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).
Przegląd badań
Status
Warunki
Interwencja / Leczenie
Typ studiów
Zapisy (Szacowany)
Faza
- Faza 3
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Amgen Call Center
- Numer telefonu: 866-572-6436
- E-mail: medinfo@amgen.com
Lokalizacje studiów
-
-
Ehime
-
Matsuyama, Ehime, Japonia, 790-0034
- Rekrutacyjny
- Mikannohana Clinic, Diabetes, Endocrinology and Metabolism
-
-
Fukuoka
-
Kitakyusyu-shi, Fukuoka, Japonia, 807-0072
- Rekrutacyjny
- Morizono Medical Clinic
-
-
Hiroshima
-
Aki-gun, Hiroshima, Japonia, 735-8585
- Rekrutacyjny
- Mazda Hospital of Mazda Motor Corporation
-
-
Ibaraki
-
Mito, Ibaraki, Japonia, 310-0826
- Rekrutacyjny
- Nakamoto Medical Clinic
-
Naka, Ibaraki, Japonia, 311-0113
- Rekrutacyjny
- Nakakinen Clinic
-
Tsuchiura-shi, Ibaraki, Japonia, 300-0835
- Rekrutacyjny
- Ohishi Naika Clinic
-
-
Kumamoto
-
Kumamoto, Kumamoto, Japonia, 860-0863
- Rekrutacyjny
- Morinaga Ueno Clinic
-
-
Osaka
-
Kashiwara-shi, Osaka, Japonia, 582-0005
- Rekrutacyjny
- Shiraiwa Medical Clinic
-
-
Shizuoka
-
Shizuoka, Shizuoka, Japonia, 424-0855
- Rekrutacyjny
- Suruga Clinic
-
-
Tokyo
-
Meguro-ku, Tokyo, Japonia, 153-0053
- Rekrutacyjny
- Yutenji Medical Clinic
-
Mitaka-shi, Tokyo, Japonia, 181-0013
- Rekrutacyjny
- Medical Corporation Ouitsukai Kanno Naika
-
-
-
-
Ontario
-
Hamilton, Ontario, Kanada, L8L 5G4
- Rekrutacyjny
- Hamilton Medical Research Group
-
-
-
-
-
San Juan, Portoryko, 00909
- Rekrutacyjny
- Latin Clinical Trial Center
-
-
-
-
Arizona
-
Gilbert, Arizona, Stany Zjednoczone, 85296
- Rekrutacyjny
- Gilbert Center for Family Medicine
-
-
California
-
Canoga Park, California, Stany Zjednoczone, 91304
- Rekrutacyjny
- San Fernando Valley Health Institute
-
Cerritos, California, Stany Zjednoczone, 90703
- Rekrutacyjny
- Core Healthcare Group
-
La Mesa, California, Stany Zjednoczone, 91942
- Rekrutacyjny
- Velocity Clinical Research Chula Vista
-
Modesto, California, Stany Zjednoczone, 95355
- Rekrutacyjny
- Paradigm Clinical Research
-
Pomona, California, Stany Zjednoczone, 91767
- Rekrutacyjny
- Empire Clinical Research
-
-
Florida
-
Miami, Florida, Stany Zjednoczone, 33135
- Rekrutacyjny
- Optimus U Corporation
-
Miami, Florida, Stany Zjednoczone, 33015
- Rekrutacyjny
- San Marcus Research Clinic Inc
-
Miami Lakes, Florida, Stany Zjednoczone, 33016
- Rekrutacyjny
- Indago Research and Health Center
-
Orlando, Florida, Stany Zjednoczone, 32825
- Rekrutacyjny
- Florida Institute for Clinical Research
-
Weston, Florida, Stany Zjednoczone, 33331
- Rekrutacyjny
- Encore Medical Research of Weston LLC
-
Winter Park, Florida, Stany Zjednoczone, 32789
- Rekrutacyjny
- Conquest Research - Winter Park
-
-
Illinois
-
Skokie, Illinois, Stany Zjednoczone, 60077
- Rekrutacyjny
- Endeavor Health
-
-
Iowa
-
West Des Moines, Iowa, Stany Zjednoczone, 50266
- Rekrutacyjny
- Iowa Diabetes Research
-
-
Kansas
-
Lenexa, Kansas, Stany Zjednoczone, 66219
- Rekrutacyjny
- JCCT- Juno Northwest Houston
-
Newton, Kansas, Stany Zjednoczone, 67114
- Rekrutacyjny
- Alliance for Multispecialty Research Newton
-
Wichita, Kansas, Stany Zjednoczone, 67226
- Rekrutacyjny
- Alliance for Multispecialty Research LLC
-
-
Louisiana
-
Monroe, Louisiana, Stany Zjednoczone, 71201
- Rekrutacyjny
- Ima Clinical Research- Monroe
-
-
Maryland
-
Annapolis, Maryland, Stany Zjednoczone, 21401
- Rekrutacyjny
- Annapolis Internal Medicine, LLC
-
-
Missouri
-
Kansas City, Missouri, Stany Zjednoczone, 64114
- Rekrutacyjny
- Alliance for Multispecialty Research - Kansas City
-
-
Nevada
-
Las Vegas, Nevada, Stany Zjednoczone, 89148
- Rekrutacyjny
