Lilly and Novo Nordisk: The Incumbents in ObesityThin moat

Amgen (AMGN) — moat facet

Amgen enters obesity against two entrenched leaders, betting that a few injections a year can pull patients away from weekly ones.

In obesity Amgen is the challenger, and the market it wants to enter is already held by two companies whose contest is described on Eli Lilly's pages in this app, Novo Nordisk and the GLP-1 War among them. Amgen's candidate, MariTide, is not yet approved; its data and the market's reaction to them are the subject of the Future Bets page. This page is about how Amgen proposes to compete.

How MariTide is positioned against the incumbentsDosingmonthly, then as few as 4 or 6 doses a yearSwitch studyfrom tirzepatide or semaglutide, every 8 weeks or quarterlyPhase 3 studies listed, Q2 20269Second candidate AMG 513discontinuedUS patent2038Amgen Q2 2026 results release; Form 10-K FY2025
Competing on how often, not whether.

The plan is dosing. Amgen describes MariTide as starting with monthly dosing, and staying on MariTide with as few as 4 or 6 doses per year1, against the weekly injections the incumbents' drugs have required. A patient who needs a few injections a year rather than one a week is an argument for switching.

Amgen is testing that argument directly. Among its Phase 3 studies is MARITIME-SWITCH, which enrolls patients moving from tirzepatide or semaglutide, the incumbents' molecules, onto MariTide given every eight weeks or quarterly2. A company that designs a trial around taking patients from rivals knows it arrives late.

It has also narrowed its bets. The second-quarter 2026 release says future development of AMG 513, a second obesity candidate, will be discontinued3.

The incumbents have scale, supply and years of prescribing behind them. What Amgen has is a different dosing schedule and a patent on MariTide's antibody-peptide conjugates to 20384. The first readout that will say whether dosing is enough is MARITIME-SWITCH; if patients switched from the incumbents keep their weight off on quarterly doses, Amgen has a place in the market, and if they do not, it has a late entry with nothing distinctive.

Moat trajectory: Holding steady

Phase 3 under way; AMG 513 dropped.

The number that tests this moat
Reported
MariTide Phase 3 studies under way
Nine listed in Q2 2026 (two ongoing, seven enrolling), three more in type 2 diabetes to start in 2026

The scale of the entry; any study stopped early would narrow the challenge.

Source: Amgen Q2 2026 results release ↗
References
  1. ReportedAmgen describes MariTide as starting with monthly dosing, and staying on MariTide with as few as 4 or 6 doses per year, against the weekly injections the incumbents' drugs have required.
    Amgen second-quarter 2026 results release, Form 8-K exhibit 99.1 - pipeline and clinical updates. — Q2 2026 · publ. 4 August 2026 · source ↗
  2. ReportedAmong its Phase 3 studies is MARITIME-SWITCH, which enrolls patients moving from tirzepatide or semaglutide, the incumbents' molecules, onto MariTide given every eight weeks or quarterly.
    Amgen second-quarter 2026 results release, Form 8-K exhibit 99.1 - pipeline and clinical updates. — Q2 2026 · publ. 4 August 2026 · source ↗
  3. ReportedThe second-quarter 2026 release says future development of AMG 513, a second obesity candidate, will be discontinued.
    Amgen second-quarter 2026 results release, Form 8-K exhibit 99.1 - pipeline and clinical updates. — Q2 2026 · publ. 4 August 2026 · source ↗
  4. ReportedWhat Amgen has is a different dosing schedule and a patent on MariTide's antibody-peptide conjugates to 2038.
    Amgen Form 10-K for fiscal 2025 - Item 1 patents, biosimilars and competitors. — FY2025 · publ. 13 February 2026 · source ↗
Sources
Generated September 28, 2026