Daunorubicin Hydrochloride

– New Drug Application for ziftomenib in adults with R/R NPM1-m AML remains under FDA Priority Review, with a PDUFA target action date of November 30, 2025 – – KOMET 017 Phase 3 trials to evaluate ziftomenib in combination with intensive and non-intensive chemotherapy in frontline AML are accelerating; ziftomenib being investigated in settings representing more than 50% of AML patients – – Two oral presentations at 2025 ASH Annual Meeting on ziftomenib in combination with venetoclax / azacitidine chemotherapy in frontline and R/R NPM1-m AML – – Clinical data at ESMO 2025 Congress highlight promise of second strategic program – FTIs darlifarnib and tipifarnib show promising safety profile and clinical activity with targeted therapies in solid tumors – – $609.7 million in pro forma cash, together with anticipated collaboration payments, expected to support ziftomenib AML program through topline results in KOMET-017 – – Management to host webcast and conference call today at 8:00 a.m. ET – SAN DIEGO , Nov. 04, 2025 (GLOBE NEWSWIRE) -- Kura Oncology, Inc. (Nasdaq: KURA), a clinical-stage biopharmaceutical company committed to realizing the promise of precision medicines for the treatment of cancer, today reported third quarter 2025 financial results and provided a corporate update. “Our momentum is accelerating across the ziftomenib program and our broader precision oncology pipeline,” said Troy Wilson , Ph.D., J.D., President and Chief Executive Officer. “With the initiation of the pivotal KOMET-017 Phase 3 trials, we are executing a robust, focused development strategy to unlock ziftomenib’s best-in-class potential across the continuum of unmet need in AML. Bolstered by a strong balance sheet and our productive partnership with Kyowa Kirin, we are well positioned to advance ziftomenib toward commercialization, accelerate our frontline Phase 3 trials and create enduring value across our pipeline for patients and other key stakeholders.” Recent Highlights In September 2025 , we announced the first patient was dosed in the Phase 3 KOMET-017 trial of ziftomenib in frontline AML (NCT07007312). KOMET-017 comprises two global, randomized, double-blind, placebo-controlled trials to evaluate ziftomenib in combination with both intensive and non-intensive chemotherapy regimens in patients with newly diagnosed NPM1-m or KMT2A-rearranged (KMT2A-r) AML. In October 2025 , we announced the first patient was dosed in the FLT3 inhibitor cohort of the KOMET-007 clinical trial (NCT05735184). The cohort evaluates ziftomenib combined with the FDA-approved FLT3 inhibitor, quizartinib, plus cytarabine and daunorubicin (7+3) induction chemotherapy in patients with newly diagnosed AML harboring FLT3-ITD / NPM1 co-mutations. In September 2025 , the Journal of Clinical Oncolog y published the full results from the pivotal KOMET-001 clinical trial (NCT04067336) evaluating ziftomenib as a monotherapy in adult patients with R/R NPM1-m AML. (Reprint) Two abstracts featuring clinical data from ziftomenib in combination with venetoclax / azacitidine (ven/aza) chemotherapy in patients with newly diagnosed and R/R NPM1-m or KMT2A-r AML were accepted for oral presentation at the 67th Annual Meeting of the American Society of Hematology (ASH) to be held in December 2025 . (Abstract ID 764; Abstract ID 766) In October 2025 , preliminary clinical data were presented at ESMO 2025, highlighting the potential of Kura’s farnesyl transferase inhibitors, darlifarnib (KO-2806) and tipifarnib, to enhance the anti-tumor activity of PI3Ka inhibitors, KRAS inhibitors and antiangiogenic tyrosine kinase inhibitors across a range of diverse tumor types by addressing a common resistance pathway. Data from the FIT-001 Phase 1 trial evaluating darlifarnib and cabozantinib in patients with renal cell carcinoma (RCC) reflect a manageable safety profile across multiple dose levels of each agent, including at the full label dose of cabozantinib. Antitumor activity was observed across all dose combinations tested, including in patients with prior exposure to cabozantinib. The objective response rate (ORR) was 33-50% in ccRCC, and 17-50% in patients with prior cabozantinib exposure. (Poster) Data from the KURRENT-HN trial evaluating tipifarnib and alpelisib in patients with PIK3CA-dependent HNSCC also reflect a manageable safety profile. An ORR of 47% was observed at a dose of tipifarnib 1200 mg/day and alpelisib 