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Moleculin Biotech (MBRX) investor relations material
Moleculin Biotech Q1 2026 earnings summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Executive summary
Lead drug candidate Annamycin advanced in pivotal Phase 2B/3 MIRACLE trial for relapsed/refractory AML, achieving enrollment of 45 subjects and reporting strong early efficacy and safety signals, with interim unblinding expected mid-2026.
Preliminary blinded data show a 40% composite complete remission rate in a difficult-to-treat AML population.
Clinical trial operations expanded in the US and Europe, with global IP strategy for Annamycin strengthened and new Hong Kong patent issued, extending protection through 2040.
Additional pipeline programs, including WP1066 and WP1122, continue development for cancer and viral diseases, with new data presented at major scientific meetings.
Closure of Australian subsidiary approved to reduce overhead, focusing resources on core US and European operations.
Financial highlights
Net loss for Q1 2026 was $12.8 million, compared to $5.9 million in Q1 2025, driven by higher R&D expenses and warrant-related charges.
Research and development expenses increased to $5.4 million from $3.4 million year-over-year, mainly due to MIRACLE trial costs in Europe.
General and administrative expenses were stable at $2.5 million year-over-year.
Cash and cash equivalents were $10.3 million as of March 31, 2026, up from $8.9 million at year-end 2025.
Net cash used in operating activities was $6.1 million, with $7.6 million raised from warrant exercises and ATM equity sales.
Outlook and guidance
MIRACLE trial interim unblinding for 45 subjects expected in Q2 2026; 90th subject enrollment and unblinding anticipated in Q3 2026.
Part B of MIRACLE trial and a pancreatic cancer clinical trial to begin in 2H 2026.
Cash on hand plus recent ATM proceeds expected to fund operations into Q3 2026; additional $25 million needed to support MIRACLE trial and operations into Q1 2027.
Rolling NDA submission for Annamycin in AML targeted for 2028.
Ongoing focus on advancing Annamycin and leveraging external funding for other pipeline assets.
- Annamycin's Phase 3 trial targets AML with early data readouts and strong remission potential.MBRX
Corporate Connect Webinar Series13 Apr 2026 - Up to 6.37M shares registered for resale from warrant exercises, supporting late-stage oncology trials.MBRX
Registration filing27 Mar 2026 - Annamycin's phase III AML trial nears key data, highlighting strong efficacy and zero cardiotoxicity.MBRX
The 38th Annual Roth Conference24 Mar 2026 - 2025 results highlight a 40% CRc rate in MIRACLE AML trial and a $33.7M net loss.MBRX
Q4 202519 Mar 2026 - Annamycin delivers high remission rates in AML and is advancing toward pivotal data in 2026.MBRX
Corporate presentation18 Mar 2026 - Annamycin delivers high remission rates in AML with no cardiotoxicity and broad market potential.MBRX
Corporate presentation9 Mar 2026 - Shareholders to vote on warrant issuance, name change, and adjournment; Board urges approval.MBRX
Proxy Filing9 Mar 2026 - Vote on warrant share issuance, company name change, and adjournment; board recommends approval.MBRX
Proxy Filing27 Feb 2026 - Annamycin delivers high remission rates in AML with no cardiotoxicity; pivotal trial underway.MBRX
Status Update3 Feb 2026
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