Brain scans reveal how Weight-Loss drug targets appetite
NCT ID NCT02400359
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study uses brain scans (fMRI) to see how the weight-loss drug lorcaserin changes activity in brain areas that control appetite and food intake. Forty obese adults will receive either lorcaserin or a placebo pill. Researchers will also measure changes in body composition. The goal is to understand the brain mechanisms behind the drug's effects.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Lorcaserin (Belviq)
- What this could lead to
- If successful, this could clarify how lorcaserin works in the brain to reduce appetite, potentially improving weight-loss treatments.
- What could go wrong
- This is a small, early-phase study focused on brain imaging, not weight loss itself. Results may not translate to real-world weight reduction or long-term safety.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
About 40 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Oct 2014
- Expected to finish
-
Jun 2027
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 65 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Obese: BMI\> 30 kg/m2 or \>27 kg/m2 with comorbidities (including but not limited to insulin resistance, hypertension, dyslipidemia, cardiovascular disease, stroke, sleep apnea, gallbladder disease, hyperuricemia and gout, and osteoarthritis). Additionally, women participants must use double barrier methods to prevent pregnancy (diaphragm with intravaginal spermicide, cervical cap, male or female condom with spermicide). If a woman suspects that she has become pregnant at any time or does not use one of the contraceptive methods recommended by the investigator, she must notify the study staff. If a woman becomes pregnant, she will be withdrawn from the study. The study staff will follow the progress of her pregnancy and the birth of her child. Exclusion Criteria: 1. Subjects using any other weight loss products (orlistat, phentermine, topiramate, fenfluramine, dexfenfluramine, amphetamines, GLP-1 agonists) or use within 3 months. 2. Women who are breastfeeding, pregnant, or wanting to become pregnant. 3. Women using IUD (intrauterine device) 4. Any change in the dosage of hormonal contraceptive medications (birth control pills, implanon). Subjects should remain on same medication/ same dose during the time of the entire study. 5. Moderate (creatinine clearance of 30-59 ml/min) and severe renal impairment (creatinine clearance below 30 ml/min) and end-stage renal disease 6. Moderate, or severe hepatic impairment 7. Hypersensitivity to the active substance or any of the excipients in lorcaserin 8. Congestive heart failure and/or pulmonary hypertension 9. Arrhythmias (bradycardia, tachycardia) and valvular heart diseases 10. Diagnosis of diabetes, defined per ADA criteria as Hba1c \> 6.5% and/or fasting glucose \> 125 mg/dL and/or random glucose \> 200 mg/dL 11. Inflammatory conditions like inflammatory bowel disease, Rheumatoid arthritis etc. 12. Alcohol consumption- the maximum quantity for men is 140g-210g per week. For women, the range is 84g-140g per week or drinking as consuming no more than two drinks a day for men and one for women. Alcohol can cause increased risk of pancreatitis and hypoglycemia. 13. Untreated thyroid disease like hypothyroidism or hyperthyroidism 14. Subjects taking the following medications: phosphodiesterase inhibitors, serotonergic medications (e.g. SSRI (selective serotonin reuptake inhibitor), SNRI, MAO (monoamine oxidase) inhibitors, bupropion, tricyclic antidepressants, St. John's Wort), valproic acid, codeine (CYP2D6 inhibition), tamoxifen, timolol, warfarin, steroids (inhaled or systemic due to reduced hypoglycemic effect), and subjects on other hormones (LHRH analogs etc). 15. Subjects with any type of bioimplant activated by mechanical, electronic, or magnetic means (e.g. cochlear implants, pacemakers, neuron or biostimulators, electronic infusion pumps, etc.) 16. Subjects with any type of metallic implant that could potentially be displaced or damaged during MRI, such as aneurysm clips, metallic skull plates, surgical implants etc. or metal containing tattoos 17. Anxiety of small spaces and/or claustrophobia 18. Uncontrolled cardiac impairment, circulatory impairment, or inability to perspire (poor thermoregulatory function) 19. Significant sensory or motor impairment 20. Epilepsy, particularly photo-sensitive epilepsy, which may place the individual at a higher risk for adverse events during fMRI scanning with visual stimulation 21. Subjects with neurological problems which may interfere with or complicate testing (e.g. presence of titubation) 22. Body weight above the limitation of the MRI scanning table (330lbs/150 Kg) or body dimensions that could difficult the performance of the scan. 23. Subjects who cannot adhere to the experimental protocol for any reason 24. Anemia with Hgb less than 10 25. Uncontrolled infectious diseases (e.g. HIV, hepatitis, chronic infections etc) 26. Any uncontrolled endocrine condition, e.g. Cushing's, Acromegaly, etc 27. Any cancers or lymphoma 28. Eating disorders like anorexia, bulimia 29. Weight loss surgery or gastrectomy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215, United States
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