Standard PCT: Nolvadex + Clomid (4 weeks)
Standard post-cycle therapy beginning after ester clearance (14-day offset). Front-loaded taper: Nolva 40mg→20mg, Clomid 100mg→50mg, each 2 weeks.
Model levels over time
% of sampled peakModel details: Nolvadex (Tamoxifen) · relative timing
Compare timing and buildup for this compound. The values are not blood concentrations or a measure of strength.
Shows a relative timing scenario; absolute blood concentrations are not calibrated.
Timing assumptions and sources
Label terminal 120–168 h;144 h midpoint is a timing assumption.
One 1 mg input peaks at 1 relative unit after a single dose. Other amounts scale proportionally; overlapping doses add when accumulation is on. Different compounds use separate relative scales.
- Timing half-life used
- 144 hours
- Absorption half-life assumed
- 0.6364052 hours
- Reference amount for the relative scale
- 1 mg
- The faster rate is inferred to match the 5 h source-scoped peak time; absorption half-life 0.6364052012164843 h is a mathematical shape parameter, not separately measured.
- A single 1-unit input has a peak of 1 relative unit; scaling and repeated-dose addition are mathematical assumptions. This normalization is independent of the example dose.
- One-compartment predicts steady mean 354.7 ng/mL (~2.91×122); biphasic parent kinetics and metabolites require more than aterminal exponential.
- Do not sum parent+N-desmethyl/endoxifen as equal drug action.
- Tablet dose is tamoxifen base equivalent, not mass of citrate salt.
- Tamoxifen citrate prescribing information
20 mg single dose parentpeak 40 ng/mL at 5 h; terminal 5–7 days;20 mg/day chronic meanparent 122 ng/mL; N-desmethyl 353 ng/mL.
nolvadex-relative-timing-2026-10 · version 1
Model details: Clomid (Clomiphene) · relative timing
Compare timing and buildup for this compound. The values are not blood concentrations or a measure of strength.
Shows a relative timing scenario; absolute blood concentrations are not calibrated.
Timing assumptions and sources
Five-day timing is a legacy illustration; no single measured half-life for the mixture accepted. The retained 120 h slower timescale is an assumption.
One 1 mg input peaks at 1 relative unit after a single dose. Other amounts scale proportionally; overlapping doses add when accumulation is on. Different compounds use separate relative scales.
- Timing half-life used
- 120 hours
- Absorption half-life assumed
- 30 hours
- Reference amount for the relative scale
- 1 mg
- Absorption half-life is assumed to be one quarter of the slower timescale (30 h); it is not a measured absorption parameter.
- A single 1-unit input has a peak of 1 relative unit; scaling and repeated-dose addition are mathematical assumptions. This normalization is independent of the example dose.
- Two separate 15 ng/mL peaks at different times are not a 30 ng/mL mixture Cmax.
- Do not model enclomiphene alone as Clomid.
- Ghobadi et al 2009: clomiphene isomers in PCOS
50 mg citrate:Zu peak 15 ng/mL at 7 h, AUC 0–456=1289; En peak 15 at 3 h, AUC 0–72=65; reliable terminal model parameters could not be obtained.
- Mikkelson 1986: clomiphene in volunteers
24 healthy women;50 mg; isomer concentrations and persistence differ.
- Clomiphene citrate label
Product is 30–50% cis isomer and 50 mgcitrate; cis persists much longer.
clomid-relative-timing-2026-10 · version 1
Different scales · each curve is normalized to its own peak. Compare timing and shape, not concentration or potency.
| Date | Clomid (Clomiphene) · Relative timing (% of sampled peak) | Nolvadex (Tamoxifen) · Relative timing (% of sampled peak) |
|---|---|---|
| W1 | 0 % of sampled peak | 0 % of sampled peak |
| W1 | 0 % of sampled peak | 0 % of sampled peak |
| W2 | 0 % of sampled peak | 0 % of sampled peak |
| W2 | 0 % of sampled peak | 0 % of sampled peak |
| W3 | 20.7048 % of sampled peak | 35.9314 % of sampled peak |
| W3 | 52.2417 % of sampled peak | 60.6589 % of sampled peak |
| W4 | 76.6215 % of sampled peak | 76.4381 % of sampled peak |
| W4 | 92.331 % of sampled peak | 86.7128 % of sampled peak |
| W5 | 98.9478 % of sampled peak | 87.5975 % of sampled peak |
| W5 | 89.761 % of sampled peak | 83.7213 % of sampled peak |
| W6 | 80.528 % of sampled peak | 76.9799 % of sampled peak |
| W6 | 73.898 % of sampled peak | 71.6109 % of sampled peak |
| W6 | 69.4544 % of sampled peak | 67.5927 % of sampled peak |
The chart uses a bounded time grid. Long horizons can miss brief peaks between samples; shorten the horizon to inspect more detail. Chart peaks are sampled values.
Protocol summary
Standard PCT: Nolvadex + Clomid (4 weeks) · 6 weeks starting Oct 30, 26
- Nolvadex (Tamoxifen) — 40.0 mg Every day, weeks 2–3.857142857142857
- Clomid (Clomiphene) — 100.0 mg Every day, weeks 2–3.857142857142857
- Nolvadex (Tamoxifen) — 20.0 mg Every day, weeks 4–5.857142857142857
- Clomid (Clomiphene) — 50.0 mg Every day, weeks 4–5.857142857142857
Protocol overview
- Category
- pct
- Duration
- 6 weeks
- Compounds
- 4
- Tags
- pct, serm, nolvadex, clomid, taper
Compounds in this protocol
- Nolvadex 40mg — 40 mg, every-day (weeks 2-3.857142857142857)
- Clomid 100mg — 100 mg, every-day (weeks 2-3.857142857142857)
- Nolvadex 20mg — 20 mg, every-day (weeks 4-5.857142857142857)
- Clomid 50mg — 50 mg, every-day (weeks 4-5.857142857142857)
How to read this protocol
The chart shows available model curves over the 6-week example. Rows whose model is unavailable are retained for context but produce no curve. Read each model’s details for what its line represents; a plotted level does not predict treatment effects or establish a suitable dose.
The peak/trough explorer examines one complete model interval. The single-dose decline explorer is a separate one-dose scenario; it does not calculate this protocol's washout or a safe treatment-change date. Read the recovery reference for PCT evidence and its limits.
Educational only. Not medical advice. These examples do not predict individual blood levels.