MaaT Pharma (MAAT) Q3 2024 TU earnings summary
Event summary combining transcript, slides, and related documents.
Q3 2024 TU earnings summary
13 Jun, 2025Executive summary
Completed enrollment in European Phase 3 ARES trial for MaaT013 in acute Graft-versus-Host Disease; topline results expected January 2025.
Positive safety review by DSMB for Phase 2b PHOEBUS trial of MaaT033; trial continues without modification.
Management changes: Eric Soyer appointed CFO, Sian Crouzet transitions to Chief of Staff after 8 years as CFO.
Financial highlights
Cash and cash equivalents at €27 million as of September 30, 2024, down from €31.2 million at June 30, 2024.
Q3 2024 revenues of €0.6 million, up from €0.4 million in Q3 2023; nine-month 2024 revenues at €2.3 million vs €1.8 million in 2023.
Net cash decrease in Q3 2024 reflects ongoing R&D investments, partially offset by public funding and R&D tax credit payments.
Outlook and guidance
Sufficient cash to fund operations and development programs into Q2 2025.
Topline results for Phase 3 ARES trial expected in January 2025.
Latest events from MaaT Pharma
- MaaT013 shows strong efficacy and safety in refractory aGvHD, with pivotal data due January 2025.MAAT
KOL Event11 Jan 2026 - 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 - Positive Phase 3 data, revenue growth, and €13M capital raise position MaaT Pharma for EU submission.MAAT
H2 20246 Jun 2025