12-week titration (subQ)
Titration (4 steps) and details
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Also known as: AED · AED peptide · Ala-Glu-Asp · T-31 · Kartalax · Alanyl-glutamyl-aspartic acid · Cartilage bioregulator
Updated 20 sources
How it is thought to work. Cartalax is said to work like other Khavinson short peptides: entering cells and nudging gene expression. In aging human stem-cell cultures, AED at 200 ng/mL raised cartilage markers such as SOX9, aggrecan, type II collagen and COMP. In aging chondrocyte and kidney cell cultures it lowered aging and apoptosis markers such as p16, p21 and p53. No receptor or target is known, and no study shows how a dose reaches cartilage in a living body.
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Doses shown are what sources report, labelled by origin. Not medical advice.
Full Cartalax dosage guideEvery titration step in syringe units, missed doses and how to mix.| Water | Strength | 2 mgdose, units | 5 mgdose, units | 10 mgdose, units |
|---|---|---|---|---|
| 10 mg vial | ||||
| 2 mLCompetitor guide | 5 mg/mL | 400.4 mL | 1001 mL | 2002 mL2 draws |
| 20 mg vial | ||||
| 2 mLCompetitor guide | 10 mg/mL | 200.2 mL | 500.5 mL | 1001 mL |
| 3 mLCompetitor guide | 6.667 mg/mL | 300.3 mL | 750.75 mL | 1501.5 mL2 draws |
| 40 mg vial | ||||
| 3 mLCompetitor guide | 13.333 mg/mL | 150.15 mL | 37.50.375 mL | 750.75 mL |
Doses shown are what sources report, labelled by origin. Not medical advice.
Calculate with this peptideYour vial, your water, your dose: Cartalax in syringe units, with the math shown.No validated rule exists. Guides advise against doubling the next dose to make up for a missed one.
From community reports and dosing guides. Not measured rates.
Occasional and mild, per guides; no study has measured a rate
How people manage it
Reported for oral use in Russian practice; usually self-limited
How people manage it
Occasional and mild, per one guide
How people manage it
Rare, per one guide; no anaphylaxis reported
How people manage it
Listed as rare on one guide
How people manage it
Pregnancy or breastfeedingCondition
No reproductive toxicology or human safety data exist.
Active bone or cartilage cancerCondition
If the peptide really changes gene activity in cartilage cells, a guide argues that is no place to experiment with a bone or cartilage tumor present. A theoretical concern, not an observed one.
Vials with unclear identity, amount or sterilitySubstance
Research vials are unregulated, and a wrong amount or contamination adds risk that has nothing to do with the peptide.
Fridge at 2 to 8 C, or -20 C for the long term, dry and out of light. One guide allows room temperature. A guide quotes 18 to 24 months of shelf life for the powder in the fridge.
Fridge at 2 to 8 C, never frozen. Guides give 14 to 30 days, and one says no stability study backs any figure, so use the short end. Discard if cloudy or particles appear.
Mixed with: Bacteriostatic water
Mixing. With 3 mL in a 20 mg vial, 1 unit on a U-100 syringe holds about 66.7 mcg, so 2 mg is 30 units and 5 mg is 75 units. Using 2 mL makes the same doses a third smaller in volume. Guides keep injections at 1 mL or less per site.
The usual joint-recovery pairing. App users co-log the two, but no study has tested the combination.
Listed by one guide as compatible in a BPC-157 and TB-500 recovery stack. No data on the combination.
Not a designed stack: app users on retatrutide are the largest group logging cartalax, likely for joints during weight loss.
Co-logged by app users in connective tissue and skin rotations.
A polypeptide complex extracted from young animals' cartilage and bone, not one defined peptide. Cell studies dosed it at 2,000 ng/mL against 200 ng/mL for AED.
Published work is cell cultures from one connected Russian research network: AED raised cartilage markers in aging stem cells and lowered aging markers in chondrocyte, kidney and skin cell cultures. A rat osteoporosis study tested a T-31 substance on bone density. A 2023 review from the same group says AED was given by mouth to older people with osteoarthritis, but no trial report with numbers is indexed. ClinicalTrials.gov lists no cartalax trials.
