Moleculin Biotech (MBRX) Q2 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q2 2026 earnings summary
14 Aug, 2026Executive summary
Interim data from the pivotal Phase 2/3 MIRACLE trial showed Annamycin achieved complete remission rates three times higher than control in relapsed/refractory AML, with strong physician and payer interest and no cardiotoxicity observed even at high doses.
MIRACLE trial enrollment is on track to reach 90 patients by September 2026, with unblinded efficacy data expected between December 2026 and February 2027.
Additional portfolios target hard-to-treat cancers and viruses, with ongoing and planned investigator-initiated trials and preclinical research.
Closed Australian subsidiary to reduce overhead, with future activities focused in the US, Europe, and possibly the Middle East.
Strong investigator engagement and enthusiasm for Annamycin, with market research indicating high intent to prescribe.
Financial highlights
Net loss for Q2 2026 was $7.96 million, compared to $17.8 million in Q2 2025; net loss for the first half of 2026 was $20.5 million, down from $23.7 million in the prior year.
Operating expenses rose to $7.6 million in Q2 2026 from $5.7 million in Q2 2025, driven by increased R&D for the MIRACLE trial.
Cash and cash equivalents were $7.3 million as of June 30, 2026, with an additional $9.3 million raised after quarter-end.
Net cash used in operating activities was $12.8 million for the first half of 2026, up from $10.1 million in 2025.
Financing activities provided $11.2 million in the first half of 2026, including warrant exercises and ATM equity sales.
Outlook and guidance
Cash on hand plus $9.3 million raised in August 2026 expected to fund operations into Q1 2027; additional $8 million needed to support operations into Q2 2027.
MIRACLE Part B initiation is planned for the first half of 2027 after optimal dose selection.
Key milestones include completion of Part A enrollment in September 2026, data unblinding by early 2027, and NDA submission beginning in 2028.
Continued focus on advancing Annamycin through MIRACLE trial and supporting other programs via external funding.
Latest events from Moleculin Biotech
- Proxy seeks approval for director elections, equity plan expansion, and a reverse stock split.MBRX
Proxy filing - Annamycin delivers superior efficacy and safety in AML, supporting broad market potential.MBRX
Corporate presentation - Biotech seeks $9.1M via stock and warrant offering to fund pivotal cancer drug trials.MBRX
Registration filing - Biotech seeks $9.1M via stock and warrant offering to advance late-stage cancer drug Annamycin.MBRX
Registration filing - Biotech seeks $9.1M via stock and warrant offering to fund late-stage AML drug trials, with high dilution risk.MBRX
Registration filing - Pivotal AML trial reached 45 enrollments, 40% remission; Q1 net loss $12.8M, more funding needed.MBRX
Q1 2026 - Annamycin delivers high remission rates in AML with no cardiotoxicity, advancing toward pivotal trial results.MBRX
Status Update - Phase 3 AML trial for Annamycin starts Q1 2025; $9.4M cash, $15M more needed for key milestones.MBRX
Q3 2024 - Annamycin showed high clinical benefit and survival in STS lung metastases with no cardiotoxicity.MBRX
Study Update