- ICH GCP
- Rejestr badań klinicznych w USA
- Badanie kliniczne NCT07829198
Efficacy of Tirzepatide for Weight Management in Patients With Suboptimal Weight Loss After Bariatric Surgery: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial (TirBaS)
Many people who have bariatric (weight-loss) surgery do not lose as much weight as expected, or they regain weight over time. This study will test whether a medicine called tirzepatide can help these patients lose more weight and improve their overall health.
Participants who had bariatric surgery at least one year ago and still have obesity with insufficient weight loss will be randomly assigned, like a coin flip, to receive either tirzepatide or a placebo (an inactive injection that looks the same). Neither participants nor study staff will know who is receiving which treatment.
Participants will inject the study medicine or placebo once a week for 52 weeks, starting at a low dose that is gradually increased. During the study, researchers will measure body weight, waist size, blood pressure, and blood tests related to metabolism and inflammation. Participants will also answer questionnaires about their quality of life.
The main goal is to find out whether tirzepatide leads to greater weight loss than placebo after one year of treatment.
Przegląd badań
Szczegółowy opis
TirBaS is a prospective, multicenter, randomized, double-blind, placebo-controlled, parallel-group clinical trial evaluating the efficacy of tirzepatide, a dual GIP/GLP-1 receptor agonist, for weight management in adults with a history of bariatric surgery (Roux-en-Y gastric bypass or sleeve gastrectomy) performed at least 12 months prior to enrollment, who present with suboptimal weight loss or weight regain.
A total of 70 participants will be randomized in a 1:1 ratio to receive either tirzepatide or matching placebo, administered once weekly by subcutaneous injection. Randomization will be stratified by type of bariatric surgery, baseline BMI category, and time since surgery. Tirzepatide will be up-titrated in 2.5 mg increments every 4 weeks, up to a maximum of 15 mg or the maximum tolerated dose, with weekly dosing continuing through week 52 of the 52-week treatment period.
The primary objective is to assess the effect of tirzepatide versus placebo on the percentage change in body weight from baseline to week 52. Secondary objectives include evaluating changes in cardiometabolic parameters (body weight, BMI, waist circumference, blood pressure, HbA1c, fasting glucose, lipid profile, kidney function, liver profile), inflammatory status (hs-CRP), the proportion of participants achieving clinically meaningful weight loss thresholds (≥5%, ≥10%, ≥15%, ≥20%), and quality of life, assessed using the IWQOL-Lite-CT, EQ-5D-5L, SF-36, and a study-specific Patient Global Impression of Status (PGIS) item.
Participants will attend six study visits over 52 weeks (Weeks 0, 8, 16, 24, 36, and 52), including anthropometric measurements, vital signs, laboratory safety assessments, and adverse event monitoring. Optional biobanking of blood and urine samples will be offered at Visits 1, 4, and 6 for future research, subject to separate informed consent.
The primary analysis will follow the intention-to-treat principle, using an analysis of covariance (ANCOVA) model adjusted for baseline weight and stratification factors. Secondary continuous outcomes will be analyzed using mixed-model repeated measures (MMRM), and categorical outcomes using logistic regression. No interim analysis is planned.
Typ studiów
Zapisy (Szacowany)
Faza
- Faza 3
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Janete Santos, PhD
- Numer telefonu: +351 220 426 569
- E-mail: investigaclinica@med.up.pt
Lokalizacje studiów
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Porto, Portugalia
- Unidade Local de Saúde de São João
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Kontakt:
- Paula Freitas
- Numer telefonu: +351 966869160
- E-mail: paula_freitas@sapo.pt
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Porto, Portugalia
- Unidade Local de Saúde de Santo António
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Kontakt:
- Teresa Pereira
- Numer telefonu: +351 961543537
- E-mail: teresa.rocha.pereira@gmail.com
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Santa Maria da Feira, Portugalia
- Unidade Local de Saúde de Entre Douro e Vouga
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Kontakt:
- Mariana Monteiro
- Numer telefonu: +351 919875148
- E-mail: mpmonteiro.icbas@gmail.com
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
- Dorosły
- Starszy dorosły
Akceptuje zdrowych ochotników
Opis
Inclusion Criteria:
- Adults (male or female) aged ≥18 years.
