iRGD
Oncology research In trials Animal studies
Also called Internalizing RGD peptide, CRGDKGPDC
A ring-shaped peptide that does not treat cancer itself — it makes tumours leaky. It docks onto integrins on tumour blood vessels, gets cut by an enzyme there, and the fragment then opens a transport route that lets whatever drug is circulating get in.
Evidence at a glance
- Evidence
- Animal studies — Not yet studied in people
- Status
- Reached clinical trials
- Dosing
- No human study has set a dose
Mouse data, from the laboratory that discovered it. It does nothing on its own — it is a delivery adjunct, and the same mechanism that improves drug entry could in principle help tumour cells spread. Human trials are early.
What studies report
- Up to 40-fold greater drug accumulation in mouse tumours when co-administered with doxorubicin, trastuzumab or nab-paclitaxel
- Matched the effect of roughly threefold higher doses of drug given alone
- Early human trials in pancreatic cancer in combination regimens
How it works
Binds integrins on tumour endothelium; protease cleavage then exposes a fragment that binds neuropilin-1, activating a transport pathway that carries co-administered drugs into the tumour.
Where it acts
Acts body-wide rather than on one organThe library groups this compound under Oncology research. The diagram shows that target, not every tissue it reaches.
Illustrated

AI-generated subject illustration; not a depiction of the compound or evidence of its effects.
Why people take it
Reasons people seek it out — not a list of proven effects.
Status: Preclinical, with early-phase human trials in combination therapy. Not approved.
- Route
- Injection, alongside the drug it is meant to assist
- Available as
- Compounded vials
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Educational information only. Nothing here is medical advice, a dosing protocol, or a recommendation to use any compound. Most entries describe substances not approved for human use. Talk to a licensed clinician before acting on anything you read here. How to read these entries.