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ACP-105

Aliases: ACP105

Last verified: 2026-09-23

PreclinicalPreclinical evidenceSARMsLow interest

The short version

A SARM from the Acadia program — anabolic potential with reportedly milder suppression; preclinical data also show cognitive/neural effects. Key fact: No controlled human trials exist. Everything known about ACP-105 in humans comes from indirect sources and self-reports. Status: preclinical. Not approved; WADA-banned (S1).

Identity & type

Molecular type
SARM
Origin
A SARM from the Acadia program — anabolic potential with reportedly milder suppression; preclinical data also show cognitive/neural effects.

Mechanism of action

Selective AR agonism; additional CNS actions (preclinical).

not confirmed in humans

Dosing & routes

Official / clinical context

No approved official document exists for ACP-105. Any protocols mentioned are to be read as information, not as a recommendation.

Regulator-approved labeling and published study designs — never a recommendation.

Community-reported practice

Community: 5–15 mg/day. Described as a "milder RAD-140": modest mass gains with little suppression; experiences limited.

Unverified self-reports. Not medical advice. Not endorsement.

Expected effects (community)

Described as a "milder RAD-140": modest mass gains with little suppression; experiences limited.

Protocol — official vs community

Official / label

No official protocol exists — this compound has no approved product.

Community (anecdotal)

5–15 mg oral daily; a minority of vendor listings go to 20 mg.

Cycle:
8 weeks.
Break:
4 weeks; milder suppression means PCT is debated rather than assumed.

Marketed as a 'milder RAD-140' — modest mass gains with comparatively little suppression. The human experience base is small, and the cognitive-angle marketing has no human data behind it.

Human evidence

No controlled human trials exist. Everything known about ACP-105 in humans comes from indirect sources and self-reports.

Preclinical evidence

Preclinical; clinical development never advanced.

Known risks

  • Unknown in humans; presumed mild suppression.characterized
  • WADA prohibition (S1 anabolic agents)characterized

Teal: characterized in clinical/labeling contexts. Amber: theoretical or reported outside controlled settings.

Unknowns & evidence gaps

  • All human pharmacokinetics, safety and efficacy

Frequently asked questions

References

Systematic references are being expanded; verify sources directly before any decision.