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HOOKIPA Pharma(HOOK) - 2024 Q3 - Quarterly Report
HOOKHOOKIPA Pharma(HOOK)2024-11-14 21:09

Financial Performance - The company reported a net loss of 13.8millionand13.8 million and 18.6 million for the three and nine months ended September 30, 2024, respectively, with an accumulated deficit of 387.8million[151].ThenetlossforthethreemonthsendedSeptember30,2024,was387.8 million [151]. - The net loss for the three months ended September 30, 2024, was 13.8 million, an improvement of 5.2millioncomparedtoanetlossof5.2 million compared to a net loss of 19.1 million in the same period of 2023 [200]. - The net loss for the nine months ended September 30, 2024, was 18.6million,comparedtoanetlossof18.6 million, compared to a net loss of 56.8 million for the same period in 2023 [229][230]. - The accumulated deficit as of September 30, 2024, was 387.8million,withexpectationsofcontinuedsignificantlossesfortheforeseeablefuture[218].Thecompanydoesnotexpectpositivecashflowsfromoperationsintheforeseeablefutureandanticipatesincurringnetoperatinglossesforatleastthenextseveralyears[214].Managementhasconcludedthatsubstantialdoubtexistsaboutthecompanysabilitytocontinueasagoingconcernforatleast12monthsfromtheissuancedateofthefinancialstatements[216].RevenueandIncomeRevenuefromcollaborationandlicensingwas387.8 million, with expectations of continued significant losses for the foreseeable future [218]. - The company does not expect positive cash flows from operations in the foreseeable future and anticipates incurring net operating losses for at least the next several years [214]. - Management has concluded that substantial doubt exists about the company's ability to continue as a going concern for at least 12 months from the issuance date of the financial statements [216]. Revenue and Income - Revenue from collaboration and licensing was 4.7 million for the three months ended September 30, 2024, down from 6.9millioninthesameperiodof2023,representingadecreaseofapproximately31.66.9 million in the same period of 2023, representing a decrease of approximately 31.6% [182]. - For the nine months ended September 30, 2024, revenue increased to 42.6 million from 12.7millionin2023,markinganincreaseofapproximately234.612.7 million in 2023, marking an increase of approximately 234.6% [182]. - The company recognized 36.4 million in revenue related to the terminated Roche Collaboration Agreement during the nine months ended September 30, 2024 [190]. - Other income for the three months ended September 30, 2024, was 1.8million,comparedtootherexpensesof1.8 million, compared to other expenses of 0.8 million for the same period in 2023, primarily due to exchange rate differences [205]. - For the nine months ended September 30, 2024, other income was 1.3million,comparedtootherexpensesof1.3 million, compared to other expenses of 1.0 million for the same period in 2023, also attributed to exchange rate differences [206]. Expenses - Research and development expenses for the three months ended September 30, 2024, totaled 15.6million,comparedto15.6 million, compared to 24.6 million for the same period in 2023 [168]. - Total research and development expenses for the nine months ended September 30, 2024, were 55.5million,comparedto55.5 million, compared to 65.3 million for the same period in 2023 [168]. - The company expects research and development expenses to increase substantially as it advances existing and future product candidates through clinical trials [165]. - General and administrative expenses increased to 6.7millionforthethreemonthsendedSeptember30,2024,comparedto6.7 million for the three months ended September 30, 2024, compared to 4.9 million in 2023, an increase of approximately 36.7% [195]. - Restructuring expenses for the three months ended September 30, 2024, were 0.9million,with0.9 million, with 0.8 million attributed to severance and other personnel costs [198]. - The company has established a full valuation allowance for deferred tax assets as of September 30, 2024, due to uncertainty in realizing benefits [180]. Cash and Funding - The company has cash, cash equivalents, and restricted cash of 60.0millionasofSeptember30,2024[147].CashusedinoperatingactivitiesfortheninemonthsendedSeptember30,2024,was60.0 million as of September 30, 2024 [147]. - Cash used in operating activities for the nine months ended September 30, 2024, was 56.0 million, an increase from 46.3millioninthesameperiodof2023[229][230].Cashusedininvestingactivitiesdecreasedto46.3 million in the same period of 2023 [229][230]. - Cash used in investing activities decreased to 0.2 million in the nine months ended September 30, 2024, from 3.7millioninthesameperiodof2023[231][232].Cashusedinfinancingactivitieswas3.7 million in the same period of 2023 [231][232]. - Cash used in financing activities was 1.3 million for the nine months ended September 30, 2024, compared to cash provided of 44.4millioninthesameperiodof2023[233][234].Thecompanyanticipatesrequiringadditionalfundingtosupportclinicalandpreclinicaldevelopment,regulatoryapprovals,andoperationalexpansions[219].Thecompanyhasnocommittedexternalsourceoffundsforitsdevelopmenteffortsandexpectstofinancefuturecashneedsthroughacombinationofequityofferings,debtfinancings,andcollaborations[225].ResearchandDevelopmentTheesebavecprogramforHPV16+headandneckcancersshowedanoverallresponserate(ORR)of55.044.4 million in the same period of 2023 [233][234]. - The company anticipates requiring additional funding to support clinical and preclinical development, regulatory approvals, and operational expansions [219]. - The company has no committed external source of funds for its development efforts and expects to finance future cash needs through a combination of equity offerings, debt financings, and collaborations [225]. Research and Development - The eseba-vec program for HPV16+ head and neck cancers showed an overall response rate (ORR) of 55.0% in the selected Phase 3 dose group, with a disease control rate (DCR) of 75% [137]. - The combination treatment of eseba-vec with pembrolizumab demonstrated a favorable safety profile, with serious adverse events in only 7.6% of participants [139]. - The company received FDA clearance for HB-700 in April 2024, targeting KRAS mutated cancers, including lung, colorectal, and pancreatic cancers [140]. - The collaboration with Gilead for the HBV program has the potential for up to 185.0 million in milestone payments, plus tiered royalties [142]. - The company regained full control of the HB-700 program after Roche terminated their collaboration agreement, receiving a non-refundable upfront payment of 25.0millionandmilestonepaymentsof25.0 million and milestone payments of 20.0 million [141]. - The company regained full control of the intellectual property portfolio associated with the terminated Roche Collaboration Agreement effective April 25, 2024 [158]. - The company recognized $0.6 million in cost reimbursements for research and development activities related to a first human trial [160]. Market Risks - The company is subject to market risks from changes in interest rates, foreign exchange rates, and inflation, which may impact financial performance [241][243]. - The company anticipates that a significant portion of its expenses will continue to be denominated in euros, exposing it to foreign currency risk [241].