Mesoblast (MSB) Q2 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q2 2026 earnings summary
29 Jan, 2026Executive summary
RyoncilⓇ net revenues reached US$30 million for the quarter ended December 31, 2025, a 60% increase over the prior quarter, driven by strong sales and expanded clinical use.
A new non-dilutive US$125 million credit line was established at a lower fixed interest rate, enhancing financial flexibility for strategic initiatives.
RyoncilⓇ remains the only FDA-approved MSC therapy for pediatric SR-aGvHD, with positive real-world outcomes and ongoing label expansion efforts.
Financial highlights
Gross sales for RyoncilⓇ were US$35 million, with net revenues of US$30 million, up 60% sequentially from the previous quarter.
Cash at quarter end was US$130 million; net operating cash spend for the quarter was US$16 million.
Net cash from operating activities for the quarter was negative US$15.6 million.
Estimated quarters of funding available is 11.6, based on current cash and financing facilities.
Outlook and guidance
Net cash spend is expected to decrease over the remainder of the fiscal period due to projected revenue receipts and tight expense control.
Pivotal trial for RyoncilⓇ in adults with SR-aGvHD to commence site enrollment this quarter, targeting a population three times larger than pediatric.
Confirmatory Phase 3 trial for rexlemestrocel-L in chronic low back pain is actively recruiting and expected to complete enrollment in three months.
Latest events from Mesoblast
- Ryoncil/RYONCIL launch drove $49M H1 FY26 revenue, 93% margin, and strong FY26 outlook.MSB
H1 202626 Feb 2026 - RYONCIL BLA resubmitted, cash burn cut 23%, and FDA decision expected by January 2025.MSB
Q4 202423 Jan 2026 - Pivotal FDA decision for pediatric GVHD expected, with major expansion and filings ahead.MSB
Maxim Group’s 2024 Healthcare Virtual Summit19 Jan 2026 - Disciplined financials, clinical progress, and FDA-focused strategies drive near-term milestones.MSB
AGM 202414 Jan 2026 - FDA approves first MSC therapy for pediatric steroid-refractory acute GVHD, with 70% response rate.MSB
FDA Announcement10 Jan 2026 - First FDA-approved allogeneic cell therapy for pediatric GVHD launching, with broad pipeline and strong cash position.MSB
Emerging Growth Conference 7923 Dec 2025 - FDA approval and $161M raise support US launch, but losses and risks remain.MSB
H1 202519 Dec 2025 - Ryoncil's robust launch and pipeline expansion drive growth, with adult trials and global filings ahead.MSB
Piper Sandler 37th Annual Healthcare Conference4 Dec 2025 - RYONCIL's US launch drives revenue growth as label expansion and pivotal trials advance.MSB
AGM 2025 Presentation25 Nov 2025