Workflow
Astria Therapeutics(ATXS) - 2024 Q3 - Quarterly Report

Financial Performance - The company reported net losses of 68.6millionfortheninemonthsendedSeptember30,2024,comparedto68.6 million for the nine months ended September 30, 2024, compared to 41.5 million for the same period in 2023[65]. - The company has an accumulated deficit of 649.2millionasofSeptember30,2024,andhasnotgeneratedanyproductrevenues[65].NetlossfortheninemonthsendedSeptember30,2024,was649.2 million as of September 30, 2024, and has not generated any product revenues[65]. - Net loss for the nine months ended September 30, 2024, was 68.63 million, an increase of 27.15millionor6527.15 million or 65% compared to a net loss of 41.48 million in the prior year[74]. - Other income, net increased by 6.0millionto6.0 million to 13.3 million for the nine months ended September 30, 2024, a 82% increase from 7.3millioninthesameperiodof2023[77].FortheninemonthsendedSeptember30,2024,netcashusedinoperatingactivitieswas7.3 million in the same period of 2023[77]. - For the nine months ended September 30, 2024, net cash used in operating activities was 63.9 million, compared to 38.2millionforthesameperiodin2023[83].Netcashusedininvestingactivitieswas38.2 million for the same period in 2023[83]. - Net cash used in investing activities was 188.1 million for the nine months ended September 30, 2024, primarily due to purchases of short-term investments totaling 3.5billion[83].Netcashprovidedbyfinancingactivitieswas3.5 billion[83]. - Net cash provided by financing activities was 157.2 million for the nine months ended September 30, 2024, driven by net proceeds from the February 2024 Financing and ATM Programs[85]. Cash and Funding - As of September 30, 2024, the company had 344.3millionincash,cashequivalents,andshortterminvestments,expectedtofundoperationsintomid2027[65].ThegrossproceedsfromtheOctober2023Financingwere344.3 million in cash, cash equivalents, and short-term investments, expected to fund operations into mid-2027[65]. - The gross proceeds from the October 2023 Financing were 64.0 million, and from the February 2024 Financing were 125.0million[64].Existingcash,cashequivalents,andshortterminvestmentsareexpectedtofundoperationsintomid2027,coveringongoingclinicaltrialsanddevelopmentactivities[86].Thecompanyexpectstofinancefuturecashneedsthroughequityofferings,debtfinancings,andcollaborations,withnocommittedexternalsourcesoffunds[88].Thecompanysold1,504,619sharesunderthe2024ATMProgramforgrossproceedsof125.0 million[64]. - Existing cash, cash equivalents, and short-term investments are expected to fund operations into mid-2027, covering ongoing clinical trials and development activities[86]. - The company expects to finance future cash needs through equity offerings, debt financings, and collaborations, with no committed external sources of funds[88]. - The company sold 1,504,619 shares under the 2024 ATM Program for gross proceeds of 15.6 million in the three months ended September 30, 2024[81]. Research and Development - Research and development expenses increased by 26.5millionto26.5 million to 56.9 million for the nine months ended September 30, 2024, representing an 87% increase compared to the same period in 2023[75]. - Research and development expenses for the three months ended September 30, 2024, were 20.5million,a5420.5 million, a 54% increase from 13.3 million in the same period of 2023[72]. - The company expects to incur significant research and development expenses in 2024 related to clinical trials for navenibart and STAR-0310, with higher expenses anticipated over the next several quarters[72]. Clinical Trials and Product Development - Navenibart achieved a 92% reduction in monthly attack rate and a 96% reduction in moderate and severe attacks in Cohort 1 after 6 months of follow-up[57]. - In Cohort 2, a 600 mg dose followed by a 300 mg dose resulted in a 96% reduction in monthly attack rate and 67% of patients were attack-free after 6 months[59]. - The company plans to initiate a Phase 1a clinical trial for STAR-0310 in healthy subjects in Q1 2025, with initial results expected in Q3 2025[63]. - The company aims to start a Phase 3 pivotal trial for Navenibart in Q1 2025, with top-line results expected by year-end 2026[59]. - STAR-0310 exhibited a long mean half-life of 26 days in preclinical studies, compared to 10-14 days for typical non-half-life extended IgG antibodies[60]. - Navenibart has received Fast Track and Orphan Drug designations from the FDA for the treatment of hereditary angioedema[57]. Operating Expenses - General and administrative expenses rose by 6.6millionto6.6 million to 25.0 million for the nine months ended September 30, 2024, a 36% increase from the prior year[77]. - General and administrative expenses for the three months ended September 30, 2024, increased by 1.6millionto1.6 million to 8.5 million, a 23% increase from the prior year[72]. - Total operating expenses for the nine months ended September 30, 2024, were 81.97million,up81.97 million, up 33.14 million or 68% from 48.83millioninthesameperiodof2023[74].TotaloperatingexpensesforthethreemonthsendedSeptember30,2024,were48.83 million in the same period of 2023[74]. - Total operating expenses for the three months ended September 30, 2024, were 29.01 million, up 8.78millionor438.78 million or 43% from 20.24 million in the same period of 2023[71]. Internal Controls - The company has not made any changes to its internal control over financial reporting that materially affected its financial reporting during the nine months ended September 30, 2024[92].