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PCT & Bloodwork Planner

Pick compounds and a length of use. The planner shows each half-life with the group it was measured in, how drug levels fall (an illustration), what studies found on suppression, which blood markers they tracked, and the drugs researched for restoring testosterone.

Key takeaways

  • Shows each compound's half-life, with the study group and route, and how long five half-lives take (about 3% left): an illustration of concentration decay, not a personal calculation.
  • Gives no figure for the whole selection when any compound has no human half-life, and names it.
  • Clearance is not recovery: the planner gives no recovery, testing or PCT date.
  • Shows what studies found on testosterone suppression (human or animal data), the blood markers they tracked and the drugs researched for restoring testosterone. It never gives a dose or a protocol.

Everything the planner shows comes from our compound records, each with its source. It shows what studies found on half-life, suppression and bloodwork; it never gives a dose, a protocol, a recovery date or a testing date.

Compounds

Selected: LGD-4033 and MK-677, 8 weeks.

Half-life and drug levels

CompoundHalf-life (study population, route)About 3% left after (5 half-lives, illustration)Suppression in studies
LGD-4033~24–36 h sourceMeasured in healthy men aged 21–50, by mouth5–7.5 daysMarked human data Yes, even at low doses. In healthy young men, 21 days of 0.1–1.0 mg/day lowered total testosterone and SHBG in a dose-dependent way. At 1.0 mg/day, FSH and free testosterone also fell. All hormones were back to baseline by day 56. This trial did not test doses above 1 mg/day. source
MK-677Not established in humansNot establishedMild human data MK-677 does not act on the androgen receptor, so it is not expected to shut down testosterone the way SARMs and steroids do. One 8-week trial in obese men found lower total testosterone than placebo, but no change in the testosterone/SHBG ratio, LH or FSH. source

An illustration of concentration decay only: half of a drug is cleared every half-life, so after five half-lives about 3% is left. Each half-life comes from one study population and route and can differ in other people. source

The whole selection

No overall figure. MK-677 has no human half-life in our records, so no time can be given for the whole selection. A figure from the other compounds would leave it out.

  • MK-677: No human plasma half-life has been published. source

Clearance is not recovery. A falling drug level does not show that your own hormone production has recovered, when a blood test reflects your own levels, or whether or when any treatment (PCT) is appropriate. In the LGD-4033 trial, drug levels and the return of hormones after the last dose were measured separately, with hormone follow-up over the following weeks. source

Bloodwork the studies tracked

Total and free testosterone, LH and FSH, SHBG, Lipid panel (HDL, LDL, triglycerides), ALT/AST (liver enzymes), Bilirubin, PSA, Hematocrit, IGF-1, Fasting glucose, HbA1c, Fasting insulin, Prolactin

Suppression, and the drugs researched for restoring testosterone

Studies report moderate or marked suppression of natural testosterone with LGD-4033.

These drugs were studied for raising or restoring testosterone, mostly in men with low testosterone. None has been tested after SARM use, and this list is the same for every selection:

Enclomiphene Selective estrogen receptor modulator (SERM); the trans-isomer of clomiphene

Total testosterone: Raised testosterone into the normal range in most men with secondary hypogonadism across Phase 2 and Phase 3 trials. source

Clomiphene Selective estrogen receptor modulator (SERM); a mixture of two isomers, enclomiphene (trans) and zuclomiphene (cis)

Total testosterone in hypogonadal men: Across 19 studies (1,642 men), testosterone, free testosterone, LH, FSH, SHBG and estradiol rose during treatment. Symptom scores (ADAM) improved. source

Tamoxifen Selective estrogen receptor modulator (SERM)

LH, FSH and testosterone in men: In healthy men, 2 weeks of tamoxifen raised LH, FSH and testosterone. The label also notes raised LH, FSH, testosterone and estrogen in oligospermic men. source

A summary of published research, not medical advice. It shows what studies found and does not tell anyone how to use these compounds.

Sarmguide is reader-supported. We may earn a commission from partner links. How we earn These listings are separate from the research above: they are the same whatever the result shows and are not a recommendation.

How the planner works

  1. Drug levels. For each compound it takes the half-life in our record, with the group and route it was measured in, and multiplies it by five. Half of what is in the body is cleared every half-life, so after five half-lives about 3% is left (StatPearls). This is an illustration of concentration decay, not a personal calculation. If any selected compound has no human half-life, the planner gives no figure for the whole selection and names the compound that is missing.
  2. Suppression. It shows our 0–3 suppression score (0 = none found, 3 = marked), whether it rests on human or animal data, and a one-line summary of the studies, with a link to the source. “Not measured” means there are no data, which is not the same as no suppression.
  3. Cycle length check. If the weeks you enter are longer than any human study of a compound in our database, it says so. Many cycles described online are longer than anything that has been studied.
  4. Bloodwork. It lists every marker the studies of your compounds tracked, combined.
  5. Drugs researched for restoring testosterone. It always lists enclomiphene, clomiphene and tamoxifen with what the evidence says about each, whatever you select. None has been tested after SARM use.
  6. Shop listings. After the result, a separate section headed “Where to buy (affiliate links)” shows partner-shop listings. It is the same for every selection and is not derived from the result.

You can share or bookmark a result: the address keeps your selection (for example LGD-4033 + MK-677 for 8 weeks).

