MaaT Pharma SA (EPA:MAAT)

France flag France · Delayed Price · Currency is EUR
7.24
-0.01 (-0.14%)
May 14, 2026, 5:35 PM CET
Market Cap136.62M +51.7%
Revenue (ttm)4.52M +40.7%
Net Income-31.06M
EPS-1.95
Shares Out18.84M
PE Ration/a
Forward PEn/a
Dividendn/a
Ex-Dividend Daten/a
Volume203,697
Average Volume81,964
Open7.34
Previous Close7.25
Day's Range7.11 - 7.82
52-Week Range3.55 - 8.62
Beta0.46
RSI75.07
Earnings DateSep 15, 2026

About MaaT Pharma

MaaT Pharma SA, a late-stage clinical company, engages in the development of gut microbiome-driven therapies to modulate the immune system and improve cancer survival. Its products pipeline includes MaaT013, that is in pivotal phase 3 clinical trial for the treatment of acute graft versus host diseases with gastrointestinal involvement; MaaT033, which is in phase 2b clinical trial for the improvement of survival at 12 months for patients with blood cancer receiving allogenic hematopoietic stem cell transplantation; and MaaT03X for the treatment... [Read more]

Industry Biotechnology
Sector Healthcare
Founded 2014
Employees 59
Stock Exchange Euronext Paris
Ticker Symbol MAAT
Full Company Profile

Financial Performance

In 2025, MaaT Pharma's revenue was 4.52 million, an increase of 40.67% compared to the previous year's 3.22 million. Losses were -31.06 million, 7.46% more than in 2024.

Financial Statements

News

MaaT Pharma Transcript: Status Update

A transformative exclusive partnership with Clinigen will drive Xervyteg’s commercialization across Europe, supported by strong early access data and a robust financial agreement. Manufacturing is ready for scale, and the deal extends cash runway into 2026, setting a benchmark for future growth and expansion.

11 months ago - Transcripts

MaaT Pharma Transcript: Study Result

The ARES phase 3 trial of MaaT013 in severe, refractory acute GVHD demonstrated a 62% GI response rate at day 28 and a 54% one-year survival, far surpassing historical outcomes. Regulatory submission in Europe is imminent, with commercialization and expansion plans supported by strong safety, robust real-world data, and a EUR 750 million market opportunity.

1 year ago - Transcripts

MaaT Pharma Transcript: KOL Event

KOLs highlighted the high unmet need in acute GVHD, with MaaT013 showing strong response and survival rates in heavily pretreated patients, especially those refractory to ruxolitinib. Upcoming phase 3 results in January 2025 are expected to be pivotal for approval and expansion.

1 year ago - Transcripts

MaaT Pharma Transcript: KOL Event

2 years ago - Transcripts

MaaT Pharma Transcript: Investor Update

3 years ago - Transcripts

MaaT Pharma Transcript: R&D Day 2022

4 years ago - Transcripts