MaaT Pharma (MAAT) KOL Event summary
Event summary combining transcript, slides, and related documents.
KOL Event summary
11 Jan, 2026Introduction and agenda
The event focused on MaaT013's development and clinical data for GVHD, featuring presentations from leading KOLs and a Q&A session.
The agenda included company introduction, KOL presentations, early access program results, unmet need, and future plans.
KOL background and credentials
Professor Mohammad Mohty is a globally recognized expert in GVHD and HSCT, with over 1,000 peer-reviewed publications.
Dr. Monzr Al-Malki is the director of blood and marrow transplant at City of Hope and the first to treat a US patient with MaaT013.
Featured speakers included Prof. Mohamad Mohty, Dr. Monzr M. Al Malki, and Hervé Affagard (Co-Founder & CEO).
Market insights and analysis
Acute GVHD affects about 12,000 patients annually in the US and Europe, with high mortality in steroid- and ruxolitinib-refractory cases.
Current standard of care is limited, with only ruxolitinib approved for second-line and no FDA-approved options for third-line.
MaaT013 is the most advanced product in third-line, with a pivotal Phase 3 trial ongoing and significant market potential estimated at €250m in 3L alone.
Revenue is currently generated in France, with €2.3m in the first nine months of 2024 and global expansion underway.
There is a significant unmet need for effective third-line therapies, especially for GI-involved GVHD.
Latest events from MaaT Pharma
- Phase 3 data show 62% GI response, 54% survival in aGvHD; EU submission planned for 2025.MAAT
Study Result10 Jan 2026 - Clinigen secures exclusive European rights to Xervyteg, targeting approval and launch by mid-2026.MAAT
Status Update14 Nov 2025 - Q3 2025 revenue up 45% year-over-year; cash runway secured through February 2026.MAAT
Q3 2025 TU4 Nov 2025 - 41% revenue growth, €15.1M net loss, and major EU deal extend cash runway to Feb 2026.MAAT
H1 202517 Sep 2025 - H1 2024 saw revenue growth, deeper R&D-driven loss, and strong progress in late-stage clinical trials.MAAT
H1 202413 Jun 2025 - Phase 3 ARES trial enrollment completed; Q3 revenues up, cash at €27M, new CFO named.MAAT
Q3 2024 TU13 Jun 2025 - Positive Phase 3 data, revenue growth, and €13M capital raise position MaaT Pharma for EU submission.MAAT
H2 20246 Jun 2025