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All peptides · Sexual health & hormones

Alprostadil

Sexual health & hormones
Prostaglandin E1 (not a peptide)

Widens blood vessels; injected or inserted to treat erectile dysfunction, and used to keep a newborn's ductus arteriosus open.

FDA-approved (e.g. Caverject, Edex); prescription-only.

Look it up on Wikipedia

2 listings across 1 independently tested vendor, ranked by price per milligram after coupon codes anyone can use. Vendors you can only order from by message are hidden.

Cheapest right now
$1,175.00 per mg
Qingdao Sigma Chemical QSC
Alprostadil 20mcg | 20-Vial Kit | Prostaglandin E1 (PGE1) Vasodilator
$470.00 for 20 × 20 mcg = 0.4 mg
Metascore 78Finnrick 64%Bought vials 103% of label · 47 testsNo report for thisOnline checkout
Go to qscpeptide.com
US compoundingFDA-approved drug

FDA-approved (Caverject, Edex, Muse); also a common ingredient in compounded erectile-dysfunction injections.

Sources: Drugs@FDA · checked 2026-10-08 · All peptides' status

Daily price tracking started October 7, 2026; a price-history chart appears here once a few days have been collected.

VendorTrustListingVialsPricePer mg
Qingdao Sigma Chemical QSC
#69 by metascore
Metascore 78Finnrick 64%Bought vials 103% of label · 47 testsNo report for thisOnline checkout
Alprostadil 20mcg | 20-Vial Kit | Prostaglandin E1 (PGE1) Vasodilator 20 × 20 mcg = 0.4 mg $470.00
$23.50 per vial
$1,175.00 Buy
Qingdao Sigma Chemical QSC
#69 by metascore
Metascore 78Finnrick 64%Bought vials 103% of label · 47 testsNo report for thisOnline checkout
Alprostadil 20mcg | 10-Vial Kit | Prostaglandin E1 (PGE1) Vasodilator 10 × 20 mcg = 0.2 mg $260.00
$26.00 per vial
$1,300.00 Buy

Mixing a 0.02 mg vial

What each common amount of bacteriostatic water gives you on a U-100 insulin syringe. Pick a vial size above to change it.

WaterStrengthPer 10 units (0.1 mL)Per unit
1 mL0.02 mg/mL2 mcg0.2 mcg
2 mL0.01 mg/mL1 mcg0.1 mcg
3 mL0.007 mg/mL0.7 mcg0.07 mcg
5 mL0.004 mg/mL0.4 mcg0.04 mcg

Doses studied in research Approved drug

What was given to people (or animals) in published studies and official labels, each linked to its source. This is not a recommendation: study products, purity and supervision differ from research-grade vials.

Caverject · erectile dysfunction

Label dosing is titrated in the prescriber's office: initial intracavernosal dose 2.5 mcg (vasculogenic, psychogenic or mixed cause) or 1.25 mcg (pure neurogenic cause, e.g. spinal cord injury), increased in steps to the lowest dose giving an erection suitable for intercourse lasting no more than 1 hour; no more than 3 injections weekly with at least 24 hours between doses; doses above 60 mcg not recommended (intracavernosal injection)

Official label
Prostin VR Pediatric · temporarily maintaining patency of the ductus arteriosus in neonates with ductal-dependent congenital heart defects

continuous intravenous infusion beginning at 0.05 to 0.1 micrograms/kg/minute, reduced after response to the lowest rate that maintains it (0.05, 0.025, 0.01 micrograms/kg/minute); up to 0.4 micrograms/kg/minute if response is inadequate (intravenous infusion (hospital use))

