Why Kura Oncology shares tumbled after securing a $1.2bn cancer-drug partnership

Why Kura Oncology shares tumbled after securing a $1.2bn cancer-drug partnership

Kura Oncology, Inc., a clinical-stage biopharmaceutical innovator, and Japan-based pharmaceutical leader Kyowa Kirin Co., Ltd., have entered into a strategic partnership that could redefine treatment for acute myeloid leukemia (AML). The collaboration focuses on ziftomenib, an investigational oral menin inhibitor that has garnered attention as a potential breakthrough therapy for genetically defined AML patients. This […]

Thermo Fisher Scientific and NCI launch myeloMATCH trial to advance AML and MDS treatment

Thermo Fisher Scientific and NCI launch myeloMATCH trial to advance AML and MDS treatment

In a significant advancement in cancer treatment, Thermo Fisher Scientific Inc. (NYSE: TMO) has partnered with the National Cancer Institute (NCI), a component of the National Institutes of Health, to launch the myeloMATCH precision medicine umbrella trial. This initiative aims to revolutionize the treatment landscape for Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome (MDS) through […]

Immune-Onc Therapeutics gets FDA orphan drug status for IO-202 in CMML

Immune-Onc Therapeutics gets FDA orphan drug status for IO-202 in CMML

Immune-Onc Therapeutics, Inc., a clinical-stage biopharmaceutical company focused on the development of innovative therapies in immunology and oncology, has achieved a significant milestone with the U.S. Food and Drug Administration’s (FDA) recent Orphan Drug Designation for IO-202. This designation is a crucial step forward in the treatment of chronic myelomonocytic leukemia (CMML), a rare form […]

Kurome Therapeutics advances with FDA-approved IND for KME-0584 in AML and HR MDS clinical trial

Kurome Therapeutics advances with FDA-approved IND for KME-0584 in AML and HR MDS clinical trial

In a significant development for cancer research, Kurome Therapeutics Inc. has announced the U.S. Food and Drug Administration (FDA) clearance of the Investigational New Drug (IND) application for KME-0584, propelling the biotech firm into a Phase 1 clinical trial for patients with relapsed/refractory (R/R) Acute Myeloid Leukemia (AML) and high-risk (HR) Myelodysplastic Syndromes (MDS). Slated […]

Hemogenyx Pharmaceuticals receives FDA nod for HEMO-CAR-T AML treatment study

Hemogenyx Pharmaceuticals receives FDA nod for HEMO-CAR-T AML treatment study

Hemogenyx Pharmaceuticals plc, a London-based biopharmaceutical company, has received approval from the U.S. Food and Drug Administration (FDA) to proceed with its Phase I clinical study of HEMO-CAR-T, marking a significant milestone in the treatment of acute myeloid leukemia (AML). This development follows the FDA’s decision to lift the clinical hold on the Investigational New […]

Invivoscribe, Complete Genomics to develop biomarker tests for oncology research

Invivoscribe, Complete Genomics to develop biomarker tests for oncology research

Invivoscribe and Complete Genomics have announced a partnership aimed at developing and commercializing biomarker tests on the latter’s next-generation sequencing (NGS) platforms. The collaboration, covering worldwide territories, focuses on oncology and cancer research. Based in California, Invivoscribe is specialized in precision diagnostics and reagents for hematologic malignancies and molecular diagnostics. Also based in California, Complete […]

Rigel Pharmaceuticals gets Rezlidhia FDA approval for AML

Rigel Pharmaceuticals gets Rezlidhia FDA approval for AML

Rigel Pharmaceuticals has received approval from the US Food and Drug Administration (FDA) for its Rezlidhia (olutasidenib) capsules for relapsed or refractory (R/R) acute myeloid leukemia (AML) in adult patients. Rezlidhia is indicated for patients with a susceptible isocitrate dehydrogenase-1 (IDH1) mutation as identified by an FDA-approved test. The oral, small molecule and mutant isocitrate […]

Medac resubmits treosulfan NDA to FDA, says Medexus Pharmaceuticals

Medac resubmits treosulfan NDA to FDA, says Medexus Pharmaceuticals

Medexus Pharmaceuticals said that its strategic partner medac has resubmitted the new drug application (NDA) for treosulfan with the US Food and Drug Administration (FDA). Treosulfan is part of a preparative regimen for allogeneic hematopoietic stem cell transplantation (allo-HSCT). It is intended to be used in combination with fludarabine for the treatment of eligible patients […]

Gilead Sciences wraps up $4.9bn acquisition of Forty Seven

Gilead Sciences wraps up $4.9bn acquisition of Forty Seven

Gilead Sciences has completed its previously announced $4.9 billion acquisition of Forty Seven, a clinical-stage immuno-oncology company based in California. The immuno-oncology company has been acquired by the US biotech company for $95.50 per share in cash to become the latter’s fully-owned subsidiary. Forty Seven will be delisted from the Nasdaq Global Select Market. The […]