PEDEvidence
Latest studiesAll common questions
FAT LOSS & EMERGING TREATMENTS · COMMON QUESTIONS

What makes amycretin, now called zenagamtide, different from tirzepatide?

Receptor targets, oral versus injectable formulations, and why headline percentages do not rank drugs.

Evidence at a glancePublished phase 2 studies; cross-trial superiority not established

Zenagamtide is the name now used for amycretin. It combines GLP-1 and amylin activity in one molecule, and the publications also describe calcitonin receptor agonism. Tirzepatide instead combines GIP and GLP-1 receptor activity. Those targets explain why the compounds are scientifically distinct, but they do not predict which is best for an individual. Zenagamtide’s oral and injectable formulations have separate clinical reports and should not be combined into a single headline result.[1][2][3][4]

The oral phase 2 study in type 2 diabetes demonstrated improved HbA1c compared with placebo; the injectable program also reported weight reductions. A glucose-control endpoint is not a direct test of fat loss or muscle preservation. Gastrointestinal adverse events and treatment discontinuations matter alongside efficacy. Comparisons with tirzepatide require attention to diabetes status, treatment duration, formulation and statistical handling of discontinued treatment. Different trials do not establish that zenagamtide is superior, and an injectable result does not establish the same effect from an oral product.[1][2][3][4]

Sources & further reading

  1. Oral zenagamtide: phase 2 trial in type 2 diabetes
  2. Oral zenagamtide phase 2 trial record
  3. Injectable zenagamtide: phase 2 publication
  4. Zenagamtide: injectable phase 2 findings

Updated September 24, 2026 · Evidence summaries for understanding research.