No approval, no trial program and not on FDA's compounding lists.
Not FDA approved, and never evaluated. Cartalax does not appear on FDA's 503A bulk substance category lists (May 14, 2026) or its compounding safety-risk page, so US pharmacies have no route to compound it. It is sold as a research chemical or as imported oral capsules.
WADA does not name cartalax. Its S0 class bans any substance with no government approval for human use, which on its wording likely covers cartalax; that is our reading, and one guide agrees it arguably applies. The same guide says it is not registered as a drug outside Russia; we did not verify its status in Russia.
WADA: Not confirmed
A synthetic tripeptide, Ala-Glu-Asp (AED), from Vladimir Khavinson's short-peptide bioregulator program in St. Petersburg. It is also sold as T-31 or Kartalax and is marketed as a cartilage bioregulator. Molecular weight about 333 g/mol.
Mostly joints: knee and hip wear, cartilage support and recovery. Research covers cartilage-cell markers and cell aging in culture. No study shows it relieves joint pain or rebuilds cartilage in people.
There is no tested human dose. Guides and communities run 2 to 5 mg once a day by subQ injection, often ramping 2, 3, 4 then 5 mg over 12 weeks. The oral format runs 20 mg a day for 10 days. One guide lists far lower subQ doses of 100 to 250 mcg.
Mixed with 3 mL of bacteriostatic water, a 20 mg vial holds about 6.67 mg/mL, so each U-100 unit is about 66.7 mcg. That makes 2 mg 30 units, 3 mg 45 units, 4 mg 60 units and 5 mg 75 units. With 2 mL it is 10 mg/mL and 100 mcg per unit.
Some commercial and community sites say so, but one guide could not trace it to any study and thinks it was borrowed from oral product directions. It would use 200 mg, ten 20 mg vials.
No. A capsule's weight can include fillers or a broader peptide complex, and pure AED's oral absorption is unproven. Do not convert a capsule label into an injection dose.
No trial report is indexed. The published work is cell cultures of stem cells, chondrocytes, kidney cells and skin fibroblasts, plus a rat bone study. A 2023 review from the developers' group says it was given by mouth to older people with osteoarthritis, without trial details. ClinicalTrials.gov lists no cartalax trials.
No study has measured them. Guides list mild injection-site redness or itch, occasional nausea or indigestion with oral use, mild headache and, rarely, a mild rash. No anaphylaxis has been reported. Missing reports partly reflect missing research.
Unknown. No human or animal pharmacokinetic study exists. Once-daily dosing is community convention, not a finding.
A tripeptide. PubChem and most guides list cartalax as Ala-Glu-Asp, 333.29 g/mol. One guide calls it a 446.5 Da tetrapeptide and gives two different sequences on the same page, which looks like an error. Check that a vial's certificate lists AED.
Cartalax is a 3-amino-acid Khavinson peptide studied in cartilage cell cultures. BPC-157 is a 15-amino-acid peptide with more animal healing studies. Neither has a proven human dose for joints, and nobody has studied the two together.
Sigumir is a peptide complex extracted from young animals' cartilage and bone. Cartalax is the single defined tripeptide AED. In stem-cell cultures the complex needed 2,000 ng/mL to match what AED did at 200 ng/mL.
No. FDA has never evaluated it, and it is not on any 503A bulk category list, so US compounding pharmacies cannot make it. It is sold as a research chemical.
WADA does not name it, but S0 bans any substance with no government approval for human use, and that likely covers cartalax. Tested athletes should assume it is prohibited.
On one tracking app, 27 users rated it 57% favorable and 43% mixed, none unfavorable, and recovery was the benefit they logged most. Self-reports are not evidence it works.
Answers come from this site's pages only, with a link to each source.
20 sources, each checked by date. Record updated Oct 24, 2026. Numbers are restated in our own words and labelled by where they came from.