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Achieve Life Sciences(ACHV) - 2024 Q3 - Quarterly Report

Financial Performance - The net loss for the nine months ended September 30, 2024, was 27.5million,withanaccumulateddeficitof27.5 million, with an accumulated deficit of 193.2 million[119]. - The company has not generated any revenue from product sales to date and has incurred operating losses each year since inception[119]. - The company expects to incur significant expenses and increasing operating losses for at least the next several years as it continues clinical development[120]. - The accumulated deficit through September 30, 2024 was 193.2million,withexpectationsofincurringsubstantialadditionallossesinthefuture[170].FortheninemonthsendedSeptember30,2024,netcashusedinoperationswas193.2 million, with expectations of incurring substantial additional losses in the future[170]. - For the nine months ended September 30, 2024, net cash used in operations was 20.6 million[170]. - The company incurred a loss on extinguishment of debt of 0.3millionforeachofthethreeandninemonthsendedSeptember30,2024[169].Substantialdoubtexistsregardingthecompanysabilitytocontinueasagoingconcernwithoutadditionalfinancing[173].CashandInvestmentsAsofSeptember30,2024,thecompanyhadcash,cashequivalents,andshortterminvestmentstotaling0.3 million for each of the three and nine months ended September 30, 2024[169]. - Substantial doubt exists regarding the company's ability to continue as a going concern without additional financing[173]. Cash and Investments - As of September 30, 2024, the company had cash, cash equivalents, and short-term investments totaling 42.9 million, and a positive working capital balance of 38.8million[119].NetcashprovidedbyfinancingactivitiesfortheninemonthsendedSeptember30,2024was38.8 million[119]. - Net cash provided by financing activities for the nine months ended September 30, 2024 was 47.8 million, significantly higher than 15.3millioninthesameperiodof2023,drivenbyproceedsfromtheFebruary2024offeringandotherfinancingactivities[199].Netcashusedininvestingactivitiesincreasedto15.3 million in the same period of 2023, driven by proceeds from the February 2024 offering and other financing activities[199]. - Net cash used in investing activities increased to 33.3 million for the nine months ended September 30, 2024, compared to only 15,000inthesameperiodof2023,attributedtotransactionsinvolvingmarketablesecurities[200].AsofSeptember30,2024,thecompanyhad15,000 in the same period of 2023, attributed to transactions involving marketable securities[200]. - As of September 30, 2024, the company had 50.0 million available under an Open Market Sale Agreement with Jefferies LLC, although no shares were sold under this agreement during the three and nine months ended September 30, 2024[197]. Clinical Trials and Drug Development - The FDA granted Breakthrough Therapy designation for cytisinicline for nicotine e-cigarette cessation, which allows expedited development of the drug[125]. - The company initiated the ORCA-OL open label trial in May 2024, enrolling 479 subjects to provide long-term safety data for cytisinicline[127]. - In the Phase 2b ORCA-1 trial, cytisinicline treatment arms showed a 74-80% median reduction in the number of cigarettes smoked compared to a 62% reduction in placebo arms[133]. - The 3 mg TID cytisinicline arm demonstrated a 50% abstinence rate at week 4, compared to 10% for placebo (p<0.0001)[135]. - The ORCA-V1 trial showed a vaping cessation rate of 31.8% for cytisinicline compared to 15.1% for placebo during weeks 9 through 12 (p=0.04)[141]. - The Phase 3 ORCA-2 trial demonstrated that subjects receiving 12 weeks of cytisinicline had a 6.3 times higher likelihood of quitting smoking compared to placebo, with an abstinence rate of 32.6% versus 7.0%[144]. - The continuous abstinence rate from week 9 to 24 for the 12-week cytisinicline arm was 21.1%, compared to 4.8% for placebo, with an odds ratio of 5.3[145]. - The Phase 3 ORCA-3 trial showed that subjects receiving 12 weeks of cytisinicline had a 4.4 times higher likelihood of quitting smoking, with a cessation rate of 30.3% compared to 9.4% for placebo[150]. - Cytisinicline was well tolerated in both ORCA-2 and ORCA-3 trials, with no treatment-related serious adverse events reported[154]. Research and Development Expenses - R&D expenses for the three months ended September 30, 2024, increased to 7.6millionfrom7.6 million from 3.6 million in the same period in 2023, primarily due to the initiation of the ORCA-OL trial[162]. - The company initiated the ORCA-OL trial in May 2024, contributing to higher R&D expenses, while costs associated with completed trials (ORCA-3 and ORCA-V1) were reduced[198]. General and Administrative Expenses - General and administrative expenses for the three months ended September 30, 2024, rose to 4.9millionfrom4.9 million from 3.0 million in the same period in 2023, attributed to higher employee and consulting costs[164]. Financing Activities - In May 2023, the company sold 3,000,000 shares of common stock at 5.50pershare,raisingapproximately5.50 per share, raising approximately 15.3 million in net proceeds after fees and expenses[194]. - In February 2024, the company sold 13,086,151 shares of common stock at 4.585pershare,resultingingrossproceedsofapproximately4.585 per share, resulting in gross proceeds of approximately 60.0 million and net proceeds of about 56.1millionafterdeductingfees[197].Thecompanyissuedunregisteredwarrantstopurchaseupto13,086,151sharesatanexercisepriceof56.1 million after deducting fees[197]. - The company issued unregistered warrants to purchase up to 13,086,151 shares at an exercise price of 4.906 per share, which are immediately exercisable and will expire under specific conditions[196]. Accounting Policies - There have been no material changes to the company's critical accounting policies since December 31, 2023, as disclosed in the Annual Report filed on March 28, 2024[202]. - The company has adopted new accounting standards in 2024, as detailed in the consolidated financial statements[203].