Official label
Who was studiedDose givenHow oftenFor how longWhat happened
men with erectile dysfunction of vasculogenic, neurogenic, psychogenic or mixed cause (three multicentre studies)
n = 1180
2.5 to 20 microg per injection (dose-response study); individually titrated doses in a 6-month self-injection study
intracavernosal
per sexual episodeup to 6 months all doses superior to placebo with a dose-response relation; sexual activity possible after 94% of self-injections; penile pain in 50% of men, prolonged erection 5%, priapism 1%PubMed
men aged 27-82 with organic erectile dysfunction
n = 234
125, 250 or 500 microg alprostadil, alone or with prazosin
transurethral
random sequence of 7 single doses in clinic4 weeks 500 microg gave full enlargement or rigidity in 51.8% of administrations vs 2.7% with placeboPubMed
men with long-standing, mainly organic erectile dysfunction
n = 68
125, 250, 500 and 1000 micrograms plus placebo, in random sequence
transurethral
single at-home doses2-4 weeks 75.4% achieved full enlargement and 49.2% an erection sufficient for intercourse; penile pain with 9.1-18.3% of administrationsPubMed
men with erectile dysfunction (double-blind crossover)
n = 45
5 or 10 micrograms vs placebo; 20 micrograms open-label if unsatisfactory
intracavernosal
single in-clinic injectionssingle-dose crossover 68.8% responded to at least one alprostadil injection; 10 micrograms effective in 55.5%PubMed
men with organic erectile dysfunction, randomised intracavernosal vs intraurethral
n = 60
20 microg intracavernosal PGE1 or 1 mg intraurethral (MUSE)
intracavernosal or intraurethral
per sexual episode at home3 months good erection in clinic in 90% (injection) vs 60% (urethral); intercourse after 85% vs 55% of administrations; urogenital pain 47% vs 7%PubMed

Approved doses differ greatly by route and indication: micrograms by penile injection, hundreds of micrograms by urethral pellet, and weight-based intravenous infusion in newborns. The MUSE urethral product is not currently listed on DailyMed.

What the research says

A
Strong human evidence
Why: Approved ED drug: placebo-controlled RCTs in over 1,100 men plus a meta-analysis of 11 RCTs consistently show erections improve, injection more than urethral forms.

Alprostadil (synthetic prostaglandin E1) is an approved erectile dysfunction treatment backed by multiple placebo-controlled human RCTs and a meta-analysis; injected into the penis it produces usable erections in most men, while urethral and topical forms are less effective but better tolerated. Penile pain is the most common side effect, with prolonged erection, priapism and penile fibrosis as less common risks.

Key papers ✓ 5~ 2

  • ✓ Positive human RCTN Engl J Med · 1996
    Efficacy and safety of intracavernosal alprostadil in men with erectile dysfunction. The Alprostadil Study Group.
    Humanssize not reportedRandomizedPlacebo-controlledSix months (self-injection study)
    Three multi-institutional prospective studies (dose-response vs placebo, dose-finding, self-injection)

    NEJM studies in over 1,100 men with ED: intracavernosal alprostadil outperformed placebo with a dose-response; in a 6-month self-injection study (683 men) sexual activity was possible after 94% of injections.

    Key resultSexual activity possible after 94 percent of injections; rated satisfactory after 87 and 86 percent by men and partners; penile pain in 50 percent of men, priapism in 1 percent

    Study details
    Studied
    Men with erectile dysfunction of vasculogenic, neurogenic, psychogenic and mixed causes
    Compared with
    Placebo (dose-response study)
    Main outcome
    Erection and satisfactory sexual activity rated by men and partners
    Sample
    Three studies: dose-response 296 men, dose-finding 201 men, six-month self-injection 683 men
    Authors' conclusion
    Intracavernosal alprostadil injection is an effective therapy for erectile dysfunction with tolerable side effects.
    Limitations
    Only the dose-response study was placebo-controlled.
  • ✓ Positive meta-analysisAndrology · 2025
    The effect of topical and intraurethral alprostadil on erectile function: A systematic review and meta-analysis.
    Humans5,869 people
    Systematic review and meta-analysis, random-effects model (PROSPERO registered)

    Meta-analysis of 11 RCTs and 4 non-randomized studies (5,869 men): topical alprostadil improved IIEF score by 4.7 points vs placebo and intraurethral alprostadil also improved ED vs placebo; study quality was low and heterogeneity high.

