Effect of Caloric Restriction on Fat Oxidation in Obese Men and Women (Magellan II) (MagellanII)
Obesity, Overweight, Metabolic Diseases
About this trial
This is an interventional basic science trial for Obesity focused on measuring fatty acid oxidation, Proton magnetic resonance spectroscopy
Eligibility Criteria
Inclusion Criteria:
- Male or female subjects between the ages of 18 and 55 years, inclusive
- Body Mass Index (BMI) 27-30 kg/m2, inclusive, with hypertension, controlled (<140 / <90) either by diet or medication.
- BMI 30-40 kg/m2, inclusive.
- An informed consent document signed and dated by the subject or a legally acceptable representative.
- Subjects who are willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
Exclusion Criteria:
- Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular (hypertension controlled (<140 / <90) either by diet or medication is acceptable), hepatic, psychiatric, neurologic, allergic, (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at time of dosing), muscle disease, diabetes, or severe uncontrolled hypertension.
- Known hypersensitivity to phentermine, lidocaine, bupivicaine or any medication component of the study procedure.
- Presence of cardiac pacemaker, implanted cardiac defibrillator, or brain aneurysm clips.
- Any significant bleeding diathesis which could preclude recovery from the biopsy procedure. ASA, ibuprofen, and any other oral anti platelet agent will be discontinued at least 7 days prior to procedure.
- Abnormal CK as per site laboratory ranges.
- Subjects with either a medical history of or physical evidence of keloid scar formation upon physical examination.
- 12-lead electrocardiogram (ECG) demonstrating a clinically significant abnormality.
- Pregnant or nursing females or females less than 6 months postpartum from the scheduled date of collection.
- Participation in non-routine rigorous exercise (e.g., road races, heavy lifting, etc.) within one week prior to the muscle biopsy procedures.
- Presence of any condition in the investigator's opinion that may negatively affect subject safety or protocol adherence.
- Females of childbearing potential (any female except those with tubal ligation, hysterectomy, or absence of menses > 2years) unwilling to use an approved method of contraception (condom, diaphragm, implantable uterine device (IUD) that does not release hormones).
- Prior participation in the Magellan I study at the Translational Research Institute for Metabolism and Diabetes.
Sites / Locations
- Translational Research Institute for Metabolism and Diabetes
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Overwight/Obese with no drug
Overweight/obese with Phentermine
After screening, overweight/obese subjects (BMI >27 - ≤40.0) subjects will be started on a low calorie diet (approximately 900-1000 kcal/d) until a target weight loss is achieved.
After screening, overweight/obese (BMI >27.0 - ≤40.0) subjects will be started on a low calorie diet (approximately 900-1000 kcal/d) until a target weight loss is achieved. Individuals not on track to achieve their target weight by four weeks will receive the drug Phentermine to promote weight loss. Then, following eight weeks LCD (or four weeks LCD + four weeks LCD+Phentermine), in the event that they did not achieve the target weight loss, subjects will be given the option to continue with the LCD + Phentermine for up to an additional 12 weeks, under a doctor's supervision.