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Moleculin Biotech Inc

Moleculin Biotech, Inc. is a late-stage pharmaceutical development company focused on therapeutic candidates for tumors and viruses. Its lead candidate, Annamycin, is an anthracycline in clinical development for relapsed or refractory acute myeloid leukemia and soft tissue sarcoma lung metastases. The company is also developing the WP1066 portfolio, including WP1066, WP1193, and WP1220, which are immune/transcription modulators designed to inhibit phosphorylated signal transducer and activator of transcription for brain tumors and pancreatic and other cancers. Additionally, it is developing the WP1122 portfolio, such as WP1122, WP1096, and WP1097, designed to exploit inhibitors of glycolysis including 2-deoxy-D-glucose to cut off the energy supply of tumors. Incorporated in 2015, the company is headquartered in Houston, Texas.

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Moleculin Biotech Q2 GAAP EPS misses by $0.53

Moleculin Biotech reported a second-quarter GAAP loss of $1.40 per share, missing expectations by $0.53. As of June 30, 2026, the company had cash and cash equivalents of approximately $7.3 million. Management believes that its cash on hand and cash equivalents as of June 30, 2026, together with $9.3 million in financing proceeds raised subsequent to the quarter, will support planned operations into the first quarter of 2027.
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Moleculin Biotech Prices $9.3 Million Public Offering

Moleculin Biotech has priced a best-efforts public offering expected to raise approximately $9.3 million. The offering consists of 12,376,667 shares of common stock, or pre-funded warrants in lieu thereof, together with warrants to purchase up to 37,130,001 additional shares, at a combined price of $0.75 per share and associated warrant. The common warrants are immediately exercisable at $0.75 per share and expire five years from the initial exercise date. The company intends to use the net proceeds to advance its lead drug candidate Annamycin through clinical development and for working capital. Roth Capital Partners is acting as exclusive placement agent, with Maxim Group LLC serving as financial advisor, and the offering is expected to close on or about August 3, 2026, subject to customary conditions.
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Moleculin reports 37% blinded CRc in MIRACLE trial for venetoclax-failed AML patients

Moleculin Biotech announced updated preliminary blinded results from Part A of its pivotal Phase 2/3 MIRACLE trial of Annamycin plus cytarabine in relapsed or refractory acute myeloid leukemia, showing a blinded composite complete remission rate of 37% among 62 evaluable subjects. Among the 30 patients who had failed prior venetoclax therapy, the blinded CRc was also 37%, essentially identical to the overall evaluable population and roughly three times the published salvage remission rate of approximately 13% for this subgroup. Enrollment has reached 74 of the planned 90 subjects, with final Part A treatment expected in September 2026 and comprehensive unblinded results anticipated between December 2026 and February 2027. No evidence of cardiotoxicity has been observed, continuing to differentiate Annamycin from conventional anthracyclines.
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Moleculin CEO Highlights Positive Preliminary MIRACLE Trial Results in Virtual Investor Segment

Moleculin Biotech announced that Chairman and CEO Walter Klemp discussed positive preliminary unblinded efficacy results from the first 45 patients enrolled in Part A of the pivotal Phase 2/3 MIRACLE trial evaluating Annamycin in relapsed or refractory acute myeloid leukemia. Klemp provided perspective on the significance of early efficacy trends observed across both Annamycin treatment arms, summarized key data, and discussed the commercial opportunity, including insights from recent market research on the potential addressable market for Annamycin if approved. The segment is available for on-demand viewing.
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