Clearance times in our records

Compound Half-life About 3% left after (5 half-lives, illustration) Source
Ostarine ~14–24 h About 3–5 days Phase 1 data (EMERALD protocol)
LGD-4033 24–36 h About 5–8 days Basaria 2013
RAD-140 ~45 h (measured in women) About 9 days Phase 1, 2022
Enclomiphene ~8–10 h About 2 days EMA 2018
Anastrozole ~50 h About 10 days label
Tamoxifen ~5–7 days (metabolite ~14 days) About 4–5 weeks (metabolite longer) label
Clomiphene No single value Not established: the zuclomiphene part lingers for weeks label
MK-677, cardarine No verified human value in our records Not established

Each figure is an illustration of how drug levels fall, based on one study population and route. They are not drug-test detection windows, which can be far longer (detection data are on each fact sheet), and they say nothing about when hormones recover.

What the planner does not do

  • It does not give doses or a PCT protocol. No PCT has been tested after SARMs, so there is no evidence-based protocol to give. The planner shows what was studied and lets the evidence speak.
  • It does not know your body. Half-lives were measured in specific groups (RAD-140 in women with cancer, for example) and vary between people.
  • It does not time bloodwork or recovery. Drug levels falling is not the same as hormones recovering (see below).
  • It cannot check what is in your bottle. In a 2017 analysis of 44 products sold online as SARMs, only 52% contained a SARM and only 41% the labeled amount (Van Wagoner 2017).
  • It is not medical advice. It summarizes published research.

Clearance is not recovery

A falling drug level and a recovering hormone system are different things. When a compound is mostly cleared, that does not show that your own testosterone, LH and FSH have recovered, that a blood test now reflects your own levels, or whether or when any treatment (PCT) is appropriate. The planner therefore gives no recovery date, no testing date and no PCT start date.

Studies measure recovery separately from drug levels. In the LGD-4033 trial in healthy young men, drug levels were measured during 21 days of dosing, and hormones were followed for five weeks after the last dose to see whether they returned to baseline (Basaria 2013). The HAARLEM study of steroid users tested hormones before the cycle, at its end, 3 months after it and one year after the start (Smit 2021). For diagnosing low testosterone, the Endocrine Society recommends a fasting morning total testosterone, repeated to confirm a low value (Bhasin 2018). Which markers studies used and how to read them: SARMs bloodwork. The evidence on PCT itself: SARMs PCT.

Other tools: Stack checker (overlapping risks of a stack) and Compare (two compounds side by side).

Frequently asked questions

Does "mostly cleared" mean my hormones have recovered?

NoEvidence: Trial

Five half-lives only describes how a drug level falls. Hormone recovery is measured separately: in the LGD-4033 trial, hormones were followed for five weeks after the last dose.

Read the full section

What does "mostly cleared" mean?

About 3% leftEvidence: Human data

Half of a drug is cleared every half-life, so after five half-lives about 3% is left. It is a standard pharmacology rule of thumb, used here only as an illustration with half-lives measured in specific study groups.

Read the full section

Why does the planner not give a PCT dose?

No PCT tested after SARMsEvidence: Limited

No PCT has been tested after SARMs, so there is no evidence-based protocol to give. The planner shows the studies that exist and leaves out protocols that have never been tested.

Read the full section

Which blood markers does the planner list?

Every marker the studies trackedEvidence: Trial

Every marker the studies of the selected compounds tracked, combined. For SARMs usually total and free testosterone, SHBG, LH, FSH, lipids, liver enzymes and bilirubin; for MK-677 also IGF-1, glucose and HbA1c.

Read the full section

Why does it say my cycle is longer than any study?

No human data at that lengthEvidence: Limited

Most human SARM studies ran from two weeks to about five months, mostly at low doses. Beyond the longest study of a compound, there is no human data on what that length does.

Read the full section

Why do some compounds show "not established"?

No verified human valueEvidence: Limited

Our records have no verified human half-life for MK-677 and cardarine, and clomiphene's half-life has no single value, so the planner says so instead of guessing. If one of them is selected, it gives no figure for the whole selection.

Read the full section

Sources

  1. Elimination Half-Life of Drugs (StatPearls, NCBI Bookshelf) 2025 · PMID 32119385
  2. EMERALD study protocol (ISRCTN12213700, University of Liverpool, version 6.0, 2021): a window of opportunity study of enobosarm in ER+/AR+ early breast cancer 2021
  3. The safety, pharmacokinetics, and effects of LGD-4033, a novel nonsteroidal oral, selective androgen receptor modulator, in healthy young men 2013 · PMID 22459616
  4. A First-in-Human Phase 1 Study of a Novel Selective Androgen Receptor Modulator (SARM), RAD140, in ER+/HER2- Metastatic Breast Cancer 2022 · PMID 34565686
  5. EnCyzix (enclomifene): public assessment report, EMA/88321/2018 2018
  6. ARIMIDEX (anastrozole) tablets – prescribing information (DailyMed, ANI) 2026
  7. Tamoxifen citrate tablets – prescribing information (DailyMed, Mylan) 2026
  8. CLOMID (clomiphene citrate) tablets – prescribing information (DailyMed) 2025
  9. Chemical Composition and Labeling of Substances Marketed as Selective Androgen Receptor Modulators and Sold via the Internet 2017 · PMID 29183075
  10. Disruption and recovery of testicular function during and after androgen abuse: the HAARLEM study 2021 · PMID 33550376
  11. Testosterone Therapy in Men With Hypogonadism: An Endocrine Society Clinical Practice Guideline 2018 · PMID 29562364