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Comprehensive guides, interactive calculators, and an encyclopedia of 296 peptides. Every claim cited. No product sales. No vendor bias.

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New · Compound Hub

The Retatrutide Hub

The complete, vendor-neutral guide to the most talked-about peptide in the world — FDA status, the record-setting TRIUMPH trial data, mechanism, dosing, side effects, and how access really works. Continuously updated.

28.7%
peak weight loss
3
receptors
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Reference · 296 Peptides

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Mechanism, dosing, evidence level, and sourced references for every peptide with published research — from FDA-approved compounds to clinical-trial candidates.

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Wire · Live

Industry news

FDA action, trial readouts, and peptide pipeline developments — by the Grey Peptides News Desk.

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May 12, 2026 Trial Data

REDEFINE-1 Body Composition Data: How CagriSema Affects Muscle Mass

New post-hoc DXA findings from Novo Nordisk's pivotal CagriSema trial, presented at the European Congress on Obesity 2026, examine the muscle-mass picture behind 20%+ weight loss.

Source: Pharmaceutical Technology / ECO 2026
May 1, 2026 Regulation

The FDA Just Proposed Ending Mass GLP-1 Compounding — Here's What It Actually Means

On April 30, the FDA published a proposed rule that would permanently exclude semaglutide, tirzepatide, and liraglutide from the 503B bulks list. The compounding workaround is closing.

Source: FDA / STAT News
Apr 24, 2026 Trial Data

PIONEER TEENS: Oral Semaglutide Posts Positive Phase 3 Results in Pediatric T2D

Novo Nordisk reported topline results from a phase 3a trial of oral semaglutide in patients aged 10 to 17 with type 2 diabetes — the first oral GLP-1 RA to clear a pivotal study in this group.

Source: Novo Nordisk
Apr 22, 2026 Regulation

FDA Pulls 12 Peptides Off Its "Do Not Compound" List — What Changes, and What Doesn't

On April 15, the FDA quietly removed twelve peptide bulk substances from Category 2 of the 503A interim policy. A July advisory-committee vote will decide what happens next.

Source: Frier Levitt / FDA
Apr 15, 2026 Regulation

Wegovy HD Cleared in 54 Days: What the FDA's New Voucher Pathway Means for Peptide Drugs

The FDA approved semaglutide 7.2 mg on March 19 — fifty-four days after filing — using the Commissioner's National Priority Voucher pathway. The precedent is more complicated than the speed.

Source: FDA
Apr 2, 2026 Approval

Foundayo (Orforglipron) Approved: The First Oral Small-Molecule GLP-1 for Weight Loss

On April 1, the FDA approved Eli Lilly's orforglipron under the brand Foundayo. Unlike oral Wegovy, it's a small-molecule pill that doesn't require an empty stomach.

Source: Eli Lilly / FDA
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