PureTech Health plc (LON:PRTC)

London flag London · Delayed Price · Currency is GBP · Price in GBX
140.20
+2.60 (1.89%)
May 26, 2026, 4:47 PM GMT
Market Cap334.94M +14.7%
Revenue (ttm)3.46M -3.5%
Net Income-81.54M
EPS-0.34
Shares Out 243.42M
PE Ration/a
Forward PEn/a
Dividendn/a
Ex-Dividend Daten/a
Volume417,601
Open139.00
Previous Close137.60
Day's Range135.46 - 140.20
52-Week Range104.71 - 148.00
Beta0.79
AnalystsStrong Buy
Price Target454.74 (+224.35%)
Earnings DateApr 29, 2026

About PureTech Health

PureTech Health plc, engages in the development and commercialization of biotechnology and pharmaceutical solutions in the United States. It is developing LYT-100, which is under Phase 2 stage, to treat idiopathic pulmonary fibrosis (IPF); and LYT-200, a IgG4 monoclonal antibody, currently under Phase 1/2 stage, targeting galectin-9 for treating solid tumors and hematological malignancies. The company also develops SPT-300, an oral drug of allopregnanolone for the treatment of anxious depression; and delivers transformative medicines for patien... [Read more]

Industry Biotechnology
Sector Healthcare
Founded 2015
Employees 56
Stock Exchange London Stock Exchange
Ticker Symbol PRTC
Full Company Profile

Financial Performance

Financial numbers in USD Financial Statements

News

PureTech to Showcase Deupirfenidone Program at the American Thoracic Society International Conference

BOSTON--(BUSINESS WIRE)--PureTech to Showcase Deupirfenidone Program at the American Thoracic Society International Conference.

13 days ago - Business Wire

PureTech Health Earnings Call Transcript: H2 2025

Refined strategy emphasizes operational efficiency, early spin-outs, and disciplined capital allocation. Cash runway extends through 2028, with major progress in Celea and Gallop clinical programs and a focus on returning capital to shareholders after significant inflows.

27 days ago - Transcripts

PureTech Health Annual report: H2 2025

PureTech Health has published its H2 2025 annual report on April 29, 2026.

27 days ago - Filings

PureTech Health Annual report: H2 2025

PureTech Health has published its H2 2025 annual report on April 29, 2026.

27 days ago - Filings

PureTech Health Annual report: H2 2025

PureTech Health has published its H2 2025 annual report on April 29, 2026.

27 days ago - Filings

PureTech Health to delist American depositary shares from Nasdaq

PureTech Health (PRTC) announced that it has notified Nasdaq of its intention to voluntarily delist its American depositary shares, each representing the right to receive 10 ordinary shares of the…

27 days ago - TheFly

PureTech Announces Annual Results for Year Ended December 31, 2025

BOSTON--(BUSINESS WIRE)--PureTech Announces Annual Results for Year Ended December 31, 2025.

27 days ago - Business Wire

PureTech Announces Intention to Voluntarily Delist American Depositary Shares from Nasdaq and Concentrate Trading on the London Stock Exchange

BOSTON--(BUSINESS WIRE)--PureTech Announces Intention to Voluntarily Delist American Depositary Shares from Nasdaq and Concentrate Trading on the London Stock Exchange.

27 days ago - Business Wire

PureTech Founded Entity Seaport Therapeutics Adds Intra-Cellular Therapies Founder and CEO, Dr. Sharon Mates, to its Board of Directors

BOSTON--(BUSINESS WIRE)--PureTech Founded Entity Seaport Therapeutics Adds Intra-Cellular Therapies Founder and CEO, Dr. Sharon Mates, to its Board of Directors.

4 weeks ago - Business Wire

PureTech Health announces data from Phase 1b trial of LYT-200

PureTech Health (PRTC) announced positive topline data from the completed Phase 1b clinical trial of LYT-200, a fully human anti-galectin-9 monoclonal antibody, in heavily pretreated patients with rel...

4 weeks ago - TheFly

PureTech Reports Positive Topline Data from Phase 1b Trial of LYT-200 in Relapsed/Refractory (R/R) High-Risk (HR) Myelodysplastic Syndrome (MDS) and R/R Acute Myeloid Leukemia (AML)

BOSTON--(BUSINESS WIRE)--PureTech Reports Positive Topline Data from Phase 1b Trial of LYT-200 in R/R High-Risk Myelodysplastic Syndrome & R/R Acute Myeloid Leukemia.

