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AVROBIO(AVRO) - 2025 Q1 - Quarterly Report
AVROAVROBIO(AVRO)2025-05-08 20:20

Financial Performance - The net loss for the company was $15.906 million for the three months ended March 31, 2025, a 5% increase from a net loss of $15.221 million in the same period of 2024[108]. - Cash used in operating activities was $13.1 million for the three months ended March 31, 2025, compared to $9.3 million for the same period in 2024, reflecting ongoing investment in product development[116][117]. - Net cash provided by financing activities was $178.1 million for the three months ended March 31, 2025, primarily from the sale of shares in a Private Placement[119]. - As of March 31, 2025, the company had $306.2 million in cash and cash equivalents and an accumulated deficit of $164.5 million[114]. - The company expects to incur significant expenses and operating losses as it advances preclinical and clinical development, necessitating additional capital through equity or debt financing[113][120]. Expenses - The company reported a 21% increase in research and development expenses, totaling $13.036 million for the three months ended March 31, 2025, compared to $10.818 million in the same period of 2024[108]. - General and administrative expenses surged by 145%, reaching $5.262 million in Q1 2025, up from $2.150 million in Q1 2024[108]. - Total operating expenses increased by 41% to $18.298 million in Q1 2025, compared to $12.968 million in Q1 2024[108]. - Total research and development expenses increased by $2.2 million, or 21%, for the three months ended March 31, 2025, compared to the same period in 2024, primarily due to increased CRO and CDMO costs related to TX2100[110]. - General and administrative expenses rose by $3.1 million, or 145%, for the three months ended March 31, 2025, driven by a 102% increase in employee-related expenses and a 266% increase in professional and consulting expenses[111]. Clinical Development - TX45 is currently being evaluated in a Phase 1b hemodynamic clinical trial, with 19 patients dosed in Part A, showing improvements in left heart function and pulmonary hemodynamics[92]. - The APEX Phase 2 clinical trial for TX45 commenced in October 2024, with topline results expected in 2026[92]. - TX2100, the second development candidate, is expected to initiate a Phase 1 clinical trial in late 2025 or early 2026, pending IND enabling study results[93]. Funding and Capital - The company completed a private placement in February 2025, raising approximately $185.0 million by issuing 3,689,465 shares of common stock[94][95]. - The merger with AVROBIO was completed on June 20, 2024, with Legacy Tectonic continuing as a wholly owned subsidiary of the surviving corporation[96]. Revenue Generation - The company has not generated any revenue since inception and does not expect to do so in the foreseeable future[97]. - The company has no approved products and has never generated revenue from product sales, relying on funding from convertible preferred stock and common stock sales[114]. - The company anticipates additional costs associated with operating as a public company and ongoing research and development activities[123]. Lease Obligations - Minimum lease payments due as of March 31, 2025, are $2.2 million in 2025, $0.5 million in 2026, and $0.1 million in 2027[127].