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Pyrilutamide

Emerging

KX-826 / 'Pyri' — Kintor Pharmaceuticals' topical AR antagonist for AGA; Phase 3 in China missed primary endpoint (2023-2024). Sister compound to topilutamide / fluridil.

Aliases (3)
KX-826 · GT20029-precursor · topical AR antagonist
TYPICAL DOSE
0.5% topical solution (community-typical resear…
0.5% solution BID
ROUTE
Topical (scalp)
Topical scalp application
CYCLE
Continuous (chronic)
Continuous chronic use
STORAGE
Cool, dry, dark; protect from heat
Cool, dry, dark

Overview

What is Pyrilutamide?

Pyrilutamide (KX-826) is Kintor Pharmaceuticals' topical AR antagonist developed for androgenetic alopecia. It is structurally distinct from but mechanistically related to topilutamide (fluridil / Eucapil) and RU58841 — all members of the topical-AR-antagonist class designed for local DHT/AR blockade at scalp follicles with reduced systemic anti-androgen activity. Pyrilutamide entered Phase 3 in China for AGA; the program reported a disappointing primary-endpoint readout in 2023-2024, with the trial failing to meet its prespecified primary efficacy endpoint despite some positive secondary trends. Not FDA-approved in the US; sold domestically as a research chemical (RUO). Hair-loss community shorthand: 'Pyri'.

Key Benefits

Topical-only AR antagonist for AGA users seeking to avoid systemic 5α-reductase inhibitor side effects. Designed for low systemic exposure. Continues to be used in the bodybuilding / PED community for AAS-cycle scalp protection despite the Phase 3 efficacy miss.

Mechanism of Action

Non-steroidal topical AR antagonist; competitively binds DHT/testosterone at scalp dermal-papilla AR to halt AGA miniaturization. Designed for local activity with rapid systemic deactivation. The 2023-2024 Kintor Phase 3 miss in China is the most salient public fact: the trial's effect size was insufficient to meet the prespecified primary endpoint, though community use and AAS-cycle adjunct application continue. For the same indication, the sister compound topilutamide (fluridil / Eucapil) has a published 3-month RCT (Sovak 2002) and ~20+ years of Czech/Slovak commercial pharmacovigilance — arguably the better-supported topical AR antagonist option.

Quality Indicators

Reputable RUO vendor with COA

Verify HPLC purity ≥98% on a recent batch COA; pyrilutamide has more counterfeiting risk than topilutamide because of community demand built up during Phase 3 hype 2020-2023.

!

Vendor with no Phase 3 awareness in marketing

Vendors still marketing pyrilutamide as 'breakthrough Phase 3 candidate' without acknowledging the 2023-2024 primary endpoint miss are red-flag for staleness or hype-cycle misrepresentation.

Missing or counterfeit COA

Pyrilutamide's pre-Phase-3 hype built a market that has continued post-failure; verify provenance carefully.

What to Expect

  • Week 1
    Tolerability and dose-response.
  • Week 2-4
    Early effect window.
  • Week 4-8
    Peak benefit assessment.
  • Week 8+
    Cycle decision point.
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