Clinical Trials - Enrollment of 68 patients completed in Phase 2 study for eseba-vec + pembrolizumab in HPV+ HNSCC, four months ahead of schedule[1] - First patients dosed in Phase 2 investigator-initiated study for eseba-vec in adjuvant therapy for head and neck cancer[3] - The HB-700 program is ready for Phase 1 trials, targeting KRAS-mutated cancers, with FDA clearance received in April 2024[5] - HOOKIPA received a 5millionmilestonepaymentfromGileadinJuly2024relatedtotheHB−500clinicaltrial[12]FinancialPerformance−RevenueforQ32024was4.7 million, a decrease of 31.6% from 6.9millioninQ32023,primarilyduetolowerpartneringrevenues[14]−NetlossforQ32024was13.8 million, compared to a net loss of 19.1millioninQ32023,representinga27.315.6 million in Q3 2024 from 24.6millioninQ32023,reflectinglowerpersonnelandlaboratory−relatedexpenses[15]−Generalandadministrativeexpensesincreasedto6.7 million in Q3 2024 from 4.9millioninQ32023,drivenbyhigherpersonnel−relatedexpensesandconsultingfees[16]CashPosition−CashpositionasofSeptember30,2024,was60.0 million, down from 117.5millionasofDecember31,2023,primarilyduetocashusedinoperatingactivities[13]−AsofSeptember30,2024,cash,cashequivalents,andrestrictedcashtotaled59,957,000, down from 117,521,000asofDecember31,2023[24]AssetsandLiabilities−Totalassetsdecreasedto109,730,000 from 161,337,000[24]−Totalliabilitiesreducedto37,928,000 compared to 71,480,000[24]−Totalstockholders′equitydeclinedto71,802,000 from $89,857,000[24] Corporate Actions - A reverse stock split of 1-for-10 was executed on July 9, 2024, to comply with Nasdaq listing requirements[11]