Skip to content
Calculator

The peptide reference that sells nothing.

Reconstitution calculator

Your vial, water and dose in. Insulin-syringe units out.

Preset dose: a commonly reported community amount, not a clinical dose.

10.0 units

0.100 mL on a 1 mL, 100-unit syringe. 2.50 mg/mL, 20 doses per vial.

102030405060708090100

It adds reverse mode, multi-vial schedules, pen dosing, cost per dose and PDF export.

350 peptides, each with an evidence grade and its sources. 3853 citations, 26 free tools and a dated regulatory tracker.

What changed, and what comes next

July 23–24, 2026 · as of September 25, 2026

FDA's compounding committee backed six of seven peptides (BPC-157 8–6, KPV 8–6, TB-500 8–6, MOTS-c 7–5, Semax 8–5, Epitalon 7–4 or 7–5) and rejected Emideltide (DSIP) 6–7. FDA has not acted on the votes.

The votes and FDA's briefing →
Comments closed July 30, 2026 · as of September 25, 2026

Compounded GLP-1s: FDA proposes not to put Semaglutide, Tirzepatide or Liraglutide on the 503B list. No final determination yet.

What it means for you →
Next: by the end of February 2027

5 more peptides await the committee (GHK-Cu (injectable), Melanotan II, Cathelicidin (LL-37), Dihexa, PEG-MGF); no meeting date has been set.

The regulatory tracker →

Start with your situation

Eight compounds to start with

Chosen by our editors from the compounds the regulatory tracker and FDA's committee cover most; we have no traffic data to rank by. Grades and statuses come from the encyclopedia.

Every tool, by what it does

Guides by journey

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
Open the hub →

Reference · 350 Peptides

Every peptide,
one reference.

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

11 Categories
350 Entries
3853 Citations
350
Encyclopedia entries
Every peptide with published research
26
Free tools
Calculators, planners, checkers and references
0
Products for sale
Pure education, zero vendor bias
Wire · Live

Industry news

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

Archive →
October 7, 2026 Trial Data

REIMAGINE 5: CagriSema vs Tirzepatide

Novo Nordisk reports that CagriSema beat tirzepatide 5 mg on weight loss in people with type 2 diabetes, 12.4% against 9.1% over 60 weeks, with similar HbA1c falls. The results are the company's and not yet published.

Source: ClinicalTrials.gov
October 5, 2026 Trial Data

Vosoritide in Hypochondroplasia: Phase 3 Growth Result

In a 52-week phase 3 trial in 81 children with hypochondroplasia, vosoritide raised yearly growth by 2.33 cm more than placebo. Vosoritide is approved for achondroplasia, not for hypochondroplasia.

Source: NEJM Evidence (PubMed)
October 5, 2026 Regulation

Saxenda to Be Discontinued; Rybelsus Tablets Replaced

Two Novo Nordisk GLP-1 products are leaving the US market according to FDA notices: Saxenda (liraglutide for weight) by January 2027, and the original Rybelsus tablets, which are being replaced by Ozempic tablets.

Source: FDA Drug Shortages database
October 2, 2026 Trial Data

EloraTZP: 23.3% Weight Loss in Type 2 Diabetes

In 367 adults with type 2 diabetes, the top EloraTZP dose cut weight 23.3% and HbA1c 2.9 points at 48 weeks, against 14.8% and 2.4 on tirzepatide 15 mg. Up to 27% stopped for side effects.

Source: Eli Lilly / ClinicalTrials.gov
October 2, 2026 Trial Data

Petrelintide's Paper: Weight Loss Levelled Off Above 5 mg

The ZUPREME-1 paper puts petrelintide's 28-week weight loss at 7.9% to 9.8% against 1.7% on placebo, with doses above 5 mg adding nothing. Other peptide data from EASD 2026 came from Hengrui, Kailera and AbbVie.

Source: Lancet Diabetes & Endocrinology / Zealand Pharma
October 1, 2026 Approval

Rusfertide Approved: The First Hepcidin Mimetic for Polycythemia Vera

FDA approved rusfertide, sold as Mimrylo, for adults with polycythemia vera on August 28. It is a weekly injected peptide that copies the iron-regulating hormone hepcidin, and in its phase 3 trial it spared far more patients from blood removal than placebo did.

Source: FDA press announcement
View all news →