- History of bariatric surgery (Roux-en-Y gastric bypass or sleeve gastrectomy) performed ≥12 months before enrollment.
- Current BMI ≥30 kg/m².
- Evidence of suboptimal weight loss, defined as percentage total weight loss (%TWL) since surgery of less than 25% (defined as the percentage of weight loss comparing current body weight with body weight before surgery).
- Absence of recent weight loss (defined as <5% reduction in body weight over the 6 months prior to screening); participants may be weight stable (<5% variation in body weight over the 6 months prior to screening) or have experienced weight gain.
- In the investigator's opinion, well-motivated, capable, and willing to comply with study procedures.
- For male participants: male participants with partners of childbearing potential should be willing to use reliable contraceptive methods throughout the study and for 5 half-lives of study drug plus 90 days, corresponding to 4 months after the last injection.
For female participants:
a. Female participants not of childbearing potential may participate and include those who are: i. infertile due to surgical sterilization (hysterectomy, bilateral oophorectomy or tubal ligation), congenital anomaly such as Mullerian agenesis ii. postmenopausal, defined as either:
- a woman at least 40 years of age with an intact uterus, not on hormone therapy, who has cessation of menses for at least 1 year without an alternative medical cause, AND a follicle-stimulating hormone ≥40mIU/mL; women in this category must test negative in pregnancy test prior to study entry
- a woman 55 or older not on hormone therapy, who has had at least 12 months of spontaneous amenorrhea
- a woman at least 55 years of age with a diagnosis of menopause prior to starting hormone replacement therapy b. Female participants of child-bearing potential (not surgically sterilized and between menarche and 1-year postmenopausal) must:
- test negative for pregnancy at Visit 1 based on a serum pregnancy test
- if sexually active, agree to use 2 forms of effective contraception, where at least 1 form is highly effective, for the duration of the trial and for 30 days thereafter
- not be breastfeeding
- Provision of written informed consent prior to any study-specific procedures.
Exclusion Criteria:
- Use of a GLP-1 receptor agonist (GLP-1 RA) or any other GLP-1-based therapy at present or within the past 6 months.
- Prescription of a GLP-1 RA or other GLP-1-based therapy within the past 12 months that could not be initiated or maintained due to drug supply shortages.
- Have a planned surgical treatment, endoscopic and/or device-based therapy for obesity during the period of the study.
- History of type 1 diabetes or uncontrolled type 2 diabetes (HbA1c >10%).
- Type 2 diabetes currently treated with insulin or sulfonylureas.
- Have a known clinically significant gastric emptying abnormality (for example, severe diabetic gastroparesis or gastric outlet obstruction) or chronically take drugs that directly affect GI motility.
- Have had a history of chronic or acute pancreatitis.
- Have NYHA Functional Classification III or IV heart failure.
- Have thyroid-stimulating hormone (TSH) outside of the reference range at screening visit.
- Have obesity induced by other endocrinologic disorders (for example, Cushing Syndrome) or diagnosed monogenetic or syndromic forms of obesity (for example, Melanocortin 4 Receptor deficiency or Prader Willi Syndrome).
- Have a history of significant active or unstable Major Depressive Disorder or other severe psychiatric disorder (for example, schizophrenia, bipolar disorder, or other serious mood or anxiety disorder) within the last 2 years.
- Have any lifetime history of a suicide attempt.
- Have a family or personal history of medullary thyroid carcinoma or Multiple Endocrine Neoplasia (MEN) Syndrome type 2.
- Involvement in the planning and/or conduct of the study (applies to both Investigator staff and/or staff at the study site).
- Participation in another clinical study with an investigational product during the last month.
- Unwilling or unable to sign the informed consent form.