    Key resultTopical alprostadil improved IIEF by 4.7 points (95% CI: 2.4-7.1, I2 = 97%); intraurethral pooled odds ratio 0.08 (95% CI: 0.04-0.16, I2 = 54%)

    Study details
    Studied
    Men with erectile dysfunction (mean age 60 ± 9.4 years)
    Compared with
    Placebo
    Main outcome
    IIEF score (topical); erectile dysfunction improvement (intraurethral)
    Sample
    11 randomized controlled trials and 4 non-randomized studies, 5869 patients
    Authors' conclusion
    Topical and intraurethral alprostadil significantly improve ED symptoms vs placebo and are generally safe with no serious adverse events; further trials are needed.
    Limitations
    Study design variability, few studies and low methodological quality; very high heterogeneity for topical (I2 = 97%).
  • ✓ Positive human RCTUrology · 1996
    A double-blind, placebo-controlled evaluation of the erectile response to transurethral alprostadil.
    Humans68 peopleRandomizedPlacebo-controlledDouble-blind2 to 4 weeks
    Prospective, multicenter, double-blind, placebo-controlled; random sequence of four doses and placebo at home

    Double-blind, placebo-controlled study in 68 men with organic ED: with transurethral alprostadil 49% achieved an erection sufficient for intercourse and 64% reported intercourse; no priapism.

    Key result75.4% (49 of 65) achieved full penile enlargement, 49.2% (32 of 65) achieved an erection sufficient for intercourse; 63.6% (42 of 66) reported intercourse

    Study details
    Studied
    Men with long-standing (mean 41 months) erectile dysfunction of primarily organic etiology
    Compared with
    Placebo
    Main outcome
    Erectile response and intercourse
    Sample
    68 men enrolled; 65-66 evaluable for outcomes
    Authors' conclusion
    Short-term transurethral alprostadil produced erections leading to intercourse in most patients with chronic ED and may be a useful option.
    Limitations
    Short-term treatment; penile pain in 9.1% to 18.3% of administrations.
  • ✓ Positive human RCTUrology · 2000
    Intracavernous alprostadil alfadex is more efficacious, better tolerated, and preferred over intraurethral alprostadil plus optional actis: a comparative, randomized, crossover, multicenter study.
    Humans111 peopleRandomizedOpen-label
    Crossover, randomized, open-label multicenter study

    Randomized crossover trial in 111 men: injected alprostadil gave erections sufficient for intercourse after 82.5% of uses vs 53.0% for intraurethral alprostadil, and was preferred by patients.

    Key resultPatients with at least one erection sufficient for intercourse: 92.6% with EDEX vs 61.8% with MUSE (P <0.0001)

    Study details
    Studied
    Patients with erectile dysfunction of at least 6 months' duration
    Compared with
    Intraurethral alprostadil (MUSE) plus optional ACTIS
    Main outcome
    Erections sufficient for intercourse, safety, patient preference
    Sample
    111 patients
    Authors' conclusion
    Intracavernous injection was more efficacious, better tolerated and preferred, so it should be offered first-choice if oral therapy fails or is contraindicated.
    Limitations
    Open-label design.
  • ~ Mixed human RCTBJU Int · 1999
    Intracavernosal versus intraurethral alprostadil: a prospective randomized study.
    Humans60 peopleRandomized3 months
    Prospective randomized study with 3-month home treatment

    60 men randomized to injected vs intraurethral alprostadil: injection worked better (intercourse after 85% vs 55% of doses) but caused more pain (47% vs 7%) and a 67% withdrawal rate.

    Key resultGood erection in outpatient dosing: 27 (90%) intracavernosal vs 18 (60%) MUSE (P<0.05); withdrawal 67% vs 17% (P<0.05)

    Study details
    Studied
    Men with organic erectile dysfunction
    Compared with
    MUSE 1 mg intraurethral alprostadil
    Main outcome
    Erection response, intercourse, adverse reactions, ease of use
    Sample
    60 men randomized (30 per group)
    Authors' conclusion
    MUSE is less effective than intracavernosal PGE1 but is more accepted as an easy method with minimal or no discomfort.
    Limitations
    High withdrawal in the injection group (10 of 30 completed).
  • ✓ Positive human RCTJ Urol · 1997
    Recovery of spontaneous erectile function after nerve-sparing radical retropubic prostatectomy with and without early intracavernous injections of alprostadil: results of a prospective, randomized trial.
    Humans30 peopleRandomized12 weeks of treatment; 6-month follow-up
    Prospective randomized trial; alprostadil injections 3 times per week vs observation

    30 men after nerve-sparing prostatectomy: 12 weeks of alprostadil injections led to more recovery of spontaneous erections at 6 months (67% vs 20% with observation).

