Magnetic Jejuno-Ileal Diversion Study ("MJI Study")

Prior treatment

• Prior intestinal, colonic or duodenal surgery, other than bariatric
• Prior surgery, trauma, prostheses, disease or genetic expression which prevent or contra-indicate the procedure, including scarring and abnormal anatomy.
• Had surgical or interventional procedure within 30 days prior to procedure
• Any scheduled surgical or interventional procedure planned within 30 days postprocedure
• Any stroke/TIA within 6 months prior to consent
• Requires chronic anticoagulation therapy (except aspirin)
• Recent tobacco or nicotine product cessation within \< 3 months prior to informed consent
• Currently participating in another clinical research study with an investigational drug or medical device

Other illness

• Type 1 diabetes
• Uncontrolled hypertension, dyslipidemia or sleep apnea
• Refractory gastro-esophageal reflux disease (GERD)
• Barrett's disease
• Helicobacter pylori positive and/or active ulcer disease
• Inflammatory bowel or colonic diverticulitis disease
• Psychiatric disorder, except well-controlled depression with medication for \> 6 months
• History of substance abuse
• Unhealed ulcers, bleeding lesions, tumor, or any other lesion at target magnet deployment site
• Active infections requiring antibiotic therapy, unless resolved before undergoing the study procedure
• Known allergies to the device components or contrast media
• Limited life expectancy due to terminal disease
• Any condition that, in the investigator's opinion, may preclude completion of followup assessments through Day 360 (e.g., a medical condition that may increase the risk associated with study participation or may interfere with interpretation of study results, inability to adhere to the visit schedule, or poor compliance with treatment regimen)

Other

• Use of injectable insulin
• Uncontrolled T2DM
• Plan to perform a sleeve gastrectomy with the jejuno-ileal anastomosis procedure
• Large hiatal hernia
• Any anomaly precluding orogastric access by gastroscope and catheters, and manipulation techniques.
• Implantable pacemaker or defibrillator
• Woman who is either pregnant or breast feeding
• Woman of childbearing potential who does not agree to use an effective method of contraception.
• Any comorbidity or current status of subject's physiological fitness that in the surgeon's or anesthesiologist's opinion represents safety concerns that make the subject medically unfit for the procedure, including any significant congenital or acquired anomalies of the GI tract at or distal to the placement of the magnets.
• Expected need for MR imaging within the first 2 months after the procedure
• Any anomaly preventing/contraindicating endoscopic or laparoscopic access and procedures
• Unable to comply with the follow-up schedule and assessments

• 18-65 years of age, inclusive, at the time of informed consent
• BMI 30-40 kg/m2
• T2DM (defined as HbA1c ≥ 6.5%) without previous sleeve gastrectomy and without plan to perform a concurrent sleeve gastrectomy
• Agrees to refrain from any type of additional bariatric or reconstructive surgery that would affect body weight for the duration of the study
• If a child-bearing female, subject must commit to not becoming pregnant and agree to use contraception for the duration of the study
• Willing and able to comply with protocol requirements