- History of active malignancy within the past 5 years (except adequately treated non-melanoma skin cancer or in situ carcinoma of the cervix).
- Known hypersensitivity or contraindication to tirzepatide or any of its excipients.
- Have severe hepatic impairment (Child-Pugh class C).
- Have severe renal impairment (eGFR <30 mL/min/1.73 m² using CKD-EPI formula).
- Are receiving or have received within 3 months prior to screening chronic (>2 weeks or 14 days) systemic glucocorticoid therapy (excluding topical, intraocular, intranasal, intra-articular, or inhaled preparations) or have evidence of a significant, active autoimmune abnormality (for example, lupus or rheumatoid arthritis) that has required (within the last 3 months) or is likely to require, in the opinion of the investigator, concurrent treatment with systemic glucocorticoids (excluding topical, intraocular, intranasal, intra-articular or inhaled preparations) in the next 12 months.
- For female patients, pregnancy, breastfeeding, or planning pregnancy during the study period.
- Any condition which, in the investigator's opinion, may jeopardize the subject's safety or compliance with the protocol (e.g., severe psychiatric illness, alcohol or substance abuse).
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Leczenie
- Przydział: Randomizowane
- Model interwencyjny: Przydział równoległy
- Maskowanie: Poczwórny
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
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Eksperymentalny: Tirzepatide
Participants will receive tirzepatide once weekly by subcutaneous injection, self-administered at home.
Treatment will start at 2.5 mg once weekly, with up-titration in 2.5 mg increments every 4 weeks (5 mg, 7.5 mg, 10 mg, 12.5 mg, up to 15 mg), according to tolerability, up to the maximum tolerated dose or 15 mg once weekly.
Treatment will continue for a total of 52 weeks.
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Dual GIP/GLP-1 receptor agonist supplied as a prefilled syringe (2.5 mg, 5 mg, 7.5 mg, 10 mg, 12.5 mg, or 15 mg) for subcutaneous injection, manufactured by Eli Lilly and Company.
Self-administered once weekly by the participant in the abdomen, thigh, or upper arm, with rotating injection sites.
Dose up-titrated every 4 weeks in 2.5 mg increments, up to a maximum of 15 mg or the maximum tolerated dose, for a total treatment duration of 52 weeks.
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Komparator placebo: Placebo
Participants will receive matching placebo (identical prefilled syringe) once weekly by subcutaneous injection, self-administered at home, following the same up-titration schedule and visit schedule as the tirzepatide arm, for a total of 52 weeks.
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Matching placebo, supplied as a prefilled syringe identical in appearance to the tirzepatide syringe, manufactured by Eli Lilly and Company.
Self-administered once weekly by subcutaneous injection, following the same up-titration schedule, injection sites, and visit schedule as the tirzepatide arm, for a total of 52 weeks
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
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Percentage Change in Body Weight from Baseline to Week 52
Ramy czasowe: Baseline (Week 0) to Week 52
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To assess the effect of tirzepatide versus placebo on the percentage change in body weight relative to baseline at week 52
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Baseline (Week 0) to Week 52
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Change in Body Weight
Ramy czasowe: From baseline to Weeks 8, 16, 24, 36, and 52
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Change in body weight (kg) from baseline.
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From baseline to Weeks 8, 16, 24, 36, and 52
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Change in Body Mass Index (BMI)
Ramy czasowe: From baseline to Weeks 8, 16, 24, 36, and 52
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Change in BMI, calculated as body weight in kilograms divided by the square of height in meters
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From baseline to Weeks 8, 16, 24, 36, and 52
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Change in Waist Circumference
Ramy czasowe: From baseline to Weeks 8, 16, 24, 36, and 52
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Change in waist circumference (cm)
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From baseline to Weeks 8, 16, 24, 36, and 52
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Change in Blood Pressure
Ramy czasowe: From baseline to Weeks 8, 16, 24, 36, and 52
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Change in systolic and diastolic blood pressure (mmHg), measured in triplicate after rest.
