Not medical advice. Talk to your provider before using any peptide.
Full disclaimerPeptide Schedule Research TeamReviewed Apr 20267 Citations
Danuglipron was Pfizer's oral small-molecule GLP-1 agonist. Phase 2b trials showed 5 to 13 percent weight loss at 32 weeks, but severe GI side effects caused over 50 percent dropout. Development stopped in April 2025 after a drug-induced liver injury signal.
10mcg · 2x Daily
Summary: Add 0mL BAC water to your 120mg vial. Draw to < 0.1 units on a U-100 syringe for a 10mcg dose. This vial will last 0 doses.
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| Level | Dose / Injection | Frequency |
|---|---|---|
| Beginner | 10mg | 2x Daily |
| Moderate | 80mg | 2x Daily |
| Aggressive | 120mg | 2x Daily |
Danuglipron is an oral tablet. No vials, no reconstitution, no bacteriostatic water. That's the entire practical appeal and why Pfizer invested in this program. The twice-daily dosing schedule matters. The half-life is roughly 6 to 8 hours, so missing a dose creates a 12 to 16 hour gap in receptor coverage. If you're reading about this compound for research context, the clinical doses ranged from 2.5 mg BID up to 200 mg BID depending on the trial and arm. The obesity trial targeted 40 to 200 mg BID. The T2D trial tested 2.5, 10, 40, 80, and 120 mg BID. Slow titration is the only tolerability strategy that showed any benefit. The 4-week titration schedule in Cohort 3 of the obesity trial [1] produced the best efficacy data (32 weeks at target dose) and better completion rates than faster titration arms. This drug is not available from compounding pharmacies. No FDA-approved reference drug exists, which means 503A and 503B pharmacies cannot legally compound it. Research chemical suppliers carry it for lab use only; those products are explicitly not for human consumption.
Dosing based on Phase 2 trial: danuglipron (PF-06882961) oral GLP-1 in adults with type 2 diabetes (2023) — 10 published references.View all sources →
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Disclaimer: This curve is a simplified first-order exponential decay model. Actual pharmacokinetics vary based on injection site, individual metabolism, body composition, and other factors. Half-life values are approximate and based on available preclinical and clinical literature. Many research peptides lack formal human pharmacokinetic studies. This is for educational purposes only — not medical advice.
Danuglipron was Pfizer's oral small-molecule GLP-1 agonist. Phase 2b trials showed 5 to 13 percent weight loss at 32 weeks, but severe GI side effects caused over 50 percent dropout. Development stopped in April 2025 after a drug-induced liver injury signal.