250 mg/day. Robust antitumor activity was observed in a heavily pretreated patient population where clinical benefit is not expected from either alpelisib or tipifarnib as monotherapy. (Poster) In October and November 2025 , Kura received two $30 million milestone payments under its agreement with Kyowa Kirin in connection with first patient dosing in the pivotal KOMET-017 clinical trial of ziftomenib with intensive and non-intensive chemotherapy in patients with frontline AML. Data from the FIT-001 Phase 1 trial evaluating darlifarnib and cabozantinib in patients with renal cell carcinoma (RCC) reflect a manageable safety profile across multiple dose levels of each agent, including at the full label dose of cabozantinib. Antitumor activity was observed across all dose combinations tested, including in patients with prior exposure to cabozantinib. The objective response rate (ORR) was 33-50% in ccRCC, and 17-50% in patients with prior cabozantinib exposure. (Poster) Data from the KURRENT-HN trial evaluating tipifarnib and alpelisib in patients with PIK3CA-dependent HNSCC also reflect a manageable safety profile. An ORR of 47% was observed at a dose of tipifarnib 1200 mg/day and alpelisib 250 mg/day. Robust antitumor activity was observed in a heavily pretreated patient population where clinical benefit is not expected from either alpelisib or tipifarnib as monotherapy. (Poster) Forecasted Milestones Continued regulatory interactions with the FDA ahead of the November 30, 2025 PDUFA target action date for ziftomenib as a monotherapy for adult patients with relapsed or refractory NPM1-m AML. Present preliminary clinical data in newly diagnosed NPM1-m AML and updated clinical data in R/R NPM1-m and KMT2A-r AML from KOMET-007 cohorts evaluating ziftomenib in combination with ven/aza at ASH Annual Meeting to be held in December 2025 . Present preliminary data from the KOMET-008 cohort evaluating ziftomenib in combination with the FLT3 inhibitor gilteritinib in patients with R/R NPM1-m AML in 2026. Initiate FIT-001 Phase 1b expansion cohorts of darlifarnib and cabozantinib in patients with advanced RCC in the first half of 2026. Present updated dose-escalation data from the combination of darlifarnib and cabozantinib in patients with advanced RCC in 2026. Present preliminary clinical data from the combination of darlifarnib and adagrasib in patients with KRASG12C-mutated solid tumor indications in 2026. Financial Results Collaboration revenue from our Kyowa Kirin partnership for the third quarter of 2025 was $20.8 million , compared to no revenue for the third quarter of 2024. Research and development expenses for the third quarter of 2025 were $67.9 million , compared to $41.7 million for the third quarter of 2024. General and administrative expenses for the third quarter of 2025 were $32.8 million , compared to $18.2 million for the third quarter of 2024. Net loss for the third quarter of 2025 was $74.1 million , compared to a net loss of $54.4 million for the third quarter of 2024. Net loss for the third quarter included non-cash share-based compensation expense of $11.0 million , compared to $8.3 million for the same period in 2024. As adjusted for the two $30 million clinical trial milestone payments earned under our collaboration agreement with Kyowa Kirin, Kura had, on a pro forma basis, cash, cash equivalents and short-term investments of $609.7 million as of September 30, 2025 . Based on our current plans, we believe that our cash, cash equivalents and short-term investments as of September 30, 2025 will be sufficient to enable us to fund our current operating expenses into 2027, and, combined with anticipated funding under our collaboration agreement with Kyowa Kirin, should support our ziftomenib AML program through topline results from KOMET-017. Conference Call and Webcast - Third Quarter 2025 Financial Results Kura’s management will host a webcast and conference call at 8:00 a.m. ET / 5:00 a.m. PT today, November 4, 2025 , to discuss the financial results for the third quarter of 2025 and to provide a corporate update. A live webcast and archived replay of the event will be available here or online from the investor relations section of the Company’s website at www.kuraoncology.com. Conference Call and Webcast – ASH 2025 Annual Meeting Kura plans to host a virtual analyst and investor event at 12:30 p.m. ET / 9:30 a.m. PT on Monday, December 8, 2025 , to discuss the Company’s