Foundayo, Wegovy, Zepbound KwikPen
$50 copay · Jul 1, 2026–Dec 31, 2027
Medicare GLP-1 Bridge
CMS describes the Medicare GLP-1 Bridge as a short-term demonstration for eligible Medicare Part D beneficiaries, running from July 1, 2026 through December 31, 2027. It operates outside the Part D benefit’s coverage and payment flow. Part D sponsors do not carry risk for these drugs and do not have to opt in.
Stated July 1, 2026. CMS: Medicare GLP-1 Bridge. Checked October 16, 2026.
Certain GLP-1 medications
Bridge open at $50 per month
Medicare GLP-1 Bridge
On July 1, 2026, CMS announced that eligible people enrolled in Medicare Part D can obtain certain GLP-1 medications to lose weight or maintain weight reduction for $50 per month through December 31, 2027. CMS said people who already receive GLP-1 medications through existing Medicare prescription drug coverage, or who are eligible for GLP-1 coverage through the Part D benefit, will not qualify.
Stated July 1, 2026. CMS: CMS Launches Medicare GLP-1 Bridge, Expanding Access to GLP-1 Medications. Checked October 16, 2026.
Mounjaro, Ozempic, Rybelsus, Wegovy, Zepbound KwikPen, Foundayo
Part D BALANCE is not launching in 2027; the Bridge runs through 2027
Medicare and Medicaid
The CMS BALANCE model page says state Medicaid agencies can join from May 2026 through January 1, 2027, and that eligible Part D beneficiaries have access through the separate Medicare GLP-1 Bridge from July 1, 2026 to December 31, 2027. CMS says the Bridge was extended through December 31, 2027 so the agency can collect GLP-1 utilization data to share with Part D sponsors ahead of potential BALANCE in Part D. CMS lists all formulations of Mounjaro, Ozempic, Rybelsus, and Wegovy, the KwikPen formulation of Zepbound, and Foundayo, for currently covered indications and for weight management. Participation is voluntary for manufacturers, state Medicaid agencies, and Part D plans. Coverage is not guaranteed for any individual.
Stated July 1, 2026. CMS: BALANCE Model. Checked October 16, 2026.
BALANCE model drugs
CMS announcement dated April 21, 2026, as reported by KFF
Medicare Part D
KFF’s brief, updated May 11, 2026, says CMS announced on April 21, 2026 — the day after the Part D sponsor application deadline — that it would not move forward with BALANCE in Medicare in 2027 and would extend the Bridge through the end of 2027. KFF says the original Medicare design ran from January 2027 through December 2031 and that implementation in Part D is now uncertain. KFF also describes cost sharing in that original Part D design: $245 for a 30-day supply in the deductible phase, then $50 per month for enhanced plans and employer group plans and $125 per month for basic plans, and $0 after the out-of-pocket maximum ($2,100 in 2026, $2,400 in 2027). Those Part D BALANCE copays are not a benefit CMS says is in effect for 2027.
Stated April 21, 2026. KFF: What to Know About the BALANCE Model for GLP-1s in Medicare and Medicaid and the Medicare GLP-1 Bridge. Checked October 16, 2026.
Foundayo, Wegovy, Zepbound KwikPen
Three products; Zepbound vials and single-dose pens excluded
Medicare GLP-1 Bridge
CMS tells pharmacies that eligible products, when used to reduce excess body weight and maintain weight reduction, are Foundayo, Wegovy (injection and tablets), and Zepbound KwikPen. The single-dose vial and single-dose pen formulations of Zepbound are not available through the Bridge. CMS says this list was updated on April 6, 2026 to include Foundayo after FDA approval and to limit Zepbound to the KwikPen. A fill is one monthly supply (28 or 30 days). Sixty- and ninety-day fills are not available. Pen needles for the KwikPen are not covered.
Stated April 6, 2026. CMS: Medicare GLP-1 Bridge: Information for Pharmacies. Checked October 16, 2026.
Foundayo (orforglipron)
Approved April 1, 2026
FDA approval
FDA announced on April 1, 2026 that it approved Foundayo (orforglipron) for use with a reduced-calorie diet and increased physical activity to reduce excess body weight and maintain weight reduction long term in adults with obesity, or in adults with overweight and at least one weight-related comorbid condition. FDA granted the approval to Eli Lilly and Company.
Stated April 1, 2026. FDA: FDA Approves First New Molecular Entity Under National Priority Voucher Program. Checked October 16, 2026.