Fundraising Fox

Pelage

Founded 2018 Β· 6 known investors

pelagepharma.com β†—

Pelage develops regenerative medicines for hair loss based on stem cell biology, with a lead candidate (PP405) that is a topical small-molecule drug designed to reactivate dormant hair follicle stem cells. It targets conditions including androgenetic alopecia, drug-induced alopecia, and telogen effluvium, and is currently in clinical trials.

Also known as Pelage Pharma Β· Pelage Pharmaceuticals

BiotechHealthtechLongevity

Founders & leadership

WLWilliam Lowry
William LowryPhD
CWChristina Weng
Christina WengChief Medical Officer
NW
Nathan WheelerChief Operating Officer
DGDaniel Gil
Daniel GilPhD

Investors Β· 6

Also in the syndicate Β· 1

Main Street Advisors

Company profile

researched Aug 2026

Pelage Pharmaceuticals is a clinical-stage regenerative medicine biotechnology company based in Los Angeles that develops treatments for hair loss grounded in stem cell biology and metabolism. Its lead program, PP405, is a non-invasive topical small molecule designed to reactivate dormant hair follicle stem cells and restore the body's natural ability to grow hair. The approach is based on UCLA research identifying a metabolic switch that governs hair follicle stem cell activation; PP405 is described as a mitochondrial pyruvate carrier (MPC) inhibitor that blocks transport of pyruvate into mitochondria, causing intracellular pyruvate build-up and increased lactate dehydrogenase activity, which switches on hair follicle stem cells.

Pelage positions PP405 against the existing treatment landscape, in which only two medicines (minoxidil and finasteride) are FDA-approved for androgenetic alopecia, only one of which is approved for women, and where existing therapies act on secondary factors such as hormones or require oral dosing or invasive procedures. PP405 is being developed as a non-hormonal option intended for all genders, skin types and hair types, and is applied topically with no systemic absorption detected in clinical testing. Company materials also reference development for other forms of hair loss including chemotherapy-induced alopecia.

The company's program has progressed from Phase 1 (data presented at AAD 2024) through a randomized, placebo-controlled Phase 2a trial in 78 men and women with androgenetic alopecia, with late-stage/Phase 3 studies planned to begin in 2026. Pelage maintains a clinical advisory board of dermatologists from Brigham and Women's Hospital, Wake Forest, Massachusetts General Hospital and private practice.

Founding story

Pelage's science originates from UCLA research on a metabolic switch controlling hair follicle stem cell activation, including published work on lactate dehydrogenase activity driving hair follicle stem cell activation (Nature Cell Biology, 2017) and the development of mitochondrial pyruvate carrier inhibitors for hair loss (Journal of Medicinal Chemistry, 2021). In 2018, Pelage licensed the intellectual property to PP405 and related topical small molecules from UCLA. Co-founders identified in company materials include William Lowry, Ph.D. (Co-Founder and President) and Michael Jung, Ph.D., Professor of Chemistry and Biochemistry at UCLA. [0][2][4][5]

Business model

Pelage is a clinical-stage biotechnology developer advancing an investigational prescription therapy through the FDA clinical development pathway; it has no disclosed marketed products and is funded by venture capital. Its core asset is intellectual property licensed from UCLA in 2018 covering PP405 and related topical small molecules. [3][4][5]

Traction

Phase 1 data presented at AAD 2024 met primary safety endpoints and showed statistically significant Ki67 activation in hair follicles after one week of dosing. The Phase 2a randomized, placebo-controlled trial enrolled 78 men and women with androgenetic alopecia dosed once daily for four weeks and followed to 12 weeks; it met its primary safety and secondary pharmacokinetic endpoints, with 31% of treated men with higher degrees of hair loss showing a greater than 20% increase in hair density at week 8 versus 0% on placebo. A three-month open-label extension for placebo participants has been completed, a full dataset is planned for a 2026 medical meeting, and late-stage/Phase 3 studies are planned for 2026. Total disclosed venture funding across Series A, A-1 and B is approximately $150.75 million. [2][3][4][5][6]

