Financial Performance - Protagonist reported cash, cash equivalents, and marketable securities of 595.4millionasofJune30,2024,upfrom341.6 million as of December 31, 2023, reflecting a significant increase due to a 300millionupfrontpaymentfromtheTakedacollaboration[7].−LicenseandcollaborationrevenueforthesixmonthsendedJune30,2024,was259.1 million, primarily from the Takeda collaboration agreement, which included 255millionrecognizedinQ12024[9].−LicenseandcollaborationrevenueforthethreemonthsendedJune30,2024,was4,167,000, compared to 0forthesameperiodin2023[15].−TotaloperatingexpensesforthethreemonthsendedJune30,2024,were42,960,000, an increase from 42,354,000inthesameperiodof2023[15].−NetlossforthethreemonthsendedJune30,2024,was30,616,000, compared to a net loss of 38,460,000forthesameperiodin2023[15].−ThenetlossforQ22024was30.6 million, or 0.50pershare,animprovementfromanetlossof38.5 million, or 0.68pershare,inQ22023[11].−InterestincomeforthethreemonthsendedJune30,2024,was7,404,000, compared to 3,913,000forthesameperiodin2023[15].Expenses−Researchanddevelopmentexpensesincreasedby6.7 million for the six months ended June 30, 2024, primarily due to higher drug discovery and pre-clinical research costs[10]. - General and administrative expenses rose by 6.6millionforthesixmonthsendedJune30,2024,mainlyduetoone−timeadvisoryandlegalfeesrelatedtotheTakedacollaboration[10].−ResearchanddevelopmentexpensesforthesixmonthsendedJune30,2024,were67,254,000, up from 60,598,000inthesameperiodof2023[15].−Stock−basedcompensationexpenseforthethreemonthsendedJune30,2024,was8,944,000, compared to 8,343,000forthesameperiodin2023[16].AssetsandEquity−TotalassetsasofJune30,2024,were614,629,000, an increase from 357,951,000asofDecember31,2023[17].−Totalstockholders′equityincreasedto541,324,000 as of June 30, 2024, from 336,677,000asofDecember31,2023[17].−TheaccumulateddeficitasofJune30,2024,was(438,986,000), down from $(615,710,000) as of December 31, 2023[17]. Clinical Development - Protagonist anticipates top-line results from the Phase 3 VERIFY study of rusfertide in polycythemia vera in Q1 2025[4]. - The primary endpoint portions of the Phase 3 ICONIC-LEAD and ICONIC-TOTAL studies for JNJ-2113 are expected to be completed in Q4 2024[5]. - Protagonist is pursuing the discovery of novel oral peptides, with a development candidate for an oral IL-17 program expected by the end of 2024[7]. - The company is currently conducting five Phase 3 trials for JNJ-2113 in psoriasis and a Phase 2b study in ulcerative colitis, with rapid enrollment progress reported[2]. Market Position - Protagonist's addition to the S&P SmallCap 600 index enhances visibility and reflects the company's value to shareholders[2].