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HormoneApproved

Oxandrolone (Anavar)

ox-AN-droh-lone

Research profile · How we handle evidence

Category

Hormone

Compound type

Phase / Status

Approved

FDA-approved for certain medical conditions. It remains a controlled prescription medication and has known risks.

Standard Dose

20-80mg/day (men) or 5-15mg/day (women)

Once or twice daily

Half-life

9-10 hours

Plasma elimination

Route(s)

IN / SU / OR

Intramuscular, Subcutaneous or Oral

Research Stage

Market Approved

Regulatory approval granted; post-market monitoring ongoing.

Overview

Oxandrolone is a prescription medication in some clinical settings. It can influence muscle and body composition but is not risk-free; monitoring may be recommended in medical use.

Plain-language summary

Oxandrolone is a prescription medication in some clinical settings. It can influence muscle and body composition but is not risk-free; monitoring may be recommended in medical use.

Administration Routes

  • Intramuscular
  • Subcutaneous
  • Oral

Also known as

AnavarVarOxandrinPrincess SteroidBaby SteroidOxanMild One

Mechanisms

1

Dihydrotestosterone (DHT) derivative that binds androgen receptors. It has low aromatization to estrogen, but androgen-related effects can still occur.

Detailed mechanism

Oxandrolone is a synthetic DHT-derived anabolic steroid that binds androgen receptors with high affinity, activating androgen-response elements in gene promoters to upregulate protein synthesis, nitrogen retention, and IGF-1 expression in skeletal muscle. Because its structure prevents aromatase-mediated conversion to estrogen, water retention and gynecomastia are less prominent than with testosterone-based compounds, though androgenic side effects such as hair loss, acne, and HPG-axis suppression remain possible. The 17-alpha-alkylation confers oral bioavailability at the cost of hepatic stress, necessitating periodic monitoring of liver enzymes and lipid panels during clinical use.

Safety

Side effects

  • Possible testosterone suppression
  • Potential liver effects because of oral steroid chemistry
  • Changes in lipid profile (e.g., HDL reduction)
  • Virilization risk in women at higher exposures
  • Hair loss/acne in susceptible individuals

Reported benefits

  • Approved medical use in selected indications
  • Can influence lean mass in appropriate patients
  • Low aromatization may reduce estrogen-related effects

Safety profile

Safety depends on patient factors, indication, dose, and monitoring. Potential risks include liver and lipid effects.

Clinical trials

Completed clinical trials leading to FDA or regulatory approval in approved indications.

Structure

View 3D structure

Verified structure

Oxandrolone (Anavar)

Exact 2D structure can be rendered from a PubChem-backed canonical SMILES string.

Verified via PubChemMatched by casNumber
Source: PubChemLookup: 53-39-4InChIKey QSLJIVKCVHQPLV-PEMPUTJUSA-N
Chemical Formula
C19H30O3
Molecular Weight
306.44 g/mol
CAS Number
53-39-4
InChIKey
QSLJIVKCVHQPLV-PEMPUTJUSA-N

Stack Context

Stacks with

CardarinePrimobolanTestosterone (at low dose)BPC-157

References

  1. 1

    The anabolic androgenic steroid oxandrolone in the treatment of wasting and catabolic disorders: a systematic review (Drug Safety)

    2004

    View source
  2. 2

    Pharmacology of anabolic steroids (British Journal of Sports Medicine)

    2008

    View source
  3. 3

    Effect of oxandrolone on the endocrinologic, inflammatory, and hypermetabolic responses during the acute phase postburn (Annals of Surgery)

    2007

    View source

This profile summarizes research literature for education only. It is not medical advice, and it does not diagnose, treat, or recommend a dose. Consult a qualified professional before changing a protocol.

Research-driven insights.Evidence-based decisions.