Dulaglutide
Also known as: Trulicity, Dulaglutida
Molecular Identifiers
Molecular Formula
C2646H4044N704O836S18
CAS Number
923950-08-7
UNII
WTT295HSY5
Molecular Weight
~59.7 kDa (59670.63 g/mol)
Overview
Long-acting GLP-1 receptor agonist composed of a GLP-1 analog fused to a modified IgG4 immunoglobulin Fc fragment. This fusion protein confers an extended half-life of approximately 5 days, enabling weekly administration. Approved for type 2 diabetes treatment and cardiovascular risk reduction in diabetic patients.
FDA-approved as Trulicity (2014) for type 2 diabetes treatment, including cardiovascular risk reduction in diabetic patients, demonstrated in the REWIND study.
The core clinical effects of dulaglutide are improved glycemic control in type 2 diabetes (HbA1c reduction of 0.7–1.6%), modest weight loss of 1–3 kg, and a reduction in major cardiovascular events demonstrated in the REWIND trial. Once-weekly administration via a pre-filled pen supports adherence compared with daily GLP-1 agonists.
Approved by the FDA in 2014 as Trulicity, it is now a first- or second-line therapy in type 2 diabetes, frequently combined with metformin. Following approval of the cardiovascular indication, it is also prescribed to diabetic patients at increased cardiovascular risk. Off-label use for weight loss alone exists but is not the approved indication and tends to give way to analogs with a dedicated obesity dossier.
Dulaglutide was developed by Eli Lilly as part of the second generation of long-acting GLP-1 agonists, using an IgG4 Fc fusion design to extend half-life without relying on albumin binding.
Among GLP-1 agonists, it occupies a middle tier: more modern and more convenient than exenatide (an older formulation with twice-daily or weekly microsphere dosing), but less potent on weight loss and glycemic control than semaglutide, which has consolidated itself as the class reference. Its current value proposition is the cardiovascular dataset in type 2 diabetes from the REWIND trial.
Fusion protein (~59.7 kDa) — GLP-1 analog fused with IgG4 Fc fragment
Half-life
~5 days
Administration Route
Subcutaneous
Category
Metabolic & Fat Loss
Mechanism of Action
- GLP-1 receptor agonism with glucose-dependent insulin secretion stimulation
- Suppression of glucagon secretion in hyperglycemic states
- Delayed gastric emptying
- Appetite and caloric intake reduction via hypothalamic signaling
- Improved insulin sensitivity in peripheral tissues
- Cardiovascular protection with reduction of major adverse cardiovascular events (MACE)
Dosage Protocol
Data compiled from the literature. This does not constitute medical advice.
| Parameter | Value |
|---|---|
| Dose | 0.75-4.5 mg per week (subcutaneous) |
| Frequency | Once weekly |
| Timing | Same day of the week, any time of day, regardless of meals |
| Duration | Continuous use (with gradual dose escalation) |
Reported Side Effects
Adverse effects described in the literature. Severity and frequency vary between individuals.
- Nausea
- Diarrhea
- Vomiting
- Abdominal pain
- Decreased appetite
- Fatigue
Product Properties
| Purity | >95% |
| Appearance | Clear to slightly opalescent, colorless to slightly yellow solution in pre-filled pen |
| Solubility | Pre-filled solution — no reconstitution required |
| Source | Recombinant DNA technology (CHO cells) |
| Storage | Refrigerated 2-8°C. Do not freeze. Protect from light. Once opened, use within 14 days at room temperature (up to 30°C). |
Presentations & Preparation
Vials of Dulaglutide found in the research market:
Reconstitution
- Diluent: Not applicable — pre-filled pen ready for use
- Volume: Single-dose pre-filled pen (0.5 ml)
- Use single-dose pre-filled pen — no reconstitution required
- Inject subcutaneously in abdomen, thigh or arm, rotating sites
- Dose escalation every 4 weeks (0.75 → 1.5 → 3.0 → 4.5 mg)
- Each pen is single-use — discard after administration
Storage
- Lyophilized: Not applicable — ready-to-use solution
- Reconstituted: Refrigerated 2-8°C (unopened); room temperature up to 14 days (maximum 30°C)
- Do not freeze — discard if frozen
- Protect from direct light
- Keep in original packaging until time of use
Scientific Studies
Published studies on Dulaglutide.
Dulaglutide and cardiovascular outcomes in type 2 diabetes (REWIND): a double-blind, randomised placebo-controlled trial
Gerstein HC, Colhoun HM, Dagenais GR, Diaz R, Lakshmanan M, Pais P, et al.
Efficacy and Safety of Dulaglutide Added Onto Pioglitazone and Metformin Versus Exenatide in Type 2 Diabetes (AWARD-1)
Wysham C, Blevins T, Arakaki R, Colon G, Garcia P, Atisso C, et al.
Related Peptides
5-Amino-1MQ
50 mg per capsule · 1-2 times daily
Adipotide
0.03 mg/kg body weight (Phase 1 trial starting dose) · Once daily
AICAR
0.1 mg/kg/min by intravenous infusion (CABG trial dose) · Single continuous infusion
AOD 9604
300-600 mcg per injection · Once daily
Cagrilintide
1.2-4.5 mg per week (subcutaneous) · Once weekly
Exenatide
5-10 mcg per injection (subcutaneous) · Twice daily (Byetta) or once weekly (Bydureon)