cafraglutide in Parent Trial)
Participants who received high dose of maridebart cafraglutide in the parent trial will be re-randomized in this trial to receive placebo SC Q4W. |
Administered subcutaneously. |
|
실험적: Maridebart Cafraglutide High Dose Q4W (Received Placebo in the Parent Trial)
Participants who received placebo in the parent trial will receive high dose of maridebart cafraglutide SC Q4W. Prior to initiating the assigned high dose, participants will undergo a dose-escalation phase gradually increasing doses. |
Administered subcutaneously.
다른 이름들:
|
|
실험적: Maridebart Cafraglutide Low Dose Q4W(Received Very Low Dose Maridebart Cafraglutide in Parent Trial)
Participants who permanently de-escalated to very low dose of maridebart cafraglutide in the parent trial will receive low dose of maridebart cafraglutide SC Q4W. |
Administered subcutaneously.
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
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Number of Participants Experiencing Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)
기간: Baseline of current trial up to 60 weeks
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Baseline of current trial up to 60 weeks
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Percent Change in Body Weight from Baseline of the Parent Trial (20210184)
기간: Baseline of parent trial (20210184) to Week 48 of current trial
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Baseline of parent trial (20210184) to Week 48 of current trial
|
2차 결과 측정
결과 측정 |
기간 |
|---|---|
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Change from Baseline of the Parent Trial in Waist Circumference
기간: Baseline of parent trial to Week 48 of current trial
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Baseline of parent trial to Week 48 of current trial
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Change from Baseline of the Parent Trial in the Impact of Weight on Quality of Life-Lite Clinical Trials Version (IWQOL-Lite-CT) Physical Function Composite Score
기간: Baseline of parent trial to Week 48 of current trial
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Baseline of parent trial to Week 48 of current trial
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Percent Change from Baseline in Body Weight
기간: Baseline of current trial to Week 48
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Baseline of current trial to Week 48
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Percentage of Participants with No Body Weight Gain of >3% From Baseline
기간: Week 48 of current trial
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Week 48 of current trial
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Percentage of Participants with No Body Weight Gain of >5% From Baseline
기간: Week 48 of current trial
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Week 48 of current trial
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Percentage of Body Weight Reduction Maintained from the Parent Trial
기간: Baseline of parent trial to Week 48 of current trial
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Baseline of parent trial to Week 48 of current trial
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Percentage of Participants Maintaining ≥ 80% of the Body Weight Reduction Achieved in the Parent Trial
기간: Baseline of parent trial to Week 48 of current trial
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Baseline of parent trial to Week 48 of current trial
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Percentage of Participants Achieving ≥ 5% Reduction in Body Weight from Baseline of the Parent Trial
기간: Baseline of parent trial to Week 48 of current trial
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Baseline of parent trial to Week 48 of current trial
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Percentage of Participants Achieving ≥ 10% Reduction in Body Weight from Baseline of the Parent Trial
기간: Baseline of parent trial to Week 48 of current trial
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Baseline of parent trial to Week 48 of current trial
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Percentage of Participants Achieving ≥ 15% Reduction in Body Weight from Baseline of the Parent Trial
기간: Baseline of parent trial to Week 48 of current trial
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Baseline of parent trial to Week 48 of current trial
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Percentage of Participants Achieving ≥ 20% Reduction in Body Weight from Baseline of the Parent Trial
기간: Baseline of parent trial to Week 48 of current trial
|
Baseline of parent trial to Week 48 of current trial
|
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Change from Baseline of the Parent Trial in Hemoglobin A1c
기간: Baseline of parent trial to Week 48 of current trial
|
Baseline of parent trial to Week 48 of current trial
|
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Change from Baseline in HbA1c
기간: Week 48 of current trial
|
Week 48 of current trial
|
공동 작업자 및 조사자
스폰서
수사관
- 연구 책임자: MD, Amgen
간행물 및 유용한 링크
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- 20210182
- 2025-524788-19-00 (씨티스)
- U1111-1332-0531 (기타 식별자: WHO/UTN Number)
- 2025 (미국 NIH 보조금/계약)
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
De-identified individual patient data for variables necessary to address the specific research question in an approved data sharing request.
IPD 공유 기간
Data sharing requests relating to this study will be considered beginning 18 months after the study has ended and either 1) the product and indication have been granted marketing authorization in both the US and Europe or 2) clinical development for the product and/or indication discontinues and the data will not be submitted to regulatory authorities. There is no end date for eligibility to submit a data sharing request for this study.
IPD 공유 액세스 기준
Qualified researchers may submit a request containing the research objectives, the Amgen product(s) and Amgen study/studies in scope, endpoints/outcomes of interest, statistical analysis plan, data requirements, publication plan, and qualifications of the researcher(s). In general, Amgen does not grant external requests for individual patient data for the purpose of re-evaluating safety and efficacy issues already addressed in the product labelling. Requests are reviewed by a committee of internal advisors. If not approved, a Data Sharing Independent Review Panel will arbitrate and make the final decision. Upon approval, information necessary to address the research question will be provided under the terms of a data sharing agreement. This may include anonymized individual patient data and/or available supporting documents, containing fragments of analysis code where provided in analysis specifications. Further details are available at the URL below.
IPD 공유 지원 정보 유형
- 연구_프로토콜
- 수액
- ICF
- CSR
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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. .