    Key result8 patients (67%) in the alprostadil group vs 3 patients (20%) in the control group recovered spontaneous erections (p <0.01)

    Study details
    Studied
    Potent men with localized prostate cancer after nerve-sparing radical retropubic prostatectomy
    Compared with
    Observation without erectogenic treatment
    Main outcome
    Recovery of spontaneous erections sufficient for intercourse
    Sample
    30 potent patients (15 per group)
    Authors' conclusion
    Early postoperative alprostadil injections significantly increased recovery of spontaneous erections after nerve-sparing prostatectomy.
    Limitations
    Small trial; only 12 of 15 treated patients completed the schedule; no blinding or placebo.
  • ~ Mixed human trialEur Urol · 2000
    Safety and efficacy of alprostadil sterile powder (S. Po., CAVERJECT) in diabetic patients with erectile dysfunction.
    Humans31 peopleNo control group6 months home phase
    Single-group long-term self-injection study with dose titration

    31 diabetic men with ED on 6 months of home injections: 76.5% of injections gave satisfactory sexual activity, but penile pain affected 61% and about half dropped out.

    Key resultSatisfactory sexual activity after 76.5% of injections (patient-assessed) and 72.5% (partner-assessed); penile pain in 19 (61%) of 31 patients; 16 patients dropped out

    Study details
    Studied
    Diabetic men aged 44-75 with erectile dysfunction of at least 4 months
    Main outcome
    Efficacy and adverse events of intracavernosal alprostadil
    Sample
    31 diabetic men
    Authors' conclusion
    Despite high penile pain incidence and higher withdrawal, intracavernosal alprostadil is relatively effective and safe in some diabetic patients if dose is titrated and they are trained.
    Limitations
    No control group; high dropout (16 of 31).

Reported side effects

40 registered human trials (3 active)

✓ positive · ✗ negative · ~ mixed · ? inconclusive, judged on each paper's own main outcome. Grades: A strong human evidence → D little or none. Papers and verdicts are drawn from PubMed, Europe PMC and Russian journals (CyberLeninka); not medical advice.

Registered clinical trials 40 on ClinicalTrials.gov · 3 active · 11 completed · 5 with posted results

TrialStatusPhasePeopleSponsor
ALP-1 Continuous Intravenous Infusion to Maintain Clinical Stability in Advanced Heart Failure
NCT00610051 · started 2026-10
Not yet recruitingPhase 3600Biopeutics Co., Ltd
Comparing MOP, Prostaglandin E1, and Calcitriol to Accelerate Orthodontic Tooth Movement
NCT07842120 · started 2026-04-16
RecruitingPhase 260Ghufran Dhari Awad
Platelet Rich Plasma (PRP) as Terapeutical Option in Erectil Disfunction (DE)
NCT06768177 · started 2023-04-01
Enrolling by invitation–60Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari
Alprostadil in Peripheral Arterial Occlusive Disease (PAOD) Stage IV
NCT00596752 · started 2004-03 · results posted
CompletedPhase 4840UCB BIOSCIENCES GmbH
Prostaglandin E1 in Outpatients With Intermittent Claudication
NCT01263925 · started 2001-04 · results posted
CompletedPhase 3561UCB Pharma
ED Recovery in Men Age </=65 Treated With Bilateral Nerve Sparing Robotic Assisted Prostatectomy for Prostate Cancer
NCT00544076 · started 2006-01 · results posted
TerminatedPhase 3110City of Hope Medical Center
Pharmacological Penile Rehabilitation in the Preservation of Erectile Function Following Bilateral Nerve-Sparing Radical Prostatectomy
NCT00955929 · started 2009-08-06 · results posted
Terminated–76Memorial Sloan Kettering Cancer Center
Alprostadil in Maculopathy Study (AIMS)
NCT00619229 · started 2006-07 · results posted
TerminatedPhase 337UCB Pharma
Topical Alprostadil for Female Sexual Arousal Disorder
NCT00324948 · started 2004-09
CompletedPhase 2300VIVUS LLC
Cervical Ripening: A Comparison Between Intravaginal Misoprostol Tablet and Intracervical Foley's Catheter and Subsequent Induction of Labor, Safety and Efficacy in Federal Teaching Hospital Abakaliki, Ebonyi State, Nigeria.
NCT02574338 · started 2015-09
Completed–135Nwali Matthew Igwe
Nerve-Sparing Radical Prostatectomy With or Without Nerve Grafting Followed by Standard Therapy for Erectile Dysfunction in Treating Patients With Localized Prostate Cancer
NCT00080808 · started 2001-08
CompletedPhase 2111M.D. Anderson Cancer Center
Intravenous Dexamethasone for Inducing Labor in Women With Term Pregnancy and Pre-Labour Rupture of Membranes
NCT07503184 · started 2025-07-15
CompletedPhase 460Nishtar Medical University

All 40 Alprostadil trials, with countries and summaries · Search ClinicalTrials.gov · Recruiting trials for every peptide

Discussions elsewhere

Experiences and questions about Alprostadil on other sites. Treat anecdotes with care.

