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MONOGRAPH No. 122
TYPE
GIP receptor agonist
MW
Peptide (undisclosed)
CAS
Not assigned
EU STATUS
Investigational · Not approved
WADA
Not listed
MIN PURITY
≥98% HPLC
⚖ GLP-1 & Weight

ZP6590 — EU research guide.

ZP6590 is Zealand Pharma's investigational long-acting GIP receptor agonist, designed not as a standalone obesity drug but as a co-formulation partner that boosts the effect of GLP-1 medicines like semaglutide.

Last reviewed:

What is ZP6590?

In preclinical models, ZP6590 has little weight-loss effect alone but substantially amplifies the weight loss produced by GLP-1 monotherapy when combined — the same ‘dual agonism’ logic behind tirzepatide, but as two separate co-dosed molecules instead of one hybrid peptide.

What does the research show?

As of Zealand Pharma's early-2026 pipeline disclosures, ZP6590 is Phase 1-ready for obesity, positioned as a future combination partner alongside the company's more advanced amylin analogue, petrelintide.

EU legal status

Not approved anywhere; a very early-stage, single-sponsor investigational candidate with no legitimate research-peptide supply route.

Early-stage investigational compound (Phase 1-ready). Not EMA/FDA-approved. No human use outside authorised trials.
✓ For the approved dual-mechanism class this compound is designed to complement, PeptideCompare tracks tirzepatide and semaglutide from EU research vendors with COA documentation.

Molecular information

Molecular weight
Peptide (undisclosed)
CAS number
Not assigned

Pharmacokinetics

No established human pharmacokinetic data. Published human PK parameters for this compound are not available; reported data are limited to animal models or absent. No curve is shown, to avoid implying data that does not exist.

GLP-1/GIP compounds across EU suppliers

COA-verified EU vendors · Updated monthly

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