BARI-OPTIMISE · ICD-10 Z98.84, E66.01 · Updated May 25

Weight regain after bariatric surgery and GLP-1.

FDA-labeled indication. Preferred drug: Wegovy (semaglutide 2.4 mg) or Zepbound (tirzepatide).

The headline trial: BARI-OPTIMISE

BARI-OPTIMISE (Semaglutide for Post-Bariatric Weight Regain)

Mok et al., Lancet Diabetes & Endocrinology, 2024

Semaglutide 2.4 mg weekly produced 8.8 percent mean body-weight reduction versus 0.5 percent for placebo over 16 weeks in adults with weight regain following bariatric surgery. Tolerability and adherence profiles were similar to non-surgical patients.

Trial enrollment criteria

  • History of Roux-en-Y gastric bypass, sleeve gastrectomy, gastric bypass or duodenal switch at least 18 months prior
  • Documented post-surgical weight nadir followed by weight regain
  • Current BMI greater than or equal to 30 (or 27 with comorbidity, FDA labeling)

Does this trial apply to you?

Bariatric surgery history (ICD-10 Z98.84) does not exclude a patient from GLP-1 therapy. The qualifying criterion is current BMI plus comorbidities, regardless of how the patient reached that BMI. Most major payers approve PA for post-bariatric patients under the standard obesity indication.

What to ask your prescriber

  1. Type and date of prior bariatric surgery
  2. Documented weight nadir and current weight
  3. Whether your bariatric surgeon or obesity medicine specialist will co-sign the PA
  4. Any post-surgical complications (dumping syndrome, nutritional deficiencies) that need consideration

Editorial notes

  • Post-bariatric patients sometimes experience more pronounced GI side effects on GLP-1. Slow titration is usually appropriate.
  • Continue bariatric multivitamin and B12/iron monitoring; rapid weight loss can mask nutritional deficiencies.
  • If the patient is within 12 months of surgery, defer the GLP-1 conversation; the surgical weight loss is still on its natural trajectory.

Clinical trials for Weight regain after bariatric surgery

Could you join a Weight regain after bariatric surgery study? GLP-1 clinical trials are enrolling now for this condition. Many cover screening and trial-related care, and many pay participants for their time.
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Take it to your prescriber: PA letter templates

Editable prior-authorization letter templates that cite the registration trial above. Pick the plan your prescriber will submit to, copy the template, fill in the patient-specific findings and have your clinician sign and submit.

Not seeing your plan? The full PA letter librarycovers 20 plans × 10 indications = 200 templates. The appeal letter library handles denials.

Other GLP-1 conditions

Editorial provenance

Editorial review by John, Editor on 2026-05-23, against BARI-OPTIMISE (Mok et al., Lancet Diabetes & Endocrinology, 2024). We do not yet have a credentialed medical reviewer on staff (actively recruiting). This page summarises public registration-trial data and FDA labeling. It is not clinician-authored medical advice.

John Samaras, founder and editor of GLP Chart
John Samaras, founder and editor. Full-time on US GLP-1 telehealth research since 2026. Editorial-only role (not a clinician). Writes from public registration-trial publications, FDA labeling, and PBM clinical-policy documents. Read more about the editorial process →
Medical reviewer position currently open and being recruited. See the role →

Educational summary of published registration trial data. Not medical advice. Not a substitute for evaluation by a treating clinician. Trial-level results do not guarantee individual outcomes. Discuss eligibility, contraindications, dose adjustments and drug interactions with your prescriber. We do not have a credentialed medical reviewer on staff yet (actively recruiting); the content below is editor-written from public registration-trial publications and FDA labeling, not clinician-authored medical advice.

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