What is EPO?
EPO (erythropoietin) is an endogenous hormone that stimulates the production of red blood cells. Medically, recombinant EPO is used mainly against anemia, for example in kidney disease or under chemotherapy. In endurance sport it is infamous as a doping agent, because more red blood cells mean more oxygen transport.
Important and honest up front: EPO thickens the blood and has serious cardiovascular risks. It is not a harmless performance agent.
Comparison
The body's own hormones as compounds
Each of these hormones has its own receptor. EPO acts almost only on blood formation.
How it works
EPO binds receptors in the bone marrow and stimulates the production and maturation of red blood cells there. More red blood cells means more hemoglobin and thus more oxygen transport, which can increase endurance performance. But exactly this raised hematocrit is also the problem: the blood gets thicker and the risk of clots rises.
Where it acts
One receptor, several consequences
Tap a point or a card. Colour = receptor, grey = observed in studies.
- Kidney
Makes EPO when oxygen is low, controlled by HIF. In kidney disease it is lacking, hence the anaemia1
Observed in trials - Bone marrow
Precursors of red blood cells survive and divide1
EPOR - Blood and vessels
Haemoglobin rises, clots in vessels occurred twice as often5
Observed in trials - Heart and circulation
Higher Hb target: more deaths, heart attacks, heart failure and strokes3
Observed in trials - Endurance
VO2max higher in the lab, mountain race not faster2
Observed in trials
Targets in the ChEMBL database8
Compound CHEMBL1201565: one recorded mechanism, agonist with direct binding to the human receptor.
- Gene
- EPOR
- UniProt
- P19235
- ChEMBL
- CHEMBL1817
- Action
- Agonist, direct binding
What you need
Supplies
2 things, numbered as in the picture
Tick off what you already have. Vial and BAC water are our real shop photos at the same size.
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EPO vial
The EPO vial (labeled in IU, often 3000 IU).
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Syringes and swabs
U-100 insulin syringes, alcohol swabs.
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Mixing and units
EPO is given in IU (international units), not in mg. Many EPO preparations come as a ready solution or with a defined IU per vial (e.g. 3000 IU per vial).
- The IU count per vial is on the label, the partial amount follows from that.
- Dose precisely, EPO is very potent in small amounts.
Step by step
Dissolving the powder
Four steps, the same for every vial size.
- 1Wipe the cap
Clean the rubber stopper with an alcohol swab.
- 2Add BAC water
Just add it, it does not matter if it hits the powder directly.
- 3Swirl or shake
Until everything has dissolved, both are fine.
- 4Draw up
With the U-100 insulin syringe.
Dosing (in IU)
Dosing
Dosing, titration and syringe
Loading the dosing information …
- Getting started and stepping up, drawn as a staircase
- Units on the U-100 syringe for every step
- How long one vial lasts
Injection
The injection is subcutaneous, into the fat layer under the skin. Common spots are the abdomen (keep about two finger-widths clear of the navel), the front and the inner side of the thigh, or the back of the upper arm.
The short version:
Injection
Where and at what angle
Pick a spot or switch the angle. Subcutaneous means: into the fat layer, not the muscle.
Rotate the spot each time, never the same one twice in a row.
Rule of thumb: where there is more fat under the skin, insert straight at 90 degrees. In lean people with little fat, 45 degrees, so the needle stays in the fat layer. Simplified diagram.
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Clean the spot with an alcohol swab and let it dry
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Pinch up a small fold of skin
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Insert the needle: at 90 degrees where there is more fat under the skin, at 45 degrees in lean people with little fat
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Inject slowly, wait a moment, then withdraw
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Put the needle straight into the sharps container
Rotate the site each time so the tissue does not get irritated. Never the same spot twice in a row.
What the research shows
EPO is very well understood as a hormone and drug (overview: Jelkmann, 2013): it is the central regulator of red blood cell formation and medically established against anemia. The performance-enhancing effect in endurance sport is real, but so are the documented cardiovascular risks from the thickened blood.
Study results
What the trials measured
Interactive: switch tabs, tap points, show or hide arms. Arms are named relative to each other, no dosing advice.
Performance after 8 weeks of EPO2
Difference from the placebo group in percent, 48 well-trained amateur cyclists
VO2max and watts calculated from the means in the abstract. Race time was 0.3 percent higher with EPO, so slightly slower, without a measurable difference. The 45-minute test just below maximal effort showed no difference either.
Blood transfusions in breast cancer5
Share of patients with a transfusion, 2,098 women on chemotherapy
Fewer transfusions with EPO. The trial missed its goal of ruling out a higher risk of tumour progression, though. The authors therefore recommend transfusions rather than EPO for this group.
Research status
Where the research stands
EPO has been approved for decades. The registry lists 658 trials with epoetin alfa and 194 with epoetin beta. Here are the large trials this page draws on. As of 26 Oct 2026. 7
- Preclinical Kidney hormone that controls red blood cell production
- Phase 1 no registered trial
- Phase 2 no registered trial
- Phase 3 3 trials, 2 completed
- Approval since 1989, only for anaemia
Show all 4 phase 3 and 4 trials on a timelineHide timeline
CREATE · NCT00321919 · 605 participants, started Jul 2000, primary endpoint reached Oct 2004.
Registry entry ↗ · Results: Drüeke et al., New England Journal of Medicine, 2006
NCT00338286 · 2,098 participants, started Mar 2006, primary endpoint reached Jul 2014.
Registry entry ↗ · Results: Leyland-Jones et al., Journal of Clinical Oncology, 2016
EPO-TRAUMA · NCT04588311 · 2,500 participants (planned), started Nov 2020, primary endpoint planned Dec 2026.
CHOIR · NCT00211120 · 1,432 participants, started Mar 2002, stopped early Aug 2005.
Registry entry ↗ · Results: Singh et al., New England Journal of Medicine, 2006, ClinicalTrials.gov, NCT00211120
Bar: start to primary endpoint (planned for running trials). Green = completed, blue = progress until 26 Oct 2026, grey = stopped early.
Side effects
- Central risk: blood too thick (high hematocrit), causing thrombosis, heart attack, stroke.
- High blood pressure.
- Flu-like symptoms, local reactions.
Tolerability
Risks in large trials
Per 100 people: how many had a serious event. Left the comparison of two Hb targets in kidney disease, right with and without EPO in breast cancer.
| Event | Lower Hb target | Higher Hb target |
|---|---|---|
| Death, heart attack, heart failure or stroke3 | 14% | 18% |
| Clots in vessels (thromboses)5 | 0% | 0% |
Values for the kidney trial calculated from the event counts (125 of 715 versus 97 of 717). The trial was stopped early because the higher target showed more harm. Raised blood pressure, headaches and flu-like symptoms come on top.364
Practice
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Without regular hematocrit control EPO is especially dangerous.
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Enough fluids, do not thicken the blood further.
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With cardiovascular risk, leave it alone.
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Banned in official competition (WADA S2).
Storage
EPO comes either as a ready-made solution or as a powder you mix yourself. Store the ready-made solution as the pack and the prescribing information say: refrigerated throughout (2 to 8 degrees), not frozen, protected from light.
Once mixed from powder, it keeps for at least 4 to 6 months in the fridge (2 to 8 °C). Here too, do not freeze and protect from light.