Prévisions

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Actualités Accéder au fil d'actualités

MaaT Pharma starts phase‑2 IMMUNOLIFE trial with MaaT033 in NSCLC

MaaT Pharma has enrolled the first patient in the randomized phase‑2 IMMUNOLIFE trial, which is testing the microbiome therapy MaaT033 in combination with cemiplimab versus the investigator’s choice of best therapy in non‑small cell lung cancer. A total of 162 patients are to be recruited across 14 centers in France; the primary endpoint is disease control rate at 12 weeks. Recruitment is expected to take around two years, an interim futility analysis is planned for H1 2027, and first results after one year of follow‑up are expected at the end of 2030. MaaT Pharma emphasizes that the study results will also support development of the next‑generation MaaT034; the company reports a market capitalization of about €93 million and revenue growth of 52.55% in the past twelve months. » Plus sur de.investing.com
MaaT Pharma: MaaT013 shows 54% one-year survival rate in phase‑3 study for GI‑aGvHD

MaaT Pharma reports that microbiome candidate MaaT013 (Xervyteg) achieved a one‑year overall survival rate of 54% in the pivotal phase‑3 ARES study in patients with steroid‑ and ruxolitinib‑refractory gastrointestinal acute graft‑versus‑host disease. The 66‑patient study across 50 sites showed a gastrointestinal response rate of 62% at day 28 and sustained remissions on follow‑up; the safety profile was deemed acceptable. MaaT013 is currently under review by the EMA, with a regulatory decision expected by mid‑2026. » Plus sur de.investing.com
MaaT Pharma: Xervyteg achieves 62% GI response rate in Phase‑3 ARES study

In the approval‑relevant Phase‑3 ARES study, Xervyteg® (MaaT013) produced an overall gastrointestinal response rate (GI‑ORR) of 62% at day 28 in refractory or ruxolitinib‑intolerant GI‑aGvHD, including 38% complete remissions and 20% very good partial remissions. Secondary endpoints showed a GI‑ORR of 49% at day 56 and 44% at three months; median duration of response was 6.4 months. Estimated 12‑month overall survival was 54% (67% for responders vs. 28% for non‑responders). The single‑arm study included 66 patients at 50 sites in Europe; an EMA decision is expected in H2 2026. In addition, the DSMB has cleared continuation of the Phase‑2b PHOEBUS study with MaaT033 without safety concerns. » Plus sur de.investing.com

Données financières de l'entreprise

Au dernier trimestre, MAAT PHARMA S.A. EO-,1 Aktie a réalisé un chiffre d'affaires de 2,10 Mio€ et un bénéfice net de −15,98 Mio€

(EUR)	déc. 2025	YoY
Chiffre d'affaires	+2,10 Mio	-
Bénéfice brut	+620,00k	-
Bénéfice net	−15,98 Mio	-
EBITDA	−16,04 Mio	-

Données fondamentales

Indicateur	Valeur
Capitalisation boursière	+56,83 Mio€
Nombre d'actions	18,82 Mio
Plus haut/bas sur 52 semaines	+8,62€ - +2,32€
Dividendes	Non
Bêta	0,4
Ratio P/E	−1,55
Ratio PEG	−0,13
Ratio P/B	+28,20
Ratio P/S	+12,56

Profil de l'entreprise

MaaT Pharma SA, ein Unternehmen in der klinischen Phase, beschäftigt sich mit der Erforschung und Entwicklung von Mikrobiom-Biotherapien zur Behandlung von soliden Krebstumoren. Seine Produktpipeline umfasst MaaT013, das klinische Studien der Phase 2 zur Behandlung von akuten Graft-versus-Host-Erkrankungen abgeschlossen hat und sich in präklinischen Studien zur Behandlung von Melanomen befindet; MaaT033, das sich in klinischen Studien der Phase 1b zur Verbesserung des Überlebens von Patienten mit akuter myeloischer Leukämie oder anderen flüssigen Tumoren nach allogener hämatopoetischer Stammzelltransplantation befindet; und MaaT03X zur Behandlung solider Tumore. Das Unternehmen wurde im Jahr 2014 gegründet und hat seinen Hauptsitz in Lyon, Frankreich.