PP-405, PP 405 (developed by Pelage Pharmaceuticals; derived from the MPC-inhibitor chemotype exemplified by UK-5099 / JXL001) · Evidence-based safety and harm-reduction overview.
| Also known as | PP-405, PP 405 (developed by Pelage Pharmaceuticals; derived from the MPC-inhibitor chemotype exemplified by UK-5099 / JXL001) |
| Category | Research Chemical |
| Drug class | Dual mitochondrial pyruvate carrier (MPC1/MPC2) inhibitor; small molecule |
| Developer | Pelage Pharmaceuticals (UCLA spinout, founded 2018) |
| Route | Topical scalp gel (reported ~0.05%), once daily |
| Indication | Androgenetic alopecia (male- and female-pattern hair loss) |
| Trial stage | Phase 1 complete; Phase 2a reported June 2025 (n=78); Phase 3 planned 2026 |
| Regulatory status | Investigational; not FDA-approved; not a dietary supplement; not for sale |
| US legal status | PP405 is an investigational drug, not an FDA-approved product and not a lawful dietary supplement. As of mid-2026 it exists only inside Pelage Pharmaceuticals' clinical program (Phase 1 completed, Phase 2a reported June 2025, Phase 3 planned for 2026) and is not sold, prescribed, or available through any legal channel. The exact chemical structure is proprietary and undisclosed. Any product marketed online as "PP405" outside of a Pelage-sponsored trial is unverified and not the genuine investigational compound. This entry is informational only; Peptropix does not sell PP405 or any research chemical. |
PP405 is a topical small-molecule candidate for androgenetic alopecia (male- and female-pattern hair loss) being developed by Pelage Pharmaceuticals, a UCLA spinout. It is described as a dual mitochondrial pyruvate carrier (MPC1/MPC2) inhibitor formulated as a low-concentration scalp gel (reported at 0.05%, once daily). The proposed idea is to metabolically "reactivate" dormant hair follicle stem cells rather than block DHT (finasteride) or act as a vasodilator/K-channel opener (minoxidil). It is early-stage and investigational, with human efficacy data limited to a small Phase 2a readout.
PP405 is described as a dual inhibitor of the mitochondrial pyruvate carrier (MPC1 and MPC2), the transporter that shuttles pyruvate into mitochondria for oxidative metabolism. By blocking pyruvate entry, the proposed mechanism diverts metabolism toward the cytoplasm: pyruvate and lactate dehydrogenase (LDH) activity rise, intracellular lactate and glycolysis increase, and this metabolic shift is thought to push quiescent (telogen) hair follicle stem cells into an activated, growth (anagen) state. This builds on UCLA research (foundational work reported around 2017) showing that LDH activity and lactate act as a metabolic switch for hair follicle stem cell activation, and on the earlier MPC-inhibitor tool compound UK-5099, which accelerated hair growth in mice by the same lactate-driving logic. The mechanism is well-motivated preclinically but its translation to durable human hair regrowth remains to be confirmed in larger trials.
The science traces to UCLA, where Bill Lowry, studying hair follicle stem cells, observed unusually high lactate dehydrogenase activity in active follicles; work by Lowry, Heather Christofk, and colleagues (reported around 2017) established lactate/LDH as a metabolic switch for follicle stem cell activation, using MPC inhibition (including the classic tool compound UK-5099) to drive lactate and stimulate hair growth in mice. Pelage Pharmaceuticals was spun out of UCLA in 2018 by Lowry, Christofk, and chemist Michael Jung; the company name comes from the French pelage ("coat of fur") and PP405 is reportedly named after the company and the 405 freeway. First-in-human trials began around 2023, Phase 2a topline results were announced in June 2025, and Pelage stated it plans to begin Phase 3 in 2026. The program has drawn significant venture funding (reported rounds led by Google Ventures, with cumulative financing cited around 120 million dollars) and mainstream press attention.
