Company
Kura Oncology
5 active trials that select patients by a biomarker on marked.bio, across 2 biomarkers; 1 in phase 3.
Counts only trials this company leads as sponsor, not partnered or academic trials of its drugs.
Biomarkers
Drugs in these trials
Targeted, immune and antibody-drug-conjugate therapies named in the company's active biomarker-selected trials (including other companies' drugs used in combination).
ziftomenib 4venetoclax 2gilteritinib 1cabozantinib 1adagrasib 1quizartinib 1
Trials
5 of 9 trials shown
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Studies to Assess Ziftomenib in Combination With Ven+Aza or 7+3 in Patients With Untreated NPM1-m or KMT2A-r AML
ziftomenib FDAvenetoclaxazacitidinedaunorubicincytarabine
…nintensive (Venetoclax+Azacitidine) or Intensive (7+3) Therapy in Patients With Untreated NPM1 Mutated or KMT2A Rearranged Acute Myeloid Leukemia
NPM1 mutationAcute Myeloid Leukemia (AML)
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First in Human Study of Ziftomenib in Relapsed or Refractory Acute Myeloid Leukemia
ziftomenib FDAmidazolamitraconazole
Patients with a documented nucleophosmin 1 mutation (NPM1-m)
NPM1 mutationAdvanced Malignant Neoplasm, Acute Myeloid Leukemia, Mixed Lineage Leukemia, Mixed Lineage Acute Leukemia
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Safety and Tolerability of Ziftomenib Combinations in Patients With Relapsed/Refractory Acute Myeloid Leukemia
ziftomenibfludarabineidarubicincytarabinegilteritinib FDA EUGranulocyte colony-stimulating factor
Has a documented FLT3 mutation (cA-3 only).
FLT3 mutation (ITD/TKD)NPM1 mutationAML, AML With Mutated NPM1, Hematologic Malignancy, KMT2Ar
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KO-2806 Monotherapy and Combination Therapies in Advanced Solid Tumors
Darlifarnibcabozantinibadagrasib FDA EU
…eceived at least 1 prior systemic therapy including available approved SOC treatments for KRAS G12C-mutant locally advanced or metastatic NSCLC, CRC, or PDAC.
KRAS G12CKRAS G12DSolid Tumors With HRAS Alterations, Non Small Cell Lung Cancer (NSCLC), Colorectal Cancer (CRC), Pancreatic Ductal Adenocarcinoma (PDAC)
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A Study to Investigate the Safety and Tolerability of Ziftomenib in Combination With Venetoclax/Azacitidine, Venetoclax, 7+3, or 7+3+Quizartinib in Patients With AML
ziftomenibvenetoclaxazacitidinedaunorubicincytarabinequizartinib FDA EU
Those intending treatment with intensive chemotherapy in Arm C should be NPM1-m and FLT3-ITD+ with an allelic ratio ≥0.05 and eligible for FLT3-targeted treatment
FLT3 mutation (ITD/TKD)NPM1 mutationAcute Myeloid Leukemia, Mixed Lineage Leukemia Gene Mutation, Refractory AML, AML With Mutated NPM1
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Combination Trial of Tipifarnib and Alpelisib in Adult Recurrent/ Metastatic Head and Neck Squamous Cell Carcinoma (R/M HNSCC)
Tipifarnibalpelisib FDA EU
…and Alpelisib for the Treatment of Adult Participants Who Have HRAS-overexpressing and/or PIK3CA-mutated and/or - Amplified Recurrent/Metastatic Head and Neck Squamous Cell Carcinoma
PIK3CA activating mutationHNSCC
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Investigation of Tipifarnib in Treatment of Subjects With Peripheral T-Cell Lymphoma (PTCL) That Have Not Responded to Standard Therapy
Tipifarnib
Anaplastic large cell lymphoma (ALCL), ALK positive
ALK fusionRelapsed or Refractory Peripheral T-Cell Lymphoma
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Tipifarnib and Osimertinib in EGFR-mutated Non-Small Cell Lung Cancer
Tipifarnibosimertinib FDA EU
The tumor harbors an Ex19del or Ex21-L858R substitution (based on tumor tissue or plasma \[ctDNA\] assessment).
EGFR exon 19 deletion / L858RNSCLC
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First-in-Human Study of KO-947 in Non-Hematological Malignancies
KO-947
Malignancy of non-squamous histology that carries a BRAF, KRAS, NRAS or HRAS mutation(s).
KRAS G12CKRAS G12DBRAF V600EAdvanced Malignant Neoplasm
No trials match these filters.