- Palm Research Center Inc
-
-
New Jersey
-
Trenton, New Jersey, Stany Zjednoczone, 08611
- Rekrutacyjny
- Premier Research
-
-
North Carolina
-
Morehead City, North Carolina, Stany Zjednoczone, 28557
- Rekrutacyjny
- West Clinical Research
-
-
Ohio
-
Cincinnati, Ohio, Stany Zjednoczone, 45242
- Rekrutacyjny
- Velocity Clinical Research - Cincinnati
-
Cincinnati, Ohio, Stany Zjednoczone, 45246
- Rekrutacyjny
- Velocity Clinical Research - Springdale
-
-
Rhode Island
-
East Greenwich, Rhode Island, Stany Zjednoczone, 02818
- Rekrutacyjny
- Velocity Clinical Research - Providence
-
-
Texas
-
Austin, Texas, Stany Zjednoczone, 78704
- Rekrutacyjny
- Elligo Clinical Research Center
-
Bellaire, Texas, Stany Zjednoczone, 77401
- Rekrutacyjny
- Johnson County Clinical Trials Juno Bellaire
-
Corpus Christi, Texas, Stany Zjednoczone, 78414
- Rekrutacyjny
- Osvaldo A Brusco MD PA
-
Denison, Texas, Stany Zjednoczone, 75020
- Rekrutacyjny
- Soma Clinical Trials, LLC
-
-
Virginia
-
Burke, Virginia, Stany Zjednoczone, 22015
- Rekrutacyjny
- Manassas Clinical Research Center Inc
-
-
-
-
-
Birmingham, Zjednoczone Królestwo, B21 9RY
- Rekrutacyjny
- FutureMeds Birmingham
-
-
Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
-
Signed informed consent form (ICF) indicating compliance with the requirements and restrictions listed in the ICF and this protocol.
-
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.
-
Participants must use protocol-specified contraception during treatment and for 16 weeks after the last dose of trial intervention.
Exclusion Criteria:
-
Planned (during the trial) surgical, endoscopic, or device-based treatment for obesity.
-
Body mass index (BMI) ≤ 18.5 kilograms per meter square (kg/m^2).
-
Participant has known sensitivity to any of the products or components to be administered during dosing.
-
History of ischemic optic neuropathy.
-
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
-
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).
-
Patient Health Questionnaire-9 (PHQ-9) score ≥ 15 at the Week 72 visit from the parent trial (20210184) before randomization.
-
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.
-
Participant unlikely to be able to complete all protocol-required procedures, restrictions and requirements, in the judgment of the individual and investigator.
-
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.
-
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.
-
Major surgical procedures planned during the trial.
-
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.
-
Investigative site personnel directly affiliated with the trial and/or their immediate family (ie, spouse, parent, child, or sibling, whether biological or legally adopted).
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Podwójnie
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
|
Eksperymentalny: 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.
Inne nazwy:
|
|
Eksperymentalny: 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.
Inne nazwy:
|
|
Eksperymentalny: 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.
Inne nazwy:
|
|
Komparator placebo: 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. |
|
Eksperymentalny: 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.
Inne nazwy:
|
|
Eksperymentalny: 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.
Inne nazwy:
|
|
Komparator placebo: 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. |
|
Eksperymentalny: 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.
Inne nazwy:
|
|
Eksperymentalny: 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.