Human data are early and thin. A Phase 1 study reported the drug was well tolerated, achieved its target pharmacokinetic profile with no detectable systemic (blood) drug levels, and produced a statistically significant increase in Ki67 (a proliferation marker) in treated follicles within about seven days, interpreted as stem-cell engagement. The Phase 2a trial was a randomized, double-blind, placebo-controlled study in 78 adults with androgenetic alopecia (men and women, diverse skin phototypes and hair textures), applying PP405 or placebo once daily for 4 weeks with follow-up to 12 weeks. Per the sponsor's June 2025 announcement, the study met its primary safety endpoint and secondary PK endpoint (no systemic absorption), and in a subgroup of men with more advanced loss, 31% of PP405-treated participants showed a greater than 20% increase in hair density at week 8 versus 0% on placebo. These are company-reported topline figures from a small, short trial; results have been publicized largely through press releases and conference/media coverage rather than a full peer-reviewed Phase 2a publication, and no robust large-scale, long-term human efficacy or durability data exist yet.
Informational only, not a protocol and not usable guidance. The formulation described in reporting is a low-concentration topical scalp gel (approximately 0.05%) applied once daily, with the Phase 2a trial using a 4-week once-daily application window followed out to 12 weeks. These figures describe a controlled clinical trial regimen for the genuine investigational compound, which is not commercially available; they are not a recommendation, and no equivalent self-administration is possible or advisable outside a sponsored trial.
This is general research/context information, not medical advice or a recommended protocol.
No stacking or combination guidance can be given. PP405 is investigational and not available; combination regimens (for example with minoxidil or finasteride) have not been tested or reported, so any "stack" would be speculative and unsupported by evidence. Peptropix does not provide combination protocols for unapproved compounds.
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Get tested with Ulta Lab Tests →No. PP405 is an investigational drug still in clinical trials (Phase 2a reported in 2025, Phase 3 planned for 2026). It is not FDA-approved, not a dietary supplement, and not legally sold. The only access to the genuine compound is through a Pelage-sponsored trial. Anything sold online as 'PP405' is unverified.
It targets a different biology. Finasteride blocks DHT and minoxidil is a topical vasodilator/potassium-channel opener; PP405 is proposed to work metabolically by inhibiting the mitochondrial pyruvate carrier to raise lactate and reactivate dormant hair follicle stem cells. Whether that translates into better or more durable regrowth than existing options is unproven and awaits larger trials.
In a randomized, double-blind, placebo-controlled study of 78 adults using the gel once daily for 4 weeks, the company reported it met its primary safety endpoint with no detectable systemic absorption, and that in a subgroup of men with more advanced loss, 31% had a greater than 20% increase in hair density at week 8 versus 0% on placebo. These are small, short-term, company-reported topline results, not a definitive efficacy dataset.
The human safety database is very limited (Phase 1 plus one ~78-person Phase 2a). Early data reported no systemic adverse events and no measurable blood levels, which is the main claimed advantage over oral drugs, but long-term and rare-event safety is unknown. This is not medical advice; safety questions should go to a licensed clinician.
We do not provide dosing guidance. Reporting describes a roughly 0.05% topical gel applied once daily in trials, but that describes a controlled study of the real investigational compound, not a protocol you can follow. There is no safe or verified way to self-administer PP405, and dosing decisions belong with a clinician and trial investigators.
Likely not where follicles are scarred or permanently lost. The proposed mechanism reactivates dormant but intact follicles, so areas with viable, merely resting follicles are the plausible targets. Regeneration of terminal hair in some previously thin/bald areas was reported in early data, but this is preliminary and not established.
Medical & legal disclaimer. This site is for informational and harm-reduction purposes only. It is not medical advice and is not a substitute for a licensed healthcare professional. The compounds discussed are largely not approved by the FDA for human use and many are sold strictly as research chemicals 'not for human consumption.' Nothing here is an endorsement to purchase, possess, or use any substance. Laws vary by jurisdiction. Always consult a qualified physician and follow the law where you live.
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