4 weeks ago - Business Wire

PureTech Health: Notice of Results

BOSTON--(BUSINESS WIRE)--PureTech Health: Notice of Results.

6 weeks ago - Business Wire

PureTech Health announces publication of Phase 2b ELEVATE IPF trial results

PureTech Health (PRTC) announced the publication of results from the Phase 2b ELEVATE IPF trial of deupirfenidone for the potential treatment of idiopathic pulmonary fibrosis in The American Journal o...

7 weeks ago - TheFly

PureTech Announces Publication of Phase 2b ELEVATE IPF Trial Results in The American Journal of Respiratory and Critical Care Medicine

BOSTON--(BUSINESS WIRE)--PureTech Announces Publication of Phase 2b ELEVATE IPF Trial Results in The American Journal of Respiratory and Critical Care Medicine.

7 weeks ago - Business Wire

PureTech Founded Entity Seaport Therapeutics Announces Publication in Science Translational Medicine Featuring GlyphAllo™ (SPT-300) as the First Triglyceride-Mimetic Prodrug to Achieve Therapeutically Relevant Drug Levels in Humans

BOSTON--(BUSINESS WIRE)--PureTech Founded Entity Seaport Therapeutics Announces Publication in Science Translational Medicine Featuring GlyphAllo (SPT-300).

2 months ago - Business Wire

PureTech Health Transcript: Leerink Global Healthcare Conference 2026

The conference highlighted a robust hub-and-spoke model driving innovation and value through spin-outs, with strong clinical progress in IPF and oncology. Deupirfenidone is poised for a pivotal phase 3 trial, and the company remains self-funded with significant future milestones expected.

2 months ago - Transcripts

PureTech to Present at the Leerink Partners Global Healthcare Conference

BOSTON--(BUSINESS WIRE)--PureTech to Present at the Leerink Partners Global Healthcare Conference.

3 months ago - Business Wire

PureTech Health announces orphan drug designation for Deupirfenidone in IPF

PureTech Health (PRTC) announced that the U.S. Food and Drug Administration and European Commission have granted Orphan Drug Designation to deupirfenidone for the treatment of idiopathic pulmonary fib...

3 months ago - TheFly

PureTech Announces Orphan Drug Designations Granted by the U.S. Food and Drug Administration and European Commission for Deupirfenidone (LYT-100) in Idiopathic Pulmonary Fibrosis

BOSTON--(BUSINESS WIRE)--PureTech Announces Orphan Drug Designations Granted by the U.S. Food and Drug Administration and European Commission for Deupirfenidone in IPF.

3 months ago - Business Wire

PureTech Health Transcript: 44th Annual J.P. Morgan Healthcare Conference

A diversified hub-and-spoke model drives innovation and financial returns by spinning out de-risked drug programs, with a strong track record of clinical and commercial success. Key assets Celea and Gallop are advancing to pivotal trials, while the company remains self-funded and focused on efficient capital allocation.

4 months ago - Transcripts

PureTech to Present at 44th Annual J.P. Morgan Healthcare Conference

BOSTON--(BUSINESS WIRE)--PureTech to Present at 44th Annual J.P. Morgan Healthcare Conference.

5 months ago - Business Wire

PureTech Health appoints Robert Lyne as CEO

PureTech Health (PRTC) announces that the board of directors has appointed Robert Lyne as CEO, and as a member of the board of directors, effective immediately. Lyne has served as…

5 months ago - TheFly

PureTech Appoints Robert Lyne as Chief Executive Officer

BOSTON--(BUSINESS WIRE)--PureTech Health plc (Nasdaq: PRTC, LSE: PRTC) ("PureTech" or the "Company"), a hub-and-spoke biotherapeutics company dedicated to giving life to science and transforming innov...

5 months ago - Business Wire

PureTech Health completes LYT-100 End-of-Phase 2 meeting with FDA

PureTech Health (PRTC) announced the completion of the End-of-Phase 2 meeting with the FDA regarding the development of deupirfenidone, or LYT-100, for the treatment of idiopathic pulmonary fibrosis. ...

6 months ago - TheFly

PureTech Announces Successful End-of-Phase 2 Meeting with FDA for Deupirfenidone (LYT-100) in Idiopathic Pulmonary Fibrosis

BOSTON--(BUSINESS WIRE)--PureTech Announces Successful End-of-Phase 2 Meeting with FDA for Deupirfenidone (LYT-100) in Idiopathic Pulmonary Fibrosis.

6 months ago - Business Wire