Inne nazwy:
|
Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Ramy czasowe |
|---|---|
|
Number of Participants Experiencing Treatment-emergent Adverse Events (TEAEs) and Serious Adverse Events (SAEs)
Ramy czasowe: Baseline of current trial up to 60 weeks
|
Baseline of current trial up to 60 weeks
|
|
Percent Change in Body Weight from Baseline of the Parent Trial (20210184)
Ramy czasowe: Baseline of parent trial (20210184) to Week 48 of current trial
|
Baseline of parent trial (20210184) to Week 48 of current trial
|
Miary wyników drugorzędnych
Miara wyniku |
Ramy czasowe |
|---|---|
|
Change from Baseline of the Parent Trial in Waist Circumference
Ramy czasowe: Baseline of parent trial to Week 48 of current trial
|
Baseline of parent trial to Week 48 of current trial
|
|
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
Ramy czasowe: Baseline of parent trial to Week 48 of current trial
|
Baseline of parent trial to Week 48 of current trial
|
|
Percent Change from Baseline in Body Weight
Ramy czasowe: Baseline of current trial to Week 48
|
Baseline of current trial to Week 48
|
|
Percentage of Participants with No Body Weight Gain of >3% From Baseline
Ramy czasowe: Week 48 of current trial
|
Week 48 of current trial
|
|
Percentage of Participants with No Body Weight Gain of >5% From Baseline
Ramy czasowe: Week 48 of current trial
|
Week 48 of current trial
|
|
Percentage of Body Weight Reduction Maintained from the Parent Trial
Ramy czasowe: Baseline of parent trial to Week 48 of current trial
|
Baseline of parent trial to Week 48 of current trial
|
|
Percentage of Participants Maintaining ≥ 80% of the Body Weight Reduction Achieved in the Parent Trial
Ramy czasowe: Baseline of parent trial to Week 48 of current trial
|
Baseline of parent trial to Week 48 of current trial
|
|
Percentage of Participants Achieving ≥ 5% Reduction in Body Weight from Baseline of the Parent Trial
Ramy czasowe: Baseline of parent trial to Week 48 of current trial
|
Baseline of parent trial to Week 48 of current trial
|
|
Percentage of Participants Achieving ≥ 10% Reduction in Body Weight from Baseline of the Parent Trial
Ramy czasowe: Baseline of parent trial to Week 48 of current trial
|
Baseline of parent trial to Week 48 of current trial
|
|
Percentage of Participants Achieving ≥ 15% Reduction in Body Weight from Baseline of the Parent Trial
Ramy czasowe: Baseline of parent trial to Week 48 of current trial
|
Baseline of parent trial to Week 48 of current trial
|
|
Percentage of Participants Achieving ≥ 20% Reduction in Body Weight from Baseline of the Parent Trial
Ramy czasowe: Baseline of parent trial to Week 48 of current trial
|
Baseline of parent trial to Week 48 of current trial
|
|
Change from Baseline of the Parent Trial in Hemoglobin A1c
Ramy czasowe: Baseline of parent trial to Week 48 of current trial
|
Baseline of parent trial to Week 48 of current trial
|
|
Change from Baseline in HbA1c
Ramy czasowe: Week 48 of current trial
|
Week 48 of current trial
|
Współpracownicy i badacze
Sponsor
Śledczy
- Dyrektor Studium: MD, Amgen
Publikacje i pomocne linki
Przydatne linki
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Rzeczywisty)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- 20210182
- 2025-524788-19-00 (Ctis)
- U1111-1332-0531 (Inny identyfikator: WHO/UTN Number)
- 2025 (Grant/umowa NIH USA)
Plan dla danych uczestnika indywidualnego (IPD)
Planujesz udostępniać dane poszczególnych uczestników (IPD)?
Opis planu IPD
De-identified individual patient data for variables necessary to address the specific research question in an approved data sharing request.
Ramy czasowe udostępniania IPD
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.
Kryteria dostępu do udostępniania IPD
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.
Typ informacji pomocniczych dotyczących udostępniania IPD
- PROTOKÓŁ BADANIA
- SOK ROŚLINNY
- ICF
- CSR
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
Te informacje zostały pobrane bezpośrednio ze strony internetowej clinicaltrials.gov bez żadnych zmian. Jeśli chcesz zmienić, usunąć lub zaktualizować dane swojego badania, skontaktuj się z register@clinicaltrials.gov. Gdy tylko zmiana zostanie wprowadzona na stronie clinicaltrials.gov, zostanie ona automatycznie zaktualizowana również na naszej stronie internetowej .