presentations from ziftomenib in combination with ven/aza chemotherapy in patients with newly diagnosed and R/R NPM1-m or KMT2A-r AML at the 67th Annual Meeting of the American Society of Hematology . A live webcast and archived replay of the event will be available online from the investor relations section of the Company’s website at www.kuraoncology.com. About Kura Oncology Kura Oncology is a clinical-stage biopharmaceutical company committed to realizing the promise of precision medicines for the treatment of cancer. The Company’s pipeline of small molecule drug candidates is designed to target cancer signaling pathways and address high-need hematologic malignancies and solid tumors. Kura is developing ziftomenib, a menin inhibitor targeting certain genetic drivers of acute myeloid leukemias, and it continues to pioneer advancements in menin inhibition for acute leukemias and solid tumors and in farnesyl transferase inhibition to address mechanisms of adaptive and innate resistance in the treatment of solid tumors. For additional information, please visit the Kura website at https://kuraoncology.com/ and follow us on X and LinkedIn. Forward-Looking Statements This news release contains certain forward-looking statements that involve risks and uncertainties that could cause actual results to be materially different from historical results or from any future results expressed or implied by such forward-looking statements. Such forward-looking statements include statements regarding, among other things, ziftomenib’s best-in-class potential across the continuum of unmet need in AML; Kura’s ability to advance ziftomenib toward commercialization, accelerate our frontline Phase 3 trials and create enduring value for patients and other stakeholders; the potential duration of FDA’s review of the NDA; the potential FDA approval of product candidates; the success and impact of interactions with the FDA; continued regulatory interactions with the FDA; the efficacy, safety and therapeutic potential of Kura’s product candidates, ziftomenib, darlifarnib and tipifarnib; the expected timing of clinical trials; the expected timing and presentation of results and data from clinical trials; the strength of Kura’s balance sheet and the sufficiency of cash, cash equivalents and short-term investments to fund Kura’s current operating expenses into 2027 and, combined with anticipated funding under our collaboration agreement with Kyowa Kirin, to support Kura’s ziftomenib AML program through topline results from KOMET-017. Factors that may cause actual results to differ materially include risks associated with the commercialization of ziftomenib, the risk that compounds that appeared promising in early research or clinical trials do not demonstrate safety and/or efficacy in later preclinical studies or clinical trials, uncertainties associated with performing clinical trials, regulatory filings, and other interactions with regulatory bodies, risks associated with reliance on third parties to successfully conduct clinical trials, the risks associated with reliance on outside financing to meet capital requirements, the risk that the collaboration with Kyowa Kirin is unsuccessful, and other risks associated with the process of discovering, developing and commercializing drugs that are safe and effective for use as human therapeutics, and in the endeavor of building a business around such drugs. You are urged to consider statements that include the words “may,” “will,” “would,” “could,” “should,” “believes,” “estimates,” “projects,” “promise,” “potential,” “expects,” “plans,” “anticipates,” “intends,” “continues,” “designed,” “goal,” or the negative of those words or other comparable words to be uncertain and forward-looking. For a further list and description of the risks and uncertainties the Company faces, please refer to the Company's periodic and other filings with the Securities and Exchange Commission, which are available at www.sec.gov. Such forward-looking statements are current only as of the date they are made, and Kura assumes no obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise. FLT3, Fms-like tyrosine kinase 3; HNSCC, head and neck squamous cell carcinoma; KMT2A, lysine methyltransferase 2A; NPM1, nucleophosmin 1; R/R, relapsed / refractory; ven/aza, venetoclax / azacitidine. Contacts Investors and media: Greg Mann 858-987-4046gmann@kuraoncology.com Source: Kura Oncology, Inc.