Latest developments

In October 2025 Pelage closed a $120 million Series B co-led by ARCH Venture Partners and GV with participation from Main Street Advisors, Visionary Ventures and YK Bioventures, appointing Cathy Friedman as Board Chair and adding Richard Heyman to the board. In February 2026 it appointed Maykin Ho, Ph.D. to the board, named Nathan Wheeler, MPH, Chief Operating Officer, and promoted Lisa Sherman to Vice President, Head of Clinical Operations, citing preparation for late-stage PP405 trials. In March 2026 it announced that PP405 and follicular regeneration would be featured in a presentation by Arash Mostaghimi at the AAD Annual Meeting in Denver on March 28, 2026. [2][3][4]

β–ΈFull profile β€” market position, technology, go-to-market, geography, history, risks & controversies

Market position

Pelage describes PP405 as the most advanced clinical-stage program with a novel target for androgenetic alopecia and as a first-in-class regenerative approach; only two drugs (minoxidil and finasteride) are FDA approved for the condition, with no new approvals for nearly three decades. The company cites a global hair loss prevention products market of $23.6 billion in 2021, projected to reach $31.5 billion by 2028, and states hair loss affects more than 80% of men and 40% of women over their lifetimes. [0][3][5][6]

Unlike minoxidil, finasteride or platelet-rich plasma, which the company characterizes as targeting secondary factors such as hormones or having unclear mechanisms, PP405 acts directly on hair follicle stem cells via a metabolic mechanism. It is non-hormonal, topically delivered without detectable systemic absorption, and in Phase 2a induced new hair growth from follicles where no hair was previously present, with clinical response observed by week eight versus the six-to-twelve months typically required with existing therapies. Pelage also promotes a Follicular Unit Count endpoint to measure activation of previously dormant follicular units. [0][3][5][6]

Technology

PP405 is a topical small molecule inhibitor of the mitochondrial pyruvate carrier, formulated as a gel applied to the scalp. Blocking pyruvate transport into mitochondria increases intracellular pyruvate and lactate dehydrogenase activity, which activates hair follicle stem cells that remain present in balding scalp. Clinical testing has shown delivery to the follicle with no detectable systemic exposure. Underlying research includes Nature Cell Biology (2017), Journal of Medicinal Chemistry (2021), and Experimental Dermatology (2021) publications from UCLA-affiliated investigators. [0][2][5][6]

Go-to-market

Development follows the FDA regulatory pathway, with company-sponsored randomized clinical trials, data presentations at dermatology meetings such as the American Academy of Dermatology annual meeting, and a clinical advisory board of dermatology key opinion leaders. Pelage operates a patient-facing registration site (pelagepp405.com) to collect interest in upcoming trials. [0][2][3][5]

Men and women with androgenetic alopecia across skin phototypes and hair textures, including groups the company describes as underserved by existing treatments such as women and people with longstanding hair loss; company materials also cite chemotherapy-induced alopecia as a target indication. [4][5][6]

Geography

Headquartered in Los Angeles, California, United States; press releases are datelined Los Angeles and coverage describes the company as Los Angeles-based. [3][4][6][7]

History

Following the 2018 license of PP405 IP from UCLA, Pelage completed a Phase 1 trial whose data were presented as a late-breaker at the American Academy of Dermatology meeting in March 2024, showing statistically significant Ki67 activation in hair follicles. In February 2024 the company announced a $16.75M Series A led by GV and appointed Christina Weng, M.D. as Chief Medical Officer. In August 2024 it dosed the first patients in its Phase 2 study alongside a $14M GV-led Series A-1. Positive Phase 2a results were announced in June 2025, followed by a $120M Series B co-led by ARCH Venture Partners and GV in October 2025, with Cathy Friedman (GV) named Board Chair and Richard Heyman (ARCH) joining the board. In February 2026 the company expanded its board and leadership, and in March 2026 announced an AAD 2026 presentation on PP405. [2][3][4][5]

Risks & controversies

PP405 remains investigational and is not FDA approved; Phase 2a was designed primarily to assess safety, with efficacy observations described as preliminary and exploratory, and dosing limited to four weeks. Efficacy signals were reported specifically in men with a higher degree of hair loss, and the full trial dataset had not yet been presented as of the October 2025 financing announcement. [4][5][6]

Compiled by commissioned research from 8 cited public sources β€” announcements, filings, and press listed under research sources below.

