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PharmaceuticalApproved

Dutasteride (Avodart)

doo-TAS-ter-ide

Research profile · How we handle evidence

Category

Pharmaceutical

Compound type

Phase / Status

Approved

FDA approved for BPH. Off-label use for hair loss prevention.

Standard Dose

0.5mg daily or every other day

Daily or EOD

Half-life

5 weeks (terminal)

Plasma elimination

Route(s)

OR

Oral

Research Stage

Market Approved

Regulatory approval granted; post-market monitoring ongoing.

Overview

Dutasteride lowers DHT by blocking both type 1 and type 2 5-alpha-reductase enzymes. It can be used to treat BPH and may help reduce DHT-related hair loss. Because it lasts a long time in the body, potential side effects may also persist after stopping.

Plain-language summary

Dutasteride lowers DHT by blocking both type 1 and type 2 5-alpha-reductase enzymes. It can be used to treat BPH and may help reduce DHT-related hair loss. Because it lasts a long time in the body, potential side effects may also persist after stopping.

Administration Routes

  • Oral

Also known as

DutaAvodartDuagenDutagenDuprostDutasDual 5-ARI

Mechanisms

1

Dual 5-alpha reductase inhibitor — inhibits both type 1 and type 2 5-AR enzymes, reducing conversion of testosterone to DHT.

Detailed mechanism

Dual 5-alpha reductase inhibitor that blocks both type 1 and type 2 enzymes, preventing conversion of testosterone to dihydrotestosterone (DHT). More complete DHT suppression than finasteride with longer duration of action.

Safety

Side effects

  • Reduced libido
  • Erectile dysfunction (in some individuals)
  • Gynecomastia (uncommon; can occur with hormonal changes)
  • Mood changes/depression in a subset of users
  • Persistent effects after discontinuation due to long half-life

Reported benefits

  • Reduces DHT levels (commonly reported around 85–90%)
  • Helps treat BPH
  • May reduce DHT-related hair loss
  • Used off-label to manage DHT-related side effects

Safety profile

Well-tolerated for many patients, but sexual side effects and persistent pharmacologic effects are possible. Discuss risks and benefits with a clinician.

Clinical trials

Completed clinical trials leading to FDA approval for BPH.

Structure

View 3D structure

Verified structure

Dutasteride (Avodart)

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

Verified via PubChemMatched by casNumber
Source: PubChemLookup: 164656-23-9InChIKey JWJOTENAMICLJG-VYZSUTEISA-N
Chemical Formula
C27H30F6N2O2
Molecular Weight
528.53 g/mol
CAS Number
164656-23-9
InChIKey
JWJOTENAMICLJG-VYZSUTEISA-N

Stack Context

Stacks with

Finasteride (generally not recommended together)TestosteroneNandrolone

References

  1. 1

    Effect of dutasteride on the risk of prostate cancer: REDUCE randomized controlled trial (New Engl J Med)

    2010

    View source
  2. 2

    Combination therapy with dutasteride and tamsulosin for BPH: CombAT randomized controlled trial (Eur Urol)

    2010

    View source
  3. 3

    Avodart (dutasteride 0.5 mg) FDA-approved prescribing information for benign prostatic hyperplasia - NDA 021319 (FDA AccessData)

    2017

    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.