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AVERY FISK · AF COACHING

SARMs

PF-06260414

An experimental SARM with phase 1 human pharmacology data, including hormone, lipid and liver findings; clinical muscle benefit was not established.

Placebo-controlled phase 1 research; biomarker and safety observations, not an efficacy trial

PF-06260414 molecular structure
Structure reference · C14H14N4O2S

Practical use

Evidence interpretation and clinical context

Identify the development phase
Read a phase 1 result as an early pharmacology study.
Name the observed safety signal
Retain liver and lipid findings in summaries of tolerability.
Check for functional endpoints
A hormone change cannot stand in for measured strength or health benefit.

Safety, Pharmacokinetic, and Pharmacodynamic Evaluation After Single and Multiple Ascending Doses of a Novel Selective Androgen Receptor Modulator in Healthy Subjects.

Regulatory status — primary or official source

Overview

PF-06260414 was studied in healthy volunteers to characterize exposure, tolerability and biological activity. Early human development can show that a compound affects androgen-related markers without showing that it improves strength or health.

Risks and limitations

The phase 1 report recorded ALT elevations in seven participants and changes in HDL cholesterol, sex hormone-binding globulin and testosterone-related measures. A small early trial cannot rule out uncommon or cumulative harms.

How to read this

Pharmacokinetics describes how exposure changes over time. Pharmacodynamics describes biological response. Neither alone demonstrates that a patient feels or functions better.

Research explained

Safety, Pharmacokinetic, and Pharmacodynamic Evaluation After Single and Multiple Ascending Doses of a Novel Selective Androgen Receptor Modulator in Healthy Subjects.

Who was studied

Healthy adult men in single- and repeated-exposure phase 1 cohorts, including a Japanese cohort.

What was found

Researchers characterized exposure and androgen-responsive biomarker changes. ALT elevations and headache were reported; no serious adverse events were reported in this study.

What it cannot establish

Small cohorts and brief follow-up limit safety conclusions. The study did not establish strength, disability or disease-treatment benefit.

Read the original study

Regulatory status

FDA states that SARMs are unapproved drugs, not dietary supplements.

Supporting source

What the hormone findings mean

Changes in circulating endocrine markers show that the intervention is not biologically confined to a muscle measurement. The trial was not designed to establish fertility outcomes.

Supporting source

Claims versus findings

Incorrect trial interpretation

A phase 1 study proves a muscle-building treatment works.

This phase evaluated pharmacology and tolerability rather than clinical muscle efficacy.

Check the evidence

Common questions

Does no serious event mean the compound is safe?

It means none was reported in these small, short cohorts. It does not quantify rare or long-term risk.

Source

Sources

Safety, Pharmacokinetic, and Pharmacodynamic Evaluation After Single and Multiple Ascending Doses of a Novel Selective Androgen Receptor Modulator in Healthy Subjects.

Regulatory status — primary or official source

Sources checked 2026-10-01.

General education; not a personal treatment plan.