What is Clomiphene?
Clomiphene (brand name Clomid) is a SERM - a selective estrogen receptor modulator. In the PCT context (post-cycle therapy) it is used to restart the body's own testosterone production after a suppressive anabolic cycle.
This information is for research and educational purposes only. No medical advice.
Comparison
Restarting the axis: routes in the lexicon
What each entry targets, as stated in the TPD lexicon. Tap a card to open its entry.
Simplified. SERMs block the estrogen signal in the brain, aromatase inhibitors lower estrogen itself, HCG replaces the LH signal directly at the testes. 74
How it works
Clomiphene blocks the estrogen receptors in the hypothalamus. The body therefore "thinks" estrogen is low and releases more GnRH. That drives LH and FSH up from the pituitary - the two signals that boost testosterone and sperm production in the testes. This restarts the HPTA axis suppressed after a cycle.
Where it acts
Where clomiphene acts
Tap a point or a card. Colour = estrogen receptor, grey = observed.
- Hypothalamus and pituitary
Estrogen signal blocked, LH and FSH rise by about 4.6 units per litre each4
ERα - Testes
More own testosterone, +11.6 nmol/l on average in obesity5
Observed in trials - Muscle
More lean and muscle mass after 12 weeks against placebo2
Observed in trials - Blood lipids
HDL cholesterol fell compared with placebo2
Observed in trials
Targets in the ChEMBL database10
Compound ChEMBL CHEMBL2355051: one recorded mechanism, Modulator, blocking in the hypothalamus.
Use and dosing
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
What the research shows
The Katz study (BJU International, 2012) examined clomiphene in young hypogonadal men and showed a clear, stable testosterone rise on 25-50mg, with good tolerability and preserved fertility. That confirms the HPTA reactivation mechanism.
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.
Rise in testosterone in obesity5
Meta-analysis, 7 studies, 292 men, 1.5 to 4 months
Values from the abstract (11.56 and 7.50 nmol/l). Without one study in severely obese men clomiphene was at 10.3 nmol/l. There were no unexpected safety findings.
Control hormones vs placebo4
Meta-analysis of randomised trials, mean difference
Values from the abstract. The analysis pools clomiphene and enclomiphene. Testosterone rose by 274 ng/dl on average against placebo.
Testosterone level compared with testosterone treatment6
Meta-analysis, 11 studies, 1,512 men, mean difference
Values from the abstract, rounded (24.29 and -290.50 ng/dl). Across all studies no clear difference. Libido was somewhat weaker on clomiphene than on testosterone.
Research status
Where the research stands
ClinicalTrials.gov lists 263 trials with clomiphene, almost all in women trying to conceive. Only trials with clomiphene in men are shown here. Enclomiphene trials belong to its own entry. As of 26 Oct 2026. 9
- Preclinical Approved for decades, early data from before the registry era
- Phase 1 no registered trial
- Phase 2 7 trials, 5 completed, 2 stopped early
- Phase 3 1 trial, 1 completed
- Approval since 1967
Show all 8 phase 2 and 3 trials on a timelineHide timeline
NCT00697814 · 15 participants, started Jun 2004, primary endpoint reached Jun 2005.
Registry entry ↗ · Results not yet in PubMed
NCT01155518 · 5 participants, started Jun 2010, stopped early Dec 2013. Tests several agents.
NCT01904734 · 42 participants, started Oct 2012, primary endpoint reached Oct 2018.
Registry entry ↗ · Results not yet in PubMed
NCT01880086 · 13 participants, started Aug 2013, primary endpoint reached Mar 2016.
Registry entry ↗ · Results not yet in PubMed
NCT03933618 · 24 participants, started Apr 2015, primary endpoint reached Mar 2017. Tests several agents.
Registry entry ↗ · Results not yet in PubMed
NCT02380755 · 78 participants, started Apr 2015, primary endpoint reached Jan 2017.
Registry entry ↗ · Results: Soares et al., International Journal of Obesity, 2018
NCT03245827 · 9 participants, started Apr 2019, stopped early Oct 2021.
NCT06564961 · 50 participants, started Jul 2022, primary endpoint reached Jun 2023.
Registry entry ↗ · Results not yet in PubMed
Bar: start to primary endpoint (planned for running trials). Green = completed, blue = progress until 26 Oct 2026, grey = stopped early.
Side effects
- Visual disturbances: at higher doses rarely flickering or blurred vision - then stop.
- Mood: some report irritability or low mood (clomiphene has estrogenic effects in the brain).
- Hot flashes, nausea: dose-dependent.
Storage
Store dry and protected from light. Out of reach of children.