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From baseline to Weeks 8, 16, 24, 36, and 52
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Change in Glycated Hemoglobin (HbA1c)
Ramy czasowe: From baseline to Week 52
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Change in HbA1c (%, mmol/mol), measured at the local laboratory
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From baseline to Week 52
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Change in Fasting Glucose
Ramy czasowe: From baseline to Week 52
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Change in fasting glucose, measured at the local laboratory.
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From baseline to Week 52
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Change in Lipid Profile
Ramy czasowe: From baseline to Week 52
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Change in lipid profile (total cholesterol, LDL-cholesterol, HDL-cholesterol, triglycerides), measured at the local laboratory.
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From baseline to Week 52
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Change in Kidney Function
Ramy czasowe: From baseline to Week 52
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Change in kidney function, including estimated glomerular filtration rate (eGFR, CKD-EPI formula) and creatinine.
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From baseline to Week 52
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Change in Liver Profile
Ramy czasowe: From baseline to Week 52
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Change in liver profile (ALT, AST, GGT, alkaline phosphatase, total bilirubin, direct bilirubin)
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From baseline to Week 52
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Change in High-Sensitivity C-Reactive Protein (hs-CRP)
Ramy czasowe: From baseline to Week 52
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Change in high-sensitivity C-reactive protein (hs-CRP), an assessment of inflammatory status.
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From baseline to Week 52
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Proportion of Participants Achieving Clinically Meaningful Weight Loss
Ramy czasowe: At Week 52
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Proportion of participants achieving weight loss thresholds of ≥5%, ≥10%, ≥15%, and ≥20% at week 52, derived from body weight measurements.
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At Week 52
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Change in Impact of Weight on Quality of Life-Lite Clinical Trials Version (IWQOL-Lite-CT) Score
Ramy czasowe: From baseline to Week 52
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Change in IWQOL-Lite-CT, a 20-item obesity-specific patient-reported outcome instrument assessing physical and psychosocial domains of health-related quality of life.
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From baseline to Week 52
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Change in EQ-5D-5L Score
Ramy czasowe: From baseline to Week 52
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Change in EQ-5D-5L, a standardized instrument assessing 5 dimensions of health (mobility, self-care, usual activities, pain/discomfort, and anxiety/depression), including index value and EQ Visual Analog Scale.
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From baseline to Week 52
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Change in Short Form 36 version 2 (SF-36v2) Score
Ramy czasowe: From baseline to Week 52
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Change in SF-36v2 (acute, 1-week recall version) across 8 domains, aggregated into Physical-Component and Mental-Component summary scores.
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From baseline to Week 52
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Change in Patient Global Impression of Status (PGIS)
Ramy czasowe: From baseline to Week 52
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Change in PGIS, a patient-rated assessment of current health limitation on a 5-point scale.
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From baseline to Week 52
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Współpracownicy i badacze
Sponsor
Współpracownicy
Śledczy
- Główny śledczy: Mariana Monteiro, Unidade Local de Saúde de Entre Douro e Vouga
- Główny śledczy: Paula Freitas, Unidade Local de Saúde de São João
- Główny śledczy: Teresa Pereira, Unidade Local de Saúde de Santo António
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
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
Dodatkowe istotne warunki MeSH
- Zaburzenia odżywiania
- Przekarmienie
- Masy ciała
- Nadwaga
- Stany patologiczne, oznaki i objawy
- Choroby żywieniowe i metaboliczne
- Objawy i symptomy
- Otyłość
- Aminokwasy, peptydy i białka
- Białka
- Receptor peptyd-1 podobny do glukagonu
- Glukagonowe receptory peptydowe
- Receptory, sprzężone z białkiem G.
- Receptory, powierzchnia komórkowa
- Białka błony
- Receptory, hormon przewodu pokarmowego
- Receptory, peptyd
- Tirzepatide
Inne numery identyfikacyjne badania
- TirBaS
- 2026-527275-29-00 (Ctis)
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
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