Alprostadil: questions people ask

What is Alprostadil?

Prostaglandin E1 (not a peptide). Widens blood vessels; injected or inserted to treat erectile dysfunction, and used to keep a newborn's ductus arteriosus open.

How much does Alprostadil cost?

The cheapest Alprostadil from an independently tested vendor is $1,175.00 per mg (Qingdao Sigma Chemical QSC, Alprostadil 20mcg | 20-Vial Kit | Prostaglandin E1 (PGE1) Vasodilator, $470.00). Across 2 listings from 1 vendors the median is $1,300.00 per mg.

Where can I buy Alprostadil?

1 vendors tested by Finnrick sell Alprostadil. The cheapest per mg right now: Qingdao Sigma Chemical QSC ($1,175.00). 0 of them publish a lab report (COA) for Alprostadil; compare lab scores and reports in the table above before buying.

Is Alprostadil FDA approved?

FDA-approved (e.g. Caverject, Edex); prescription-only.

Can Alprostadil be compounded in the US?

FDA-approved (Caverject, Edex, Muse); also a common ingredient in compounded erectile-dysfunction injections. Compounding status for every peptide.

Does Alprostadil work? What does the research say?

Evidence grade A (strong human evidence), from 7 papers: Approved ED drug: placebo-controlled RCTs in over 1,100 men plus a meta-analysis of 11 RCTs consistently show erections improve, injection more than urethral forms. Alprostadil (synthetic prostaglandin E1) is an approved erectile dysfunction treatment backed by multiple placebo-controlled human RCTs and a meta-analysis; injected into the penis it produces usable erections in most men, while urethral and topical forms are less effective but better tolerated. Penile pain is the most common side effect, with prolonged erection, priapism and penile fibrosis as less common risks. See the papers.

Are there clinical trials of Alprostadil?

ClinicalTrials.gov lists 40 registered trials of Alprostadil: 3 active, 11 completed, 5 in phase 3, 5 with posted results. Examples: ALP-1 Continuous Intravenous Infusion to Maintain Clinical Stability in Advanced Heart Failure (Not yet recruiting, Phase 3, 600 people); Comparing MOP, Prostaglandin E1, and Calcitriol to Accelerate Orthodontic Tooth Movement (Recruiting, Phase 2, 60 people); Platelet Rich Plasma (PRP) as Terapeutical Option in Erectil Disfunction (DE) (Enrolling by invitation, 60 people).

What dose of Alprostadil was used in studies?

Alprostadil is an approved drug. Caverject: Label dosing is titrated in the prescriber's office: initial intracavernosal dose 2.5 mcg (vasculogenic, psychogenic or mixed cause) or 1.25 mcg (pure neurogenic cause, e.g. spinal cord injury), increased in steps to the lowest dose giving an erection suitable for intercourse lasting no more than 1 hour; no more than 3 injections weekly with at least 24 hours between doses; doses above 60 mcg not recommended; Prostin VR Pediatric: continuous intravenous infusion beginning at 0.05 to 0.1 micrograms/kg/minute, reduced after response to the lowest rate that maintains it (0.05, 0.025, 0.01 micrograms/kg/minute); up to 0.4 micrograms/kg/minute if response is inadequate; men with erectile dysfunction of vasculogenic, neurogenic, psychogenic or mixed cause (three multicentre studies): 2.5 to 20 microg per injection (dose-response study); individually titrated doses in a 6-month self-injection study per sexual episode. These are amounts used in published studies or official labels, not a recommendation.

What are the side effects of Alprostadil?

Reported in the research: Penile pain; Hematoma or ecchymosis at injection site; Prolonged erection; Penile fibrosis / nodule; Priapism.

More on Alprostadil