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Harm-reduction information only — not medical advice. In crisis or experiencing adverse effects, contact a healthcare professional or your local emergency services immediately.

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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.

Concentration over time

Concentration values over time. Rows are sampled dates; columns are compounds.
DateNolvadex (Tamoxifen)Clomid (Clomiphene)
W10.000.00
W10.000.00
W20.000.00
W31050.810.00
W41085.820.00
W51053.28258.96
W5736.58353.92
W6706.48479.64
W4491.81
W5435.33
W5367.51
W6359.30
W6321.43

Protocol summary

Standard PCT: Nolvadex + Clomid (4 weeks) · 6 weeks starting Jul 20, 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 above shows the modeled blood concentration of each compound over the 6-week duration. Each compound accumulates toward steady state (roughly 5 half-lives). The peak-to-trough ratio within each dose interval depends on the injection frequency relative to the half-life.

Use the [peak-trough estimator](/tools/peak-trough) to see predicted levels at any point, or the [clearance calculator](/tools/clearance) to estimate washout after the protocol ends. The [PCT planner](/pct-planner) estimates when to start post-cycle therapy.

Educational only. Not medical advice. Concentration values are modeled estimates based on population pharmacokinetics, not predictions of individual blood levels.