Dulaglutide — reference
Dulaglutide: glp-1 receptor agonist (fc fusion), approximate mass 59.7 kDa, 5 days half-life. Identity, evidence base, analytical considerations and limitations.
Scope
A maintained identity and evidence reference for Dulaglutide. It is deliberately narrow: what the molecule is, what has been published about it, and what an analytical report on it can and cannot establish. It contains no dosing recommendations and is not advice about anyone's care.
Where a figure is approximate this page says so. Where something is unknown, it says that instead of filling the gap.
Identity
| Field | Value |
|---|---|
| Class | GLP-1 receptor agonist (Fc fusion) |
| Approximate molecular mass | ≈ 59.7 kDa |
| Elimination half-life | ≈ 5 days |
| Route and schedule | Subcutaneous weekly |
| Regulatory status | Licensed for type 2 diabetes |
Masses quoted here are approximate and are given for orientation when reading an analytical report. For a mass-error calculation, use the exact monoisotopic mass computed from the elemental composition rather than a rounded figure from a reference page, including this one.
What it is
Dulaglutide is structurally quite different from the acylated peptides: two GLP-1 analogue peptides fused to an immunoglobulin Fc fragment. The size accounts for the long half-life by a different route — reduced renal clearance and Fc-mediated recycling rather than albumin binding.
That structural difference matters analytically. A protein of this size behaves nothing like a 40-residue peptide on a reversed-phase column and requires different methods entirely.
Evidence base
Published studies and programmes most relevant to this compound:
- AWARD programme
- REWIND
REWIND is the relevant cardiovascular outcome trial and included a substantial primary-prevention population, which distinguishes it from several other trials in the class.
Individual digests for several of these are maintained separately in this commons and are linked from the evidence category. A digest is a summary with its criticisms attached; it is not a substitute for reading the paper.
Analytical considerations
Reversed-phase HPLC with ultraviolet detection at 214 nm is the usual purity method, and electrospray mass spectrometry the usual identity method. A purity figure is an area percentage at a stated wavelength under a stated gradient, and it is not interchangeable with a content determination.
Three things a purity assay on this compound will not tell you: how much peptide is in the container (that requires a content assay), what the counter-ion is (that requires ion chromatography or NMR), and whether anything is present that does not elute under the method used.
See Reversed-phase HPLC for peptides and LC-MS identity confirmation for the method detail.
Status and legality
Licensed for type 2 diabetes.
Material sold as research-use-only is not a licensed medicine, whatever it contains and however good its certificate is. That is a statement about regulatory status rather than about quality, and it is true of high-purity material as much as of poor material.
Limitations of this page
This is a reference page maintained by volunteers, reviewed on the date shown, and it will be out of date at some point after that date. It summarises published work rather than reproducing it, and a summary always loses something. Where the summary and the source disagree, the source is right.
If you find an error, the fastest route to fixing it is a topic in doc review naming the sentence and the source. The maintainers named above are notified.
Revision history
| 2025-12-01 | excursion_check | Restructured into shorter sections so the outline navigation is usable. |
| 2025-09-16 | np_gilmore | Removed a paragraph that duplicated a linked page, and linked it instead. |
| 2025-04-21 | d.szymanski | Reverted an unsourced change and asked the editor to re-apply it with a citation. |
| 2024-12-23 | a.reyes | Plain-language pass on the opening section after feedback from a newcomer. |
| 2024-09-23 | batchlog | Initial promotion from the source topic. Structure taken from the marked solution. |
Every edit to a maintained document records its author and a note explaining the change. An edit without a note may be reverted by any wiki editor under R9, and the revert is logged. Disagreements about content belong on the source topic rather than in the revision history (R10).
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