BOSTON & SALT LAKE CITY--(BUSINESS WIRE)--Corventum, Inc., a new medicines company advancing novel therapies to make existing cancer treatments safer and more effective, today announced the clearance by the U.S. Food and Drug Administration (FDA) of the Investigational New Drug (IND) application for CVT-130 for the prevention of anthracycline-related cardiotoxicity. CVT-130 is a first-in-class metabolic modulator being developed to protect against chemotherapy-induced cardiac injury and to address additional diseases involving mitochondrial dysfunction. The company plans to initiate a first-in-human Phase 1 clinical trial in the second quarter of 2026. “Our preclinical data show that CVT-130 prevents cardiac injury while maintaining full anti-tumor potency, a balance that no therapy has achieved to date,” said Aarti Asnani, M.D., Corventum co-founder and Chair of the Cardio-Oncology Committee of the AHA. “Anthracyclines have saved countless lives, yet the use of these highly effective chemotherapies is limited by cumulative heart damage that can appear months or years after treatment,” said Randall Peterson, Ph.D., Corventum co-founder, CVT-130 co-inventor, and Dean of the University of Utah College of Pharmacy. “CVT-130 was designed to protect cardiac cells from damage caused by anthracyclines, potentially allowing more patients to benefit from these widely used cancer treatments and enabling retreatment in recurrent disease.” “Our preclinical data show that CVT-130 prevents cardiac injury while maintaining full anti-tumor potency, a balance that no therapy has achieved to date,” said Aarti Asnani, M.D., Corventum co-founder, CVT-130 co-inventor, and Chair of the Cardio-Oncology Committee of the American Heart Association. “With FDA clearance of the IND, we can now advance CVT-130 to the clinic and take the next step toward delivering a therapy that could benefit millions of patients worldwide who depend on anthracyclines for cancer treatment.” The planned randomized, placebo-controlled Phase 1 clinical trial will evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of CVT-130 in healthy volunteers, along with cardiac and mitochondrial biomarkers. The study is designed to identify an optimal dose for a subsequent Phase 2 trial in cancer patients. Corventum worked closely with the FDA to align on the Phase 1 study design, which reflects the intended dosing strategy for the Phase 2 clinical trial. About Anthracycline Cardiotoxicity Anthracyclines, including doxorubicin, epirubicin, and daunorubicin, are among the most effective cancer drugs developed and are used in more than two million patients each year. Their clinical utility, however, is limited by cumulative, dose-dependent cardiac damage that can lead to heart failure and reduced long-term survival. Once patients reach their lifetime anthracycline dose limit, retreatment is often impossible, even if their cancer recurs, forcing reliance on less effective alternatives. About CVT-130 CVT-130 is a novel small molecule that has demonstrated robust preclinical cardioprotection with no loss of anthracycline efficacy. It is designed to modulate mitochondrial and metabolic pathways to prevent anthracycline-induced cardiac injury and preserve mitochondrial function. CVT-130’s room-temperature stable formulation allows rapid injection prior to anthracycline chemotherapy administration. About Corventum, Inc. Corventum is a new medicines company committed to developing novel therapies that make cancer treatments safer and more effective. The company's lead program, CVT-130, is designed to prevent anthracycline-induced cardiotoxicity and improve outcomes for patients receiving these cornerstone chemotherapies. For more information, visit www.corventum.com.