Key figures

latest reported
FDA-approved drugs for androgenetic alopeciaOct 20252 drugs
Global hair loss prevention products marketJan 2021$23.6B
Global hair loss prevention products market (projected)Jan 2028$31.5B
HeadcountAug 202617
Lifetime hair loss prevalence, menOct 2025$80
Lifetime hair loss prevalence, womenOct 2025$40
Men with higher degree of hair loss achieving >20% increase in hair density at wJun 20250%
Phase 2a trial enrollmentJun 202578 participants
Total disclosed venture funding (Series A + A-1 + B)Oct 2025$150.8M

Company-reported or press-reported figures, each dated to when it was claimed β€” not independently audited.

Timeline Β· 11

launches, deals, and filings
Mar 2026
PP405 follicular regeneration data to be presented at AAD 2026

Presentation on emerging treatments for hair loss targeting dormant follicles, delivered by Arash Mostaghimi on March 28, 2026 at the AAD Annual Meeting in Denver, Colorado.

source β†—

Feb 2026
Board expansion and executive leadership promotions

Maykin Ho, Ph.D. appointed to the board of directors; Nathan Wheeler, MPH appointed Chief Operating Officer; Lisa Sherman promoted to Vice President, Head of Clinical Operations, ahead of late-stage PP405 trials.

source β†—

Oct 2025
$120M Series B co-led by ARCH Venture Partners and GV

Financing to support advancement of PP405 into Phase 3 trials in 2026; Cathy Friedman appointed Board Chair and Richard Heyman joined the board.

$120M source β†—

Oct 2025
Cathy Friedman appointed Board Chair; Richard Heyman joins board

Cathy Friedman of GV, who led the Series A, became Chair of the Board; Richard Heyman of ARCH Venture Partners joined the board alongside CEO Daniel Gil and Co-Founder and President William Lowry.

source β†—

Jun 2025
Positive Phase 2a results announced for PP405

Trial in 78 participants met primary safety and secondary pharmacokinetic endpoints; 31% of treated men with higher degree of hair loss showed >20% increase in hair density at week 8 versus 0% on placebo.

source β†—

Aug 2024
$14M Series A-1 led by GV

$14M source β†—

Aug 2024
First patients dosed in Phase 2 study of PP405

Phase 2 trial recruiting women and men with androgenetic alopecia to evaluate safety and preliminary efficacy of topical PP405; leaders in dermatology joined the Clinical Advisory Board.

source β†—

Mar 2024
Late-breaking Phase 1 and ex vivo data presented at AAD 2024

Pelage presented data showing PP405, a topical MPC inhibitor, activates human hair follicle stem cells ex vivo and in a Phase 1 clinical study, with statistically significant Ki67 activation in the hair follicle.

source β†—

Feb 2024
$16.75M Series A led by GV

Series A financing led by GV; announced alongside Phase 1 data and the appointment of Christina Weng, M.D. as Chief Medical Officer.

$16.8M source β†—

Feb 2024
Qing Yu Christina Weng, M.D. appointed Chief Medical Officer

source β†—

Jan 2018
Licensed PP405 intellectual property from UCLA

Pelage licensed the intellectual property to PP405 and related topical small molecules from UCLA.

source β†—

Dated company events from announcements, filings, and press; legal rows summarize public dockets and regulator releases.

In the news

β–ΈResearch sources Β· 8

primary sources listed
  • Pelagepelagepharma.com Β· web

8 public sources were cited for this profile; the first-party ones are listed here.

Frequently asked questions

What does Pelage do?
Los Angeles clinical-stage biotech developing PP405, a topical small molecule that reactivates dormant hair follicle stem cells.
Who are Pelage's investors?
Pelage's investors include GV (Google Ventures), ARCH Venture Partners, HAWKTAIL, Visionary Ventures, YK Bioventures.