MaaT Pharma (MAAT) KOL Event summary
Event summary combining transcript, slides, and related documents.
KOL Event summary
9 Jul, 2026Introduction and agenda
The event focused on MaaT013's development and clinical data for GVHD, featuring presentations from Prof. Mohamad Mohty, Dr. Monzr M. Al Malki, and Hervé Affagard, with a Q&A session.
The agenda included company introduction, KOL presentations, early access program results, unmet need for MaaT013 in GVHD, and discussion of next steps.
KOL background and credentials
Professor 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 patient with MaaT013 in the U.S.
Market insights and analysis
Acute GVHD affects 20-50% of allogeneic HSCT patients, with about 12,000 cases annually in the US and Europe and high mortality, especially with GI involvement.
There is a significant unmet need for effective third-line therapies, as current options have limited efficacy, no FDA approval, and 85% one-year mortality.
MaaT013 is positioned as the most advanced product in 3L, with increasing demand, global early access, and estimated €250m market potential in 3L alone.
Increasing clinical adoption and revenue growth for MaaT013, with €2.3m generated in France and in the first nine months of 2024.
Latest events from MaaT Pharma
- Pivotal trial success and EMA review position XervytegⓇ for market entry in high-need aGvHD.MAAT
Corporate presentation29 Jul 2026 - Clinigen secures exclusive European rights to Xervyteg, with strong financial and regulatory momentum.MAAT
Status Update8 Jul 2026 - Revenue up 38%, net loss deepened, all major resolutions approved with 65% quorum.MAAT
AGM 202620 Jun 2026 - Q1 2026 revenue was €0.8M, with cash runway extended to November 2026 amid regulatory challenges.MAAT
Q1 2026 TU26 May 2026 - Pivotal trial success, EMA review, and 38% revenue growth extend cash runway to August 2026.MAAT
H2 202531 Mar 2026 - Phase 3 data show 62% GI response, 54% survival in aGvHD; EU submission planned for 2025.MAAT
Study Result10 Jan 2026 - 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