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Kura Oncology (KUR) Drug Pipeline

Drug pipeline
Drug NameConditionStageStatusStudy NameTrial Start DateArticle
Venetoclax, Daunorubicin, Azacitidine (Aza), ziftomenib, Ziftomenib, Cytarabine (Ara-C)Acute Myeloid Leukemia (Aml)Phase IIIRecruitingStudies to Assess Ziftomenib in Combination With Ven+Aza or 7+3 in Patients With Untreated NPM1-m or KMT2A-r AMLMay 16, 2025―
ziftomenib, Ziftomenib, Imatinib MesylateGastrointestinal Stromal Tumor (Gist), Gastrointestinal Stromal Tumor (Gist) Of The Gastrointestinal Tract, Gastrointestinal Stromal Cancer, Gastrointestinal Stromal Neoplasm, Gastrointestinal Stromal Tumor, Malignant, Gastrointestinal Stromal Cell TumorsPhase IRecruitingA Study of Ziftomenib, an Oral Menin Inhibitor, in Combination With Imatinib in Patients With Advanced Gastrointestinal Stromal Tumors (GIST)Oct 14, 2024―
Cabozantinib, Adagrasib, DarlifarnibColorectal Cancer (Crc), Pancreatic Ductal Adenocarcinoma (Pdac), Non Small Cell Lung Cancer (Nsclc), Clear Cell Renal Cell Carcinoma (Ccrcc), Renal Cell Carcinoma (Kidney Cancer), Solid Tumors With Hras AlterationsPhase IRecruitingKO-2806 Monotherapy and Combination Therapies in Advanced Solid TumorsAug 17, 2023―
Gilteritinib, Fludarabine, Cytarabine, Idarubicin, ziftomenib, Ziftomenib, Granulocyte Colony-Stimulating FactorAcute Myeloid Leukemia, Leukemia, Myeloid, Acute, Neoplasms By Histologic Type, Leukemia, Leukemia, Myeloid, Hematologic Malignancy, Acute Leukemia, Aml, Aml With Mutated Npm1, Kmt2ar, Npm1 Mutation, Mll RearrangementPhase IRecruitingSafety and Tolerability of Ziftomenib Combinations in Patients With Relapsed/Refractory Acute Myeloid LeukemiaAug 07, 2023―
Azacitidine, Cytarabine, Venetoclax, Quizartinib, Daunorubicin, ziftomenib, ZiftomenibAcute Myeloid Leukemia, Refractory Aml, Acute Myeloid Leukemia, In Relapse, Aml With Mutated Npm1, Kmt2ar, Npm1 Mutation, Mixed Lineage Leukemia Gene Mutation, Acute Myeloid Leukemia Recurrent, Myeloid Sarcoma, Nucleophosmin 1-Mutated Acute Myeloid LeukemiaPhase IRecruitingA Study to Investigate the Safety and Tolerability of Ziftomenib in Combination With Venetoclax/Azacitidine, Venetoclax, 7+3, or 7+3+Quizartinib in Patients With AMLFeb 09, 2023―
Alpelisib, TipifarnibHnsccphase1AndPhase2Active Not RecruitingCombination Trial of Tipifarnib and Alpelisib in Adult Recurrent/ Metastatic Head and Neck Squamous Cell Carcinoma (R/M HNSCC)Jul 27, 2021―
Midazolam, Itraconazole, ziftomenib, ZiftomenibAcute Myeloid Leukemia, Acute Lymphoblastic Leukemia, Advanced Malignant Neoplasm, Mixed Lineage Leukemia, Mixed Lineage Acute Leukemia, Acute Leukemia Of Ambiguous Lineage, Mixed Phenotype Acute Leukemiaphase1AndPhase2RecruitingFirst in Human Study of Ziftomenib in Relapsed or Refractory Acute Myeloid LeukemiaJun 25, 2019―

FAQ

What are the FDA phases for drug approval?
The FDA approval process for new drugs is divided into several phases: a. Preclinical testing b. Phase 1 – Safety and dosage c. Phase 2 – Effectiveness and side effects d. Phase 3 – Confirmation of effectiveness, monitoring of adverse reactions, and comparison with existing treatments e. Phase 4 – Post-marketing studies to track long-term safety and effectiveness
What is a clinical trial?
A clinical trial is a carefully designed study in which researchers test a drug, treatment, or medical device in people to evaluate its safety, effectiveness, and potential side effects. These trials are essential for determining whether a new treatment should be approved for widespread use.
What drugs does Kura Oncology (DE:KUR) have in its pipeline
Kura Oncology DE:KUR is currently developing the following drugs: Venetoclax, Daunorubicin, Azacitidine (Aza), ziftomenib, Ziftomenib, Cytarabine (Ara-C), ziftomenib, Ziftomenib, Imatinib Mesylate, Cabozantinib, Adagrasib, Darlifarnib, Gilteritinib, Fludarabine, Cytarabine, Idarubicin, ziftomenib, Ziftomenib, Granulocyte Colony-Stimulating Factor, Azacitidine, Cytarabine, Venetoclax, Quizartinib, Daunorubicin, ziftomenib, Ziftomenib, Alpelisib, Tipifarnib, Midazolam, Itraconazole, ziftomenib, Ziftomenib. These drug candidates are in various stages of clinical development as the company works toward FDA approval.